Stehlík P, Hapala J, Cepeláková H
Výzkumný ústav pro farmacii a biochemii, Praha.
Cesk Farm. 1990 Feb;39(1):22-4.
An analytical method of the assay of isosorbide dinitrate in the human plasma was developed. The analytical method is based on the extraction of the plasma with toluene and direct injection of the toluene phase on the packed column (3% SE 30) of a gas chromatographic apparatus. After separation, detection is carried out with a detector of electron capture. The reported method is rapid (period of analysis = 10 min), sensitive (limit of detection = 0.1 ng/ml of plasma) and sufficiently precise (error of the method, 12%). The precision of the method during the day and between days is presented. The application of the method is shown in a comparison of a Czechoslovak preparation in advance development with the foreign preparation Iso-Mack. The results after administration of 5 mg of the Czechoslovak and foreign sublingual form of the preparation in a group of ten volunteers are documented with the course of the levels in the individual experimental subjects and the principal pharmacokinetic derived from the one-compartmental model.
建立了一种人血浆中异山梨醇二硝酸酯的分析方法。该分析方法基于用甲苯萃取血浆,并将甲苯相直接注入气相色谱仪的填充柱(3% SE 30)。分离后,用电子捕获检测器进行检测。所报道的方法快速(分析周期 = 10分钟)、灵敏(检测限 = 0.1 ng/ml血浆)且足够精确(方法误差为12%)。给出了该方法在日间和日间的精密度。该方法的应用体现在将一种处于前期开发阶段的捷克斯洛伐克制剂与国外制剂Iso - Mack进行比较。在一组十名志愿者中给予5毫克捷克斯洛伐克制剂和国外制剂的舌下剂型后,记录了个体实验对象中药物水平的变化过程以及源自单室模型的主要药代动力学情况。