Yuan J, Bucher J R, Goehl T J, Dieter M P, Jameson C W
National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709.
J Anal Toxicol. 1992 Nov-Dec;16(6):359-62. doi: 10.1093/jat/16.6.359.
A rapid and sensitive high performance liquid chromatographic (HPLC) method is described for the quantitation of cinnamaldehyde (CNMA) in rat blood at concentrations of 0.1-100 micrograms/mL. One of the metabolites of CNMA, cinnamic acid, can also be quantified simultaneously. CNMA is unstable in rat blood, probably because of rapid oxidation to cinnamic acid by enzymatic catalysis and nonenzymatic Schiff base formation with free amine groups of blood proteins. The disappearance of CNMA from rat blood follows first-order reaction kinetics with a half-life of 9 min at room temperature. The current analysis method involves the addition of an agent that will prevent CNMA degradation by denaturing protein and competitively blocking nucleophilic addition reactions, resulting in the nearly complete recovery of CNMA from blood. Recovery of cinnamic acid was approximately 80% at concentrations of 1-10 micrograms/mL.
描述了一种快速灵敏的高效液相色谱(HPLC)方法,用于定量大鼠血液中浓度为0.1 - 100微克/毫升的肉桂醛(CNMA)。CNMA的一种代谢产物肉桂酸也可同时进行定量。CNMA在大鼠血液中不稳定,可能是由于酶催化快速氧化为肉桂酸,以及与血液蛋白质的游离胺基发生非酶席夫碱形成反应。CNMA在大鼠血液中的消失遵循一级反应动力学,在室温下半衰期为9分钟。当前的分析方法包括添加一种试剂,该试剂通过使蛋白质变性并竞争性阻断亲核加成反应来防止CNMA降解,从而使CNMA从血液中几乎完全回收。在1 - 10微克/毫升的浓度下,肉桂酸的回收率约为80%。