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Plasma L-Ergothioneine Measurement by High-Performance Liquid Chromatography and Capillary Electrophoresis after a Pre-Column Derivatization with 5-Iodoacetamidofluorescein (5-IAF) and Fluorescence Detection

机译:5-碘乙酰氨基荧光素(5-IAF)柱前衍生化和荧光检测后通过高效液相色谱和毛细管电泳测定血浆L-麦角硫氨酸

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摘要

Two sensitive and reproducible capillary electrophoresis and high-performance liquid chromatography-fluorescence procedures were established for quantitative determination of L-egothioneine in plasma. After derivatization of L-ergothioneine with 5-iodoacetamidofluorescein, the separation was carried out by HPLC on an ODS-2 C-18 sperisorb column by using a linear gradient elution and by HPCE on an uncoated fused silica capillary, 50 µm id, and 60 cm length. The methods were validated and found to be linear in the range of 0.3 to 10 µmol/l. The limit of quantification was 0.27 µmol/l for HPCE and 0.15 µmol/l for HPLC. The variations for intra- and inter-assay precision were around 6 RSD%, and the mean recovery accuracy close to 100% (96.11%).
机译:建立了两种灵敏且可重现的毛细管电泳和高效液相色谱-荧光程序,用于定量测定血浆中的L-蛋氨酸。用5-碘乙酰酰胺基荧光素衍生L-麦角硫氨酸后,使用线性梯度洗脱法在ODS-2 C-18吸附柱上通过HPLC进行分离,并在未涂覆的熔融石英毛细管,内径50 µm和60上通过HPCE进行分离厘米长。方法经过验证,发现线性范围为0.3至10 µmol / l。 HPCE的定量限为0.27 µmol / l,HPLC的定量限为0.15 µmol / l。批内和批间精密度的差异约为6 RSD%,平均回收准确度接近100%(96.11%)。

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