Lewis P A, Woodward A J, Maddock J
J Pharm Sci. 1984 Jul;73(7):996-8. doi: 10.1002/jps.2600730736.
A sensitive high-performance liquid chromatographic (HPLC) assay for N-acetylcysteine in human plasma and urine has been developed. The method employs a prechromatographic stage to produce the dinitrophenyl derivative of N-acetylcysteine, which is chromatographed on a 5-microns C18 bonded reverse-phase column using an external standard method. The derivatized N-acetylcysteine molecule has a retention time of congruent to 13 min at a flow rate of 1.0 mL/min for a mobile phase of methanol-aqueous 0.05 M citrate-0.001 M EDTA buffer pH 7.0 (30:70). In a multistep extraction procedure, which is slightly modified for the N-acetylcysteine assay in urine, the limits of sensitivity for the plasma and urine assays were found to be congruent to 60 ng/mL and congruent to 200 micrograms/mL, respectively. Preliminary data from pilot studies in human subjects are presented.
已开发出一种用于测定人血浆和尿液中N-乙酰半胱氨酸的灵敏高效液相色谱(HPLC)分析法。该方法采用色谱分离前步骤制备N-乙酰半胱氨酸的二硝基苯基衍生物,然后使用外标法在5微米C18键合反相柱上进行色谱分离。对于甲醇-0.05M柠檬酸-0.001M EDTA缓冲液pH 7.0(30:70)的流动相,在流速为1.0 mL/min时,衍生化的N-乙酰半胱氨酸分子保留时间约为13分钟。在一个多步萃取程序中(该程序针对尿液中N-乙酰半胱氨酸测定略有修改),血浆和尿液分析的灵敏度极限分别约为60 ng/mL和约200微克/mL。文中给出了人体受试者初步研究的初步数据。