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首页> 外文期刊>Journal of AOAC International >Determination of metformin hydrochloride and glyburide in an antihyperglycemic binary mixture using high-performance liquid chromatographic-UV and spectrometric methods.
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Determination of metformin hydrochloride and glyburide in an antihyperglycemic binary mixture using high-performance liquid chromatographic-UV and spectrometric methods.

机译:使用高效液相色谱-紫外和光谱法测定抗血糖二元混合物中的盐酸二甲双胍和格列本脲。

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摘要

Three methods were developed for simultaneous determination of metformin hydrochloride and glyburide in an antihyperglycemic binary mixture without previous separation. In the first method, a reversed-phase HPLC column with acetonitrile-water (60 + 40, v/v) mobile phase at 0.9 mL/min flow rate was used to separate both compounds, with UV detection at 254 nm. Linearity was obtained in the concentration range of 0.06--0.24 microg/mL for glyburide and 1.5-6.0 microg/mL for metformin hydrochloride. The second method depended on first- and second-derivative UV spectrometry with zero-crossing measurements. The first-derivative amplitude at 261 nm was selected for the assay of glyburide, and the second-derivative amplitude at 235 nm was selected for the assay of metformin hydrochloride. The third method depended on measuring the first derivative of the ratio-spectra at 241 nm for glyburide and 227 nm for metformin hydrochloride. For the second and third methods, Beer's law was obeyed in the range of 10-55 microg/mL for glyburide and 20-200 microg/mL for metformin. The proposed methods were extensively validated and applied for the analysis of some pharmaceutical formulations containing binary mixtures of the mentioned drugs.
机译:开发了三种方法,无需预先分离即可同时测定降血糖二元混合物中的盐酸二甲双胍和格列本脲。在第一种方法中,使用反相乙腈-水(60 + 40,v / v)流动相,流速为0.9 mL / min的反相HPLC柱分离两种化合物,并在254 nm处进行UV检测。格列本脲在0.06--0.24 microg / mL的浓度范围内,盐酸二甲双胍在1.5-6.0 microg / mL的浓度范围内获得线性度。第二种方法取决于具有零交叉测量的一阶和二阶UV光谱法。选择在261 nm处的一阶导数振幅用于格列本脲的测定,在235 nm处选择二阶导数振幅用于盐酸二甲双胍的测定。第三种方法取决于在241 nm处测定格列本脲和227 nm时盐酸二甲双胍的比光谱的一阶导数。对于第二种方法和第三种方法,格列本脲的比尔定律在10-55微克/毫升的范围内,二甲双胍的遵守在20-200微克/毫升的范围内。所提出的方法得到了广泛的验证,并被用于分析含有所述药物的二元混合物的某些药物制剂。

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