单扫描极谱法测定药物中苯佐卡因和普鲁卡因的新方法

IF 2.3 Q3 ELECTROCHEMISTRY
S. Plotycya, Oksana Strontsitska, Solomiya Pysarevska, M. Blazheyevskiy, L. Dubenska
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引用次数: 9

摘要

用过一硫酸钾极谱还原苯并卡因和普鲁卡因的化学氧化产物,建立了测定苯并卡因、普鲁卡因的新极谱法。探讨了影响苯甲卡因和普鲁卡因氧化产物定量产率的实验条件,如рH、氧化时间、试剂浓度和温度。结果表明,在1·10−6-5·10−5 mol L−1的浓度范围内,还原电流随麻醉剂浓度的增加呈线性变化(R=0.999)。苯佐卡因和普鲁卡因的检测限分别为5.6·10−6和6·10−6mol L−1。本研究采用极谱法定量测定法瑞西片、Septolete Plus含片和普鲁卡因注射液中苯佐卡因的含量。分析结果与质量证书中描述的产品规格非常一致。证实了定量测定药物中苯佐卡因和普鲁卡因的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A New Approach for the Determination of Benzocaine and Procaine in Pharmaceuticals by Single-Sweep Polarography
A new polarographic method for the determination of benzocaine and procaine based on the polarographic reduction of their chemically obtained oxidation products with potassium peroxymonosulfate is developed. Experimental conditions affecting quantitative yield of benzocaine and procaine oxidation products such as рH, oxidation time, reagents’ concentration, and temperature are explored. It is shown that the reduction current changes in a linear fashion (R=0.999) with increasing concentration of anesthetics over a concentration range of 1·10−6 - 5·10−5 mol L−1. The calculated limits of detection (LOD) for benzocaine and procaine are found to be 5.6·10−6 and 6·10−6 mol L−1, respectively. In the present study, quantitative polarographic determination of benzocaine in Farisil tablets and “Septolete Plus” lozenges and procaine in solution for injections is performed. The results of the analysis are in good agreement with the product specifications described in the quality certificates. The possibility of quantitative determination of benzocaine and procaine in pharmaceuticals is confirmed.
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