Okuno A, Yano K, Inyaku F, Suzuki Y, Taguchi T, Murata M, Momotani N
Nihon Naibunpi Gakkai Zasshi. 1984 Aug 20;60(8):985-94. doi: 10.1507/endocrine1927.60.8_985.
An improved method for plasma methimazole assay using high performance liquid chromatography is described. The plasma samples were treated with sodium bisulfite and ammonium sulfate prior to extraction with chloroform. This pretreatment of the samples raised the extraction coefficient to 90%, while simple extraction yielded only 55%. The minimal detection limit was 0.02 microgram/ml, and the coefficient of variation at the level of 0.2 and 1.0 microgram/ml was less than 5%. Pharmacokinetics of methimazole was studied after a single oral dose (20 mg/m2) in six subjects including two healthy adults and four thyrotoxic children. Plasma levels of methimazole showed a peak concentration of 1.03 +/- 0.25 microgram/ml approximately one hour after the drug administration. Plasma half-life, area under the curve and distribution volume were 4.56 +/- 0.71 hr, 7.05 +/- 0.95 microgram/ml X hr, and 630 +/- 110 ml/kg respectively.
描述了一种使用高效液相色谱法测定血浆中甲巯咪唑的改进方法。血浆样品在用氯仿萃取前先用亚硫酸氢钠和硫酸铵处理。样品的这种预处理将萃取系数提高到了90%,而单纯萃取仅产生55%的萃取率。最低检测限为0.02微克/毫升,在0.2和1.0微克/毫升水平的变异系数小于5%。在包括两名健康成年人和四名甲状腺毒症儿童在内的六名受试者中,单次口服剂量(20毫克/平方米)后研究了甲巯咪唑的药代动力学。给药后约一小时,甲巯咪唑的血浆水平显示出峰值浓度为1.03±0.25微克/毫升。血浆半衰期、曲线下面积和分布容积分别为4.56±0.71小时、7.05±0.95微克/毫升×小时和630±110毫升/千克。