Simultaneous estimation of two anti-diabetic drugs; Linagliptin and empagliflozin in their tablet by chemometric spectrophotometry.

Amira H Kamal, Sherin F Hammad, Mohamed M Salim, Mahmoud M Elkhodary, Aya A Marie
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Abstract

Four spectrophotometric approaches had been established and optimized for the simultaneous estimation of two anti-diabetic drugs; linagliptin (LIN) and empagliflozin (EMP) in their bulk and tablet dosage form. LIN concentration could be first determined from the zero order spectra at its λmax (293 nm) without interference from EMP as at this wavelength EMP showed zero absorbance. The LIN and EMP zero order absorption spectra displayed considerable overlap which hindered the direct determination of EMP. Thus, four indirect spectrophotometric approaches were established and optimized for the determination and quantification of EMP concentrations in presence of LIN. Method (I) was ratio difference method (RD) which depended on the determination of difference amplitudes in the ratio spectra (ΔP) at 236 nm and 227 nm; ΔP(236-227) was directly proportional to EMP concentration. Method (II) was ratio derivative method (1DD) based on the measuring of the amplitude of first derivative of ratio spectra at 243 nm which was directly proportional to EMP concentration. For determination of EMP concentration using both method (I) and (II); LIN 7 µg/mL was used as the divisor. Method (III) was area under curve method (AUC) which depended on the measurement of area confined between 220 and 230 nm and 273-290 nm. Method (IV) was dual wavelength method (DWL) which based on measurement of absorbance difference (ΔA) in zero order spectra between 239.8 and 282.6 nm which was directly proportional to EMP concentration. The four developed methods were optimized and entirely validated regarding to ICH guidelines. The proposed spectrophotometric approaches were used for the quantification of LIN and EMP simultaneously in their tablet dosage form. F-test and t-test were applied for statistical comparison between the results obtained by the proposed approaches and that obtained by the reported method. There was no significant difference concerning to precision and accuracy.

两种抗糖尿病药物的同时评价;化学计量分光光度法测定利那列汀和恩帕列嗪片剂中利那列肽和恩帕列嗪的含量。
建立并优化了四种分光光度法同时测定两种抗糖尿病药物;利格列汀(LIN)和恩帕列嗪(EMP)的散装和片剂剂型。在没有EMP干扰的情况下,可以首先从λmax(293nm)的零阶光谱中测定LIN浓度,因为在该波长下,EMP显示出零吸光度。LIN和EMP的零级吸收光谱显示出相当大的重叠,这阻碍了EMP的直接测定。因此,建立并优化了四种间接分光光度法来测定和定量在LIN存在下的EMP浓度。方法(I)为比值差法(RD),该方法依赖于测定236 nm和227 nm处比值光谱(ΔP)的差幅;ΔP(236-227)与EMP浓度成正比。方法(II)是基于在243nm处测量与EMP浓度成正比的比率光谱的一阶导数幅度的比率导数方法(1DD)。用于使用方法(I)和(II)测定EMP浓度;LIN 7µg/mL用作除数。方法(III)是曲线下面积法(AUC),其取决于限制在220和230nm以及273-290nm之间的面积的测量。方法(IV)是双波长法(DWL),其基于在239.8和282.6nm之间的零阶光谱中的吸光度差(ΔA)的测量,该吸光度差与EMP浓度成正比。根据ICH指南,对四种开发的方法进行了优化和完全验证。将所提出的分光光度法同时用于片剂中LIN和EMP的定量。使用F检验和t检验对所提出的方法和所报道的方法获得的结果进行统计比较。在精确度和准确性方面没有显著差异。
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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