Drnevich D, Vary T C
Department of Cellular and Molecular Physiology, College of Medicine, Pennsylvania State University, Hershey 17033.
J Chromatogr. 1993 Mar 5;613(1):137-44. doi: 10.1016/0378-4347(93)80207-k.
A method is described for the measurement of the specific radioactivity of primary amino acids in physiological samples. The amino acids were dabsylated followed by separation using high-performance liquid chromatography. We measured the concentration of amino acids from rat plasma or liver samples. Chromatographic analyses resolved phenylalanine from a mixture of amino acids in plasma within 30 min. An extended chromatographic gradient program completely separated all physiological amino acids within 75 min. This method is as sensitive as any current method of amino acid analysis and offers several advantages including (1) simple pre-column derivatization and (2) stability of derivatized samples.
本文描述了一种用于测量生理样品中一级氨基酸比放射性的方法。氨基酸经丹磺酰化后,采用高效液相色谱进行分离。我们测定了大鼠血浆或肝脏样品中氨基酸的浓度。色谱分析在30分钟内从血浆中的氨基酸混合物中分离出苯丙氨酸。一个扩展的色谱梯度程序在75分钟内完全分离了所有生理氨基酸。该方法与目前任何氨基酸分析方法一样灵敏,并具有几个优点,包括(1)简单的柱前衍生化和(2)衍生化样品的稳定性。