含有泮托拉唑钠的抗胃微粒:稳定性研究和体内抗溃疡活性

R. Raffin, L. M. Colomé, E. Schapoval, D. S. Jornada, A. Pohlmann, S. Guterres
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引用次数: 21

摘要

本研究的目的是验证载泮托拉唑微颗粒在体内保护胃粘膜免受溃疡形成的能力,并评估其在加速条件下的稳定性。以Eudragit®S100为聚合物,采用喷雾干燥法制备了载泮托拉唑微颗粒。装有载药微粒的透明玻璃小瓶在40°C和75% RH条件下保存6个月。在UVA光下测试了其光稳定性。大鼠口服无水乙醇诱导溃疡。检测碳酸氢钠溶液、泮托拉唑溶液和载药微粒。在加速稳定性研究中,药物含量表现出完全的包封性,认为是稳定的。泛托拉唑的微胶囊化降低了其光降解。体内评价表明,微颗粒的溃疡指数低于溶液。肠道微颗粒在加速条件下具有可接受的稳定性,并且有效地保护胃免受乙醇引起的溃疡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Gastro-Resistant Microparticles Containing Sodium Pantoprazole: Stability Studies and In Vivo Anti-Ulcer Activity
The aim of the present work was to verify the in vivo capacity of pantoprazole-loaded microparticles to protect the gastric mucosa against ulcer formation and to evaluate their stability under accelerated conditions. Pantoprazole- loaded microparticles were prepared by spray-drying in pilot scale, using Eudragit ® S100 as polymer. Transparent glass vials containing drug-loaded microparticles were stored for 6 months at 40°C and 75% RH. Photostability was tested un- der UVA light. Ulcers were induced by the oral administration of absolute ethanol to rats. Sodium bicarbonate solution, pantoprazole solution and drug-loaded microparticles were tested. Regarding the drug content during the accelerate stabil- ity study, samples showed complete encapsulation efficiency and were considered stable. The microencapsulation of pan- toprazole reduced its photodegradation. The in vivo evaluation showed that the microparticles presented ulcer index lower than the solutions. Enteric microparticles had acceptable stability under accelerated conditions and were efficient in pro- tecting the stomach against ulceration caused by ethanol.
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