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可注射聚乳酸-乙醇酸共聚物阿德福韦微球:慢性乙型肝炎长期治疗的新途径。

Injectable PLGA Adefovir microspheres; the way for long term therapy of chronic hepatitis-B.

机构信息

Department of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmacy, Zagazig University, Zagazig, Egypt.

Department of Internal Medicine, Faculty of Medicine, Zagazig University, Zagazig, Egypt.

出版信息

Eur J Pharm Sci. 2018 Jun 15;118:24-31. doi: 10.1016/j.ejps.2018.03.016. Epub 2018 Mar 16.

Abstract

For patient convenience, sustained release Adefovir Poly-d,l-lactic-co-glycolic acid (PLGA) microspheres were formulated to relieve the daily use of the drug which is a problem for patients treated from chronic hepatitis-B. PLGA microspheres were prepared and characterized by entrapment efficiency, particle size distribution and scanning electron microscopy (SEM). In-vitro release and in-vivo studies were carried out. Factors such as drug: polymer ratio, polymer viscosity and polymer lactide content were found to be important variables for the preparation of PLGA Adefovir microspheres. Fourier transform infrared (FTIR) analysis and differential scanning calorimetry (DSC) were performed to determine any drug-polymer interactions. One way analysis of variance (ANOVA) was employed to analyze the pharmacokinetic parameters after intramuscular injection of the pure drug and the selected PLGA microspheres into rats. FTIR and DSC revealed a significant interaction between the drug and the polymer. Reports of SEM before and after 1 and 24 h release showed that the microspheres had nonporous smooth surface even after 24 h release. The entrapment efficiency ranged between 55.83 and 86.95% and in-vitro release studies were continued for 16, 31 and 90 days. The pharmacokinetic parameters and statistical analysis showed a significant increase in the T AUC and MRT, and a significant decrease in the C of the tested formulation (p < 0.05). Results demonstrated that PLGA Adefovir microspheres could be used for long-term treatment of chronic hepatitis-B instead of the daily dose used by the patient.

摘要

为了方便患者,研制了阿德福韦酯聚(丙交酯-乙交酯)(PLGA)缓释微球,以缓解慢性乙型肝炎患者每天使用药物的问题。通过包封效率、粒径分布和扫描电子显微镜(SEM)对 PLGA 微球进行了表征。进行了体外释放和体内研究。发现药物:聚合物比、聚合物粘度和聚合物丙交酯含量等因素是制备 PLGA 阿德福韦微球的重要变量。进行了傅里叶变换红外(FTIR)分析和差示扫描量热法(DSC)以确定药物-聚合物相互作用。采用单因素方差分析(ANOVA)分析肌肉内注射纯药物和选定的 PLGA 微球后大鼠的药代动力学参数。FTIR 和 DSC 显示药物和聚合物之间存在显著相互作用。释放前和释放 1 和 24 小时后的 SEM 报告显示,即使在释放 24 小时后,微球仍具有无孔光滑的表面。包封效率在 55.83%至 86.95%之间,体外释放研究持续了 16、31 和 90 天。药代动力学参数和统计分析显示,测试制剂的 T AUC 和 MRT 显著增加,C 显著降低(p<0.05)。结果表明,PLGA 阿德福韦酯微球可用于慢性乙型肝炎的长期治疗,而不是患者每天使用的剂量。

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