首页> 美国卫生研究院文献>International Journal of Biomedical Science : IJBS >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
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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

机译:分光光度法测定盐酸二甲双胍二元混合物中的利格列汀高效液相色谱法同时测定利格列汀和盐酸二甲双胍。

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摘要

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.
机译:已经开发了简单,准确和精确的零阶一阶导数分光光度法和色谱方法,用于测定利格列汀(LNG)和盐酸二甲双胍(MET)的有效性。零阶和一阶导数分光光度法分别通过测量299 nm和311处的吸光度来测定5-30μgmL -1 范围内的LNG。此外,还描述了一种反相液相色谱(RP-LC)方法同时测定LNG和MET的方法。在Symmetry ® Waters C18色谱柱(150 mm×4.6 mm,5μm)上进行色谱分离。在流速为1 mLmin -1 的条件下,基于磷酸二氢钾缓冲液pH(4.6)-甲醇(30:70,v / v)进行等度洗脱,并在260 nm处进行UV检测。 LNG和MET的浓度范围分别为0.125-4μgmL -1 和20-800μgmL -1 时,线性,准确性和精密度均可接受。使用单向方差分析(ANOVA)对结果进行统计比较。验证了优化的方法,并证明了其药物制剂中药物质量控制的特异性,鲁棒性,精确性和准确性。

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