以强力霉素为原料制备注射用冻干粉的研制与评价

E. A. Saliy, A. Y. Honcharuk, O. Getalo, H. Tarasenko
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引用次数: 1

摘要

乌克兰药品市场上多西环素药物的范围非常有限,以固体形式(胶囊和片剂)为代表,而通过肠外给药可以提供药物的快速效果和最大的生物利用度。本研究的对象是将盐酸强力霉素以冻干液的形式制备注射用溶液。在药物的开发过程中,考虑到多西环素水溶液是pH依赖性的,并且在长期储存过程中倾向于改变溶液的pH值。因此,辅料,如稳定剂和抗氧化剂提供缓冲性能和稳定性的溶液被引入到组合物。根据研究结果,选择了冻干粉的最佳配方,开发了活性炭固溶阶段的生产工艺,使冻干粉具有孔隙结构良好、无裂开、裂纹和裂隙、耐震动的特点,制备的肠外给药液在加速贮藏过程中以“着色度”质量指标稳定。研究发现,冻干剂形式的多西环素水合物具有广泛的抗菌活性。两种药物的体外比较研究证实了它们对引起人类传染病的细菌的抑菌作用是等效的,这两种药物分别是注射用冻干液和100毫克水合强力霉素硬明胶胶囊。
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DEVELOPMENT AND EVALUATION OF LYOPHILIZED POWDER TO PREPARE SOLUTION FOR INJECTIONS BASED ON DOXYCYCLINE
The range of doxycycline drugs on the pharmaceutical market of the Ukraine is very limited and is represented by solid forms (capsules and tablets) while a rapid effect and maximum bioavailability of the drug can be provided by parenteral administration. The object of the study is the drug doxycycline hyclate in the form of lyophilisate to prepare solution for injections. During the development of the drug it was taken into account that aqueous doxycycline solution is pH dependent and tends to shift the solution pH during long-term storage. Therefore, excipients such as stabilizer and antioxidant providing buffering properties and stability of the solution were introduced into the composition. According to the research results an optimal composition of lyophilized powder was selected, the production technology with the stage of solution treatment with activated carbon was developed which allowed to obtain lyophilized powder with a well-formed porous mass without splits, cracks and fissures, resistant to shaking, and the prepared solution for parenteral administration is stable by the «Degree of coloration» quality indicator during accelerated storage regimen. It was found that doxycycline hyclate in the form of a lyophilisate shows a wide range of antibacterial activity. Comparative studies in vitro for two drugs, in the form of lyophilisate with doxycycline hyclate for injections and hard gelatin capsules with 100 mg of doxycycline hyclate, confirm equivalence of their bacteriostatic action against bacteria causing infectious diseases in humans.
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