首页> 美国卫生研究院文献>International Journal of Biomedical Science : IJBS >Spectroflourometric and Spectrophotometric Methods for the Determination of Sitagliptin in Binary Mixture with Metformin and Ternary Mixture with Metformin and Sitagliptin Alkaline Degradation Product
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Spectroflourometric and Spectrophotometric Methods for the Determination of Sitagliptin in Binary Mixture with Metformin and Ternary Mixture with Metformin and Sitagliptin Alkaline Degradation Product

机译:分光光度法和分光光度法测定二甲双胍与二甲双胍和西格列汀碱性降解产物三元混合物中西格列汀的含量。

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摘要

Simple, accurate and precise spectroflourometric and spectrophotometric methods have been developed and validated for the determination of sitagliptin phosphate monohydrate (STG) and metformin HCL (MET). Zero order, first derivative, ratio derivative spectrophotometric methods and flourometric methods have been developed. The zero order spectrophotometric method was used for the determination of STG in the range of 50-300 μg mL-1. The first derivative spectrophotometric method was used for the determination of MET in the range of 2–12 μg mL-1 and STG in the range of 50-300 μg mL-1 by measuring the peak amplitude at 246.5 nm and 275 nm, respectively. The first derivative of ratio spectra spectrophotometric method used the peak amplitudes at 232 nm and 239 nm for the determination of MET in the range of 2–12 μg mL-1. The flourometric method was used for the determination of STG in the range of 0.25-110 μg mL-1. The proposed methods used to determine each drug in binary mixture with metformin and ternary mixture with metformin and sitagliptin alkaline degradation product that is obtained after alkaline hydrolysis of sitagliptin. The results were statistically compared using one-way analysis of variance (ANOVA). The methods developed were satisfactorily applied to the analysis of the pharmaceutical formulations and proved to be specific and accurate for the quality control of the cited drugs in pharmaceutical dosage forms.
机译:已经开发出简单,准确和精确的分光光度法和分光光度法,用于测定西他列汀磷酸一水合物(STG)和二甲双胍盐酸盐(MET)的含量。已经开发了零阶,一阶导数,比例导数分光光度法和荧光法。零级分光光度法测定STG的范围为50-300μgmL -1 。一阶导数分光光度法用于测定2–12μgmL -1 范围内的MET和50-300μgmL -1 范围内的STG。通过分别测量246.5 nm和275 nm处的峰值幅度。比率光谱分光光度法的一阶导数使用232 nm和239 nm处的峰幅度测定2–12μgmL -1 范围内的MET。用荧光法测定STG的范围为0.25-110μgmL -1 。拟议的方法用于测定西他列汀碱性水解后获得的二甲双胍与二甲双胍和西他列汀三元混合物中的每种药物的碱性降解产物。使用单向方差分析(ANOVA)对结果进行统计比较。所开发的方法已令人满意地应用于药物制剂的分析,并被证明对药物剂型中所引用药物的质量控制具有特异性和准确性。

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