Development of the spectrophotometric method for the determination of metoprolol in tablets by using bromophenol blue

Q3 Pharmacology, Toxicology and Pharmaceutics
M. Horyn, Liubomyr Kryskiw, T. Kucher, O. Poliak, N. Zarivna, Hryhorii Zahrychuk, D. Korobko, K. Peleshok, L. Logoyda
{"title":"Development of the spectrophotometric method for the determination of metoprolol in tablets by using bromophenol blue","authors":"M. Horyn, Liubomyr Kryskiw, T. Kucher, O. Poliak, N. Zarivna, Hryhorii Zahrychuk, D. Korobko, K. Peleshok, L. Logoyda","doi":"10.15587/2519-4852.2022.270311","DOIUrl":null,"url":null,"abstract":"The aim of the work was to develop a simple, economical and eco-friendly spectrophotometric method for determining metoprolol tartrate in tablets based on the reaction with bromophenol blue (BPB). \nMaterial and methods: A double–beam Shimadzu UV-Visible spectrophotometer, with a spectral bandwidth of 1 nm wavelength accuracy ±0.5 nm, Model –UV 1800 (Japan), Software UV-Probe 2.62, and a pair of 1 cm matched quartz cells, was used to measure the absorbance of the resulting solution. All the chemicals were used in analytical reagent grade. Pharmacopeial standard samples of metoprolol tartrate and bromophenol blue (BPB) were provided by Sigma-Aldrich (≥ 98%, HPLC). The used dosage forms of metoprolol tartrate are tablets of Metoprolol 50 mg and 100 mg. \nResults and discussion: The method of spectrophotometric determination of the quantitative content of metoprolol tartrate based on its reaction with BPB in a methanol solution 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. The developed method of quantitative determination of metoprolol tartrate was validated. The linearity regression equation was y = 0.0373x + 0.0038, and the obtained correlation coefficient was R2=0.9984. A linear relationship was found between absorbance at λmax and concentration of metoprolol tartrate in the range of 9.56-15.02 µg/mL. The LOD and LOQ values were calculated to be 0.81 µg/mL and 2.67 µg/mL. \nConclusions. A simple, economical and eco-friendly spectrophotometric method has been developed for the quantitative determination of metoprolol tartrate in tablets based on the reaction with BPB. The developed method of quantitative determination of metoprolol tartrate was validated in accordance with the requirements of SPhU. We suggest our work with offered detailed and successful solutions for the mentioned aim with less sophisticated equipment for QC lab for routine manufacturing control","PeriodicalId":21674,"journal":{"name":"ScienceRise: Pharmaceutical Science","volume":"38 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-12-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ScienceRise: Pharmaceutical Science","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15587/2519-4852.2022.270311","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Pharmacology, Toxicology and Pharmaceutics","Score":null,"Total":0}
引用次数: 1

Abstract

The aim of the work was to develop a simple, economical and eco-friendly spectrophotometric method for determining metoprolol tartrate in tablets based on the reaction with bromophenol blue (BPB). Material and methods: A double–beam Shimadzu UV-Visible spectrophotometer, with a spectral bandwidth of 1 nm wavelength accuracy ±0.5 nm, Model –UV 1800 (Japan), Software UV-Probe 2.62, and a pair of 1 cm matched quartz cells, was used to measure the absorbance of the resulting solution. All the chemicals were used in analytical reagent grade. Pharmacopeial standard samples of metoprolol tartrate and bromophenol blue (BPB) were provided by Sigma-Aldrich (≥ 98%, HPLC). The used dosage forms of metoprolol tartrate are tablets of Metoprolol 50 mg and 100 mg. Results and discussion: The method of spectrophotometric determination of the quantitative content of metoprolol tartrate based on its reaction with BPB in a methanol solution 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. The developed method of quantitative determination of metoprolol tartrate was validated. The linearity regression equation was y = 0.0373x + 0.0038, and the obtained correlation coefficient was R2=0.9984. A linear relationship was found between absorbance at λmax and concentration of metoprolol tartrate in the range of 9.56-15.02 µg/mL. The LOD and LOQ values were calculated to be 0.81 µg/mL and 2.67 µg/mL. Conclusions. A simple, economical and eco-friendly spectrophotometric method has been developed for the quantitative determination of metoprolol tartrate in tablets based on the reaction with BPB. The developed method of quantitative determination of metoprolol tartrate was validated in accordance with the requirements of SPhU. We suggest our work with offered detailed and successful solutions for the mentioned aim with less sophisticated equipment for QC lab for routine manufacturing control
溴酚蓝分光光度法测定片剂中美托洛尔的含量
建立了一种简单、经济、环保的基于溴酚蓝(BPB)反应测定酒石酸美托洛尔片剂中酒石酸美托洛尔含量的分光光度法。材料与方法:采用双光束Shimadzu紫外可见分光光度计,光谱带宽为1 nm,波长精度为±0.5 nm,型号为-UV 1800(日本),软件UV-Probe 2.62,一对1 cm匹配的石英细胞,测量所得溶液的吸光度。所有化学试剂均为分析试剂级。酒石酸美托洛尔和溴酚蓝(BPB)药典标准品采用Sigma-Aldrich(≥98%,高效液相色谱)。酒石酸美托洛尔的常用剂型是片剂美托洛尔50毫克和100毫克。结果与讨论:建立了酒石酸美托洛尔在甲醇溶液中与BPB反应的分光光度法测定酒石酸美托洛尔定量含量的方法。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。对建立的酒石酸美托洛尔的定量测定方法进行了验证。线性回归方程为y = 0.0373x + 0.0038,相关系数R2=0.9984。λmax吸光度与酒石酸美托洛尔浓度在9.56 ~ 15.02µg/mL范围内呈线性关系。定量限和定量限分别为0.81µg/mL和2.67µg/mL。结论。建立了一种简单、经济、环保的分光光度法测定酒石酸美托洛尔片剂中酒石酸美托洛尔的含量。根据SPhU的要求,对所建立的酒石酸美托洛尔的定量测定方法进行了验证。我们建议我们的工作为上述目标提供详细和成功的解决方案,为QC实验室提供不太复杂的设备,用于日常生产控制
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
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
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信