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高效液相色谱法测定普伐他汀钠片的溶出度
引用本文:龙汉金. 高效液相色谱法测定普伐他汀钠片的溶出度[J]. 中国现代药物应用, 2009, 3(20): 47-48
作者姓名:龙汉金
作者单位:湖南省醴陵市中医院药剂科,412200
摘    要:目的建立高效液相色谱法测定普伐他汀钠片的溶出度试验方法。方法色谱柱为kromasil C18柱(4.6×250mm,5μm);流动相为磷酸盐缓冲液(pH3.5).甲醇(45:55);检测波长:238nm。结果普伐他汀钠在0.03—0.36mg/ml范围内线性关系较好,r=0.9999,回收率为99.6%,RSD为1.27%。结论本方法简便、快速、准确、重复性好,可作为普伐他汀钠片的溶出度的检测方法。

关 键 词:普伐他汀钠片  溶出度  高效液相色谱法

Determination of Dissolution of Pravastatin Sodium Tablets by HPLC
LONG Han-jin. Determination of Dissolution of Pravastatin Sodium Tablets by HPLC[J]. Chinese Journal of Modern Drug Application, 2009, 3(20): 47-48
Authors:LONG Han-jin
Affiliation:LONG Han-jin.( Department of Pharmacy, Liling Chinese Medicine Hospital, Liling 412200, China)
Abstract:Objective To establish HPLC method for detecting dissolution of Pravastatin Sodium tablets. Methods kromasil C18 colunm(4. 6 ×250 mm,5 μm) was used, the mobile phase was phosphate buffer solution(pH3.5)-methanol (45 : 55 ), the detection wavelength was 238 nm. Results The linear range of Pravastatin Sodium was 0. 03 - 0. 36 mg/ml, coefficient correlation r was 0. 9999, the average recovery of Pravastatin Sodium was 99. 6% with RSD 1.27%. Condusion The method is simple, rapid, accurate and repreatable. It can be used for detecting dissolution of Pravastatin Sodium tablets.
Keywords:Pravastatin Sodium tablets  Dissolution  HPLC
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