Fleuren H L, Van Rossum J M
J Chromatogr. 1978 May 11;152(1):41-54. doi: 10.1016/s0021-9673(00)85332-7.
A sensitive and selective gas chromatographic method is described for determining the diuretic and antihypertensive drug chlorthalidone in plasma, urine and erythrocytes. Use is made of an alkali flame ionization detector (nitrogen detector), and the chlorthalidone and internal standard are chromatographed as methyl derivatives. Down to 10 ng of drugs in the biological sample can be measured accurately, with a standard deviation of 5%. Because the concentration of chlorthalidone found in erythrocytes is 50-100 times higher than that in plasma, the influence of haemolysis on the plasma concentration has been investigated. In addition, a pharmacokinetic study with human volunteers revealed that the apparent concentration of the drug found in plasma can be much too low (by more than 50%), if the plasma is not separated from the erythrocytes immediately after venipuncture. Precautions to be observed to ensure correct handling of blood samples (so that results for plasma concentrations will be reliable) are stressed. The findings have application in kinetic studies on chlorthalidone.
本文描述了一种灵敏且具选择性的气相色谱法,用于测定血浆、尿液及红细胞中的利尿降压药氯噻酮。采用碱火焰离子化检测器(氮检测器),氯噻酮和内标物以甲基衍生物形式进行色谱分析。生物样品中低至10 ng的药物均可准确测定,标准偏差为5%。由于红细胞中氯噻酮的浓度比血浆中高50 - 100倍,因此研究了溶血对血浆浓度的影响。此外,一项针对人类志愿者的药代动力学研究表明,如果静脉穿刺后血浆未立即与红细胞分离,血浆中药物的表观浓度可能会低得多(超过50%)。强调了为确保正确处理血样(以便血浆浓度结果可靠)而需注意的预防措施。这些发现可应用于氯噻酮的动力学研究。