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盐酸丁咯地尔缓释片的制备及体外释放度研究 被引量:4

Preparation and in vitro Release of Buflomedil Hydrochloride Sustained-release Tablets
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摘要 以羟丙甲纤维素和丙烯酸树脂为骨架材料 ,5 %乙基纤维素乙醇溶液作为粘合剂 ,采用湿法制粒压片 ,制备盐酸丁咯地尔缓释片 ,进行体外释放度试验 ,并与进口缓释片进行比较。结果表明 :研制缓释片的缓释效果良好 ,药物的释放符合一级动力学规律。 With hydroxypropylmethylcellulose and Eudragit RS PO as carriers, and 5% ethanolic ethylcellulose solution as adhesive, buflomedil hydrochloride sustained release tablets were prepared by wetting granulation method. The release rates of the tablets were determined and compared with imported sustained release tablets. The results indicated that the sustained release tablets had an expected sustained release quality, and the drug release pattern was in accorded with the first order kinetics.
出处 《中国医药工业杂志》 CAS CSCD 北大核心 2002年第6期286-287,290,共3页 Chinese Journal of Pharmaceuticals
关键词 盐酸丁咯地尔缓释片 制备 体外释放度 羟丙甲纤维素 丙烯酸树脂 动脉血管活性剂 buflomedil hydrochloride sustained release tablets hydroxypropylmethylcellulose(HPMC) Eudragit RS PO
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  • 1董志超,国外医药,1993年,14卷,41页
  • 2董志超,药物分析杂志,1993年,13卷,37页
  • 3U. Gundert-Remy,E. Weber,G. Lam,W. L. Chiou,W. Mann,G. H. Aynilian. The clinical pharmacokinetics of buflomedil in normal subjects after intravenous and oral administration[J] 1981,European Journal of Clinical Pharmacology(6):459~463

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