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异烟肼控释片剂的研制
引用本文:孙殿甲,崔玉琴. 异烟肼控释片剂的研制[J]. 新疆医科大学学报, 1989, 12(3): 171-173
作者姓名:孙殿甲  崔玉琴
作者单位:新疆医学院药学系药剂学教研室,新疆医学院药学系药剂学教研室,新疆医学院药学系药剂学教研室,新疆医学院药学系药剂学教研室,新疆医学院药学系药剂学教研室
摘    要:
本文研究了异烟肼控释片剂的处方组成、制备工艺、体外溶出度及在兔体内的血药浓度。数据按单室模型进行处理,求得动力学参数。结果表明:控释片剂1h达有效血药浓度,浓度维持在5~15μg/m1以上达24h。控释片体内外具有相关性,因此溶出度可作为控制控释片剂的质量标准。

关 键 词:异烟肼  控释片剂  溶出度  药物动力学参数

Studies on Controlled Release Isoniazid Tablets
Sun Dianjia,et al. Studies on Controlled Release Isoniazid Tablets[J]. Journal of Xinjiang Medical University, 1989, 12(3): 171-173
Authors:Sun Dianjia  et al
Affiliation:Sun Dianjia,et al Department of Pharmacy,Xinjiang Medical College
Abstract:
The formulation, preparation process, dissolution rate and plasma le-vel in rabbit of controlled release isoniazid tablets were studied. The phar-macokinetic parameters were fitted in the basis of one compartment model.The therapeutic plasma level of controlled-release isoniazid tablets was att ained at lh and then maintained over 5-15ug/ml for up to 24h. The corre lation between dissolution rate and plasma levels was good. Then the dis solution rate referred to controlling controlled-release isoniazid tablets as quality standard.
Keywords:controlled release isoniazid tablets  dissolution rate  pharmacokinetic parameter
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