CN1078452A - Implantable porous ceramic anti-tuberculosis, anti-cancer, anti-inflammatory sustained-release body - Google Patents
Implantable porous ceramic anti-tuberculosis, anti-cancer, anti-inflammatory sustained-release body Download PDFInfo
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- CN1078452A CN1078452A CN 92111035 CN92111035A CN1078452A CN 1078452 A CN1078452 A CN 1078452A CN 92111035 CN92111035 CN 92111035 CN 92111035 A CN92111035 A CN 92111035A CN 1078452 A CN1078452 A CN 1078452A
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Abstract
植入式多孔陶瓷抗痨抗癌抗炎缓释体,本发明涉 及骨结核、骨肿瘤、骨髓炎病灶内释放药物的植入式 缓释体,其主要克服常规治疗用药,其病灶内浓度低, 难以控制残余细菌的生存繁殖,以致造成患者截肢致 残等问题,本发明提供一种由羟基磷灰石、磷酸铝为 主晶相,加入适量的氧化硅,氧化钙、碳酸钾,混合煅 烧成的多孔陶瓷缓释体,其缓释体中空圆柱腔内有药 物,将它植入骨病患者病灶局部,使之缓慢释放,治疗 骨结核有效率95.4%,骨肿瘤有效率82%。Implantable porous ceramic anti-tuberculosis, anti-cancer and anti-inflammatory sustained-release body, the invention relates to and bone tuberculosis, bone tumors, and implantable drugs that release drugs in lesions of osteomyelitis Sustained-release body, which mainly overcomes conventional treatment drugs, and its concentration in the lesion is low, It is difficult to control the survival and reproduction of residual bacteria, resulting in amputation of patients Residual problems, the present invention provides a kind of hydroxyapatite, aluminum phosphate as Main crystal phase, add appropriate amount of silicon oxide, calcium oxide, potassium carbonate, mix and calcined Sintered porous ceramic sustained-release body, the hollow cylindrical cavity of the slow-release body has drug implanted into the lesion of patients with bone disease, so that it can be released slowly, and the treatment The effective rate of bone tuberculosis is 95.4%, and the effective rate of bone tumor is 82%.
Description
本发明涉及骨结核、骨肿痛、骨髓炎病灶内释放药物的植入式缓释体。The invention relates to an implantable slow-release body for releasing drugs in bone tuberculosis, bone swelling and pain, and osteomyelitis lesions.
目前对骨结核、骨肿痛、骨髓炎等常见病的治疗,通常采用常规的手术病灶清除手术后,不但大量长期应用抗痨药,抗结核药,因此易产生药的副作用,而且疗效也不佳,容易复发,甚至有些患者数十年不愈,经常用药(注射、口服)病灶内浓度低,难以控制残余细菌的生长繁殖。对于恶性骨肿瘤的治疗方法,往往采取截肢,致残率高。At present, the treatment of common diseases such as bone tuberculosis, bone swelling and pain, osteomyelitis, etc. usually adopts conventional surgical focus debridement. It is easy to relapse, and even some patients have not healed for decades, and the concentration in the lesion is low due to frequent medication (injection, oral administration), making it difficult to control the growth and reproduction of residual bacteria. For the treatment of malignant bone tumors, amputation is often adopted, and the disability rate is high.
本发明的目的是,提供一种多孔陶瓷体,使陶瓷体内的药物缓慢释放,能在病灶局部有效地杀灭病菌和肿瘤细胞,同时使病变区浓度高,全身浓度低,又可防止药物副作用,以达到提高治俞率,重建肢体的功能的目的。The purpose of the present invention is to provide a porous ceramic body, which can release the medicine in the ceramic body slowly, and can effectively kill the bacteria and tumor cells in the local lesion, and at the same time, the concentration in the lesion area is high, the concentration in the whole body is low, and the side effects of the medicine can be prevented. , in order to achieve the purpose of improving the treatment rate and rebuilding the functions of the limbs.
实现本发明的具体技术方案是,这种多孔陶瓷药物载体,由羟基磷灰石、磷酸铝为主晶相,加入适量的熔剂氧化物进行混合配制,在高温煅烧下,制成一个中空圆柱体,其中空圆柱体四周有均布的释放微孔。The specific technical solution for realizing the present invention is that the porous ceramic drug carrier is made of hydroxyapatite and aluminum phosphate as the main crystal phase, mixed and prepared by adding an appropriate amount of flux oxide, and is calcined at a high temperature to form a hollow cylinder , where the hollow cylinder is surrounded by evenly distributed release micropores.
多孔陶瓷载体的制备及实施例:Preparation and Examples of Porous Ceramic Carriers:
它由羟基磷灰石、磷酸铝、氧化硅、氧化钙、磷酸钾组成,其配方:It is composed of hydroxyapatite, aluminum phosphate, silicon oxide, calcium oxide, potassium phosphate, its formula:
以羟基磷灰石及磷酸铝为主要原料,加入适量的熔剂氧化物,配制下列两种配方:Using hydroxyapatite and aluminum phosphate as the main raw materials, adding an appropriate amount of flux oxides, the following two formulas are prepared:
制备工艺:Preparation Process:
配料→混合均匀 (950℃~1000℃)/(保温1hr) 煅烧→冷却 (120℃烘干2hr)/(加0.7%油酸) 球磨→加石腊和蜂蜡(干料量的30%)→加热熔化→搅拌→热压注成型→装钵(埋在Al2O3中烧成) (200~600℃)/() 排蜡 (1160~1200℃)/() 烧成→产品→超声波清洗→烘干→备用 Ingredients→mix evenly (950℃~1000℃)/(keep heat for 1hr) calcining→cooling (dry at 120℃ for 2hr)/(add 0.7% oleic acid) ball mill→add paraffin and beeswax (30% of dry material)→ Heating and melting→stirring→hot press injection molding→bottling (buried in Al 2 O 3 and firing) (200~600℃)/() wax removal (1160~1200℃)/() firing→product→ultrasonic cleaning →Drying→Standby
本发明提供的附图,为植入式多孔陶瓷缓释体结构图。图中,(1)缓释体,(2)圆柱空腔,(3)盖。The drawings provided by the present invention are structural diagrams of implantable porous ceramic slow-release bodies. In the figure, (1) slow-release body, (2) cylindrical cavity, (3) cover.
本发明多孔陶瓷药物载体的理化性能及临床效果:Physicochemical properties and clinical effects of the porous ceramic drug carrier of the present invention:
气孔率(%) 孔径(μm) 耐蚀性 生物相容性 毒性Porosity (%) Pore Size (μm) Corrosion Resistance Biocompatibility Toxicity
10~20 <50 良好 好 无10~20 <50 Good Good No
经200系列临床证明,作为抗结核(即抗痨)抗癌,抗炎药的载体,能在体内病灶局部持续半年释放高浓度的药物,无毒副作用,治疗骨结核有效率95.4%,骨肿瘤82%。It has been clinically proven by the 200 series that as a carrier of anti-tuberculosis (ie anti-tuberculosis) anti-cancer and anti-inflammatory drugs, it can release high-concentration drugs in local lesions in the body for half a year without toxic side effects, and the effective rate of treating bone tuberculosis is 95.4%. 82%.
Claims (4)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 92111035 CN1078452A (en) | 1992-09-21 | 1992-09-21 | Implantable porous ceramic anti-tuberculosis, anti-cancer, anti-inflammatory sustained-release body |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 92111035 CN1078452A (en) | 1992-09-21 | 1992-09-21 | Implantable porous ceramic anti-tuberculosis, anti-cancer, anti-inflammatory sustained-release body |
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| Publication Number | Publication Date |
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| CN1078452A true CN1078452A (en) | 1993-11-17 |
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| CN 92111035 Pending CN1078452A (en) | 1992-09-21 | 1992-09-21 | Implantable porous ceramic anti-tuberculosis, anti-cancer, anti-inflammatory sustained-release body |
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Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1069887C (en) * | 1998-11-26 | 2001-08-22 | 瑞安大药厂股份有限公司 | Process for preparing porous ceramic material |
| CN1537526B (en) * | 1995-06-13 | 2010-12-08 | Z·曼索尔 | Method for delivering substances to the skin and compositions used therein |
| CN104220649A (en) * | 2012-04-09 | 2014-12-17 | 株式会社小糸制作所 | Apatite crystal |
| CN104446399A (en) * | 2014-11-14 | 2015-03-25 | 苏州蔻美新材料有限公司 | Composite biological ceramic material and preparation method thereof |
| CN106691598A (en) * | 2017-02-06 | 2017-05-24 | 浙江荣诚医疗科技有限公司 | Gold mark with coating and coating location device |
-
1992
- 1992-09-21 CN CN 92111035 patent/CN1078452A/en active Pending
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1537526B (en) * | 1995-06-13 | 2010-12-08 | Z·曼索尔 | Method for delivering substances to the skin and compositions used therein |
| CN1069887C (en) * | 1998-11-26 | 2001-08-22 | 瑞安大药厂股份有限公司 | Process for preparing porous ceramic material |
| CN104220649A (en) * | 2012-04-09 | 2014-12-17 | 株式会社小糸制作所 | Apatite crystal |
| US9371231B2 (en) | 2012-04-09 | 2016-06-21 | Koito Manufacturing Co., Ltd. | Apatite crystal |
| CN104446399A (en) * | 2014-11-14 | 2015-03-25 | 苏州蔻美新材料有限公司 | Composite biological ceramic material and preparation method thereof |
| CN106691598A (en) * | 2017-02-06 | 2017-05-24 | 浙江荣诚医疗科技有限公司 | Gold mark with coating and coating location device |
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