Vielhauer S, Rudolphi A, Boos K S, Seidel D
Institut für Klinische Chemie, Ludwig-Maximilians-Universität, München, Germany.
J Chromatogr B Biomed Appl. 1995 Apr 21;666(2):315-22. doi: 10.1016/0378-4347(94)00578-s.
A fully automated coupled-column HPLC method for on-line sample processing and determination of the photoreactive drug 8-methoxypsoralen (8-MOP) in plasma has been developed. The method is based on the novel internal-surface reversed-phase precolumn packing materials Alkyl-Diol Silica (ADS). This new family of restricted-access materials has a hydrophilic, electroneutral outer particle surface and a hydrophobic internal pore surface. The supports tolerate the direct and repetitive injection of proteinaceous fluids such as plasma and allow a classical C18-, C8- or C4-reversed-phase partitioning at the internal (pore) surface. The total protein load, i.e. the lifetime of the precolumn used in this study (C8-Alkyl-Diol Silica, 25 microns, 25 x 4 mm I.D.), exceeds more than 100 ml of plasma. 8-MOP was detected by its native fluorescence (excitation 312 nm, emission 540 nm). Validation of the method revealed a quantitative and matrix-independent recovery (99.5-101.3% measured at five concentrations between 21.3 and 625.2 ng of 8-MOP per milliliter of plasma), linearity over a wide range of 8-MOP concentrations (1.2-3070 ng of 8-MOP/ml, r = 0.999), low limits of detection (0.39 ng of 8-MOP/ml) and quantitation (0.79 ng of 8-MOP/ml) and a high between-run (C.V. 1.47%, n = 10) and within-run (C.V. 1.33%, n = 10) reproducibility. This paper introduces coupled-column HPLC as a suitable method for on-site analysis of drug plasma profiles (bedside-monitoring).
已开发出一种全自动耦合柱高效液相色谱法,用于在线样品处理并测定血浆中的光反应性药物8-甲氧基补骨脂素(8-MOP)。该方法基于新型内表面反相预柱填充材料烷基二醇硅胶(ADS)。这类新型的受限进样材料具有亲水性、电中性的外颗粒表面和疏水性的内孔表面。这些载体能够耐受直接且重复地进样含蛋白质的流体,如血浆,并允许在内部(孔)表面进行经典的C18、C8或C4反相分配。总的蛋白负载量,即本研究中使用的预柱(C8-烷基二醇硅胶,25微米,内径25×4毫米)的使用寿命,超过100毫升血浆。通过其自身荧光(激发波长312纳米,发射波长540纳米)检测8-MOP。该方法的验证显示出定量且与基质无关的回收率(在每毫升血浆中21.3至625.2纳克8-MOP的五个浓度下测得的回收率为99.5 - 101.3%)、在很宽的8-MOP浓度范围内(1.2 - 3070纳克8-MOP/毫升,r = 0.999)呈线性、低检测限(0.39纳克8-MOP/毫升)和定量限(0.79纳克8-MOP/毫升)以及高的批间(变异系数1.47%,n = 10)和批内(变异系数1.33%,n = 10)重现性。本文介绍了耦合柱高效液相色谱法作为一种适用于现场分析药物血浆谱(床边监测)的方法。