Department of Chemistry, University of Pittsburgh, Pittsburgh, Pennsylvania 15260, USA.
Anal Chem. 2010 Sep 1;82(17):7267-73. doi: 10.1021/ac101182r.
Reduced glutathione (GSH) has been determined by fluorescence detection after derivatization together with a variety of separations. The reactions between GSH and fluorescent reagents usually are carried out during the sample pretreatment and require minutes to hours for complete reactions. For continuous monitoring of GSH, it would be very convenient to have an integrated microdevice that could perform online precolumn derivatization, separation, and detection. Heretofore, thiol-specific fluorogenic reagents require fairly long reaction times, preventing effective online precolumn derivatization. We demonstrate here that the fluorogenic, thiol-specific reagent, ThioGlo-1, reacts rapidly enough for efficient precolumn derivatization. The second order rate constant for the reaction of GSH and reagent (pH 7.5, room temperature) is 2.1 x 10(4) M(-1)s(-1). The microchip integrates this precolumn derivatization, continuous flow gated sampling, separation, and detection on a single device. We have validated this device for monitoring GSH concentration continuously by studying the kinetics of glutathione reductase (EC 1.8.1.7), an enzyme that catalyzes the reduction of oxidized glutathione (GSSG) to GSH in the presence of beta-NADPH (beta-nicotinamide adenine dinucleotide phosphate, reduced form) as a reducing cofactor. During the experiment, GSH being generated in the enzymatic reaction was labeled with ThioGlo-1 as it passed through a mixing channel on the microfluidic chip. Derivatization reaction products were introduced into the analysis channel every 10 s using flow gated injections of 0.1 s. Baseline separation of the internal standard, ThioGlo-1, and the fluorescently labeled GSH was successfully achieved within 4.5 s in a 9 mm separation channel. Relative standard deviations of the peak area, peak height, and full width at half-maximum (fwhm) for the internal standard were 2.5%, 2.0%, and 1.0%, respectively, with migration time reproducibility for the internal standard of less than 0.1% RSD in any experiment. The GSH concentration and mass detection limit were 4.2 nM and approximately 10(-18) mol, respectively. The Michaelis constants (K(m)) for GSSG and beta-NADPH were found to be 40 +/- 11 and 4.4 +/- 0.6 muM, respectively, comparable with those obtained from UV/vis spectrophotometric measurements. These results show that this system is capable of integrating derivatization, injection, separation, and detection for continuous GSH determinations.
还原型谷胱甘肽(GSH)通过与各种分离物一起衍生化后的荧光检测来确定。GSH 与荧光试剂之间的反应通常在样品预处理过程中进行,需要几分钟到几小时才能完成完全反应。为了连续监测 GSH,拥有一个可以在线进行预柱衍生化、分离和检测的集成微器件将非常方便。迄今为止,硫醇特异性荧光试剂需要相当长的反应时间,从而阻止了有效的在线预柱衍生化。我们在此证明,硫醇特异性荧光试剂 ThioGlo-1 的反应速度足够快,可以进行有效的预柱衍生化。在 pH7.5,室温下,GSH 和试剂之间的二级反应速率常数为 2.1 x 10(4) M(-1)s(-1)。微芯片在单个器件上集成了这种预柱衍生化、连续流门控采样、分离和检测。我们通过研究催化氧化型谷胱甘肽(GSSG)还原为 GSH 的酶谷胱甘肽还原酶(EC 1.8.1.7)的动力学,验证了该装置连续监测 GSH 浓度的能力,该酶在作为还原辅助因子的β-NADPH(β-烟酰胺腺嘌呤二核苷酸磷酸,还原形式)存在下。在实验中,在酶反应中生成的 GSH 在通过微流控芯片上的混合通道时用 ThioGlo-1 标记。衍生化反应产物使用 0.1 s 的流门控注入每 10 s 引入分析通道。在 9 毫米分离通道内成功实现了内标物、ThioGlo-1 和荧光标记的 GSH 的基线分离,仅需 4.5 秒。内标物的峰面积、峰高和半峰宽(fwhm)的相对标准偏差分别为 2.5%、2.0%和 1.0%,任何实验中内标物的迁移时间重现性均小于 0.1%RSD。GSH 浓度和质量检测限分别为 4.2 nM 和约 10(-18)mol。发现 GSSG 和β-NADPH 的米氏常数(K(m))分别为 40 ± 11 和 4.4 ± 0.6 μM,与紫外/可见分光光度法测量得到的值相当。这些结果表明,该系统能够集成衍生化、进样、分离和检测,用于连续的 GSH 测定。