US20190269609A1

US20190269609A1 - A multi-component injection

Info

Publication number: US20190269609A1
Application number: US15/737,808
Authority: US
Inventors: Xiaoqing YAO; Changhai SUN; Kai Dong; Chuan Li; Guiping Zhang; Tianhao DONG; Jing Cao; Qiyun WANG; Xianjun Li; Junmin GAO; Mingzhen SUN
Original assignee: Tianjin Chase Sun Pharmaceutical Co Ltd
Current assignee: Tianjin Chase Sun Pharmaceutical Co Ltd
Priority date: 2016-12-28
Filing date: 2017-06-23
Publication date: 2019-09-05
Also published as: WO2018120683A1; US20210346281A1; US11986553B2; CN106727649A

Abstract

The invention relates to the technical field of medicines, and particularly relates to a multi-component injection and preparation processes and applications thereof. In the present invention, the effective ingredients of safflower carthamus. Red Paeony Root, Ligusticum wallichii, radix salviae miltiorrhizae and Angelica sinensis are analyzed and a multi-component injection is prepared via the modern pharmaceutical preparation technology. The study proves that the multi-component injection of the invention has therapeutic effects on Sepsis.

Description

I. TECHNICAL FIELD

The present invention relates to the technical field of medical technology, and particularly relates to a multi-component injection and preparation processes and applications thereof.

II. BACKGROUND OF THE INVENTION

Sepsis is a fatal organ dysfunction caused by the reaction disorder of the infected hosts, with a hospital mortality of more than 10%, which has posed a huge threat to human health, becoming a focus to which the medical field pays close attention [see JAMA. 2016 Feb. 23; 315(8):801-10]. Under the big data retrospective analysis in combination with the microarray technology and analysis of leukocyte gene expression, people gradually realize that Sepsis is not only a process of systemic inflammatory reaction or immune disorder, but also a complex chronic critical disease combining sustained inflammation, immunosuppression and catabolism. [See J Trauma Acute Care Surg. 2012 June; 72(6): 1491-501, BMJ. 2016 May 23; 353: i1585 and Medicine (Baltimore). 2015 December; 94(50):e2044.].
For many years, antibiotics, antiviral medicines, vasopressor medicines, etc. are used for the traditional treatment of Sepsis. However, there are not enough specific medicines put into clinical practice aiming at the pathogenesis of Sepsis. [See Crit Care Med. 2013 February; 41(2):580-637]. How to timely correct the systemic inflammatory reaction, coagulation disorders and immune dysfunction in the development process of Sepsis, restore proinflammatory-anti-inflammatory dynamic balance of organisms as early as possible, and effectively improve the prognosis of patients have become the important issues to be solved in the research and development of Sepsis treatment medicines.
In 1970s, Professor Jinda Wang, a Chinese famous first-aid medical expert, presented the rules of treatment by traditional Chinese medicine for treating acute and critical diseases: the method of heat-clearing and detoxicating remedy is used for treating toxic-heat syndrome, the method for promoting blood circulation and removing blood-stasis is used for treating syndrome of blood stasis, and the method for supporting the healthy energy is used for treating acute asthenic symptoms, i.e., “Three Syndromes and Three Methods”, which are used as the basic methods of clinical practice for treating Sepsis [See China first-aid medicine of critical diseases, 2006, 18 (11): 643-4]. In 1975, he firstly confirmed that endotoxemia was the initial etiology of infectious multiple system organ failure, and proposed a new treatment strategy of “Treatment for both germs andendotoxin”. As he realized that the harm of endotoxin to organisms included inducing the production of in-vivo inflammatory media and then showing toxic effects, he further proposed treatment for bacteria, endotoxin and inflammatory media together, i.e., “Treatment for bacteria, endotoxin and inflammatory media together” [See Chinese Journal of Surgery of Integrated Traditional and Western Medicine, 2012, 18 (6): 553-554].
“Xuebijing injection” is an intravenous injection developed on the basis of “Xuefu Zhuyu Decoction” recorded in Wang Qingren's “Corrections on the Errors of Medical Works” in Qing Dynasty in accordance with the syndrome differentiation principle of “Three Syndromes and Three Methods” under the theoretical guidance of “Treatment for bacteria, endotoxin and inflammatory media together”. The “Xuebijing injection” is prepared from five medicinal materials, i.e., safflower carthamus, Red Paeony Root, Ligusticum wallichii, radix salviae miltiorrnhizae and Chinese angelica, via extraction, refining, drying, blending and other modern techniques. The “Xuebijing injection” belongs to the traditional Chinese medicine for dispersing blood stasis and detoxifying, which is applied for warm heat diseases, such as fever, dyspnea, tachypnea, palpitation, dysphoria and other syndromes of intermingling of blood statsis and toxin, and is suitable for the systemic inflammatory reaction syndrome induced by infection. The Xuebijing injection can also be used during the period of organ function lesion for treatment of multi-organ disfunction syndrome. The “Xuebijing injection” has the pharmacological actions of antagonizing bacterial endotoxin [See Chinese critical care medicine, 2006, 18 (11): 643-4], inhibiting inflammatory factors from being released excessively [See Chinese critical care medicine, 2006, 18 (11): 643-4, Evid Based Complement Alternat Med. 2015; 2015:860259 and Chin J Integr Med. 2009; 15(1): 13-5], overcoming coagulation disorders [See Chinese Journal of Experimental Surgery, 2010, 27 (1): 32-4 and Chinese Journal of Integrated traditional and Western Medicine in Critical Care, 2009, 16 (4): 218-22], protecting vascular endothelial cells [See Chinese Journal of Integrated traditional and Western Medicine in Critical Care, 2009, 16 (4): 218-22], improving the microcirculation of tissue [See J Surg Res. 2016 May 1; 202(1):147-54], and improving immune dysfunction [see Chinese Journal of Surgery, 2009, 47 (1): 58-61 and Evid Based Complement Alternat Med. 2015; 2015:352642], which fully embodies the integrated regulatory effects of having multiple components, multiple links, multiple channels and multiple target points of traditional Chinese medicine. The results of the multi-centric clinical study with large sample sizes and meta analysis (Meta) indicate that it can reduce the 28 d case fatality rate and incidence rate of complication of Sepsis patients, shorten the average hospital stay, effectively improve the clinical indexes including systemic inflammatory response, coagulation function of patients, and the scoring of the scoring system II for acute physiology and chronic health condition (APACHE II), protect organ function, and significantly improve the clinical effect on the basis of the conventional comprehensive treatment in combination with the use of the “Xuebijing injection” [See Chinese critical care medicine 2015, 27(6): 465-76, Chinese Journal of Emergency Medicine, 2013, 22 (2): 130-5 and Medical Journal of Chinese People's Liberation Army, 2010, 35 (1): 9-12].
In 2003, Chinese patent 03104977.X disclosed “a Chinese medicinal preparation for treating Sepsis and a preparation method thereof”, i.e., a preparation method for the “Xuebijing injection”, and its preparation process has been very matured. With the progress and innovation of science and technology, we carry out optimization on the process and elaboration of technological parameters, i.e., changing the removal of the heat source by 1% activated carbon in the original preparation process into ultrafiltration, thereby ensuring the safety of finished products and uniform and stable quality. The inventors, by means of the advanced research concept and instrument and equipment, have achieved the full-ingredient testing of such injection. We acquire a bran-new multi-component injection via the study on the material basis of the Xuebijing injection, in which the effective ingredients of the original “Xuebijing injection” are reserved.

III. SUMMARY OF THE INVENTION

The invention provides a multi-component injection, which is characterized by comprising the following active ingredients, by weight: 8.66-35.26 parts of albiflorin std, 1000.0-1700.0 parts of paeoniflorin, 11.13-68.07 parts of Oxypaeoniflorin, 12.20-52.98 parts of Benzoylpaeoniflorin, 0.667-1.617 parts of Benzoyloxypaeoniflorin, 1.915-3.202 parts of Mudanpioside J, 10.63-20.13 parts of galloylpaeoniflorin, 0.804-1.338 parts of Mudanpioside C, 10.0-200.0 parts of benzoic acid, 0.21-15.88 parts of gallic acid, 0.2396-0.6860 parts of ethyl gallate, and 1.31-12.60 parts of catechin.
The above-mentioned multi-component injection is characterized in that the preparation method thereof comprises the following steps:
providing 100 g of Red Paeony Root decoction pieces; heating and boiling the Red Paeony Root decoction pieces with process water of 10 times the weight of the Red Paeony Root decoction pieces to obtain a first decoction after 2 hours slight boiling; filtering the first decoction to obtain filtrate I and a first dreg; boiling the first dreg with process water of 8 times the weight of the first dreg to obtain a second decoction after 1 hour slight boiling; filtering the second decoction to obtain filtrate II and a second dreg; mixing filtrate I and filtrate II to obtain a mixture; concentrating the mixture to obtain a first concentrate of 100 ml; adding a proper amount of gelatin solution to the first concentrate under stirring to obtain a gelatin-containing first concentrate; adding 95% ethanol to the gelatin-containing first concentrate to obtain an ethanol-containing first concentrate having an ethanol volume content of 70%; storing the ethanol-containing first concentrate under cooling condition for 24 hours to obtain a cool ethanol-containing first concentrate; filtering and concentrating the cool ethanol-containing first concentrate to obtain a second concentrate of 100 ml; extracting the second concentrate with water-saturated n-butanol for 4 times and using water-saturated n-butanol of 50 ml for each time; combining extract liquors of the 4 times extraction to obtain a combined extract liquor; recycling n-butanol from the combined extract liquor to obtain a n-butanol-reduced extract liquor without alcohol taste; and vacuum drying the n-butanol-reduced extract liquor to obtain a Red Paeony Root dry paste;
providing a proper amount of the Red Paeony Root dry paste; dissolving the Red Paeony Root dry paste in injection water to obtain a dilute of 200 ml; storing the dilute under cooling condition to obtain a first cool liquid; adding glucosum anhydricum of an amount in accordance with 4.5% mass fraction of the multi-component injection and injection water to the first cool liquid to obtain a 1000 ml liquid; adjusting the pH value of the 1000 ml liquid to 5.5-7.0 with a sodium hydroxide solution of 10% mass fraction to obtain a pH adjusted liquid; storing the pH adjusted liquid under cooling condition to obtain a second cool liquid; subjecting the second cool liquid to ultrafiltration to obtain an ultrafiltrate; adding a proper amount of solubilizing auxiliary materials which are dissolved in a proper amount of injection water into the ultrafiltrate to obtain a solubilizing auxiliary materials-containing ultrafiltrate; adjusting the pH value of the solubilizing auxiliary materials-containing ultrafiltrate to 5.5-7.0 using the sodium hydroxide solution of 10% mass fraction to obtain a pH adjusted ultrafiltrate; filtering the pH adjusted ultrafiltrate to obtain a filtrate; encapsulating and sterilizing the filtrate to obtain the multi-component injection.
On the basis of the above-mentioned multi-component injection, the present invention further provides a multi-component injection, which is characterized by comprising the following active ingredients, by weight: 8.66-35.26 parts of albiflorin std, 1000.0-1700.0 parts of paeoniflorin, 11.13-68.07 parts of Oxypaeoniflorin, 12.20-52.98 parts of Benzoylpaeoniflorin, 0.667-1.617 parts of Benzoyloxypaeoniflorin, 1.915-3.202 parts of Mudanpioside J, 10.63-20.13 parts of galloylpaeoniflorin, 0.804-1.338 parts of Mudanpioside C, 10.0-200.0 parts of benzoic acid, 0.21-15.88 parts of gallic acid, 0.2396-0.6860 parts of ethyl gallate, 1.31-12.60 parts of catechin, 1.232-3.547 parts of Kaempferol-3-0-glucoside, 0.0500-0.4184 parts of scutellarin, 0.755-2.570 parts of quercetin-3-0-glucoside, 8.42-29.40 parts of Kaempferol-3-0-rutinoside, 4.036-7.695 parts of Kaempferol-3-0-sophoroside, 1.517-5.598 parts of quercetin-3-0-rutinoside, 200.0-500.0 parts of Hydroxysafflor yellow A, 0.316-0.774 parts of uracil, 13.77-30.56 parts of adenine, 20.50-44.99 parts of phenylalanine, 11.44-27.13 parts of uridine, 5.07-12.63 parts of adenosine, 8.00-24.11 parts of guanosine, 4.96-16.86 parts of butanedioic acid, 2.384-5.404 parts of p-hydroxybenzoic acid, 3.00-17.98 parts of p-coumaric acid, 4.837-7.806 parts of caffeic acid and 3.83-8.59 parts of chlorogenic acid.
The above-mentioned multi-component injection is characterized in that the preparation method thereof comprises the following steps:
providing 100 g of safflower carthamus decoction pieces; leaching the safflower carthamus decoction pieces with 30% ethanol of 8 times the weight of the safflower carthamus decoction pieces for 8 hours to obtain a leach liquor; filtering the leach liquor to obtain a liquid medicine of 4-6 times the weight of the safflower carthamus decoction pieces; adding 95% ethanol to the liquid medicine to obtain an ethanol-containing liquid medicine having an ethanol volume content of 70%; storing the ethanol-containing liquid medicine under cooling condition for 48 hours to obtain a cool ethanol-containing liquid medicine; filtering the cool ethanol-containing liquid medicine to obtain a first filtrate; concentrating the first filtrate under reduced pressure to obtain a concentrate of 100 ml; adding 95% ethanol to the concentrate to obtain an ethanol-containing concentrate having an ethanol volume content of 80%; storing the ethanol-containing concentrate under cooling condition for 48 hours to obtain a cool ethanol-containing concentrate; filtering the cool ethanol-containing concentrate to obtain a second filtrate; recycling ethanol from the second filtrate to obtain an ethanol-reduced filtrate; concentrating and vacuum drying the ethanol-reduced filtrate to obtain a safflower carthamus dry paste;
providing 100 g of Red Paeony Root decoction pieces; heating and boiling the Red Paeony Root decoction pieces with process water of 10 times the weight of the Red Paeony Root decoction pieces to obtain a first decoction after 2 hours slight boiling; filtering the first decoction to obtain filtrate I and a first dreg; boiling the first dreg with process water of 8 times the weight of the first dreg to obtain a second decoction after 1 hour slight boiling; filtering the second decoction to obtain filtrate II and a second dreg; mixing filtrate I and filtrate II to obtain a mixture; concentrating the mixture to obtain a first concentrate of 100 ml; adding a proper amount of gelatin solution to the first concentrate under stirring to obtain a gelatin-containing first concentrate; adding 95% ethanol to the gelatin-containing first concentrate to obtain an ethanol-containing first concentrate having an ethanol volume content of 70%; storing the ethanol-containing first concentrate under cooling condition for 24 hours to obtain a cool ethanol-containing first concentrate; filtering and concentrating the cool ethanol-containing first concentrate to obtain a second concentrate of 100 ml; extracting the second concentrate with water-saturated n-butanol for 4 times and using 50 ml water-saturated n-butanol for each time; combining extract liquors of the 4 times extraction to obtain a combined extract liquor; recycling n-butanol from the combined extract liquor to obtain a n-butanol-reduced extract liquor without alcohol taste; and vacuum drying the n-butanol-reduced extract liquor to obtain a Red Paeony Root dry paste;
providing the safflower carthamus dry paste and the Red Paeony Root dry paste each of a proper amount; dissolving the two dry pastes in injection water to obtain a dilute of 200 ml; storing the dilute under cooling condition to obtain a first cool liquid; adding glucosum anhydricum of an amount in accordance with 4.5% mass fraction of the multi-component injection and injection water to the first cool liquid to obtain a 1000 ml liquid; adjusting the pH value of the 1000 ml liquid to 5.5-7.0 with a sodium hydroxide solution of 10% mass fraction to obtain a pH adjusted liquid; storing the pH adjusted liquid under cooling condition to obtain a second cool liquid; subjecting the second cool liquid to ultrafiltration to obtain an ultrafiltrate; adding a proper amount of solubilizing auxiliary materials which are dissolved in a proper amount of injection water into the ultrafiltrate to obtain a solubilizing auxiliary materials-containing ultrafiltrate; adjusting the pH value of the solubilizing auxiliary materials-containing ultrafiltrate to 5.5-7.0 using the sodium hydroxide solution of 10% mass fraction to obtain a pH adjusted ultrafiltrate; filtering the pH adjusted ultrafiltrate to obtain a filtrate; encapsulating and sterilizing the filtrate to obtain the multi-component injection.
On the basis of the above-mentioned multi-component injection, the present invention further provides a multi-component injection, which is characterized by comprising the following active ingredients, by weight: 8.66-35.26 parts of albiflorin std, 1000.0-1700.0 parts of paeoniflorin, 11.13-68.07 parts of Oxypaeoniflorin, 12.20-52.98 parts of Benzoylpaeoniflorin, 0.667-1.617 parts of Benzoyloxypaeoniflorin, 1.915-3.202 parts of Mudanpioside J, 10.63-20.13 parts of galloylpaeoniflorin, 0.804-1.338 parts of Mudanpioside C, 10.0-200.0 parts of benzoic acid, 0.21-15.88 parts of gallic acid, 0.2396-0.6860 parts of ethyl gallate, 1.31-12.60 parts of catechin, 1.232-3.547 parts of Kaempferol-3-0-glucoside, 0.0500-0.4184 parts of scutellarin, 0.755-2.570 parts of quercetin-3-0-glucoside, 8.42-29.40 parts of Kaempferol-3-0-rutinoside, 4.036-7.695 parts of Kaempferol-3-0-sophoroside, 1.517-5.598 parts of quercetin-3-0-rutinoside, 200.0-500.0 parts of Hydroxysafflor yellow A, 0.316-0.774 parts of uracil, 13.77-30.56 parts of adenine, 20.50-44.99 parts of phenylalanine, 11.44-27.13 parts of uridine, 5.07-12.63 parts of adenosine, 8.00-24.11 parts of guanosine, 4.96-16.86 parts of butanedioic acid, 2.384-5.404 parts of p-hydroxybenzoic acid, 3.00-17.98 parts of p-coumaric acid, 4.837-7.806 parts of caffeic acid, 3.83-8.59 parts of chlorogenic acid, 6.51-69.39 parts of senkyunolide I (42), 1.55-18.27 parts of senkyunolide H, 4.30-14.22 parts of senkyunolide N, 2.460-5.648 parts of open-loop senkyunolide I, 1.55-10.74 parts of senkyunolide G, 1.43-8.67 parts of 3-hydroxyl-3-butylphthalide, 0.10-0.961 parts of senkyunolide A, and 7.66-47.15 parts of ferulaic acid.
The above-mentioned multi-component injection is characterized in that the preparation method thereof comprises the following steps:
taking 100 g of Ligusticum wallichii and Angelica sinensis decoction pieces respectively, treating in accordance with the Red Paeony Root process, keeping 300 ml of concentrated solution every time, and extracting with 150 ml of water saturated normal butanol each time to prepare dry paste;
providing 100 g of safflower carthamus decoction pieces; leaching the safflower carthamus decoction pieces with 30% ethanol of 8 times the weight of the safflower carthamus decoction pieces for 8 hours to obtain a leach liquor; filtering the leach liquor to obtain a liquid medicine of 4-6 times the weight of the safflower carthamus decoction pieces; adding 95% ethanol to the liquid medicine to obtain an ethanol-containing liquid medicine having an ethanol volume content of 70%; storing the ethanol-containing liquid medicine under cooling condition for 48 hours to obtain a cool ethanol-containing liquid medicine; filtering the cool ethanol-containing liquid medicine to obtain a first filtrate; concentrating the first filtrate under reduced pressure to obtain a concentrate of 100 ml; adding 95% ethanol to the concentrate to obtain an ethanol-containing concentrate having an ethanol volume content of 80%; storing the ethanol-containing concentrate under cooling condition for 48 hours to obtain a cool ethanol-containing concentrate; filtering the cool ethanol-containing concentrate to obtain a second filtrate; recycling ethanol from the second filtrate to obtain an ethanol-reduced filtrate; concentrating and vacuum drying the ethanol-reduced filtrate to obtain a safflower carthamus dry paste;
providing 100 g of Red Paeony Root decoction pieces; heating and boiling the Red Paeony Root decoction pieces with process water of 10 times the weight of the Red Paeony Root decoction pieces to obtain a first decoction after 2 hours slight boiling; filtering the first decoction to obtain filtrate I and a first dreg; boiling the first dreg with process water of 8 times the weight of the first dreg to obtain a second decoction after 1 hour slight boiling; filtering the second decoction to obtain filtrate II and a second dreg; mixing filtrate I and filtrate II to obtain a mixture; concentrating the mixture to obtain a first concentrate of 100 ml; adding a proper amount of gelatin solution to the first concentrate under stirring to obtain a gelatin-containing first concentrate; adding 95% ethanol to the gelatin-containing first concentrate to obtain an ethanol-containing first concentrate having an ethanol volume content of 70%; storing the ethanol-containing first concentrate under cooling condition for 24 hours to obtain a cool ethanol-containing first concentrate; filtering and concentrating the cool ethanol-containing first concentrate to obtain a second concentrate of 100 ml; extracting the second concentrate with water-saturated n-butanol for 4 times and using 50 ml water-saturated n-butanol for each time; combining extract liquors of the 4 times extraction to obtain a combined extract liquor; recycling n-butanol from the combined extract liquor to obtain a n-butanol-reduced extract liquor without alcohol taste; and vacuum drying the n-butanol-reduced extract liquor to obtain a Red Paeony Root dry paste;
providing 100 g of Ligusticum wallichii decoction pieces and 100 g of Angelica sinensis decoction pieces; treating the Ligusticum wallichii decoction pieces and Angelica sinensis decoction pieces with a same treatment process as the Red Paeony Root decoction pieces except for keeping 300 ml of concentrate every time and extracting with 150 ml of water-saturated n-butanol each time, to obtain a third dry paste;
providing the safflower carthamus dry paste, the Red Paeony Root dry paste and the third dry paste each of a proper amount; dissolving the three dry pastes in injection water to obtain a dilute of 200 ml; storing the dilute under cooling condition to obtain a first cool liquid; adding glucosum anhydricum of an amount in accordance with 4.5% mass fraction of the multi-component injection and injection water to the first cool liquid to obtain a 1000 ml liquid; adjusting the pH value of the 1000 ml liquid to 5.5-7.0 with a sodium hydroxide solution of 10% mass fraction to obtain a pH adjusted liquid; storing the pH adjusted liquid under cooling condition to obtain a second cool liquid; subjecting the second cool liquid to ultrafiltration to obtain an ultrafiltrate; adding a proper amount of solubilizing auxiliary materials which are dissolved in a proper amount of injection water into the ultrafiltrate to obtain a solubilizing auxiliary materials-containing ultrafiltrate; adjusting the pH value of the solubilizing auxiliary materials-containing ultrafiltrate to 5.5-7.0 using the sodium hydroxide solution of 10% mass fraction to obtain a pH adjusted ultrafiltrate; filtering the pH adjusted ultrafiltrate to obtain a filtrate; encapsulating and sterilizing the filtrate to obtain the multi-component injection.
On the basis of the above-mentioned multi-component injections, the present invention further provides a multi-component injection, which is characterized by comprising the following active ingredients, by weight: 8.66-35.26 parts of albiflorin std, 1000.0-1700.0 parts of paeoniflorin, 11.13-68.07 parts of Oxypaeoniflorin, 12.20-52.98 parts of Benzoylpaeoniflorin, 0.667-1.617 parts of Benzoyloxypaeoniflorin, 1.915-3.202 parts of Mudanpioside J, 10.63-20.13 parts of galloylpaeoniflorin, 0.804-1.338 parts of Mudanpioside C, 10.0-200.0 parts of benzoic acid, 0.21-15.88 parts of gallic acid, 0.2396-0.6860 parts of ethyl gallate, 1.31-12.60 parts of catechin, 1.232-3.547 parts of Kaempferol-3-0-glucoside, 0.0500-0.4184 parts of scutellarin, 0.755-2.570 parts of quercetin-3-0-glucoside, 8.42-29.40 parts of Kaempferol-3-0-rutinoside, 4.036-7.695 parts of Kaempferol-3-0-sophoroside, 1.517-5.598 parts of quercetin-3-0-rutinoside, 200.0-500.0 parts of Hydroxysafflor yellow A, 0.316-0.774 parts of uracil, 13.77-30.56 parts of adenine, 20.50-44.99 parts of phenylalanine, 11.44-27.13 parts of uridine, 5.07-12.63 parts of adenosine, 8.00-24.11 parts of guanosine, 4.96-16.86 parts of butanedioic acid, 2.384-5.404 parts of p-hydroxybenzoic acid, 3.00-17.98 parts of p-coumaric acid, 4.837-7.806 parts of caffeic acid, 3.83-8.59 parts of chlorogenic acid, 6.51-69.39 parts of senkyunolide I (42), 1.55-18.27 parts of senkyunolide H, 4.30-14.22 parts of senkyunolide N, 2.460-5.648 parts of open-loop senkyunolide I, 1.55-10.74 parts of senkyunolide G, 1.43-8.67 parts of 3-hydroxyl-3-butylphthalide, 0.10-0.961 parts of senkyunolide A, 7.66-47.15 parts of ferulaic acid, 1.43-17.25 parts of protocatechualdehyde, 2.361-4.030 parts of protocatechuic acid, 2.776-6.845 parts of tanshinol, 5.07-12.78 parts of rosmarinic acid, 0.0697-0.4005 parts of salvianolic acid D, 1.123-4.732 parts of salvianolic acid C, 0.366-2.505 parts of salvianolic acid A, 0.429-0.945 parts of alkannic acid, and 4.00-11.00 parts of salvianolic acid B.
The above-mentioned multi-component injection is characterized in that the preparation method thereof comprises the following steps:
providing 100 g of safflower carthamus decoction pieces; leaching the safflower carthamus decoction pieces with 30% ethanol of 8 times the weight of the safflower carthamus decoction pieces for 8 hours to obtain a leach liquor; filtering the leach liquor to obtain a liquid medicine of 4-6 times the weight of the safflower carthamus decoction pieces; adding 95% ethanol to the liquid medicine to obtain an ethanol-containing liquid medicine having an ethanol volume content of 70%; storing the ethanol-containing liquid medicine under cooling condition for 48 hours to obtain a cool ethanol-containing liquid medicine; filtering the cool ethanol-containing liquid medicine to obtain a first filtrate; concentrating the first filtrate under reduced pressure to obtain a concentrate of 100 ml; adding 95% ethanol to the concentrate to obtain an ethanol-containing concentrate having an ethanol volume content of 80%; storing the ethanol-containing concentrate under cooling condition for 48 hours to obtain a cool ethanol-containing concentrate; filtering the cool ethanol-containing concentrate to obtain a second filtrate; recycling ethanol from the second filtrate to obtain an ethanol-reduced filtrate; concentrating and vacuum drying the ethanol-reduced filtrate to obtain a safflower carthamus dry paste;
providing 100 g of Red Paeony Root decoction pieces; heating and boiling the Red Paeony Root decoction pieces with process water of 10 times the weight of the Red Paeony Root decoction pieces to obtain a first decoction after 2 hours slight boiling; filtering the first decoction to obtain filtrate I and a first dreg; boiling the first dreg with process water of 8 times the weight of the first dreg to obtain a second decoction after 1 hour slight boiling; filtering the second decoction to obtain filtrate II and a second dreg; mixing filtrate I and filtrate II to obtain a mixture; concentrating the mixture to obtain a first concentrate of 100 ml; adding a proper amount of gelatin solution to the first concentrate under stirring to obtain a gelatin-containing first concentrate; adding 95% ethanol to the gelatin-containing first concentrate to obtain an ethanol-containing first concentrate having an ethanol volume content of 70%; storing the ethanol-containing first concentrate under cooling condition for 24 hours to obtain a cool ethanol-containing first concentrate; filtering and concentrating the cool ethanol-containing first concentrate to obtain a second concentrate of 100 ml; extracting the second concentrate with water-saturated n-butanol for 4 times and using 50 ml water-saturated n-butanol for each time; combining extract liquors of the 4 times extraction to obtain a combined extract liquor; recycling n-butanol from the combined extract liquor to obtain a n-butanol-reduced extract liquor without alcohol taste; and vacuum drying the n-butanol-reduced extract liquor to obtain a Red Paeony Root dry paste;
providing 100 g of Ligusticum wallichii decoction pieces, 100 g of radix salviae miltiorrhizae and 100 g of Angelica sinensis decoction pieces; treating the three decoction pieces with a same treatment process as the Red Paeony Root decoction pieces except for keeping 300 ml of concentrate every time and extracting with 150 ml of water-saturated n-butanol each time, to obtain a third dry paste; providing the safflower carthamus dry paste, the Red Paeony Root dry paste and the third dry paste each of a proper amount; dissolving the three dry pastes in injection water to obtain a dilute of 200 ml; storing the dilute under cooling condition to obtain a first cool liquid; adding glucosum anhydricum of an amount in accordance with 4.5% mass fraction of the multi-component injection and injection water to the first cool liquid to obtain a 1000 ml liquid; adjusting the pH value of the 1000 ml liquid to 5.5-7.0 with a sodium hydroxide solution of 10% mass fraction to obtain a pH adjusted liquid; storing the pH adjusted liquid under cooling condition to obtain a second cool liquid; subjecting the second cool liquid to ultrafiltration to obtain an ultrafiltrate; adding a proper amount of solubilizing auxiliary materials which are dissolved in a proper amount of injection water into the ultrafiltrate to obtain a solubilizing auxiliary materials-containing ultrafiltrate; adjusting the pH value of the solubilizing auxiliary materials-containing ultrafiltrate to 5.5-7.0 using the sodium hydroxide solution of 10% mass fraction to obtain a pH adjusted ultrafiltrate; filtering the pH adjusted ultrafiltrate to obtain a filtrate; encapsulating and sterilizing the filtrate to obtain the multi-component injection.
Any one of multi-component injections of the invention is characterized in that the administration way thereof is injection administration.
Any one of multi-component injections of the invention is used for preparing medicines for treating Sepsis.
As the active ingredients in the multi-component injections of the invention are known substances, which can be acquired via the known methods, the preparation method for the multi-component injections of the invention also comprises the steps: mixing the above active ingredients which are purchased or prepared, and preparing the injection via the conventional technology of pharmaceutics.
The technical solution of the invention patent is further described via the following experiments: The multi-component injection of the present invention has therapeutic effects on the Sepsis cell model and the Sepsis mouse model, indicating that the multi-component injection of the present invention has therapeutic effects on the Sepsis of mammals, thereby achieving therapeutic effects on the Sepsis of human bodies.
The advantages of the present invention will be further detailed via the following experiment data:

Experiment I Effects of the Multi-Component Injection on the Death of Endotoxin Induced Sepsis Mice

Experiment Animals
Balb/C male mice (purchased from Laboratory Animal Center of Peking Union Medical College), cleaning level, 6-8 weeks, weight of 19-23 g, adaptive feeding for 3 days.
Medicine and Reagent
The medicines of the invention are prepared in accordance with the embodiments 2-5, and endotoxin is purchased from U.S. Sigma Company.
Experiment Method
3.1 Grouping and Intervention
280 mice are divided into a normal group, a model group, experimental groups 1-12 randomly, and there are 20 mice in each group. The mice are prohibited from being fed for 12 h before the experiment, weighed and subjected to grouping in accordance with the table of random numbers. In the model group, only the modeling of counteracting toxic substances by endotoxin is carried out; in experimental groups 1-12, 12 batches of multi-component injections in embodiments 2-5 are received respectively for medicine intervention with administration by injection (the first batch in the embodiment 2 to the third batch of the embodiment 5 are assigned to the experiment groups 1-12 successively) after the modeling of counteracting toxic substances by endotoxin has been carried out; and the normal group is not subjected to additional intervention. The modeling process of counteracting toxic substances by endotoxin is as below: the mixed solution of ketamine hydrochloride:sumianxin II:PBS (phosphate buffer)=1:1.5:2.5 is selected as anaesthetic, and intramuscular injection is carried out for anesthesia in a dose of 2 mL/kg. After anesthesia is satisfied, the mice are fixed on the operating table, and 10 mg/kg of endotoxin is injected to the enterocoelia of the mice. In experimental groups 1-12, 12 batches of multi-component injections in embodiments 2-5 are injected at the auricular vein with a dose of 4 mL/kg (by weight) at 30 min and 60 min before counteracting toxic substances by endotoxin and 30 min after counteracting toxic substances by endotoxin respectively; in the model group, normal saline are injected at auricular vein with 4 mL/kg (by weight) at 30 min and 60 min before counteracting toxic substances by endotoxin and 30 min after counteracting toxic substances by endotoxin.
3.2 Observation and Statistics of Death Rate
Dead mice are observed and counted every 24 h. Statistic analysis is carried out by Kaplan-Merer method (statistics software is SPSS 16.0), and p<0.05 indicates significant difference.
Experiment Results
The results indicate that the death rate of the Sepsis model group is 100%, within 7 days after the injection of endotoxin, whereas the death rates of the experimental groups 1-12 are shown as the table below, which are obviously lower than that of the Sepsis model group (p<0.05).
The above results prompt that in embodiments 2-5, 12 batches of multi-component injections have the protective effects on Sepsis mice caused by endotoxin.

TABLE 1

The effects of 12 batches of multi-component injections in embodiments
2-5 on the death of Sepsis mice caused by endotoxin.

		Death number of the
		7th day after being
		attacked
Group	Quantity	by endotoxin	Death rate (%)

Normal group	20	0	0
Model group	20	20	100
Experimental group 1	20	7	35*
Experimental group 2	20	8	40*
Experimental group 3	20	9	45*
Experimental group 4	20	8	40*
Experimental group 5	20	8	40*
Experimental group 6	20	9	45*
Experimental group 7	20	8	40*
Experimental group 8	20	8	40*
Experimental group 9	20	7	35*
Experimental group 10	20	7	35*
Experimental group 11	20	7	35*
Experimental group 12	20	7	35*

Note:
*indicates p < 0.05 compared with the model group.

Experiment II Effects of the Multi-Component Injection on the Death of Cecal Ligation and Puncture Mediated Sepsis Mice

Experiment Animals
Balb/C male mice (purchased from Laboratory Animal Center of Peking Union Medical College), cleaning level, 6-8 weeks, weight of 19-23 g, adaptive feeding for 3 days.
Medicine and Reagent
The medicines of the invention are prepared in accordance with the embodiments 2-5.
Experiment Method
3.1 Grouping and Intervention
280 mice are divided into a control group, a model group, experimental groups 1-12 randomly, and there are 20 mice in each group. The mice are prohibited from being fed for 12 h before the experiment, weighed and subjected to grouping in accordance with the table of random numbers. In the control group, only the same operation process is carried out, but neither ligation nor puncture is carried out on caecum; in the model group, the cecal ligation and puncture (CLP) is carried out; for experimental groupsl-12, 12 batches of multi-component injections in embodiments 2-5 are injected respectively (the first batch in the embodiment 2 to the third batch of the embodiment 5 are administered to the experimental groups 1-12 successively) for medicine intervention after CLP modeling. The CLP modeling process is as below: the mixed solution of ketamine hydrochloride:sumianxin II:PBS=1:1.5:2.5 is selected as anaesthetic, and intramuscular injection is carried out for anesthesia at a dose of 2 mL/kg. After anesthesia is satisfied, the mice are fixed on the operating table, thorax and abdomen of the mice are subjected to conventional disinfection for draping, the median abdominal incision is carried out at a position 1 cm below the xiphoid, with an incision length of 1.5 cm. The cecum is exposed and is subjected to ligation at ½ position, and a 21 G syringe needle penetrates through ligated cecum and aviods blood vessels. After it is confirmed that there is no active bleeding, the cecum is returned to the enterocoelia, and the incision of abdominal wall is sutured. The postoperation skin behind the neck is subjected to conventional disinfection, 1 mL normal saline is subcutaneous injected for anabiosis, and after coming round from anesthesia, each of the mice is raised in a single cage. After the mice are subjected to the CLP operation, 12 batches of multi-component injections in embodiments 2-5 are respectively injected from the auricular vein in the experimental groupsl-12, at 0.5 h, 12 h, 24 h, 36 h, 48 h, 60 h, 72 h, 84 h and 96 h after the operation, with dosage of 4 mL/kg; and in the model group and the control group, 4 ml/kg (by weight) of normal saline is injected from the auricular vein at corresponding time.
3.2 Observation and Statistics of Death Rate
Dead mice are observed and counted every 24 h. Statistic analysis is carried out via the Kaplan-Merer method (statistics software is SPSS 16.0), and p<0.05 indicates significant difference.
Experiment Results
The results indicate that the death rate of the Sepsis model group is 70%, within 7 days after CLP operation, whereas the death rates of the experimental groups 1-12 are shown as the table below. Where, the death rates of the experimental groups 7-12 are obviously lower than that of the Sepsis model group (p<0.05). It indicates that in the embodiment 4 (experiment groups 7-9) and embodiment 5 (experiment groups 10-12), a plurality of batches of multi-component injections have the protective effects on the Sepsis mice caused by endotoxin.

TABLE 2

The effects of 12 batches of multi-component injections in embodiments
2-5 on the death of CLP mediated Sepsis mice.

		Death number of the
		7th day after CLP
Group	Quantity	operation	Death rate (%)

Control group	20	0	0
Model group	20	14	70
Experimental group 1	20	10	50
Experimental group 2	20	11	55
Experimental group 3	20	10	50
Experimental group 4	20	8	40
Experimental group 5	20	8	40
Experimental group 6	20	8	40
Experimental group 7	20	5	25*
Experimental group 8	20	6	30*
Experimental group 9	20	6	30*
Experimental group 10	20	5	25*
Experimental group 11	20	5	25*
Experimental group 12	20	5	25*

Note:
*indicates P < 0.05 compared with the Sepsis model group.

Experiment III the Effects of the Multi-Component Injection on the Expression of High-Mobility Family Protein B1 of Sepsis Rats

Experiment Animals
Wistar male rats (purchased from Experimental Animal Research Institute of Chinese Academy of Medical Sciences), cleaning level, weight of 180-220 g, adaptive feeding for 1 week.
Medicine and Reagent
The medicines of the present invention are prepared in accordance with the embodiments 2-5; the kit for high-mobility family protein B1 (HMGB) enzyme linked immunosorbent assay (ELISA) (Japanese Shino-Test Company).
Experiment Method
3.1 Grouping and Intervention
140 rats are divided into a control group, a model group, experimental groups 1-12 randomly, and there are 10 rats in each group. The rats are prohibited from being fed for 12 h before the experiment, weighed and subjected to grouping in accordance with the table of random numbers. In the control group, laparotomy is carried out to expose the cecum, the skin is sutured, and then, 10 ml of normal saline is subcutaneous injected for anabiosis; in the Sepsis model group, the cecal ligation and puncture (CLP) is carried out for modeling; and in experimental groups 1-12, 12 batches of multi-component injections in embodiments 2-5 are injected respectively (the first batch in the embodiment 2 to the third batch of the embodiment 5 are administered to the experiment groups 1-12 successively) for medicine intervention after CLP modeling. In the CLP modeling process, the mixed solution of ketamine injection+sumianxin II injection of 2:1 is subjected to intramuscular injection to anesthetize rats, and the Sepsis animal model is prepared using CLP. At the joint of the ligated cecum and the ileum, the No. 18 syringe needle penetrates through the cecum for 2 times to form intestinal fistula, 2 drainage strips (0.5 cm×2.0 cm) are indwelled to prevent needle hole from healing, then, skin is sutured layer by layer, and 10 mL of normal saline is immediately subcutaneously injected for anabiosis after the operation. After the rats are subjected to the CLP operation, in the experiment groupsl-12, at 2 h, 12 h, 24 h, 36 h, 48 h and 60 h, after the operation, 12 batches of multi-component injections in embodiments 2-5 are respectively injected from the dorsal vein of penis, with a dose of 4 mL/kg; and in the model group and the control group, 4 mL/kg (by weight) of normal saline is injected from the dorsal vein of penis at the corresponding time.
3.2 Blood Sampling and Testing
Animals of each group, which are anesthetized, are subjected to sterile blood sampling with 3 mL at abdominal aorta at 2 h, 8 h, 24 h, 48 h and 72 h after CLP, and plasma HMGB1 content is detected via the enzyme linked immunosorbent assay (ELISA).
Experiment Results
The results indicate that in the control group, plasma contains a little amount of HMGB1; in the early stage after the CLP operation, HMGB1 content in the model group is obviously increased, the HMGB1 level at 8 h is further improved, and is gradually reduced after 24 h, but is still higher than that of the control group at 72 h after the operation. There is statistical significance between the two groups (p<0.05). While in the experiment groups 1-12 with intervention treatment via 12 batches of multi-component injection in embodiments 2-5, the plasma content at 2 h after the operation is obviously lower than that of the model group (p<0.05), HMGB1 is reduced more obviously (p<0.01) after 24 h, which is close to the level of the control group. The results prompt that 12 batches of multi-component injections in embodiments 2-5 have the inhibiting effects on the expression of HMGB1 during Sepsis.

TABLE 3

The effects of 12 batches of multi-component injections in embodiments 2-5 on the HMGB1
level of Sepsis rat plasma (x ± s, n = 10) Unit: μg/L

	2 h after	8 h after	24 h after	48 h after	72 h after
Group	operation	operation	operation	operation	operation

Control group	8.2 ± 2.8	8.3 ± 2.5	8.0 ± 2.3	8.1 ± 1.6	8.2 ± 2.2
Model group	28.8 ± 10.8#	31.7 ± 7.2#	23.2 ± 6.3#	15.3 ± 1.3#	17.3 ± 1.1#
Experimental group 1	15.3 ± 5.2*	17.4 ± 3.3*	8.2 ± 1.7*	8.0 ± 2.2*	8.1 ± 1.3*
Experimental group 2	17.2 ± 5.7*	19.2 ± 7.8*	8.4 ± 2.0*	6.8 ± 1.5*	10.5 ± 1.4*
Experimental group 3	17.0 ± 5.3*	19.5 ± 6.1*	9.0 ± 2.7*	7.1 ± 2.2*	10.7 ± 2.5*
Experimental group 4	16.3 ± 5.5*	19.0 ± 3.9*	8.4 ± 2.7*	7.9 ± 2.0*	8.9 ± 1.8*
Experimental group 5	15.9 ± 5.4*	19.4 ± 3.9*	8.5 ± 2.4*	7.2 ± 1.9*	10.1 ± 1.4*
Experimental group 6	17.0 ± 5.5*	18.7 ± 3.9*	8.5 ± 1.7*	7.9 ± 1.9*	10.4 ± 1.9*
Experimental group 7	15.3 ± 5.6*	19.2 ± 5.6*	9.0 ± 2.2*	6.9 ± 2.0*	10.4 ± 1.7*
Experimental group 8	17.0 ± 5.3*	18.0 ± 6.6*	8.9 ± 2.4*	7.4 ± 2.0*	8.3 ± 1.6*
Experimental group 9	17.2 ± 5.6*	18.9 ± 7.5*	8.8 ± 2.6*	7.7 ± 2.0*	9.4 ± 2.5*
Experimental group 10	16.4 ± 5.3*	19.2 ± 5.4*	8.9 ± 2.5*	7.6 ± 1.5*	9.6 ± 1.6*
Experimental group 11	16.3 ± 5.3*	18.5 ± 6.0*	8.4 ± 2.5*	7.7 ± 2.1*	9.7 ± 1.4*
Experimental group 12	16.2 ± 5.5*	17.6 ± 6.4*	8.5 ± 2.5*	7.4 ± 1.5*	10.1 ± 2.4*

Note:
#indicates that p < 0.05 compared with the control group;
*indicates p < 0.05 compared with the model group.

Experiment IV the Effects of the Multi-Component Injection on the Expression of Monocyte Protease Activated Receptor-1 and Tissue Factors of Sepsis Rats

Experiment Animals
Wistar male rats (purchased from Experimental Animal Research Institute of Chinese Academy of Medical Sciences), cleaning level, weight of 180-220 g, adaptive feeding for 1 week.
Medicine and Reagent
The medicines of the invention are prepared in accordance with the embodiments 2-5; the kit for tissue factor (TF) enzyme linked immunosorbent assay (ELISA) (USA USCN Company); fluorescein isothiocyanate (FITC) labelled anti-rat monocyte protease activated receptor-1 (PAR-1) antibody (USA Santa Cruz Company).
Experiment Method
3.1 Grouping and Intervention
140 rats are divided into a control group, a model group, experimental groups 1-12 randomly, and there are 10 rats in each group. The rats are prohibited from being fed for 12 h before the experiment, weighed and subjected to grouping in accordance with the table of random numbers. In the control group, laparotomy is carried out to expose the cecum, after that, the skin is sutured, and then, 10 mL of normal saline is injected subcutaneously for anabiosis; in the Sepsis model group, the cecal ligation and puncture (CLP) is carried out for modeling; and in experiment groups 1-12, 12 batches of multi-component injections in embodiments 2-5 are injected respectively (the first batch in the embodiment 2 to the third batch of the embodiment 5 are administered to the experiment groups 1-12 successively) for medicine intervention after CLP modeling. In the CLP modeling process, the mixed solution of ketamine injection:sumianxin II injection=2:1 is used to intramuscular injection to anesthetize rats, and the Sepsis animal model is prepared using CLP. At the joint of the ligated cecum and the ileum, the No. 18 syringe needle penetrates through the cecum for 2 times to form intestinal fistula, 2 drainage strips (0.5 cm×2.0 cm) are indwelled to prevent needle hole from healing, then, skin is sutured layer by layer, and 10 mL of normal saline is immediately subcutaneously injected for anabiosis after the operation. After the rats are subjected to the CLP operation, in the experimental groups 1-12, 12 batches of multi-component injections in embodiments 2-5 are respectively injected from the dorsal vein of penis, with a dose of 4 mL/kg at 2 h, 12 h, 24 h, 36 h, 48 h and 60 h, after the operation; and in the model group and the control group, 4 mL/kg (by weight) of normal saline is injected from the dorsal vein of penis at the corresponding time.
3.2 Blood Sampling and Testing
Animals of each group, which are anesthetized, are subjected to sterile blood sampling with 3 mL at aorta abdominalis at 12 h, 24 h, 48 h, 48 h and 72 h after CLP. The expression of the plasma monocyte protease activated receptor-1 (PAR-1) is detected by using the flow immumofluorescence method; and the content of plasma tissue factors (TF) are detected by using the enzyme linked immunosorbent assay (ELISA).
Detection of PAR-1 expression: taking 2 mL of heparin for anticoagulant, and separating mono karyocyte by using rat lymphocyte separating medium; resuspendeding mono karyocyte by using 10% of the full cell culture fluid of fetal calf serum-RPMI 1640, adjusting cell density to be 4×106/mL, and washing a cell culture plate using the cell culture fluid after incubating for 2 h; adding 0.25% trypsin-EDTA digestive juice for digesting 3 min, after majority of cells exfoliating, adding 2 mL of full cell culture fluid of 10% fetal calf serum-RPMI 1640, and terminating digesting; washing using phosphate buffer (PBS) for 3 times to acquire peripheral blood mononuclear cells; adding 1 μg/1×106 cell fluorescein isothiocyanate (FITC) into cell suspension to mark the anti-rat PAR-1 antibody, incubating away from light at 4° C. for 15 min, adding 2 mL of PBS to wash for 1 time, adding 0.4 mL of PBS, and detecting its average fluorescence intensity on the flow cytometry.
Experiment Results
The results indicate that the mononuclear cells PAR-1 in the control group have a certain expression; there is no statistical significance for difference of the expression quantity of PAR-1 at 12 h after the operation between the model group and the control group upon comparison, the average fluorescence intensity is significantly higher than that of the control group at 24 h, 48 h and 72 h after the operation (p<0.05), and gradually increased with the extension of postoperation time. The average fluorescence intensities of PAR-1 at 24 h and 48 h in the experiment groups 1-3 are lower than that of the model group, with no significant difference; and the fluorescence intensities of the experiment groups at 72 h are significantly lower than that of the model group (p<0.05). The average fluorescence intensities of PAR-1 of nine intervention groups of the experiment groups 4-12 at 24 h, 48 h and 72 h are significantly reduced (p<0.05) by comparison to that of the model group.
The mononuclear cells TF in the control group have a certain expression; the expression of TF at 12 h, 24 h, 48 h and 72 h after the operation in the model group are significantly higher than that of the control group (p<0.05), which is gradually increased with the extension of postoperation time, and reach a peak at 48 h. The expression of TF at 12 h and 72 h in the experiment groups 1-3 are lower than that of the model group, with no significant difference; and the expression intensities of the experiment groups at 24 h and 48 h are significantly higher than that of the model group (p<0.05). The expression of TF of nine intervention groups of the experiment groups 4-12 at 24 h, 48 h and 72 h are significantly reduced (p<0.05) by comparison to that of the model group.
The results indicate that the 9 batches of multi-component injections in embodiments 3-5 can reduce the expression of Sepsis induced monocyte PAR-1, thereby obviously reducing the secretion of TF, and improving the monocyte mediated coagulation dysfunction.

TABLE 4-1

The effects of multi-component injections on the expression of Sepsis rats
PAR-1 (x ± s, n = 10)

	12 h after	24 h after	48 h after	72 h after
Group	operation	operation	operation	operation

Control group	20.0 ± 0.7	17.6 ± 2.0	15.7 ± 0.2	16.8 ± 2.9
Model group	19.8 ± 1.1	21.9 ± 1.1#	24.2 ± 0.7#	29.7 ± 0.4#
Experimental	19.6 ± 1.9	20.2 ± 2.3	22.9 ± 2.0	22.6 ± 2.3*
group 1
Experimental	20.8 ± 2.1	20.4 ± 1.7	23.1 ± 1.8	21.6 ± 2.2*
group 2
Experimental	20.7 ± 3.3	20.9 ± 1.6	22.7 ± 2.7	22.8 ± 1.5*
group 3
Experimental	20.0 ± 3.2	18.6 ± 1.7*	20.7 ± 2.2*	18.0 ± 2.1*
group 4
Experimental	20.2 ± 2.9	18.8 ± 1.7*	18.6 ± 2.6*	18.3 ± 1.7*
group 5
Experimental	20.3 ± 2.3	19.2 ± 1.8*	18.3 ± 2.5*	18.1 ± 2.2*
group 6
Experimental	20.2 ± 2.7	19.1 ± 1.9*	20.6 ± 2.0*	17.9 ± 2.1*
group 7
Experimental	20.7 ± 2.2	18.7 ± 1.7*	21.4 ± 2.3*	17.9 ± 1.5*
group 8
Experimental	20.0 ± 2.5	18.4 ± 2.0*	18.7 ± 2.1*	17.7 ± 1.7*
group 9
Experimental	19.9 ± 2.4	18.4 ± 1.6*	18.0 ± 2.2*	17.9 ± 2.3*
group 10
Experimental	20.3 ± 2.5	18.7 ± 1.9*	21.5 ± 2.1*	17.8 ± 2.1*
group 11
Experimental	20.7 ± 2.6	18.5 ± 2.3*	18.1 ± 1.9*	17.7 ± 2.2*
group 12

Note:
#indicates that p < 0.05 compared with the control group;
*indicates p < 0.05 compared with the model group.

TABLE 4-2

The effects of multi-component injections on the expression of TF of Sepsis rats (x ± s,
n = 10) Unit: ng/L

	12 h after	24 h after	48 h after	72 h after
Groups	operation	operation	operation	operation

Control group	238.3 ± 15.6	221.8 ± 40.7	259.0 ± 27.57	240.5 ± 34.4
Model group	324.0 ± 18.9#	505.2 ± 82.8#	695.4 ± 138.9#	342.9 ± 36.3#
Experimental group 1	299.3 ± 29.6	370.0 ± 22.3*	377.8 ± 26.1*	319.7 ± 28.3
Experimental group 2	296.4 ± 32.3	366.7 ± 19.3*	380.7 ± 41.3*	313.9 ± 25.3
Experimental group 3	297.7 ± 33.3	374.3 ± 21.3*	381.0 ± 19.7*	320.0 ± 31.2
Experimental group 4	283.5 ± 24.6*	273.2 ± 20.8*	281.4 ± 39.2*	252.5 ± 23.8*
Experimental group 5	285.3 ± 29.1*	273.7 ± 21.4*	282.6 ± 31.3*	255.8 ± 19.4*
Experimental group 6	279.7 ± 26.5*	268.6 ± 21.1*	284.9 ± 39.6*	257.1 ± 20.0*
Experimental group 7	283.3 ± 31.9*	270.5 ± 20.7*	284.0 ± 20.0*	251.7 ± 25.4*
Experimental group 8	284.2 ± 30.7*	273.0 ± 21.2*	280.2 ± 31.5*	254.8 ± 29.7*
Experimental group 9	281.9 ± 29.7*	273.4 ± 20.8*	280.5 ± 40.0*	252.1 ± 25.2*
Experimental group 10	284.5 ± 23.9*	271.1 ± 19.5*	281.8 ± 30.3*	250.8 ± 26.3*
Experimental group 11	283.9 ± 31.2*	270.1 ± 19.9*	286.1 ± 21.4*	250.1 ± 27.5*
Experimental group 12	282.7 ± 20.3*	268.5 ± 19.9*	283.7 ± 39.4*	252.8 ± 19.8*

Note:
#indicates that p < 0.05 compared with the control group;
*indicates p < 0.05 compared with the model group.

Experiment V the Effects of the Multi-Component Injection on Regulating T Cell Apoptosis and T Helper Cell Drift of Sepsis Rats

Experiment Animals
Wistar male rats (purchased from Experimental Animal Research Institute of Chinese Academy of Medical Sciences), cleaning level, weight of 180-220 g, adaptive feeding for 1 week.
Medicine and Reagent
The medicines of the invention are prepared in accordance with the embodiments 2-5; phycoerythrin (PE)-anti-rat CD25, fluorescein isothiocyanate (FITC) labeled anti-rat CD4, allophycocyanin (APC) labeled Annexin V apoptosis reagent kit (USA BD Company); rat anti-PE reagent kit, CD4 magnetic beads, MiniMACS magnetic separation apparatus and separation column (Germany MiltenyiBiotec Company); PE labeled forkhead winged helix transcription factor (Foxp3) reagent kit, PE labeled T lymphocytotoxicity related antigen 4 (CTLA-4), anti-rat CD3 monoclonal antibody, anti-rat CD28 monoclonal antibody (USA eBioscience Company); interferon (IFN)-7, IL-4, IL-10 enzyme linked immunosorbent assay (ELISA) reagent kits (USA Biosource Company); IL-17 ELISA reagent kit (USA Usenlife Science Company); Trypan Blue (USA Sigma Company).
Experiment Method
3.1 Grouping and Intervention
140 rats are divided into a control group, a model group, experimental groups 1-12 randomly, and there are 10 rats in each group. The rats are prohibited from being fed for 12 h before the experiment, weighed and subjected to grouping in accordance with the table of random numbers. In the control group, laparotomy is carried out to expose the cecum, after that, the skin is sutured, and then, 10 mL of normal saline is injected subcutaneously for anabiosis; in the Sepsis model group, the cecal ligation and puncture (CLP) is carried out for modeling; and in experiment groups 1-12, 12 batches of multi-component injections in embodiments 2-5 are injected respectively (the first batch in the embodiment 2 to the third batch of the embodiment 5 are administered to the experiment groups 1-12 successively) for medicine intervention after CLP modeling. In the CLP modeling process, the mixed solution of ketamine injection:sumianxin II injection of 2:1 is intramuscular injected to anesthetize rats, and the Sepsis animal model is prepared by using CLP. At the joint of the ligated cecum and the ileum, the No. 18 syringe needle penetrates through the cecum for 2 times to form intestinal fistula, 2 drainage strips (0.5 cm×2.0 cm) are indwelled to prevent needle hole from healing, then, skin is sutured layer by layer, and 10 mL of normal saline is immediately injected subcutaneously for anabiosis after the operation. After the rats are subjected to the CLP operation, in the experiment groupsl-12, after the operation, 12 batches of multi-component injections in embodiments 2-5 are respectively injected from the dorsal vein of penis, with a dose of 4 mL/kg; and in the model group and the control group, 4 mL/kg (by weight) of normal saline is injected from the dorsal vein of penis at the corresponding time.
3.2 Cell Separation and Culture
Take spleen from each group of rats after breaking necks to death under the sterile condition, grinding the spleen, sieve it with a 400-mesh sieve, centrifuge cell suspension, add lymphocyte separating medium for centrifuging, and obtain white cells in the middle layer. Add PE-anti-CD25 and PE magnetic beads, carry out positive selection (positive) to obtain CD25+T cells, and carry out negative selection (negative) to obtain CD25-T cell. After carrying out dissociation by CD25+T cell dissociation reagent, carry out positive selection on negatively selected cells using FITC-anti-CD4 and CD4 magnetic beads to obtain CD4+CD25+Treg; and carry out positive selection on CD25-T cells using FITC-anti-CD4 and CD4 magnetic beads to obtain CD4+CD25-T cells. Test the purity of double positive cells via the flow cytometry. Dye CD4+CD25+Treg using 0.4% (mass fraction) of Trypan Blue, and observe cell survival rate. Put RPM11640 culture solution containing 20% (volume fraction) fetal bovine serum in a 48-pore culture plate, and culture in a CO₂incubator. Separate CD4+CD25+Treg in each group at the 3rd day for culturing for 12 h, adjust the concentration of CD4+CD25+Treg and CD4+CD25-T cells by using the culture solution to be 1:1 for culturing, stimulate using sword bean A (Con A, 5 mg/L), culture in a CO₂incubator at 37° C. for 68 h, centrifuge to get a supernate which is frozen at −70° C. for testing.
3.3 Detection and Analysis
Testing of Treg apoptosis rate: culturing the separated cells for 12 h, washing the suspending CD4+CD25+Treg (1×10⁹/L) 2 times with phosphate buffer (PBS), adding 100 L of binding buffer and 10 L of APC labeled Annexin V (20 mg/L), keeping in the dark place at room temperature for 30 min, then, adding 10 L of actinomycin D (7-AAD), keeping in the dark place for reaction for 5 min, adding 400 μL of binding buffer, selecting 7-AAD negative Annexin V positive cells as apoptotic cells by the flow cytometry, and testing the cell apoptosis rate.
Testing of Foxp3 and CTLA-4 expression: Adding 1 ml of newly prepared film-breaking liquid into 100 μL prepared CD4+CD25+Treg (1×109/L), keeping in the dark place at 4° C. for incubating for 2 h, and washing with 2 mL of film-breaking buffer; adding PE-anti-Foxp3, incubating in the dark place at 4° C. for 30 min, washing with 2 mL of film-breaking buffer, centrifuging and discarding supernate, adding 0.5 mL of PBS, and testing the average fluorescence intensity of Foxp3 by the flow cytometry. Directly adding PE-CTLA-4 into the resuspended cells (1×109/L), keeping in the dark place at 4° C. for incubating for 30 min, and testing the average fluorescence intensity of CTLA-4.
Testing of cell factors: including main inhibitory cell factor IL-10 secreted by Treg, IFN-γ secreted by Th1, and IL-4 secreted by Th2. The IL-10 specimen is from supernate collected after the separated Treg is cultured for 12 h in each group, IFN-γ and IL-4 specimens are from supernate collected after CD4+CD25+Treg and CD4+CD25-T cells are subjected to co-culture for 68 h. Tests are performed by using the ELISA reagent kit in accordance with the specification, the standard curve and the regression equation are calculated respectively, the absorbancy of the samples is substituted into the standard curve, and the protein concentration of cell factors in the samples are calculated.
Experiment Results
The results indicate that the apoptosis rate of Treg in the model group is obviously lower than that of the control group (p<0.05), the apoptosis rates of the experimental groups 4-12 are significantly higher than that of the model group (p<0.05), and the trends of the experimental groups 1-3 are close, without significant difference. The expression of Foxp3 and CTLA-4 in the model group is obviously higher than that of the control group (p<0.05), the expression of the experimental groups 4-12 are significantly lower than that of the model group (p<0.05), and the trends of the experimental groups 1-3 are close, without significant difference. The secretion level of IL-10 in the model group is obviously higher than that of the control group (p<0.05), the secretion level of the experimental groups 4-12 are significantly lower than that of the model group (p<0.05), and the trends of the experimental groups 1-3 are close, without significant difference. The levels of IFN-γ and IL-4 in the model group are substantially increased compared with the control group, and the levels of IFN-γ and IL-4 in the experimental groups 4-12 are further increased. Compared with the model group, there are statistical significance for difference (p<0.05). The trends of experimental groups 1-3 are close, without significant difference.
The results indicate that 9 batches of multi-component injections in embodiments 3-5 can promote the apoptosis of Sepsis Treg and improve the secretion of cell factors of Treg and effector T cells, and are conducive to correcting the inhibitory state of cellular immunity of organisms.

TABLE 5-1

The effects of 12 batches of multi-component injections in embodiments
2-5 on the apoptosis rate of Treg and the expression of Foxp3 and
CTLA-4 of Sepsis rats (x ± s, n = 10) Unit: %

Group	Apoptosis rate	Foxp3	CTLA

Control group	9.48 ± 2.2	126.5 ± 12.2	119.1 ± 6.4
Model group	5.9 ± 1.5#	175.0 ± 19.6#	172.0 ± 10.1#
Experimental group 1	7.1 ± 3.0	159.8 ± 13.3	159.7 ± 14.1
Experimental group 2	7.3 ± 2.5	159.7 ± 16.8	161.4 ± 19.9
Experimental group 3	7.0 ± 2.3	158.5 ± 15.1	160.0 ± 20.7
Experimental group 4	17.4 ± 2.5*	118.9 ± 14.4*	118.3 ± 15.2*
Experimental group 5	17.9 ± 3.0*	118.8 ± 14.1*	116.2 ± 18.3*
Experimental group 6	17.9 ± 2.9*	119.6 ± 14.1*	116.4 ± 15.6*
Experimental group 7	28.0 ± 2.9*	59.7 ± 4.2*	55.5 ± 6.5*
Experimental group 8	27.3 ± 2.4*	58.9 ± 5.5*	55.6 ± 6.3*
Experimental group 9	27.4 ± 2.8*	58.6 ± 6.3*	56.3 ± 6.6*
Experimental group 10	27.9 ± 2.9*	59.0 ± 3.5*	58.6 ± 5.8*
Experimental group 11	27.8 ± 2.5*	59.5 ± 5.8*	56.5 ± 7.4*
Experimental group 12	27.2 ± 3.0*	59.5 ± 3.3*	56.8 ± 4.2*

Note:
#indicates that p < 0.05 compared with the control group;
*indicates p < 0.05 compared with the model group.

TABLE 5-2

The effects of 12 batches of multi-component injections in embodiments
2-5 on the level of secretory cell factors of Treg and effector T cells of
Sepsis rats (x ± s, n = 10) Unit: ng/L

Group	IL-10	IFN-γ	IL-4

Control group	133.7 ± 25.7	19.0 ± 6.7	5.4 ± 0.7
Model group	318.1 ± 28.3#	254.7 ± 44.9#	8.8 ± 0.6#
Experimental group 1	299.3 ± 22.3	311.6 ± 75.2	9.3 ± 0.9
Experimental group 2	300.6 ± 22.1	321.5 ± 84.3	9.5 ± 1.2
Experimental group 3	302.6 ± 22.5	322.8 ± 88.9	9.3 ± 1.1
Experimental group 4	245.2 ± 22.5*	414.7 ± 82.2*	10.4 ± 0.8*
Experimental group 5	251.5 ± 22.2*	413.2 ± 78.2*	10.3 ± 1.0*
Experimental group 6	251.6 ± 19.3*	408.8 ± 84.1*	10.5 ± 1.3*
Experimental group 7	51.2 ± 2.5*	498.7 ± 81.7*	10.5 ± 1.2*
Experimental group 8	49.6 ± 2.2*	494.2 ± 85.3*	10.7 ± 1.1*
Experimental group 9	52.2 ± 2.3*	495.6 ± 81.9*	10.6 ± 0.9*
Experimental group 10	50.3 ± 2.1*	499.4 ± 85.6*	10.8 ± 1.4*
Experimental group 11	49.3 ± 2.3*	501.4 ± 87.6*	10.7 ± 1.1*
Experimental group 12	51.7 ± 2.1*	494.5 ± 81.0*	10.8 ± 1.3*

Note:
#indicates that p < 0.05 compared with the control group;
*indicates p < 0.05 compared with the model group.

After related testing, we find that the multi-component injections of the present invention have the characteristics of stable quality, simple production process, convenience for production, safety, effectiveness, etc.
The summary of relevant compounds presented in the present application:


Name	CAS	Molecular formula	Structural formula

Kaempferol-3-0-glucoside	480-10-4	C₂₁H₂₀O₁₁

Scutellarin	27740-01-8	C₂₁H₁₈O₁₂

Quercetin-3-0-glucoside	482-35-9	C₂₁H₂₀O₁₂

Kaempferol-3-0-rutinoside	17650-84-9	C₂₇H₃₀O₁₅

Kaempferol-3-0-sophoroside	19895-95-5	C₂₇H₃₀O₁₆

Quercetin-3-0-rutinoside	949926-49-2	C₂₇H₃₀O₁₆

Hydroxysafflor yellowA	78281-02-4	C₂₇H₃₂O₁₆

Uracil	66-22-8	C₄H₄N₂O₂

Adenine	73-24-5	C₅H₅N₅

Phenylalanine	167088-01-9	C₉H₁₁NO₂

Uridine	58-96-8	C₉H₁₂N₂O₆

Adenosine	58-61-7	C₁₀H₁₃N₅O₄

Guanosine	118-00-3	C₁₀H₁₃N₅O₅

Butanedioic acid	110-15-6	C₄H₆O₄

p-hydroxybenzoic acid	99-96-7	C₇H₆O₃

p-coumaric acid	501-98-4	C₉H₈O₃

Caffeic acid	331-39-5	C₉H₈O₄

Chlorogenic acid	327-97-9	C₁₆H₁₈O₉

Albiflorin std	39011-90-0	C₂₃H₂₈O₁₁

Paeoniflorin	23180-57-6	C₂₃H₂₈O₁₁

Oxypaeoniflorin	39011-91-1	C₂₃H₂₈O₁₂

Benzoylpaeoniflorin	38642-49-8	C₃₀H₃₂O₁₂

Benzoyloxy paeoniflorin	72896-40-3	C₃₀H₃₂O₁₃

Mudanpioside J	262350-52-7	C₃₁H₃₄O₁₄

Galloylpaeoniflorin	122965-41-7	C₃₀H₃₂O₁₅

Mudanpioside C	172760-03-1	C₃₀H₃₂O₁₃

Benzoic acid	65-85-0	C₇H₆O₂

Gallic acid	149-91-7	C₇H₆O₅

Ethyl gallate	831-61-8	C₉H₁₀O₅

Catechin	154-23-4	C₁₅H₁₄O₆

Protocatechualdehyde	139-85-5	C₇H₆O₃

Protocatechuic acid	99-50-3	C₇H₆O₄

Tanshinol	76822-21-4	C₉H₁₀O₅

Rosmarinic acid	537-15-5	C₁₈H₁₆O₈

Salvianolic acid D	142998-47-8	C₂₀H₁₈O₁₀

Salvianolic acid C	115841-09-3	C₂₆H₂₀O₁₀

Salvianolic acid A	96574-01-5	C₂₆H₂₂O₁₀

Alkannic acid	28831-65-4	C₂₇H₂₂O₁₂

Salvianolic acid B	121521-90-2	C₃₆H₃₀O₁₆

Senkyunolide I	94596-28-8	C₁₂H₁₆O₄

Senkyunolide H	94596-27-7	C₁₂H₁₆O₄

Senkyunolide N	140694-58-2	C₁₂H₁₈O₄

Open-loop senkyunolide I	1809299-03-3	C₁₂H₁₈O₅

Senkyunolide G	94530-85-5	C₁₂H₁₆O₃

3-hydroxy-3-Butylphthalide	162050-42-2	C₁₂H₁₄O₃

Senkyunolide A	62006-39-7	C₁₂H₁₆O₂

Ferulaic acid	1135-24-6	C₁₀H₁₀O₄

IV. DESCRIPTION OF THE DRAWINGS

FIG. 1 Comparison of survival rates of endotoxin induced Sepsis mice among groups Note: compared with the model group, the experimental groups 1-12 have the significant statistical difference (p<0.05).

FIG. 2 Comparison of the survival rates of cecal ligation and puncture mediated Sepsis mice among groups

Note: compared with the model group, the experimental groups 7-12 have the significant statistical difference (p<0.05).

V. DETAILED DESCRIPTION OF THE EMBODIMENTS

There is a further description to the invention via the following specific embodiments, which is not used as limits.

Embodiment 1 Testing Method for Effective Ingredients in Injection

Method 1: Chromatographic Separation Conditions for Analyzing Ingredients of Safflower Carthamus and Red Paeony Root
Chromatographic column: Waters HSS T3 UPLC C18 Chromatographic column (100 mm×2.1 mm; 1.8 μM, Waters, USA);
Column temperature: 45° C.;
Mobile phase: A: H₂O (containing 25 mM HCOOH, B: MeOH (containing 25 mM HCOOH);
Gradient elute is shown in Table 6; flow velocity: 0.35 mL/min; injection volume: 5 μL; analysis time: 13 min.

TABLE 6

Liquid-phase gradient elute conditions of ingredients of safflower
carthamus and Red Paeony Root

Time (min)	Solvent A	Solvent B

0.0	98%	2%
8.0	30%	70%
11.0	2%	98%
13.0	98%	2%

Method 2: Chromatographic Separation Conditions for Analyzing Ingredients of Radix Salviae Miltiorrhizae
Chromatographic column: Waters HSS T3 UPLC C18 Chromatographic column (100 mm×2.1 mm; 1.8 μM, Waters, USA);
Column temperature: 45° C.;
Mobile phase: A: H₂O (containing 25 mM HCOOH), B: MeOH (containing 25 mM HCOOH);
Gradient elute is shown in Table 7; flow velocity: 0.35 ml/min; injection volume: 5 μL; analysis time: 20 min.

TABLE 7

Liquid-phase gradient elute conditions of ingredients of radix
salviae miltiorrhizae

Time (min)	Solvent A	Solvent B

0.0	98%	2%
1.0	98%	2%
15.0	30%	70%
17.0	2%	98%
20.0	98%	2%

Method 3: Chromatographic Separation Conditions for Analyzing Ingredients of Ligusticum wallichii and Angelica sinensis, Adenine and Adenosine
Chromatographic column: Waters HSS T3 UPLC C18 Chromatographic column (100 mm×2.1 mm; 1.8 μM, Waters, USA);
Column temperature: 45° C.;
Mobile phase: A: MeOH—H₂O (v/v, 1:99), including 1 mM HCOOH and 25 μM, CH₃COOLi; B: MeOH—H₂O (v/v, 99:1), including 1 mM HCOOH and 25 μM, CH3COOLi; Gradient elute is shown in Table 8; flow velocity: 0.35 mL/min; injection volume: 5 μL; analysis time: 8 min.

TABLE 8

Liquid-phase gradient elute conditions of ingredients of Ligusticum
wallichii and Angelica sinensis, adenine and adenosine

Time (min)	Solvent A	Solvent B

0.0	94%	6%
7.0	5%	95%
8.0	94%	6%

Embodiment 2 Preparation of Multi-Component Injection

providing 100 g of Red Paeony Root decoction pieces; heating and boiling the Red Paeony Root decoction pieces with process water of 10 times the weight of the Red Paeony Root decoction pieces to obtain a first decoction after 2 hours slight boiling; filtering the first decoction to obtain filtrate I and a first dreg; boiling the first dreg with process water of 8 times the weight of the first dreg to obtain a second decoction after 1 hour slight boiling; filtering the second decoction to obtain filtrate II and a second dreg; mixing filtrate I and filtrate II to obtain a mixture; concentrating the mixture to obtain a first concentrate of 100 ml; adding a proper amount of gelatin solution to the first concentrate under stirring to obtain a gelatin-containing first concentrate; adding 95% ethanol to the gelatin-containing first concentrate to obtain an ethanol-containing first concentrate having an ethanol volume content of 70%; storing the ethanol-containing first concentrate under cooling condition for 24 hours to obtain a cool ethanol-containing first concentrate; filtering and concentrating the cool ethanol-containing first concentrate to obtain a second concentrate of 100 ml; extracting the second concentrate with water-saturated n-butanol for 4 times and using water-saturated n-butanol of 50 ml for each time; combining extract liquors of the 4 times extraction to obtain a combined extract liquor; recycling n-butanol from the combined extract liquor to obtain a n-butanol-reduced extract liquor without alcohol taste; and vacuum drying the n-butanol-reduced extract liquor to obtain a Red Paeony Root dry paste;
providing a proper amount of the Red Paeony Root dry paste; dissolving the Red Paeony Root dry paste in injection water to obtain a dilute of 200 ml; storing the dilute under cooling condition to obtain a first cool liquid; adding glucosum anhydricum of an amount in accordance with 4.5% mass fraction of the multi-component injection and injection water to the first cool liquid to obtain a 1000 ml liquid; adjusting the pH value of the 1000 ml liquid to 5.5-7.0 with a sodium hydroxide solution of 10% mass fraction to obtain a pH adjusted liquid; storing the pH adjusted liquid under cooling condition to obtain a second cool liquid; subjecting the second cool liquid to ultrafiltration to obtain an ultrafiltrate; adding a proper amount of solubilizing auxiliary materials which are dissolved in a proper amount of injection water into the ultrafiltrate to obtain a solubilizing auxiliary materials-containing ultrafiltrate; adjusting the pH value of the solubilizing auxiliary materials-containing ultrafiltrate to 5.5-7.0 using the sodium hydroxide solution of 10% mass fraction to obtain a pH adjusted ultrafiltrate; filtering the pH adjusted ultrafiltrate to obtain a filtrate; encapsulating and sterilizing the filtrate to obtain the multi-component injection.
Three batches of injections are prepared in accordance with the process, and the testing results of the effective ingredients are as below:


Effective	The First	The
ingredient (Unit ug/ml)	batch	Second batch	The Third batch

Albiflorin std	8.66	9.51	11.98
Paeoniflorin	1000.0	1010.7	1051.6
Oxypaeoniflorin	11.13	14.43	14.45
Benzoylpaeoniflorin	12.20	15.48	18.09
Benzoyloxypaeoniflorin	0.667	0.711	0.753
Mudanpioside J	1.915	1.934	1.960
Galloylpaeoniflorin	10.63	11.03	11.15
Mudanpioside C	0.804	0.805	0.941
Benzoic acid	10.0	20.4	30.1
Gallic acid	0.21	0.73	0.77
Ethyl gallate	0.2396	0.2428	0.2526
Catechin	1.31	1.91	1.60

Embodiment 3 Preparation Process of Multi-Component Injection

providing 100 g of safflower carthamus decoction pieces; leaching the safflower carthamus decoction pieces with 30% ethanol of 8 times the weight of the safflower carthamus decoction pieces for 8 hours to obtain a leach liquor; filtering the leach liquor to obtain a liquid medicine of 4-6 times the weight of the safflower carthamus decoction pieces; adding 95% ethanol to the liquid medicine to obtain an ethanol-containing liquid medicine having an ethanol volume content of 70%; storing the ethanol-containing liquid medicine under cooling condition for 48 hours to obtain a cool ethanol-containing liquid medicine; filtering the cool ethanol-containing liquid medicine to obtain a first filtrate; concentrating the first filtrate under reduced pressure to obtain a concentrate of 100 ml; adding 95% ethanol to the concentrate to obtain an ethanol-containing concentrate having an ethanol volume content of 80%; storing the ethanol-containing concentrate under cooling condition for 48 hours to obtain a cool ethanol-containing concentrate; filtering the cool ethanol-containing concentrate to obtain a second filtrate; recycling ethanol from the second filtrate to obtain an ethanol-reduced filtrate; concentrating and vacuum drying the ethanol-reduced filtrate to obtain a safflower carthamus dry paste;
providing 100 g of Red Paeony Root decoction pieces; heating and boiling the Red Paeony Root decoction pieces with process water of 10 times the weight of the Red Paeony Root decoction pieces to obtain a first decoction after 2 hours slight boiling; filtering the first decoction to obtain filtrate I and a first dreg; boiling the first dreg with process water of 8 times the weight of the first dreg to obtain a second decoction after 1 hour slight boiling; filtering the second decoction to obtain filtrate II and a second dreg; mixing filtrate I and filtrate II to obtain a mixture; concentrating the mixture to obtain a first concentrate of 100 ml; adding a proper amount of gelatin solution to the first concentrate under stirring to obtain a gelatin-containing first concentrate; adding 95% ethanol to the gelatin-containing first concentrate to obtain an ethanol-containing first concentrate having an ethanol volume content of 70%; storing the ethanol-containing first concentrate under cooling condition for 24 hours to obtain a cool ethanol-containing first concentrate; filtering and concentrating the cool ethanol-containing first concentrate to obtain a second concentrate of 100 ml; extracting the second concentrate with water-saturated n-butanol for 4 times and using 50 ml water-saturated n-butanol for each time; combining extract liquors of the 4 times extraction to obtain a combined extract liquor; recycling n-butanol from the combined extract liquor to obtain a n-butanol-reduced extract liquor without alcohol taste; and vacuum drying the n-butanol-reduced extract liquor to obtain a Red Paeony Root dry paste;
providing the safflower carthamus dry paste and the Red Paeony Root dry paste each of a proper amount; dissolving the two dry pastes in injection water to obtain a dilute of 200 ml; storing the dilute under cooling condition to obtain a first cool liquid; adding glucosum anhydricum of an amount in accordance with 4.5% mass fraction of the multi-component injection and injection water to the first cool liquid to obtain a 1000 ml liquid; adjusting the pH value of the 1000 ml liquid to 5.5-7.0 with a sodium hydroxide solution of 10% mass fraction to obtain a pH adjusted liquid; storing the pH adjusted liquid under cooling condition to obtain a second cool liquid; subjecting the second cool liquid to ultrafiltration to obtain an ultrafiltrate; adding a proper amount of solubilizing auxiliary materials which are dissolved in a proper amount of injection water into the ultrafiltrate to obtain a solubilizing auxiliary materials-containing ultrafiltrate; adjusting the pH value of the solubilizing auxiliary materials-containing ultrafiltrate to 5.5-7.0 using the sodium hydroxide solution of 10% mass fraction to obtain a pH adjusted ultrafiltrate; filtering the pH adjusted ultrafiltrate to obtain a filtrate; encapsulating and sterilizing the filtrate to obtain the multi-component injection.
Three batches of injections are prepared in accordance with the above process, and the testing results of the effective ingredients are as below:


Effective	The First	The Second	The
ingredient (Unit ug/ml)	batch	batch	Third batch

Albiflorin std	13.58	15.46	15.01
Paeoniflorin	1119.7	1139.7	1209.5
Oxypaeoniflorin	21.45	24.17	24.24
Benzoylpaeoniflorin	21.20	21.55	24.19
Benzoyloxypaeoniflorin	0.820	0.844	0.904
Mudanpioside J	2.083	2.463	2.480
Galloylpaeoniflorin	11.48	11.81	13.96
Mudanpioside C	0.942	1.031	1.048
Benzoic acid	84.8	85.8	100.2
Gallic acid	6.68	5.72	8.41
Ethyl gallate	0.3083	0.3967	0.4453
Catechin	4.01	5.86	5.97
Kaempferol-3-0-glucoside	1.232	1.440	1.506
Scutellarin	0.0500	0.0570	0.1033
Quercetin-3-0-glucoside	0.755	0.859	0.973
Kaempferol-3-0-rutinoside	8.42	11.02	12.59
Kaempferol-3-0-sophoroside	4.036	4.369	4.954
Quercetin-3-0-rutinoside	1.517	1.529	1.774
Hydroxysafflor yellow A	200.0	225.5	229.8
Uracil	0.316	0.338	0.424
Adenine	13.77	14.31	16.45
Phenylalanine	20.50	24.22	36.02
Uridine	11.44	13.25	14.26
Adenosine	5.07	5.59	5.70
Guanosine	8.00	9.06	10.02
Butanedioic acid	4.96	5.67	8.23
p-hydroxybenzoic acid	2.384	2.997	3.040
p-coumaric acid	3.00	3.23	3.79
Caffeic acid	4.837	5.298	5.584
Chlorogenic acid	3.83	3.86	4.28

Embodiment 4 Preparation Process of Multi-Component Injection

providing 100 g of safflower carthamus decoction pieces; leaching the safflower carthamus decoction pieces with 30% ethanol of 8 times the weight of the safflower carthamus decoction pieces for 8 hours to obtain a leach liquor; filtering the leach liquor to obtain a liquid medicine of 4-6 times the weight of the safflower carthamus decoction pieces; adding 95% ethanol to the liquid medicine to obtain an ethanol-containing liquid medicine having an ethanol volume content of 70%; storing the ethanol-containing liquid medicine under cooling condition for 48 hours to obtain a cool ethanol-containing liquid medicine; filtering the cool ethanol-containing liquid medicine to obtain a first filtrate; concentrating the first filtrate under reduced pressure to obtain a concentrate of 100 ml; adding 95% ethanol to the concentrate to obtain an ethanol-containing concentrate having an ethanol volume content of 80%; storing the ethanol-containing concentrate under cooling condition for 48 hours to obtain a cool ethanol-containing concentrate; filtering the cool ethanol-containing concentrate to obtain a second filtrate; recycling ethanol from the second filtrate to obtain an ethanol-reduced filtrate; concentrating and vacuum drying the ethanol-reduced filtrate to obtain a safflower carthamus dry paste;
providing 100 g of Red Paeony Root decoction pieces; heating and boiling the Red Paeony Root decoction pieces with process water of 10 times the weight of the Red Paeony Root decoction pieces to obtain a first decoction after 2 hours slight boiling; filtering the first decoction to obtain filtrate I and a first dreg; boiling the first dreg with process water of 8 times the weight of the first dreg to obtain a second decoction after 1 hour slight boiling; filtering the second decoction to obtain filtrate II and a second dreg; mixing filtrate I and filtrate II to obtain a mixture; concentrating the mixture to obtain a first concentrate of 100 ml; adding a proper amount of gelatin solution to the first concentrate under stirring to obtain a gelatin-containing first concentrate; adding 95% ethanol to the gelatin-containing first concentrate to obtain an ethanol-containing first concentrate having an ethanol volume content of 70%; storing the ethanol-containing first concentrate under cooling condition for 24 hours to obtain a cool ethanol-containing first concentrate; filtering and concentrating the cool ethanol-containing first concentrate to obtain a second concentrate of 100 ml; extracting the second concentrate with water-saturated n-butanol for 4 times and using 50 ml water-saturated n-butanol for each time; combining extract liquors of the 4 times extraction to obtain a combined extract liquor; recycling n-butanol from the combined extract liquor to obtain a n-butanol-reduced extract liquor without alcohol taste; and vacuum drying the n-butanol-reduced extract liquor to obtain a Red Paeony Root dry paste;
providing 100 g of Ligusticum wallichii decoction pieces and 100 g of Angelica sinensis decoction pieces; treating the Ligusticum wallichii decoction pieces and Angelica sinensis decoction pieces with a same treatment process as the Red Paeony Root decoction pieces except for keeping 300 ml of concentrate every time and extracting with 150 ml of water-saturated n-butanol each time, to obtain a third dry paste;
providing the safflower carthamus dry paste, the Red Paeony Root dry paste and the third dry paste each of a proper amount; dissolving the three dry pastes in injection water to obtain a dilute of 200 ml; storing the dilute under cooling condition to obtain a first cool liquid; adding glucosum anhydricum of an amount in accordance with 4.5% mass fraction of the multi-component injection and injection water to the first cool liquid to obtain a 1000 ml liquid; adjusting the pH value of the 1000 ml liquid to 5.5-7.0 with a sodium hydroxide solution of 10% mass fraction to obtain a pH adjusted liquid; storing the pH adjusted liquid under cooling condition to obtain a second cool liquid; subjecting the second cool liquid to ultrafiltration to obtain an ultrafiltrate; adding a proper amount of solubilizing auxiliary materials which are dissolved in a proper amount of injection water into the ultrafiltrate to obtain a solubilizing auxiliary materials-containing ultrafiltrate; adjusting the pH value of the solubilizing auxiliary materials-containing ultrafiltrate to 5.5-7.0 using the sodium hydroxide solution of 10% mass fraction to obtain a pH adjusted ultrafiltrate; filtering the pH adjusted ultrafiltrate to obtain a filtrate; encapsulating and sterilizing the filtrate to obtain the multi-component injection.
Three batches of injections are prepared in accordance with the process, and the testing results of the effective ingredients are as below:

Albiflorin std	19.06	22.10	22.27
Paeoniflorin	1227.3	1263.2	1286.0
Oxypaeoniflorin	40.38	43.28	43.69
Benzoylpaeoniflorin	32.04	34.49	35.72
Benzoyloxypaeoniflorin	1.364	1.396	1.436
Mudanpioside J	2.516	2.729	2.773
Galloylpaeoniflorin	15.07	15.71	16.16
Mudanpioside C	1.060	1.074	1.170
Benzoic acid	153.4	165.4	176.3
Gallic acid	8.80	10.12	13.70
Ethyl gallate	0.5517	0.5527	0.5863
Catechin	9.95	10.37	10.45
Kaempferol-3-0-glucoside	1.646	1.723	1.898
Scutellarin	0.1236	0.1307	0.1766
Quercetin-3-0-glucoside	1.482	1.775	1.918
Kaempferol-3-0-rutinoside	13.87	14.82	14.93
Kaempferol-3-0-sophoroside	5.321	5.542	5.619
Quercetin-3-0-rutinoside	2.669	2.788	3.150
Hydroxysafflor yellow A	250.4	311.5	329.9
Uracil	0.440	0.476	0.477
Adenine	16.56	17.27	19.82
Phenylalanine	31.17	31.85	32.93
Uridine	14.78	15.23	19.32
Adenosine	6.66	6.72	7.24
Guanosine	10.07	10.81	11.95
Butanedioic acid	9.51	9.78	10.04
p-hydroxybenzoic acid	3.054	3.447	3.712
p-coumaric acid	10.61	12.46	12.55
Caffeic acid	5.627	5.971	6.212
Chlorogenic acid	4.32	4.53	4.68
Senkyunolide I	6.51	7.72	8.06
Senkyunolide H	1.55	2.93	2.51
Senkyunolide N	4.30	4.86	6.17
Open-loop senkyunolide I	2.460	3.037	3.132
Senkyunolide G	1.55	2.06	2.12
3-hydroxy-3-Butylphthalide	1.43	1.7	2.38
Senkyunolide A	0.10	0.183	0.203
Ferulaic acid	7.66	8.41	10.23

Embodiment 5 Preparation Process of Multi-Component Injection

providing 100 g of safflower carthamus decoction pieces; leaching the safflower carthamus decoction pieces with 30% ethanol of 8 times the weight of the safflower carthamus decoction pieces for 8 hours to obtain a leach liquor; filtering the leach liquor to obtain a liquid medicine of 4-6 times the weight of the safflower carthamus decoction pieces; adding 95% ethanol to the liquid medicine to obtain an ethanol-containing liquid medicine having an ethanol volume content of 70%; storing the ethanol-containing liquid medicine under cooling condition for 48 hours to obtain a cool ethanol-containing liquid medicine; filtering the cool ethanol-containing liquid medicine to obtain a first filtrate; concentrating the first filtrate under reduced pressure to obtain a concentrate of 100 ml; adding 95% ethanol to the concentrate to obtain an ethanol-containing concentrate having an ethanol volume content of 80%; storing the ethanol-containing concentrate under cooling condition for 48 hours to obtain a cool ethanol-containing concentrate; filtering the cool ethanol-containing concentrate to obtain a second filtrate; recycling ethanol from the second filtrate to obtain an ethanol-reduced filtrate; concentrating and vacuum drying the ethanol-reduced filtrate to obtain a safflower carthamus dry paste;
providing 100 g of Red Paeony Root decoction pieces; heating and boiling the Red Paeony Root decoction pieces with process water of 10 times the weight of the Red Paeony Root decoction pieces to obtain a first decoction after 2 hours slight boiling; filtering the first decoction to obtain filtrate I and a first dreg; boiling the first dreg with process water of 8 times the weight of the first dreg to obtain a second decoction after 1 hour slight boiling; filtering the second decoction to obtain filtrate II and a second dreg; mixing filtrate I and filtrate II to obtain a mixture; concentrating the mixture to obtain a first concentrate of 100 ml; adding a proper amount of gelatin solution to the first concentrate under stirring to obtain a gelatin-containing first concentrate; adding 95% ethanol to the gelatin-containing first concentrate to obtain an ethanol-containing first concentrate having an ethanol volume content of 70%; storing the ethanol-containing first concentrate under cooling condition for 24 hours to obtain a cool ethanol-containing first concentrate; filtering and concentrating the cool ethanol-containing first concentrate to obtain a second concentrate of 100 ml; extracting the second concentrate with water-saturated n-butanol for 4 times and using 50 ml water-saturated n-butanol for each time; combining extract liquors of the 4 times extraction to obtain a combined extract liquor; recycling n-butanol from the combined extract liquor to obtain a n-butanol-reduced extract liquor without alcohol taste; and vacuum drying the n-butanol-reduced extract liquor to obtain a Red Paeony Root dry paste;
providing 100 g of Ligusticum wallichii decoction pieces, 100 g of radix salviae miltiorrhizae and 100 g of Angelica sinensis decoction pieces; treating the three decoction pieces with a same treatment process as the Red Paeony Root decoction pieces except for keeping 300 ml of concentrate every time and extracting with 150 ml of water-saturated n-butanol each time, to obtain a third dry paste; providing the safflower carthamus dry paste, the Red Paeony Root dry paste and the third dry paste each of a proper amount; dissolving the three dry pastes in injection water to obtain a dilute of 200 ml; storing the dilute under cooling condition to obtain a first cool liquid; adding glucosum anhydricum of an amount in accordance with 4.5% mass fraction of the multi-component injection and injection water to the first cool liquid to obtain a 1000 ml liquid; adjusting the pH value of the 1000 ml liquid to 5.5-7.0 with a sodium hydroxide solution of 10% mass fraction to obtain a pH adjusted liquid; storing the pH adjusted liquid under cooling condition to obtain a second cool liquid; subjecting the second cool liquid to ultrafiltration to obtain an ultrafiltrate; adding a proper amount of solubilizing auxiliary materials which are dissolved in a proper amount of injection water into the ultrafiltrate to obtain a solubilizing auxiliary materials-containing ultrafiltrate; adjusting the pH value of the solubilizing auxiliary materials-containing ultrafiltrate to 5.5-7.0 using the sodium hydroxide solution of 10% mass fraction to obtain a pH adjusted ultrafiltrate; filtering the pH adjusted ultrafiltrate to obtain a filtrate; encapsulating and sterilizing the filtrate to obtain the multi-component injection.
Three batches of injections are prepared in accordance with the process, and the testing results of the effective ingredients are as below:

Albiflorin std	34.94	32.30	35.26
Paeoniflorin	1588.2	1677.0	1700.0
Oxypaeoniflorin	59.42	64.52	68.07
Benzoylpaeoniflorin	47.98	48.27	52.98
Benzoyloxypaeoniflorin	1.452	1.551	1.617
Mudanpioside J	2.775	3.030	3.202
Galloylpaeoniflorin	18.37	19.71	20.13
Mudanpioside C	1.225	1.277	1.338
Benzoic acid	186.2	191.9	200.0
Gallic acid	13.85	15.40	15.88
Ethyl gallate	0.6277	0.6633	0.6860
Catechin	11.48	11.94	12.60
Kaempferol-3-0-glucoside	2.859	3.328	3.547
Scutellarin	0.2824	0.3620	0.4184
Quercetin-3-0-glucoside	2.295	2.263	2.570
Kaempferol-3-0-rutinoside	22.90	26.66	29.40
Kaempferol-3-0-sophoroside	7.384	7.667	7.695
Quercetin-3-0-rutinoside	4.420	5.288	5.598
Hydroxysafflor yellow A	422.4	476.9	500.0
Uracil	0.723	0.758	0.774
Adenine	24.44	28.49	30.56
Phenylalanine	38.44	40.78	44.99
Uridine	23.22	26.86	27.13
Adenosine	10.34	12.28	12.63
Guanosine	20.68	22.95	24.11
Butanedioic acid	15.29	15.44	16.86
p-hydroxybenzoic acid	4.690	5.363	5.404
p-coumaric acid	15.63	17.92	17.98
Caffeic acid	6.909	7.774	7.806
Chlorogenic acid	7.74	8.48	8.59
Senkyunolide I	60.32	63.21	69.39
Senkyunolide H	15.76	17.29	18.27
Senkyunolide N	13.36	14.18	14.22
Open-loop senkyunolide I	5.126	5.190	5.648
Senkyunolide G	10.31	10.68	10.74
3-hydroxy-3-Butylphthalide	7.02	7.08	8.67
Senkyunolide A	0.656	0.938	0.961
Ferulaic acid	35.62	42.68	47.15
Protocatechualdehyde	1.435	8.511	17.25
Protocatechuic acid	2.361	2.469	4.030
Tanshinol	2.776	4.150	6.845
Rosmarinic acid	5.07	9.57	12.78
Salvianolic acid D	0.0697	0.2892	0.4005
Salvianolic acid C	1.123	2.185	4.732
Salvianolic acid A	0.366	1.508	2.505
Alkannic acid	0.429	0.480	0.945
Salvianolic acid B	4.00	8.96	11.00

Claims

1. A multi-component injection comprising the following ingredients, by weight: 8.66-35.26 parts of albiflorin std, 1000.0-1700.0 parts of paeoniflorin, 11.13-68.07 parts of Oxypaeoniflorin, 12.20-52.98 parts of Benzoylpaeoniflorin, 0.667-1.617 parts of Benzoyloxypaeoniflorin, 1.915-3.202 parts of Mudanpioside J, 10.63-20.13 parts of galloylpaeoniflorin, 0.804-1.338 parts of Mudanpioside C, 10.0-200.0 parts of benzoic acid, 0.21-15.88 parts of gallic acid, 0.2396-0.6860 parts of ethyl gallate, and 1.31-12.60 parts of catechin.

2. The multi-component injection according to claim 1, which is prepared by a method comprising the following steps of:

providing 100 g of Red Paeony Root decoction pieces; heating and boiling the Red Paeony Root decoction pieces with process water of 10 times the weight of the Red Paeony Root decoction pieces to obtain a first decoction after 2 hours slight boiling; filtering the first decoction to obtain filtrate I and a first dreg; boiling the first dreg with process water of 8 times the weight of the first dreg to obtain a second decoction after 1 hour slight boiling; filtering the second decoction to obtain filtrate II and a second dreg; mixing filtrate I and filtrate II to obtain a mixture; concentrating the mixture to obtain a first concentrate of 100 ml; adding a proper amount of gelatin solution to the first concentrate under stirring to obtain a gelatin-containing first concentrate; adding 95% ethanol to the gelatin-containing first concentrate to obtain an ethanol-containing first concentrate having an ethanol volume content of 70%; storing the ethanol-containing first concentrate under cooling condition for 24 hours to obtain a cool ethanol-containing first concentrate; filtering and concentrating the cool ethanol-containing first concentrate to obtain a second concentrate of 100 ml; extracting the second concentrate with water-saturated n-butanol for 4 times and using water-saturated n-butanol of 50 ml for each time; combining extract liquors of the 4 times extraction to obtain a combined extract liquor; recycling n-butanol from the combined extract liquor to obtain a n-butanol-reduced extract liquor without alcohol taste; and vacuum drying the n-butanol-reduced extract liquor to obtain a Red Paeony Root dry paste;

providing a proper amount of the Red Paeony Root dry paste; dissolving the Red Paeony Root dry paste in injection water to obtain a dilute of 200 ml; storing the dilute under cooling condition to obtain a first cool liquid; adding glucosum anhydricum of an amount in accordance with 4.5% mass fraction of the multi-component injection and injection water to the first cool liquid to obtain a 1000 ml liquid; adjusting the pH value of the 1000 ml liquid to 5.5-7.0 with a sodium hydroxide solution of 10% mass fraction to obtain a pH adjusted liquid; storing the pH adjusted liquid under cooling condition to obtain a second cool liquid;

subjecting the second cool liquid to ultrafiltration to obtain an ultrafiltrate; adding a proper amount of solubilizing auxiliary materials which are dissolved in a proper amount of injection water into the ultrafiltrate to obtain a solubilizing auxiliary materials-containing ultrafiltrate; adjusting the pH value of the solubilizing auxiliary materials-containing ultrafiltrate to 5.5-7.0 using the sodium hydroxide solution of 10% mass fraction to obtain a pH adjusted ultrafiltrate; filtering the pH adjusted ultrafiltrate to obtain a filtrate; encapsulating and sterilizing the filtrate to obtain the multi-component injection.

3. A multi-component injection comprising the following ingredients, by weight: 8.66-35.26 parts of albiflorin std, 1000.0-1700.0 parts of paeoniflorin, 11.13-68.07 parts of Oxypaeoniflorin, 12.20-52.98 parts of Benzoylpaeoniflorin, 0.667-1.617 parts of Benzoyloxypaeoniflorin, 1.915-3.202 parts of Mudanpioside J, 10.63-20.13 parts of galloylpaeoniflorin, 0.804-1.338 parts of Mudanpioside C, 10.0-200.0 parts of benzoic acid, 0.21-15.88 parts of gallic acid, 0.2396-0.6860 parts of ethyl gallate, 1.31-12.60 parts of catechin, 1.232-3.547 parts of Kaempferol-3-0-glucoside, 0.0500-0.4184 parts of scutellarin, 0.755-2.570 parts of quercetin-3-0-glucoside, 8.42-29.40 parts of Kaempferol-3-0-rutinoside, 4.036-7.695 parts of Kaempferol-3-0-sophoroside, 1.517-5.598 parts of quercetin-3-0-rutinoside, 200.0-500.0 parts of Hydroxysafflor yellow A, 0.316-0.774 parts of uracil, 13.77-30.56 parts of adenine, 20.50-44.99 parts of phenylalanine, 11.44-27.13 parts of uridine, 5.07-12.63 parts of adenosine, 8.00-24.11 parts of guanosine, 4.96-16.86 parts of butanedioic acid, 2.384-5.404 parts of p-hydroxybenzoic acid, 3.00-17.98 parts of p-coumaric acid, 4.837-7.806 parts of caffeic acid, and 3.83-8.59 parts of chlorogenic acid.

4. The multi-component injection according to claim 3, which is prepared by a method comprising the following steps of:

providing 100 g of safflower carthamus decoction pieces; leaching the safflower carthamus decoction pieces with 30% ethanol of 8 times the weight of the safflower carthamus decoction pieces for 8 hours to obtain a leach liquor; filtering the leach liquor to obtain a liquid medicine of 4-6 times the weight of the safflower carthamus decoction pieces; adding 95% ethanol to the liquid medicine to obtain an ethanol-containing liquid medicine having an ethanol volume content of 70%; storing the ethanol-containing liquid medicine under cooling condition for 48 hours to obtain a cool ethanol-containing liquid medicine; filtering the cool ethanol-containing liquid medicine to obtain a first filtrate; concentrating the first filtrate under reduced pressure to obtain a concentrate of 100 ml; adding 95% ethanol to the concentrate to obtain an ethanol-containing concentrate having an ethanol volume content of 80%; storing the ethanol-containing concentrate under cooling condition for 48 hours to obtain a cool ethanol-containing concentrate;

filtering the cool ethanol-containing concentrate to obtain a second filtrate;

recycling ethanol from the second filtrate to obtain an ethanol-reduced filtrate;

concentrating and vacuum drying the ethanol-reduced filtrate to obtain a safflower carthamus dry paste;

providing 100 g of Red Paeony Root decoction pieces; heating and boiling the Red Paeony Root decoction pieces with process water of 10 times the weight of the Red Paeony Root decoction pieces to obtain a first decoction after 2 hours slight boiling; filtering the first decoction to obtain filtrate I and a first dreg; boiling the first dreg with process water of 8 times the weight of the first dreg to obtain a second decoction after 1 hour slight boiling; filtering the second decoction to obtain filtrate II and a second dreg; mixing filtrate I and filtrate II to obtain a mixture; concentrating the mixture to obtain a first concentrate of 100 ml; adding a proper amount of gelatin solution to the first concentrate under stirring to obtain a gelatin-containing first concentrate; adding 95% ethanol to the gelatin-containing first concentrate to obtain an ethanol-containing first concentrate having an ethanol volume content of 70%; storing the ethanol-containing first concentrate under cooling condition for 24 hours to obtain a cool ethanol-containing first concentrate; filtering and concentrating the cool ethanol-containing first concentrate to obtain a second concentrate of 100 ml; extracting the second concentrate with water-saturated n-butanol for 4 times and using 50 ml water-saturated n-butanol for each time; combining extract liquors of the 4 times extraction to obtain a combined extract liquor; recycling n-butanol from the combined extract liquor to obtain a n-butanol-reduced extract liquor without alcohol taste; and vacuum drying the n-butanol-reduced extract liquor to obtain a Red Paeony Root dry paste;

providing the safflower carthamus dry paste and the Red Paeony Root dry paste each of a proper amount; dissolving the two dry pastes in injection water to obtain a dilute of 200 ml; storing the dilute under cooling condition to obtain a first cool liquid; adding glucosum anhydricum of an amount in accordance with 4.5% mass fraction of the multi-component injection and injection water to the first cool liquid to obtain a 1000 ml liquid; adjusting the pH value of the 1000 ml liquid to 5.5-7.0 with a sodium hydroxide solution of 10% mass fraction to obtain a pH adjusted liquid; storing the pH adjusted liquid under cooling condition to obtain a second cool liquid; subjecting the second cool liquid to ultrafiltration to obtain an ultrafiltrate; adding a proper amount of solubilizing auxiliary materials which are dissolved in a proper amount of injection water into the ultrafiltrate to obtain a solubilizing auxiliary materials-containing ultrafiltrate; adjusting the pH value of the solubilizing auxiliary materials-containing ultrafiltrate to 5.5-7.0 using the sodium hydroxide solution of 10% mass fraction to obtain a pH adjusted ultrafiltrate; filtering the pH adjusted ultrafiltrate to obtain a filtrate; encapsulating and sterilizing the filtrate to obtain the multi-component injection.

5. A multi-component injection comprising the following ingredients, by weight: 8.66-35.26 parts of albiflorin std, 1000.0-1700.0 parts of paeoniflorin, 11.13-68.07 parts of Oxypaeoniflorin, 12.20-52.98 parts of Benzoylpaeoniflorin, 0.667-1.617 parts of Benzoyloxypaeoniflorin, 1.915-3.202 parts of Mudanpioside J, 10.63-20.13 parts of galloylpaeoniflorin, 0.804-1.338 parts of Mudanpioside C, 10.0-200.0 parts of benzoic acid, 0.21-15.88 parts of gallic acid, 0.2396-0.6860 parts of ethyl gallate, 1.31-12.60 parts of catechin, 1.232-3.547 parts of Kaempferol-3-0-glucoside, 0.0500-0.4184 parts of scutellarin, 0.755-2.570 parts of quercetin-3-0-glucoside, 8.42-29.40 parts of Kaempferol-3-0-rutinoside, 4.036-7.695 parts of Kaempferol-3-0-sophoroside, 1.517-5.598 parts of quercetin-3-0-rutinoside, 200.0-500.0 parts of Hydroxysafflor yellow A, 0.316-0.774 parts of uracil, 13.77-30.56 parts of adenine, 20.50-44.99 parts of phenylalanine, 11.44-27.13 parts of uridine, 5.07-12.63 parts of adenosine, 8.00-24.11 parts of guanosine, 4.96-16.86 parts of butanedioic acid, 2.384-5.404 parts of p-hydroxybenzoic acid, 3.00-17.98 parts of p-coumaric acid, 4.837-7.806 parts of caffeic acid, 3.83-8.59 parts of chlorogenic acid, 6.51-69.39 parts of senkyunolide I (42), 1.55-18.27 parts of senkyunolide H, 4.30-14.22 parts of senkyunolide N, 2.460-5.648 parts of open-loop senkyunolide I, 1.55-10.74 parts of senkyunolide G, 1.43-8.67 parts of 3-hydroxyl-3-butylphthalide, 0.10-0.961 parts of senkyunolide A, and 7.66-47.15 parts of ferulaic acid.

6. The multi-component injection according to claim 5, which is prepared by a method comprising the following steps of:

filtering the cool ethanol-containing concentrate to obtain a second filtrate;

providing 100 g of Ligusticum wallichii decoction pieces and 100 g of Angelica sinensis decoction pieces; treating the Ligusticum wallichii decoction pieces and Angelica sinensis decoction pieces with a same treatment process as the Red Paeony Root decoction pieces except for keeping 300 ml of concentrate every time and extracting with 150 ml of water-saturated n-butanol each time, to obtain a third dry paste;

providing the safflower carthamus dry paste, the Red Paeony Root dry paste and the third dry paste each of a proper amount; dissolving the three dry pastes in injection water to obtain a dilute of 200 ml; storing the dilute under cooling condition to obtain a first cool liquid; adding glucosum anhydricum of an amount in accordance with 4.5% mass fraction of the multi-component injection and injection water to the first cool liquid to obtain a 1000 ml liquid; adjusting the pH value of the 1000 ml liquid to 5.5-7.0 with a sodium hydroxide solution of 10% mass fraction to obtain a pH adjusted liquid; storing the pH adjusted liquid under cooling condition to obtain a second cool liquid; subjecting the second cool liquid to ultrafiltration to obtain an ultrafiltrate; adding a proper amount of solubilizing auxiliary materials which are dissolved in a proper amount of injection water into the ultrafiltrate to obtain a solubilizing auxiliary materials-containing ultrafiltrate;

adjusting the pH value of the solubilizing auxiliary materials-containing ultrafiltrate to 5.5-7.0 using the sodium hydroxide solution of 10% mass fraction to obtain a pH adjusted ultrafiltrate; filtering the pH adjusted ultrafiltrate to obtain a filtrate;

encapsulating and sterilizing the filtrate to obtain the multi-component injection.

7. A multi-component injection comprising the following ingredients, by weight: 8.66-35.26 parts of albiflorin std, 1000.0-1700.0 parts of paeoniflorin, 11.13-68.07 parts of Oxypaeoniflorin, 12.20-52.98 parts of Benzoylpaeoniflorin, 0.667-1.617 parts of Benzoyloxypaeoniflorin, 1.915-3.202 parts of Mudanpioside J, 10.63-20.13 parts of galloylpaeoniflorin, 0.804-1.338 parts of Mudanpioside C, 10.0-200.0 parts of benzoic acid, 0.21-15.88 parts of gallic acid, 0.2396-0.6860 parts of ethyl gallate, 1.31-12.60 parts of catechin, 1.232-3.547 parts of Kaempferol-3-0-glucoside, 0.0500-0.4184 parts of scutellarin, 0.755-2.570 parts of quercetin-3-0-glucoside, 8.42-29.40 parts of Kaempferol-3-0-rutinoside, 4.036-7.695 parts of Kaempferol-3-0-sophoroside, 1.517-5.598 parts of quercetin-3-0-rutinoside, 200.0-500.0 parts of Hydroxysafflor yellow A, 0.316-0.774 parts of uracil, 13.77-30.56 parts of adenine, 20.50-44.99 parts of phenylalanine, 11.44-27.13 parts of uridine, 5.07-12.63 parts of adenosine, 8.00-24.11 parts of guanosine, 4.96-16.86 parts of butanedioic acid, 2.384-5.404 parts of p-hydroxybenzoic acid, 3.00-17.98 parts of p-coumaric acid, 4.837-7.806 parts of caffeic acid, 3.83-8.59 parts of chlorogenic acid, 6.51-69.39 parts of senkyunolide I (42), 1.55-18.27 parts of senkyunolide H, 4.30-14.22 parts of senkyunolide N, 2.460-5.648 parts of open-loop senkyunolide I, 1.55-10.74 parts of senkyunolide G, 1.43-8.67 parts of 3-hydroxyl-3-butylphthalide, 0.10-0.961 parts of senkyunolide A, 7.66-47.15 parts of ferulaic acid, 1.43-17.25 parts of protocatechualdehyde, 2.361-4.030 parts of protocatechuic acid, 2.776-6.845 parts of tanshinol, 5.07-12.78 parts of rosmarinic acid, 0.0697-0.4005 parts of salvianolic acid D, 1.123-4.732 parts of salvianolic acid C, 0.366-2.505 parts of salvianolic acid A, 0.429-0.945 parts of alkannic acid, and 4.00-11.00 parts of salvianolic acid B.

8. The multi-component injection according to claim 7, which is prepared by a method comprising the following steps:

filtering the cool ethanol-containing concentrate to obtain a second filtrate;

providing 100 g of Ligusticum wallichii decoction pieces, 100 g of radix salviae miltiorrhizae and 100 g of Angelica sinensis decoction pieces; treating the three decoction pieces with a same treatment process as the Red Paeony Root decoction pieces except for keeping 300 ml of concentrate every time and extracting with 150 ml of water-saturated n-butanol each time, to obtain a third dry paste;

9. The multi-component injection according to claim 1, wherein the multi-component injection is administered via an injection.

10. A method for treating sepsis in a subject in need thereof comprising administering to the subject the multi-component injection according to claim 1.

11. The multi-component injection according to claim 3, wherein the multi-component injection is administered via an injection.

12. The multi-component injection according to claim 5, wherein the multi-component injection is administered via an injection.

13. The multi-component injection according to claim 7, wherein the multi-component injection is administered via an injection.

14. A method for treating sepsis in a subject in need thereof comprising administering to the subject the multi-component injection according to claim 3.

15. A method for treating sepsis in a subject in need thereof comprising administering to the subject the multi-component injection according to claim 5.

16. A method for treating sepsis in a subject in need thereof comprising administering to the subject the multi-component injection according to claim 7.

17. A method of preparing a multi-component injection of claim 1 comprising the following steps:

providing 100 g of Red Paeony Root decoction pieces; heating and boiling the Red Paeony Root decoction pieces with process water of 10 times the weight of the Red Paeony Root decoction pieces to obtain a first decoction after 2 hours slight boiling;

filtering the first decoction to obtain filtrate I and a first dreg; boiling the first dreg with process water of 8 times the weight of the first dreg to obtain a second decoction after 1 hour slight boiling; filtering the second decoction to obtain filtrate II and a second dreg; mixing filtrate I and filtrate II to obtain a mixture; concentrating the mixture to obtain a first concentrate of 100 ml; adding a proper amount of gelatin solution to the first concentrate under stirring to obtain a gelatin-containing first concentrate; adding 95% ethanol to the gelatin-containing first concentrate to obtain an ethanol-containing first concentrate having an ethanol volume content of 70%;

storing the ethanol-containing first concentrate under cooling condition for 24 hours to obtain a cool ethanol-containing first concentrate; filtering and concentrating the cool ethanol-containing first concentrate to obtain a second concentrate of 100 ml;

extracting the second concentrate with water-saturated n-butanol for 4 times and using water-saturated n-butanol of 50 ml for each time; combining extract liquors of the 4 times extraction to obtain a combined extract liquor; recycling n-butanol from the combined extract liquor to obtain a n-butanol-reduced extract liquor without alcohol taste; and vacuum drying the n-butanol-reduced extract liquor to obtain a Red Paeony Root dry paste;

providing a proper amount of the Red Paeony Root dry paste; dissolving the Red Paeony Root dry paste in injection water to obtain a dilute of 200 ml; storing the dilute under cooling condition to obtain a first cool liquid; adding glucosum anhydricum of an amount in accordance with 4.5% mass fraction of the multi-component injection and injection water to the first cool liquid to obtain a 1000 ml liquid; adjusting the pH value of the 1000 ml liquid to 5.5-7.0 with a sodium hydroxide solution of 10% mass fraction to obtain a pH adjusted liquid; storing the pH adjusted liquid under cooling condition to obtain a second cool liquid; subjecting the second cool liquid to ultrafiltration to obtain an ultrafiltrate; adding a proper amount of solubilizing auxiliary materials which are dissolved in a proper amount of injection water into the ultrafiltrate to obtain a solubilizing auxiliary materials-containing ultrafiltrate; adjusting the pH value of the solubilizing auxiliary materials-containing ultrafiltrate to 5.5-7.0 using the sodium hydroxide solution of 10% mass fraction to obtain a pH adjusted ultrafiltrate; filtering the pH adjusted ultrafiltrate to obtain a filtrate; encapsulating and sterilizing the filtrate to obtain the multi-component injection.

18. A method of preparing a multi-component injection of claim 3 comprising the following steps:

providing 100 g of safflower carthamus decoction pieces; leaching the safflower carthamus decoction pieces with 30% ethanol of 8 times the weight of the safflower carthamus decoction pieces for 8 hours to obtain a leach liquor; filtering the leach liquor to obtain a liquid medicine of 4-6 times the weight of the safflower carthamus decoction pieces; adding 95% ethanol to the liquid medicine to obtain an ethanol-containing liquid medicine having an ethanol volume content of 70%; storing the ethanol-containing liquid medicine under cooling condition for 48 hours to obtain a cool ethanol-containing liquid medicine; filtering the cool ethanol-containing liquid medicine to obtain a first filtrate; concentrating the first filtrate under reduced pressure to obtain a concentrate of 100 ml; adding 95% ethanol to the concentrate to obtain an ethanol-containing concentrate having an ethanol volume content of 80%; storing the ethanol-containing concentrate under cooling condition for 48 hours to obtain a cool ethanol-containing concentrate; filtering the cool ethanol-containing concentrate to obtain a second filtrate; recycling ethanol from the second filtrate to obtain an ethanol-reduced filtrate; concentrating and vacuum drying the ethanol-reduced filtrate to obtain a safflower carthamus dry paste;

extracting the second concentrate with water-saturated n-butanol for 4 times and using 50 ml water-saturated n-butanol for each time; combining extract liquors of the 4 times extraction to obtain a combined extract liquor; recycling n-butanol from the combined extract liquor to obtain a n-butanol-reduced extract liquor without alcohol taste; and vacuum drying the n-butanol-reduced extract liquor to obtain a Red Paeony Root dry paste;

providing the safflower carthamus dry paste and the Red Paeony Root dry paste each of a proper amount; dissolving the two dry pastes in injection water to obtain a dilute of 200 ml; storing the dilute under cooling condition to obtain a first cool liquid;

adding glucosum anhydricum of an amount in accordance with 4.5% mass fraction of the multi-component injection and injection water to the first cool liquid to obtain a 1000 ml liquid; adjusting the pH value of the 1000 ml liquid to 5.5-7.0 with a sodium hydroxide solution of 10% mass fraction to obtain a pH adjusted liquid; storing the pH adjusted liquid under cooling condition to obtain a second cool liquid; subjecting the second cool liquid to ultrafiltration to obtain an ultrafiltrate; adding a proper amount of solubilizing auxiliary materials which are dissolved in a proper amount of injection water into the ultrafiltrate to obtain a solubilizing auxiliary materials-containing ultrafiltrate; adjusting the pH value of the solubilizing auxiliary materials-containing ultrafiltrate to 5.5-7.0 using the sodium hydroxide solution of 10% mass fraction to obtain a pH adjusted ultrafiltrate; filtering the pH adjusted ultrafiltrate to obtain a filtrate; encapsulating and sterilizing the filtrate to obtain the multi-component injection.

19. A method of preparing a multi-component injection of claim 5 comprising the following steps:

providing the safflower carthamus dry paste, the Red Paeony Root dry paste and the third dry paste each of a proper amount; dissolving the three dry pastes in injection water to obtain a dilute of 200 ml; storing the dilute under cooling condition to obtain a first cool liquid; adding glucosum anhydricum of an amount in accordance with 4.5% mass fraction of the multi-component injection and injection water to the first cool liquid to obtain a 1000 ml liquid; adjusting the pH value of the 1000 ml liquid to 5.5-7.0 with a sodium hydroxide solution of 10% mass fraction to obtain a pH adjusted liquid; storing the pH adjusted liquid under cooling condition to obtain a second cool liquid; subjecting the second cool liquid to ultrafiltration to obtain an ultrafiltrate; adding a proper amount of solubilizing auxiliary materials which are dissolved in a proper amount of injection water into the ultrafiltrate to obtain a solubilizing auxiliary materials-containing ultrafiltrate; adjusting the pH value of the solubilizing auxiliary materials-containing ultrafiltrate to 5.5-7.0 using the sodium hydroxide solution of 10% mass fraction to obtain a pH adjusted ultrafiltrate; filtering the pH adjusted ultrafiltrate to obtain a filtrate; encapsulating and sterilizing the filtrate to obtain the multi-component injection.

20. A method of preparing a multi-component injection of claim 7 comprising the following steps: