甘油溶剂钛水化配合物药物中卡维地洛的分光光度分析

M. I. Popova, T. Kobeleva, A. Sichko
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引用次数: 0

摘要

目的建立基于甘油溶剂钛水化配合物的“卡维地洛”药物中卡维地洛的定量分光光度分析方法。材料和方法。在分析过程中,我们使用了原料药“卡维地洛”,凝胶“Tizol”,软膏“卡维地洛”组成0.5% β受体阻滞剂在钛甘油水凝胶。采用分光光度法,在SF-2000分光光度计上进行了光密度和电子能谱的配准。选择以下参数进行方法学验证:特异性、线性度、精密度、正确性。结果。卡维地洛的分析波长为243 nm,定量限为0.761 g/ml。研究结果表明,根据软剂型的监管文件(2015年10月26日俄罗斯联邦卫生部第751n号命令),软膏中卡维地洛的重量在可接受范围内(0.0404-0.0548 g)。结论。选择了分光光度法测定卡维地洛软膏中卡维地洛含量的最佳实施条件,相对误差不超过1.80%。
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Spectrophotometric analysis of carvedilol in a medication based on aquacomplex of titanium glycerosolvate
Aim to develop a methodology for quantitative spectrophotometric analysis of carvedilol in the "Carvedilosol" medication based on aquacomplex of titanium glycerosolvate. Material and methods. During the analysis we used the pharmaceutical substance "Carvedilol", gel "Tizol", ointment "Carvedilosol" consisting of 0.5% beta-blocker in titanium glycerohydrogel. The spectrophotometry was applied, registration of optical density and electron spectra was performed on spectrophotometer SF-2000. The following parameters were chosen for validation of the methodology: specificity, linearity, precision, correctness. Results. It is reasonable to analyze Carvedilol at a wavelength of 243 nm with the limit of quantitative determination of 0.761 g/ml. The results of the study showed that the weight of carvedilol in the ointment is within acceptable limits (0.0404-0.0548 g) according to the regulatory documentation for soft dosage forms (Order of the Ministry of Health of the Russian Federation No. 751n dated 26.10.2015). Conclusion. Optimal conditions for the implementation of spectrophotometric method of analysis were selected for detection of the content of carvedilol in the ointment "Carvedilosol" with a relative error not exceeding 1.80 %.
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