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布洛芬原位凝胶体外溶蚀和药物释放度考察 被引量:7

Study of in vitro dissolution and drug release for ibuprofen in-situ gel
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摘要 目的对布洛芬原位凝胶剂进行体外溶蚀和释放度考察,探索处方中布洛芬与PVP K30的最佳比例。方法采用无膜溶出法,根据公式凝胶累积溶蚀百分率=(W1-Wt)/(W1-W0)来计算溶蚀率;根据标准曲线,利用峰面积计算药物累积释放率。结果当布洛芬∶PVP K30=1∶1时,制成的凝胶的性质最好。随着时间的递增,凝胶的溶蚀率和释放率显著增加。结论布洛芬凝胶剂具有良好的缓释效果。 Objective The erosion and dissolution for in-situibuprofen was studied in order to optimize the ratio of ibuprofen and PVP K30 in the prescription.Method The membrane-free method was used.The erosion rate was calculated according to the formula,cumulative erosion percentage=(W1-Wt)/(W1-W0).The drug cumulative release rate was calculated by using the peak area according to the standard curve.Results When the proportion of ibuprofen and PVP K30 was 1∶1,the ratio of erosion and release increased significantly with the increase of time.Conclusion The in situibuprofen gels showed excellent sustained release characteristics.
出处 《西北药学杂志》 CAS 2013年第5期513-514,共2页 Northwest Pharmaceutical Journal
基金 陕西省科学技术研究发展计划项目(编号:2009k19-03) 陕西省创新能力建设项目--陕药集团技术中心.原位凝胶制剂研究(2010)
关键词 布洛芬 原位凝胶 溶蚀率 释放度 ibuprofen in situ gel erosion rate release rate
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