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作 者:陈小伟 Chen Xiaowei(Lunan Pharmaceutical Group Co.,Ltd.,Linyi 276000,China)
机构地区:[1]鲁南制药集团股份有限公司,山东临沂276000
出 处:《山东化工》2021年第17期61-62,共2页Shandong Chemical Industry
摘 要:目的:制备复方阿昔莫司缓释微丸并对其体外释放特性进行研究。方法:采用流化床包衣技术制备阿托伐他汀钙速释微丸;挤出滚圆法制备阿昔莫司载药丸芯,以乙基纤维素N-100为缓释包衣材料,流化床包衣技术制备阿昔莫司缓释微丸;高效液相色谱法测定阿托伐他汀钙、阿昔莫司的释放度。结果:阿托伐他汀钙微丸溶出迅速,阿昔莫司缓释微丸具有较好的缓释效果。结论:制备的复方阿昔莫司缓释微丸具有较理想的释放效果。Objective:To prepare compound acipimox sustained-release pellets and investigate the drug release mechanism in vitro.Methods:At first,atorvastatin calcium pellets were prepared by the fluid-bed.Acipimox pellets were prepared by extrusion-spheronization equipment,and then coated by ethylcellulose N-100 and hydroxypropyl cellulose as porogen using the fluid-bed.The dissolution of the pellets were determined by HPLC respectively.Results:Atorvastatin calcium released immediately and the acipimox pellets had a remarkable sustained-release property in vitro.Conclusion:The preprared pellets exhibited more ideal release characteristics in vitro.
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