Steele K M, Lunte C E
Department of Chemistry, University of Kansas, Lawrence 66045, USA.
J Pharm Biomed Anal. 1995 Feb;13(2):149-54. doi: 10.1016/0731-7085(94)00135-o.
Microdialysis sampling has been coupled on-line to microbore liquid chromatography for pharmacokinetic investigations in awake, freely-moving animals. Valve systems are described which provide continuous collection of the microdialysis sample for injection into the chromatographic system. One valve system consisted of two six-port valves used in tandem. The other valve system consisted of an eight-port valve with two sample loops. The eight-port valve system provided better precision than the dual six-port valve system yet worse than an autosampler. However, when used for dialysis samples, the precision of the various injection methods was equivalent. The on-line system was capable of rapidly following changes in the dialysate concentration and provided near real-time analysis of the plasma concentration of analytes. The system was evaluated by monitoring the pharmacokinetics of acetaminophen in awake, freely-moving rats.
微透析采样已与微径液相色谱在线联用,用于清醒、自由活动动物的药代动力学研究。文中描述了阀门系统,该系统可连续收集微透析样品以注入色谱系统。一种阀门系统由两个串联使用的六通阀组成。另一种阀门系统由一个带有两个样品环的八通阀组成。八通阀系统的精度优于双六通阀系统,但比自动进样器差。然而,当用于透析样品时,各种进样方法的精度相当。该在线系统能够快速跟踪透析液浓度的变化,并提供分析物血浆浓度的近实时分析。通过监测清醒、自由活动大鼠体内对乙酰氨基酚的药代动力学对该系统进行了评估。