Herfst M J, Edelbroek P M, de Wolff F A
Clin Chem. 1980 Dec;26(13):1825-8.
A method is described for determination of 8-methoxypsoralen to 0.2 mL of suction-blister fluid or 1 mL of serum from psoriatic patients being treated with this drug. The drug is extracted from the biological matrix at pH 9.0 with a mixture of dichloromethane and light petroleum ether. 5-Methoxypsoralen is used as internal standard. Separation and quantitation are performed on a "high-performance" liquid chromatograph with use of an RP 18 reversed-phase column and detection at 245 nm. Accuracy and precision are good. Some benzodiazepines and their metabolites interfere. The lowest detectable concentration is 10 microgram/L, which means that the method is sufficiently sensitive to measure the drug concentrations in serum and suction-blister fluid for pharmacokinetic studies in patients being treated with a therapeutic dosage.
本文描述了一种测定方法,用于测定接受该药物治疗的银屑病患者0.2 mL吸疱液或1 mL血清中的8-甲氧基补骨脂素。该药物在pH 9.0条件下,用二氯甲烷和轻质石油醚的混合物从生物基质中萃取。5-甲氧基补骨脂素用作内标。使用RP 18反相柱并在245 nm处进行检测,在“高效”液相色谱仪上进行分离和定量。准确度和精密度良好。一些苯二氮䓬类药物及其代谢物会产生干扰。最低可检测浓度为10微克/升,这意味着该方法灵敏度足够高,可用于测定接受治疗剂量治疗的患者血清和吸疱液中的药物浓度,以进行药代动力学研究。