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通过析因设计实验测定维格列汀和沙格列汀的兼容验证荧光分光光度法和分光光度法。

Compatible validated spectrofluorimetric and spectrophotometric methods for determination of vildagliptin and saxagliptin by factorial design experiments.

作者信息

Abdel-Aziz Omar, Ayad Miriam F, Tadros Mariam M

机构信息

Analytical Chemistry Department, Faculty of Pharmacy, Ain Shams University, Abbassia, Cairo 11566, Egypt.

Analytical Chemistry Department, Faculty of Pharmacy, Ain Shams University, Abbassia, Cairo 11566, Egypt.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2015 Apr 5;140:229-40. doi: 10.1016/j.saa.2014.12.102. Epub 2015 Jan 5.

Abstract

Simple, selective and reproducible spectrofluorimetric and spectrophotometric methods have been developed for the determination of vildagliptin and saxagliptin in bulk and their pharmaceutical dosage forms. The first proposed spectrofluorimetric method is based on the dansylation reaction of the amino group of vildagliptin with dansyl chloride to form a highly fluorescent product. The formed product was measured spectrofluorimetrically at 455 nm after excitation at 345 nm. Beer's law was obeyed in a concentration range of 100-600 μg ml(-1). The second proposed spectrophotometric method is based on the charge transfer complex of saxagliptin with tetrachloro-1,4-benzoquinone (p-chloranil). The formed charge transfer complex was measured spectrophotometrically at 530 nm. Beer's law was obeyed in a concentration range of 100-850 μg ml(-1). The third proposed spectrophotometric method is based on the condensation reaction of the primary amino group of saxagliptin with formaldehyde and acetyl acetone to form a yellow colored product known as Hantzsch reaction, measured at 342.5 nm. Beer's law was obeyed in a concentration range of 50-300 μg ml(-1). All the variables were studied to optimize the reactions' conditions using factorial design. The developed methods were validated and proved to be specific and accurate for quality control of vildagliptin and saxagliptin in their pharmaceutical dosage forms.

摘要

已开发出简单、选择性好且可重现的荧光分光光度法和分光光度法,用于测定原料药以及其药物剂型中的维格列汀和沙格列汀。所提出的第一种荧光分光光度法基于维格列汀氨基与丹磺酰氯的丹磺酰化反应,以形成高荧光产物。在345nm激发后,于455nm处用荧光分光光度法测定所形成的产物。在100 - 600μg ml(-1)的浓度范围内符合比尔定律。所提出的第二种分光光度法基于沙格列汀与四氯-1,4-苯醌(对氯苯醌)形成的电荷转移络合物。在530nm处用分光光度法测定所形成的电荷转移络合物。在100 - 850μg ml(-1)的浓度范围内符合比尔定律。所提出的第三种分光光度法基于沙格列汀的伯氨基与甲醛和乙酰丙酮的缩合反应,形成一种黄色产物,即汉奇反应,在342.5nm处测定。在50 - 300μg ml(-1)的浓度范围内符合比尔定律。使用因子设计研究了所有变量以优化反应条件。所开发的方法经过验证,证明对维格列汀和沙格列汀药物剂型的质量控制具有特异性和准确性。

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