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机构地区:[1]华侨大学生物医学学院,福建泉州362021 [2]广州优米健医药科技有限公司,广东广州510060
出 处:《华侨大学学报(自然科学版)》2017年第2期175-179,共5页Journal of Huaqiao University(Natural Science)
基 金:福建省自然科学基金资助项目(2015J01342)
摘 要:采用粉末直接压片法制备二乙基三胺五乙酸(DTPA)胃漂浮囊心缓释片,并对其进行体外漂浮性能、释放性能和释药机理研究.结果表明:DTPA胃漂浮囊心缓释片在人工胃液中可以立即起漂,持续漂浮时间长达24h,其释药过程用Korsmeyer-Peppas(T_(lag))模型拟合的拟合度最好;同时,应用Harland方程进行验证,证明该制剂的释药过程主要为扩散和骨架溶蚀共同作用.通过该法制备的胃漂浮囊心缓释片具有起漂时间短、持续漂浮时间长、缓释效果好,漂浮性能不受制剂辅料和制备工艺的影响等优点.Diethylene triamine pentaacetic acid(DTPA)intragastric floating sustained-release and capsuleheart tablets were prepared by pressing the powder directly,and the in vitro floatation,release characteristics and release mechanism were studied.Results indicated that DTPA intragastric floating sustained-release and capsule-heart tablets could float immediately in the simulated gastric fluid,floating up to 24 hours continuously,and the in vitro drug release with Korsmeyer-Peppas(T(lag))model fitting was the best.At the same time,it was proved that the drug release was controlled by diffusion and matrix erosion together using Harland equation for validation.In conclusion,intragastric floating sustained-release and capsule-heart tablets have the advantages of short floating lag time,long floating duration and good sustained-release effect.In addition,the floating characteristics were not affected by the excipients and the preparation technologies.
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