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CN105560234A - Medicine composition for treating oral and maxillofacial inflammation - Google Patents

Medicine composition for treating oral and maxillofacial inflammation Download PDF

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Publication number
CN105560234A
CN105560234A CN201610091522.6A CN201610091522A CN105560234A CN 105560234 A CN105560234 A CN 105560234A CN 201610091522 A CN201610091522 A CN 201610091522A CN 105560234 A CN105560234 A CN 105560234A
Authority
CN
China
Prior art keywords
compound
oral
pharmaceutical composition
maxillofacial surgery
treatment
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN201610091522.6A
Other languages
Chinese (zh)
Inventor
郑海英
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to CN201610091522.6A priority Critical patent/CN105560234A/en
Publication of CN105560234A publication Critical patent/CN105560234A/en
Pending legal-status Critical Current

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Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/438The ring being spiro-condensed with carbocyclic or heterocyclic ring systems
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Preparation (AREA)

Abstract

The invention relates to a medicine composition for treating the oral and maxillofacial inflammation. The composition is prepared from an effective quantity of a compound and a pharmaceutically-acceptable carrier. The compound has the structure (shown in the description). The compound has a remarkable effect on pathogenic bacteria causing the oral and maxillofacial inflammation, and a clinically-effective new medicine composition can be developed.

Description

A kind of pharmaceutical composition for the treatment of oral and maxillofacial surgery inflammation
Technical field
The present invention relates to field of medicaments, specifically, the present invention relates to a kind of pharmaceutical composition for the treatment of oral and maxillofacial surgery inflammation.
Background technology
The teeth inflammation disease that oral and maxillofacial surgery inflammation is mainly caused by local factor.As failed treatment in time, inflammation can be diffused into periodontal membrane, alveolar bone and cementum by gingiva to deep layer and develop into oral and maxillofacial surgery inflammation.
Summary of the invention
The object of the present invention is to provide a kind of pharmaceutical composition for the treatment of oral and maxillofacial surgery inflammation.
In order to realize object of the present invention, the invention provides a kind of compound for the treatment of oral and maxillofacial surgery inflammation, this compound has having structure:
The present invention also provides a kind of pharmaceutical composition for the treatment of oral and maxillofacial surgery inflammation, and described pharmaceutical composition includes the compound of effective amount and pharmaceutically acceptable carrier, and described compound has having structure:
Preferably, described pharmaceutically acceptable carrier is diluent, disintegrating agent, binding agent, lubricant, stabilizing agent or corrigent.
Preferably, described diluent is sugar derivatives, starch derivatives or cellulose derivative.
Preferably, described diluent is lactose.
Preferably, described pharmaceutical composition is powder, microgranule, granule, capsule or tablet.
The present invention also provides the purposes of compound in the medicine of preparation treatment oral and maxillofacial surgery inflammation, and this compound has having structure:
Preferably, described infection is caused by day ditch dimension enterobacteria ATCC33028.
The present invention also provides the purposes of compound in the medicine of preparation vitro inhibition day ditch dimension enterobacteria ATCC33028, and this compound has having structure:
Term used herein " pharmaceutically acceptable " refers to not eliminate the biologic activity of compound as herein described or the material of character, as carrier or diluent.This kind of material is applied to and individual does not cause undesirable biological action or not with harmful way and any component interaction comprised in its compositions.
" pharmaceutically acceptable carrier " comprises any and all solvents as the term is employed herein, disperse medium, coating material, surfactant, antioxidant, antiseptic (such as antibacterial, antifungal), isotonic agent, absorption delay agent, salt, antiseptic, drug stabilizing agent, binding agent, excipient, disintegrating agent, lubricant, sweeting agent, correctives, dyestuff etc. and its combination, this is well-known to those skilled in the art (for example, see Remington'sPharmaceuticalSciences, 18thEd.MackPrintingCompany, 1990, pp.1289-1329).Except with except the inconsistent carrier of active component, consider to use any conventional carrier in treatment or pharmaceutical composition.
Compound of the present invention, for the pathogen Be very effective causing oral and maxillofacial surgery inflammation, can be developed to pharmaceutical composition effectively new clinically.
Detailed description of the invention
Below by way of the description of detailed description of the invention, the invention will be further described, but this is not limitation of the present invention, those skilled in the art are according to basic thought of the present invention, various amendment or improvement can be made, but only otherwise depart from basic thought of the present invention, all within the scope of the present invention.
The research of the purposes of experimental example the compounds of this invention in the medicine of preparation vitro inhibition day ditch dimension enterobacteria ATCC33028
Bacteriostatic test
Use following compounds, adopt filter paper enzyme classical in this area to carry out bacteriostatic test, wherein:
The structural formula of target compound is:
For examination strain day ditch dimension enterobacteria ATCC33028 purchased from Feng Shou (Shanghai) bio tech ltd.
Culture fluid
Nutrient agar and nutrient broth, purchased from Chen Yu experimental facilities company limited of BeiJing ZhongKe.
Test method
Day ditch dimension enterobacteria ATCC33028 is inoculated in agar plate nutritional solution plane, evenly gathers during inoculation.
Take target compound 0.01 gram, add 25000 ml sterile waters, ultrasonic 30 minutes, then the filtering with microporous membrane of 0.22 μm, obtained solution.The aseptic circular filter paper sheet of tweezer, sprays above-mentioned solution to complete wetting, is attached in the agar plate nutritional solution plane of inoculated bacteria.Agar plate is placed in the incubator of 37 DEG C, incubation 4 hours.Measure the diameter of bacterial restrain.Measure and average for 3 times.
1.4 result
The average diameter of the bacterial restrain of day ditch dimension enterobacteria ATCC33028 is 14.26mm, and this shows that target compound has the effect of extremely strong vitro inhibition day ditch dimension enterobacteria ATCC33028.

Claims (9)

1. treat a compound for oral and maxillofacial surgery inflammation, it is characterized in that, this compound has having structure:
2. treat a pharmaceutical composition for oral and maxillofacial surgery inflammation, it is characterized in that, described pharmaceutical composition includes the compound of effective amount and pharmaceutically acceptable carrier, and described compound has having structure:
3. the pharmaceutical composition for the treatment of oral and maxillofacial surgery inflammation according to claim 2, is characterized in that, described pharmaceutically acceptable carrier is diluent, disintegrating agent, binding agent, lubricant, stabilizing agent or corrigent.
4. the pharmaceutical composition for the treatment of oral and maxillofacial surgery inflammation according to claim 3, is characterized in that, described diluent is sugar derivatives, starch derivatives or cellulose derivative.
5. the pharmaceutical composition for the treatment of oral and maxillofacial surgery inflammation according to claim 4, is characterized in that, described diluent is lactose.
6. the pharmaceutical composition for the treatment of oral and maxillofacial surgery inflammation according to claim 3, is characterized in that, described pharmaceutical composition is powder, microgranule, granule, capsule or tablet.
7. the purposes of compound in the medicine of preparation treatment oral and maxillofacial surgery inflammation, it is characterized in that, this compound has having structure:
8. purposes according to claim 7, is characterized in that, described infection is tieed up enterobacteria ATCC33028 by day ditch and caused.
9. the purposes of compound in the medicine of preparation vitro inhibition day ditch dimension enterobacteria ATCC33028, it is characterized in that, this compound has having structure:
CN201610091522.6A 2016-02-18 2016-02-18 Medicine composition for treating oral and maxillofacial inflammation Pending CN105560234A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201610091522.6A CN105560234A (en) 2016-02-18 2016-02-18 Medicine composition for treating oral and maxillofacial inflammation

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201610091522.6A CN105560234A (en) 2016-02-18 2016-02-18 Medicine composition for treating oral and maxillofacial inflammation

Publications (1)

Publication Number Publication Date
CN105560234A true CN105560234A (en) 2016-05-11

Family

ID=55871259

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201610091522.6A Pending CN105560234A (en) 2016-02-18 2016-02-18 Medicine composition for treating oral and maxillofacial inflammation

Country Status (1)

Country Link
CN (1) CN105560234A (en)

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1994029317A1 (en) * 1993-06-10 1994-12-22 Merck & Co., Inc. Process of making spirocycles and analogs thereof
WO2004092179A1 (en) * 2003-04-14 2004-10-28 Nippon Soda Co. Ltd. Spiro derivative, production process, and antioxidant
WO2011047481A1 (en) * 2009-10-23 2011-04-28 Merck Frosst Canada Ltd. Novel spiro compounds useful as inhibitors of stearoyl-coenzyme a delta-9 desaturase
WO2011141474A1 (en) * 2010-05-12 2011-11-17 Boehringer Ingelheim International Gmbh Novel ccr2 receptor antagonists, method for producing the same, and use thereof as medicaments

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1994029317A1 (en) * 1993-06-10 1994-12-22 Merck & Co., Inc. Process of making spirocycles and analogs thereof
WO2004092179A1 (en) * 2003-04-14 2004-10-28 Nippon Soda Co. Ltd. Spiro derivative, production process, and antioxidant
WO2011047481A1 (en) * 2009-10-23 2011-04-28 Merck Frosst Canada Ltd. Novel spiro compounds useful as inhibitors of stearoyl-coenzyme a delta-9 desaturase
WO2011141474A1 (en) * 2010-05-12 2011-11-17 Boehringer Ingelheim International Gmbh Novel ccr2 receptor antagonists, method for producing the same, and use thereof as medicaments

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
AHMED H. ABDELAZEEM,ET AL.: "Novel pyrazolopyrimidine derivatives targeting COXs and iNOS enzymes; design, synthesis and biological evaluation as potential anti-inflammatory agents", 《EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES》 *

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Legal Events

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PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication

Application publication date: 20160511

RJ01 Rejection of invention patent application after publication