Salamoun J, Remien J
Walther-Straub Institute of Pharmacology and Toxicology, Munich, Germany.
J Pharm Biomed Anal. 1992 Oct-Dec;10(10-12):931-6. doi: 10.1016/0731-7085(91)80101-e.
The inhibiting compounds were separated by micro-column liquid chromatography in the mobile phase containing the natural substrate acetylcholine. A home-made packed bed microbioreactor system containing immobilized enzyme acetylcholinesterase (ACHE) in human red blood cell membrane and choline oxidase (CHO) from alcaligenes was used for the post-column conversion of acetylcholine to hydrogen peroxide which was detected by an electrochemical detector. The inhibition effect of the solutes caused a decrease in the acetylcholinesterase activity, a decrease in the formation of hydrogen peroxide and also a decrease in the response corresponding to the concentration of the solutes. The rate of the enzyme regeneration was also recorded. The micro-system was compared with a conventional LC system comprising commercially prepared enzyme reactor. The stability of the enzymes is at least 3 weeks at ambient temperature. The limit of detection depends on biological activity of inhibition and for galanthamine was 1 pmol.
在含有天然底物乙酰胆碱的流动相中,通过微柱液相色谱法分离抑制性化合物。使用一种自制的填充床微生物反应器系统,该系统在人红细胞膜中固定化了乙酰胆碱酯酶(ACHE)以及来自产碱杆菌的胆碱氧化酶(CHO),用于将柱后流出的乙酰胆碱转化为过氧化氢,然后通过电化学检测器进行检测。溶质的抑制作用导致乙酰胆碱酯酶活性降低、过氧化氢生成量减少以及与溶质浓度相对应的响应降低。同时还记录了酶的再生速率。将该微系统与包含商业制备酶反应器的传统液相色谱系统进行了比较。在环境温度下,酶的稳定性至少为3周。检测限取决于抑制的生物活性,加兰他敏的检测限为1皮摩尔。