片剂中索他洛尔的分光光度定量测定方法

Q3 Pharmacology, Toxicology and Pharmaceutics
Olena Maletska, S. Vasyuk
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引用次数: 0

摘要

工作的目的。建立重氮盐分光光度法测定索他洛尔的方法。建立药物中索他洛尔含量测定的最佳条件。验证开发的方法。材料和方法。研究中使用的试剂和溶剂为:二唑红2J(来自NVF“Sinbias”)、“索他洛尔山德士”片剂40 mg (Salyutas Pharma GmbH,系列JZ1188)、“索他洛尔山德士”片剂80 mg (Salyutas Pharma GmbH,系列KA0464)和“索他洛尔山德士”片剂160 mg (Salyutas Pharma GmbH,系列JY3504)、甲醇(LAB-SCAN,爱尔兰,批号5120/13)、碳酸钠(Sinbias)和纯净水。分析设备:分光光度计“SPECORD-200”(Analytic Jena AG,德国),实验室电子秤RADWAG XA 210.4Y,浴超声波Sonorex Digitec DT100H,实验室a级玻璃器皿。所有研究在中国国立医科大学科学医学检验中心(SMLC)实验药物研究部进行。结果和讨论。建立了水-甲醇介质中索他洛尔与红二唑反应的分光光度法定量测定索他洛尔含量的方法。通过连续变化法和饱和法得到反应组分的化学计量比为1:1。对所开发的方法进行了线性、精密度、正确性和鲁棒性等指标的验证。根据这些数据,所建立的方法是正确的,可用于化工和制药企业的质量控制部门。建立了“索他洛尔山德士”40 mg、“索他洛尔山德士”80 mg和“索他洛尔山德士”160 mg片剂中索他洛尔的定量分光光度测定方法,考察了方法的线性度、精密度、正确性、适用范围和鲁棒性
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Spectrophotometric methods for quantitative determination of sotalol in tablets
The aim of the work. To develop a method for spectrophotometric determination of sotalol with diazonium salts. Establish optimal conditions for the quantitative determination of sotalol in drugs. Validate the developed methodology. Materials and methods. Reagents and solvents used in the study were: diazole red 2J (obtained from NVF “Sinbias”), tablets “Sotalol Sandoz” 40 mg (Salyutas Pharma GmbH, series JZ1188), “Sotalol Sandoz” 80 mg (Salyutas Pharma GmbH, series KA0464) and “Sotalol Sandoz” 160 mg (Salyutas Pharma GmbH, series JY3504), methanol (LAB-SCAN, Ireland, batch № 5120/13), sodium carbonate (Sinbias) and purified water were also used. Analytical equipment: spectrophotometer “SPECORD-200” (Analytic Jena AG, Germany), scales laboratory electronic RADWAG XA 210.4Y, bath ultrasonic Sonorex Digitec DT100H, laboratory glassware of class A. All studies were conducted in the experimental pharmaceutical research department of the scientific medical laboratory center (SMLC) of the Zaporizhzhia State Medical University. Results and discussion. The technique of spectrophotometric determination of the quantitative content of sotalol based on its reaction with red diazole in water-methanol medium has been developed. The stoichiometric ratios of the reactive components as 1:1 were obtained by the methods of continuous changes and the saturation method. Validation of the developed on such indicators as linearity, precision, correctness and robustness is carried out. Based on these data, the developed method is correct and could be used in the quality control departments of chemical and pharmaceutical companies. Conclusions. A method of quantitative spectrophotometric determination of sotalol in the tablet dosage form “Sotalol Sandoz” 40 mg, “Sotalol Sandoz” 80 mg and “Sotalol Sandoz” 160 mg of industrial production was developed, validation characteristics were investigated: linearity, precision, correctness, range of application and robustness
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来源期刊
ScienceRise: Pharmaceutical Science
ScienceRise: Pharmaceutical Science Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
1.70
自引率
0.00%
发文量
39
审稿时长
6 weeks
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