Quantitative estimation of sitagliptin and dapagliflozin propanediol monohydrate in synthetic mixture using 1 order derivative spectroscopy simultaneous spectrophotometric analysis

S. Jani, Rashmi Shukla, Pinak Patel, Binny Mehta, Krunal Detholia
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引用次数: 2

Abstract

Current research paper describes highly specific and reproducible 1 order derivative spectroscopic method for quantitative analysis of Sitagliptin which is a DPP4 inhibitors and Dapagliflozin which is SGLT2 inhibitors from its synthetic mixture. Both drugs are from Anti Diabetics class. Present analytical method was developed on Shimadzu double beam spectrophotometer equipped with UV probe 2.42 as software using methyl alcohol as solvent. Quantification of Sitagliptin was carried out at zero cross over point of Dapagliflozin that is 275 nm and for Dapagliflozin, it was achieved at 232 nm which is zero cross over point of Sitagliptin. Method shows linear response in the range of 25-125 µg/mL of Sitagliptin and 2.5-12.5 µg/mL of Dapagliflozin. Method was found to be accurate with recovery between 99.3 – 100.1 % for Sitagliptin and 98.2 – 100.7 % for Dapagliflozin. The developed method was validated as per ICH Q2 R1 guidelines and was successfully applied for quantitative analysis of synthetic mixture of Sitagliptin and Dapagliflozin.
合成混合物中西格列汀和达格列净丙二醇一水合物的一阶导数光谱同时分光光度定量分析
本研究描述了一种高特异性和可重复性的1阶导数光谱方法,用于从其合成混合物中定量分析DPP4抑制剂西格列汀和SGLT2抑制剂达格列净。这两种药都属于抗糖尿病类。本方法采用岛津双光束分光光度计,以甲醇为溶剂,以2.42紫外探针为软件。西格列汀的定量在达格列净的零交叉点275 nm处进行,达格列净的定量在232 nm处进行,这是西格列汀的零交叉点。方法在西格列汀25 ~ 125µg/mL和达格列净2.5 ~ 12.5µg/mL范围内呈线性响应。方法精密度为99.3% ~ 100.1%,达格列净为98.2% ~ 100.7%。该方法按照ICH Q2 R1指南进行了验证,并成功用于西格列汀和达格列净合成混合物的定量分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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