Gabrielsson M, Hoffmann K J, Regårdh C G
Astra Hässle Research Laboratories, Department of Pharmacokinetics and Drug Metabolism, Mölndal, Sweden.
J Chromatogr. 1992 Jan 17;573(2):265-74. doi: 10.1016/0378-4347(92)80128-d.
A reversed-phase high-performance liquid chromatography method with ultraviolet detection at 220 nm was developed to determine four carboxylic acid metabolites in plasma following therapeutic doses of the calcium antagonist felodipine. After the addition of an internal standard the analytes were isolated by liquid-liquid and solid-phase extraction. The metabolites were applied to a C2 cartridge in their free acid form, but they were transformed and retained as ion pairs with tetrabutylammonium during a wash with phosphate buffer (pH 7), prior to automated elution and injection by the Varian AASP system onto the analytical C18 column. Using a sample volume of 1 ml of plasma, the lower limit of determination for the metabolites was about 20 nmol/l. The influence of the pH of the mobile phase on the retention time of the metabolites and the structural requirements for the internal standard were studied. The method was applied to plasma samples from four dogs collected after an oral dose of felodipine. The plasma concentration-time profiles of the metabolites gave useful information about the mechanisms by which they were formed and eliminated.
建立了一种反相高效液相色谱法,采用220 nm紫外检测,用于测定治疗剂量的钙拮抗剂非洛地平给药后血浆中的四种羧酸代谢物。加入内标后,通过液-液萃取和固相萃取分离分析物。代谢物以游离酸形式应用于C2柱,但在用磷酸盐缓冲液(pH 7)洗涤期间,它们会转化并作为与四丁基铵的离子对保留,然后通过Varian AASP系统自动洗脱并注入分析C18柱。使用1 ml血浆的进样体积,代谢物的测定下限约为20 nmol/l。研究了流动相pH对代谢物保留时间的影响以及内标的结构要求。该方法应用于口服非洛地平后采集的四只犬的血浆样本。代谢物的血浆浓度-时间曲线提供了有关其形成和消除机制的有用信息。