SECOND-ORDER DERIVATIVE UV SPECTROPHOTOMETRIC AND RP-HPLC METHODS FOR THE ANALYSIS OF VILDAGLIPTIN AND APPLICATION FOR DISSOLUTION STUDY

A. Barden, B. Piccoli, N. Volpato, M. Steppe
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引用次数: 4

Abstract

This study describes two analytical methods, by second-order derivative UV spectrophotometric by HPLC, for determination of vildagliptin, a drug used for treatment of type 2 Diabetes Mellitus that belongs to a therapeutic class called inhibitors of dipeptidyl peptidase 4. The methods were validated in accordance with ICH and USP requirements. Analyses by UV derivative method were performed at 220 nm, which was the zero crossing point of excipient solutions. HPLC was optimized and the analysis was carried out using a Zorbax Eclipse Plus RP-C8 column (150 mm × 4.6 mm, 5 μm), detection at 207 nm, and potassium phosphate buffer solution pH 7.0 : acetonitrile (85:15, v/v) as mobile phase. In dissolution test, the conditions used were 0.01 mol L-1 hydrochloric acid in 900 mL of dissolution medium, USP apparatus 2 (paddle) and 50 rpm stirring speed. Both methods were successfully applied for analysis of dissolution samples from marketed vildagliptin tablets.
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二阶导数紫外分光光度法和反相高效液相色谱法分析维格列汀及其溶出度研究
维格列汀是一种用于治疗2型糖尿病的药物,属于二肽基肽酶4抑制剂,本研究描述了用高效液相色谱法二阶导数紫外分光光度测定维格列汀的两种分析方法。方法按照ICH和USP的要求进行了验证。用紫外导数法在220 nm处进行分析,220 nm为赋形剂溶液的零交叉点。HPLC优化,色谱柱为Zorbax Eclipse Plus RP-C8 (150 mm × 4.6 mm, 5 μm),检测波长为207 nm,流动相为磷酸钾缓冲液pH 7.0:乙腈(85:15,v/v)。溶出试验条件为:盐酸浓度为0.01 mol L-1,溶解介质为900 mL, USP装置2(桨叶),搅拌速度为50 rpm。两种方法均可用于市售维格列汀片溶出度分析。
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