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Thermal Analysis and Validation of UV and Visible Spectrophotometric Methods for the Determination of New Antibiotic Tigecycline in Pharmaceutical Product

机译:紫外可见分光光度法测定药品中新抗生素替加环素的热分析及验证

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摘要

This work has proposed the development and validation of ultraviolet (UV) and visible spectrophotometric methods for determination of tigecycline in lyophilized powder. In UV method tigecycline showed absorption maximum at 245 nm, in aqueous medium, where as in visible spectrophotometric method it reacts with copper acetate reagent, under acid conditions, forming a greenish coloured solution with absorption maximum at 378 nm. Thermogravimetric Analysis and Differencial Scanning Calorimetry (TGA-DSC) techniques were studied to determine the thermal analysis of tigecycline. The methods were completely validated according to the International Conference on Harmonization (ICH) guidelines, showing good accuracy, precision, selectivity, robustness and linearity. Therefore the methods were found to be simple, economic and free of polluting reagents, being suitable for the analysis of the lyophilized powder formulation, contributing to improve the quality control and to assure its therapeutic efficacy.
机译:这项工作提出了开发和验证紫外线(UV)和可见分光光度法测定冻干粉中的替加环素的方法。在紫外法中,替加环素在水性介质中显示在245 nm处有最大吸收,在可见光下,它与乙酸铜试剂在酸性条件下反应,在酸性条件下会形成绿色的绿色溶液,在378 nm处有最大吸收。研究了热重分析和差示扫描量热法(TGA-DSC)技术来确定替加环素的热分析。该方法已根据国际协调会议(ICH)指南进行了完全验证,显示出良好的准确性,精密度,选择性,鲁棒性和线性。因此,发现该方法简单,经济并且不含污染试剂,适合于冻干粉末制剂的分析,有助于改善质量控制并确保其治疗功效。

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