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分光光度法测定与盐酸二甲双胍二元混合物中的利那格列汀以及使用高效液相色谱法同时测定利那格列汀和盐酸二甲双胍

Spectrophotometric Methods for the Determination of Linagliptin in Binary Mixture with Metformin Hydrochloride and Simultaneous Determination of Linagliptin and Metformin Hydrochloride using High Performance Liquid Chromatography.

作者信息

El-Bagary Ramzia I, Elkady Ehab F, Ayoub Bassam M

机构信息

Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Cairo University, Kasr El-Aini St., Cairo 11562, Egypt.

出版信息

Int J Biomed Sci. 2013 Mar;9(1):41-7.

Abstract

Simple, accurate and precise Zero order, first derivative spectrophotometric and chromatographic methods have been developed and validated for the determination of linagliptin (LNG) and metformin HCl (MET). The zero order and first derivative spectrophotometric methods were used for the determination of LNG in the range of 5-30 μg mL(-1) by measuring the absorbance at 299 nm and 311 respectively. Besides, a reversed-phase liquid chromatographic (RP-LC) method is described for the simultaneous determination of LNG and MET. Chromatographic separation was achieved on a Symmetry(®) Waters C18 column (150 mm × 4.6 mm, 5 μm). Isocratic elution based on potassium dihydrogen phosphate buffer pH (4.6) - methanol (30:70, v/v) at a flow rate of 1 mLmin(-1) with UV detection at 260 nm was performed. Linearity, accuracy and precision were found to be acceptable over the concentration ranges of 0.125-4 μg mL(-1) and 20-800 μg mL(-1) for LNG and MET, respectively. The results were statistically compared using one-way analysis of variance (ANOVA). The optimized methods were validated and proved to be specific, robust, precise and accurate for the quality control of the drugs in their pharmaceutical preparation.

摘要

已开发并验证了简单、准确且精密的零阶、一阶导数分光光度法和色谱法,用于测定利格列汀(LNG)和盐酸二甲双胍(MET)。零阶和一阶导数分光光度法通过分别在299 nm和311 nm处测量吸光度,用于测定5 - 30 μg mL⁻¹范围内的LNG。此外,还描述了一种反相液相色谱(RP-LC)法,用于同时测定LNG和MET。色谱分离在Symmetry(®) Waters C18柱(150 mm × 4.6 mm,5 μm)上进行。以磷酸二氢钾缓冲液pH(4.6) - 甲醇(30:70,v/v)为流动相,流速为1 mL min⁻¹,在260 nm处进行紫外检测,进行等度洗脱。发现LNG和MET在浓度范围分别为0.125 - 4 μg mL⁻¹和20 - 800 μg mL⁻¹时,线性、准确度和精密度均可接受。使用单向方差分析(ANOVA)对结果进行统计学比较。所优化的方法经过验证,证明对于药物制剂中药物的质量控制具有特异性、稳健性、精密性和准确性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0b0/3644414/6c4794a77efb/IJBS-9-41-g001.jpg

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