Aslanoglu Mehmet, Peker Nesrin
Department of Chemistry, Harran University, 63100 Sanliurfa, Turkey.
J Pharm Biomed Anal. 2003 Dec 4;33(5):1143-7. doi: 10.1016/s0731-7085(03)00431-x.
The determination of methimazole was investigated by potentiometric titration in an alkaline medium involving its reaction with iodine and square wave voltammetry (SWV) in 0.1 mol/l Tris-HCl buffer at pH 7.2. In potentiometric titration, the range of determination was 10-500 micromol. A stoichiometric reaction was obtained within the concentration range 0.75-1.25 mol/l of sodium hydroxide by potentiometric titration. A linear calibration graph was obtained over the concentration range 1-700 micromol/l by SWV. The lowest concentration of methimazole detected was 0.5 micromol/l. The relative standard deviations (R.S.D.) were 0.81% in potentiometric titration and 2.89% in square wave voltammetric analysis of thyromazol tablets. The data showed that potentiometric titration using iodine in sodium hydroxide can be used for the determination of methimazole in drug samples without prior separation.
研究了在碱性介质中通过电位滴定法(涉及甲巯咪唑与碘的反应)以及在pH 7.2的0.1 mol/l Tris-HCl缓冲液中采用方波伏安法(SWV)对甲巯咪唑进行测定。在电位滴定中,测定范围为10 - 500微摩尔。通过电位滴定在0.75 - 1.25 mol/l氢氧化钠浓度范围内获得了化学计量反应。通过SWV在1 - 700微摩尔/升的浓度范围内获得了线性校准曲线。检测到的甲巯咪唑最低浓度为0.5微摩尔/升。在甲巯咪唑片的电位滴定中相对标准偏差(R.S.D.)为0.81%,在方波伏安分析中为2.89%。数据表明,在氢氧化钠中使用碘的电位滴定法可用于无需预先分离即可测定药物样品中的甲巯咪唑。