Cracco A T, Dall'Amico R, Ferrari V, Bottaro S, Zacchello G, Chiandetti L, Zacchello F
Department of Pediatrics, University of Padua, Italy.
J Chromatogr. 1992 Feb 7;574(1):156-60. doi: 10.1016/0378-4347(92)80112-4.
A sensitive and accurate assay was developed for the measurement of 8-methoxypsoralen in plasma using electron-impact positive-ion mass fragmentography. 4,5,8-Trimethylpsoralen was used as an internal standard. Sample preparation consisted of a two-step liquid phase extraction using acetonitrile and methylene chloride. The calibration curve showed a linear relationship between the peak areas of 8-methoxypsoralen and 4,5,8-trimethylpsoralen over a wide range of 8-methoxypsoralen concentrations (1-500 ng/ml). With-in- and between-run precisions, measured at five different drug concentrations, varied from 0.82 to 1.41% and from 0.82 to 1.86%, respectively.
采用电子轰击正离子质量碎片分析法,开发了一种灵敏且准确的血浆中8-甲氧基补骨脂素的测定方法。使用4,5,8-三甲基补骨脂素作为内标。样品制备包括使用乙腈和二氯甲烷的两步液相萃取。校准曲线表明,在8-甲氧基补骨脂素的广泛浓度范围(1-500 ng/ml)内,8-甲氧基补骨脂素和4,5,8-三甲基补骨脂素的峰面积之间呈线性关系。在五个不同药物浓度下测得的批内精密度和批间精密度分别在0.82%至1.41%和0.82%至1.86%之间变化。