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METHOD FOR QUANTITATIVE DETERMINATION OF TRIAZAVIRIN BY VOLTAMMETRY (VERSIONS)

机译:伏安法(含量)定量测定三唑嗪的方法。

摘要

FIELD: chemistry.;SUBSTANCE: invention relates to analytical chemistry, in particular, to voltametric method for determining drug triazavirin. Method can be used for quantitative determination of said compound in powder and its medicinal forms. Invention can be used in pharmaceutical industry for controlling technological processes and quality of pharmaceutical drugs, waste water and air zone of chemical-pharmaceutical enterprises, in pharmaceutical control laboratories for determination of active substances of medicinal agents. Invention is based on capacity of triazavirin to be recovered at various types of graphite electrodes and comprises converting triazavirin from a sample into an aqueous solution and direct (without preliminary accumulation on an electrode) voltammetric determination of triazavirin in it on a background of 0.1 mol/l nitric acid with registration of cathode peaks in square-wave mode capturing voltametric curves in range from 0.2 to (-0.6) V at a rate of potential sweep 160 mV/s. Concentration of triazavirin is determined by peak height in potential range from 0.10 to (-0.40) V relative to a silver chloride electrode by triazavirin standard addition method.;EFFECT: invention enables design a sensitive and rapid method for quantitative determination of triazavirin by voltammetry in substance and dosage form for controlling quality of drug.;2 cl, 1 dwg, 3 tbl, 2 ex
机译:技术领域本发明涉及分析化学,尤其涉及测定药物三氮唑林的伏安法。该方法可用于定量测定粉末及其药用形式的所述化合物。发明可用于制药工业中,用于控制药品的工艺过程和质量,化学制药企业的废水和空气区,在制药控制实验室中用于确定药物活性成分。本发明基于在各种类型的石墨电极上回收的triazavirin的能力,包括将样品中的triazavirin转换成水溶液,并在0.1 mol / ml的背景下直接(无需在电极上初步积累)伏安法测定triazavirin l在方波模式下具有阴极峰配准的硝酸,以160 mV / s的电位扫描速率捕获了0.2至(-0.6)V范围内的伏安曲线。相对于氯化银电极,通过Triazavirin标准添加方法,峰高在0.10至(-0.40)V的电位范围内确定峰高;效果:本发明能够设计一种灵敏而快速的伏安法定量测定Triazavirin的方法用于控制药物质量的物质和剂型。; 2 cl,1 dwg,3 tbl,2 ex

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