Piepponen T P, Skujins A
Department of Pharmacy, University of Helsinki, Finland.
J Chromatogr B Biomed Sci Appl. 2001 Jun 15;757(2):277-83. doi: 10.1016/s0378-4347(01)00156-6.
We developed a rapid step-gradient HPLC method for determination of glutamate, glycine and taurine, and a separate method for determination of gamma-aminobutyric acid (GABA) in striatal microdialysates. The amino acids were pre-column derivatized with o-phthalaldehyde-2-mercaptoethanol by using an automated refrigerated autoinjector. Separation of the amino acids was established with a non-porous ODS-II HPLC column, late-eluting substances were washed out with a one-step low-pressure gradient. Concentrations of the amino acids were determined with a fixed-wavelength fluorescence detector. The detection limit for GABA was 80 fmol in a 15 microl sample, detection limits for glutamate, glycine and taurine were not determined because their concentrations in striatal perfusates were far above their detection limits. Total analysis time was less than 12 min, including the wash-out step. The methods described are relatively simple, sensitive, inexpensive, and fast enough to keep up with the microdialysis sampling.
我们开发了一种快速梯度高效液相色谱法用于测定纹状体微透析液中的谷氨酸、甘氨酸和牛磺酸,以及一种单独的方法用于测定γ-氨基丁酸(GABA)。氨基酸通过自动制冷自动进样器用邻苯二甲醛-2-巯基乙醇进行柱前衍生。使用无孔ODS-II高效液相色谱柱对氨基酸进行分离,后期洗脱的物质通过一步低压梯度洗脱。氨基酸浓度通过固定波长荧光检测器测定。在15微升样品中,GABA的检测限为80飞摩尔,谷氨酸、甘氨酸和牛磺酸的检测限未测定,因为它们在纹状体灌注液中的浓度远高于其检测限。总分析时间少于12分钟,包括洗脱步骤。所描述的方法相对简单、灵敏、廉价且速度足够快,能够跟上微透析采样的速度。