Application of a sorbent based on hypromellose for the quantitative determination of procaine in pharmaceutical formulation

M. N. Kachalkin, Aleksander Vasilievich Voronin
{"title":"Application of a sorbent based on hypromellose for the quantitative determination of procaine in pharmaceutical formulation","authors":"M. N. Kachalkin, Aleksander Vasilievich Voronin","doi":"10.35693/avp619759","DOIUrl":null,"url":null,"abstract":"Aim. The aim is to assess the selectivity and metrological characteristics of the spectrophotometric determination method of procaine in certain combined pharmaceutical preparations using a solid-phase extraction sorbent based on hypromellose. \nMaterial and methods. To obtain the solid-phase extraction sorbent, hypromellose and ethyl cyanoacrylate were used along with procaine hydrochloride and sodium hydroxide for the formation of active centers. The sorbent was prepared using a known method. The sorption capacity of the obtained sorbent samples for procaine was 10.2 1.0 g/g. Combined drugs containing procaine and its salts, such as \"Menovazin,\" \"Sulfocamphocaine,\" and \"Otolorin,\" were selected for the study. Eluate optical density registration was performed using a SF-56 spectrophotometer (OKB SPECTR LLC). To evaluate the selectivity (specificity) of sample preparation in chromatographic separation of combined drugs, absorption spectra were registered in the wavelength range of 200-400 nm for eluates obtained using purified water and a 0.1 M hydrochloric acid solution. Procaine and benzocaine identification in the eluate was performed based on the presence of absorption maxima at wavelengths of 222 and 286 nm for benzocaine, and 228 and 292 nm for procaine, respectively. The statistical processing of experimental results and determination of metrological characteristics of the analysis method were carried out in accordance with OFS.1.1.0013 \"Statistical Processing of results of physical, physicochemical, and chemical tests.\" \nResults. The selectivity of the spectrophotometric determination method of procaine in certain combined drugs using a solid-phase extraction sorbent based on hypromellose was demonstrated. Selective binding of the analyzed substance with active centers in the sorbent and stepwise elution with purified water and a 0.1 M hydrochloric acid solution during solid-phase extraction eliminates the interfering effect of pharmaceutical components during the UV-spectrophotometry of procaine. The use of a sorbent based on hypromellose leads to improved metrological characteristics and reduces the systematic error of the quantitative determination method by an average of 14.4%.","PeriodicalId":183034,"journal":{"name":"Aspirantskiy Vestnik Povolzhiya","volume":" 5","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-04-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Aspirantskiy Vestnik Povolzhiya","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.35693/avp619759","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Aim. The aim is to assess the selectivity and metrological characteristics of the spectrophotometric determination method of procaine in certain combined pharmaceutical preparations using a solid-phase extraction sorbent based on hypromellose. Material and methods. To obtain the solid-phase extraction sorbent, hypromellose and ethyl cyanoacrylate were used along with procaine hydrochloride and sodium hydroxide for the formation of active centers. The sorbent was prepared using a known method. The sorption capacity of the obtained sorbent samples for procaine was 10.2 1.0 g/g. Combined drugs containing procaine and its salts, such as "Menovazin," "Sulfocamphocaine," and "Otolorin," were selected for the study. Eluate optical density registration was performed using a SF-56 spectrophotometer (OKB SPECTR LLC). To evaluate the selectivity (specificity) of sample preparation in chromatographic separation of combined drugs, absorption spectra were registered in the wavelength range of 200-400 nm for eluates obtained using purified water and a 0.1 M hydrochloric acid solution. Procaine and benzocaine identification in the eluate was performed based on the presence of absorption maxima at wavelengths of 222 and 286 nm for benzocaine, and 228 and 292 nm for procaine, respectively. The statistical processing of experimental results and determination of metrological characteristics of the analysis method were carried out in accordance with OFS.1.1.0013 "Statistical Processing of results of physical, physicochemical, and chemical tests." Results. The selectivity of the spectrophotometric determination method of procaine in certain combined drugs using a solid-phase extraction sorbent based on hypromellose was demonstrated. Selective binding of the analyzed substance with active centers in the sorbent and stepwise elution with purified water and a 0.1 M hydrochloric acid solution during solid-phase extraction eliminates the interfering effect of pharmaceutical components during the UV-spectrophotometry of procaine. The use of a sorbent based on hypromellose leads to improved metrological characteristics and reduces the systematic error of the quantitative determination method by an average of 14.4%.
应用基于聚甲基丙烯酸酯的吸附剂定量测定药物制剂中的普鲁卡因含量
研究目的目的是评估使用基于高美胶糖的固相萃取吸附剂的分光光度法测定某些复方药物制剂中普鲁卡因的选择性和计量学特性。材料和方法为了获得固相萃取吸附剂,使用了次聚乳胶和氰基丙烯酸乙酯以及盐酸普鲁卡因和氢氧化钠来形成活性中心。吸附剂采用已知方法制备。所得吸附剂样品对普鲁卡因的吸附容量为 10.2 1.0 克/克。研究选择了含有普鲁卡因及其盐类的复合药物,如 "美诺伐嗪"、"磺胺卡因 "和 "奥托洛林"。使用 SF-56 分光光度计(OKB SPECTR LLC)进行洗脱液光密度登记。为评估样品制备在色谱分离复方药物时的选择性(特异性),对使用纯化水和 0.1 M 盐酸溶液获得的洗脱液在 200-400 nm 波长范围内进行了吸收光谱登记。洗脱液中普鲁卡因和苯佐卡因的鉴别依据分别是苯佐卡因在波长 222 纳米和 286 纳米处、普鲁卡因在波长 228 纳米和 292 纳米处出现的吸收最大值。根据 OFS.1.1.0013 "物理、理化和化学测试结果的统计处理",对实验结果进行统计处 理,并确定分析方法的计量特性。结果使用基于低聚果糖的固相萃取吸附剂的分光光度法测定某些复方药物中的普鲁卡因的选择性得到了证实。在固相萃取过程中,被分析物质与吸附剂中的活性中心选择性结合,并用纯净水和 0.1 M 盐酸溶液逐步洗脱,消除了药物成分在普鲁卡因紫外分光光度法中的干扰作用。使用基于超美胶糖的吸附剂可改善计量特性,并将定量测定方法的系统误差平均降低 14.4%。
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
自引率
0.00%
发文量
0
×
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:604180095
Book学术官方微信