Vuckovic Dajana, Pawliszyn Janusz
Department of Chemistry, University of Waterloo, Waterloo, Ontario, Canada.
J Pharm Biomed Anal. 2009 Nov 1;50(4):550-5. doi: 10.1016/j.jpba.2008.08.023. Epub 2008 Aug 29.
An automated ligand-receptor binding study was performed for the first time using solid-phase microextraction (SPME) coupled to liquid chromatography-tandem mass spectrometry. A new multi-fibre SPME system, which relies on multi-well plate technology and allows parallel preparation of up to 96 samples was used in order to obtain all data points of the binding curve in a single experiment. The binding of diazepam to human serum albumin was used as the model system in order to evaluate the performance of automated SPME. The time required to establish equilibrium was 30 min; this was verified experimentally by constructing extraction time profiles in the presence and absence of receptor molecules. Fibre constant calibration was used to remove inter-fibre variability from the binding data. Using a simple one-site binding model, a binding constant of 9.1 x 10(5)+/-3 x 10(5)l/mol was obtained. This result is in excellent agreement with values for equilibrium dialysis and manual SPME procedures reported in the literature. The proposed method can be further extended to study plasma-protein binding or drug binding to whole blood. In comparison to other methods, SPME is simpler, faster and fully automated, can be combined with any analytical detection method, and can be used to directly study complex samples.
首次使用与液相色谱-串联质谱联用的固相微萃取(SPME)进行了自动化配体-受体结合研究。使用了一种基于多孔板技术的新型多纤维SPME系统,该系统允许并行制备多达96个样品,以便在单个实验中获得结合曲线的所有数据点。以地西泮与人血清白蛋白的结合作为模型系统来评估自动化SPME的性能。建立平衡所需的时间为30分钟;通过在有和没有受体分子的情况下构建萃取时间曲线进行了实验验证。使用纤维常数校准来消除结合数据中的纤维间变异性。使用简单的单点结合模型,获得的结合常数为9.1×10⁵±3×10⁵ l/mol。该结果与文献中报道的平衡透析和手动SPME程序的值非常一致。所提出的方法可以进一步扩展用于研究血浆蛋白结合或药物与全血的结合。与其他方法相比,SPME更简单、更快且完全自动化,可以与任何分析检测方法结合使用,并且可用于直接研究复杂样品。