Department of Pharmacodynamics, Semmelweis University, Budapest, Hungary.
Electrophoresis. 2011 Oct;32(20):2816-22. doi: 10.1002/elps.201100032.
Three different fluorescent tags have been compared for the quantitative analysis of aspartate and glutamate in brain microdialysate samples. Separation conditions have been optimized to achieve short analysis time using reversed polarity separation in coated capillary. Method validation has revealed similar quantification limit of 0.1 μM of analytes using either of the labels, although LOD values were different: 7.8-9.8 nM for 4-fluoro-7-nitro-2,1,3-benzoxadiazole, 3.5 nM for fluorescein-5-isothiocyanate and 1.3-1.5 nM for carboxyfluorescein succinimidyl ester derivatives. The almost two orders of magnitude difference between LOD and LOQ values is likely due to the unreliable derivatization reaction at low sample concentration. Based on the superior stability, FITC derivatization was used for the analysis of biological samples. The applicability of the method has been demonstrated by analyzing basal and potassium evoked amino acid concentrations in individual brain microdialysate samples.
已比较了三种不同的荧光标记物,用于定量分析脑微透析样品中的天冬氨酸和谷氨酸。优化了分离条件,以使用涂层毛细管中的反相分离实现短的分析时间。方法验证表明,使用任一种标记物都具有相似的定量限(0.1 μM),尽管检测限(LOD)值不同:4-氟-7-硝基-2,1,3-苯并恶二唑为 7.8-9.8 nM,荧光素-5-异硫氰酸酯为 3.5 nM,羧基荧光素琥珀酰亚胺酯衍生物为 1.3-1.5 nM。LOD 和 LOQ 值之间的两个数量级的差异可能是由于在低样品浓度下衍生化反应不可靠。基于优越的稳定性,FITC 衍生化用于分析生物样品。通过分析个体脑微透析样品中的基础和钾诱发的氨基酸浓度,证明了该方法的适用性。