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液相色谱法测定血清中的阿米替林及其代谢物,使玻璃吸附作用降至最低。

Liquid-chromatographic determination of amitryptyline and its metabolites in serum, with adsorption onto glass minimized.

作者信息

Edelbroek P M, de Haas E J, de Wolff F A

出版信息

Clin Chem. 1982 Oct;28(10):2143-8.

PMID:7127744
Abstract

To study correlations between the concentrations, in serum, of amitriptyline and its most important metabolites with clinical response in patients, we developed a "high-performance" liquid-chromatographic method for routine determination of amitriptyline, nortriptyline, total 10-hydroxy-amitriptyline, desmethylnortriptyline, and E(trans)- and Z(cis)-10-hydroxynortriptyline. These compounds are extracted from 1 mL of alkalinized serum into hexane/isoamyl alcohol (99/1 by vol). Perazine is the internal standard. To minimize irreversible adsorption of the drugs onto the glassware, 5 micrograms of maprotiline is added to the organic phase just before evaporation. After a 10-min resolution on a silica column eluted with acetonitrile/methanol/NH4OH (1 mol/L), absorbance is measured at 240 nm. Only chlorimipramine, doxepin, procainamide, and N-acetylprocainamide may interfere with assay of the compounds that probably are therapeutically relevant: amitriptyline, nortriptyline, and E-10-hydroxynortriptyline. Uremia, lipemia, and icterus also do not affect the analysis.

摘要

为了研究患者血清中阿米替林及其最重要代谢物的浓度与临床反应之间的相关性,我们开发了一种“高效”液相色谱法,用于常规测定阿米替林、去甲替林、总10 - 羟基阿米替林、去甲去甲替林以及E(反式)-和Z(顺式)-10 - 羟基去甲替林。这些化合物从1 mL碱化血清中萃取到己烷/异戊醇(体积比99/1)中。奋乃静为内标。为了使药物在玻璃器皿上的不可逆吸附降至最低,在蒸发前向有机相中加入5微克马普替林。在以乙腈/甲醇/NH4OH(1 mol/L)洗脱的硅胶柱上分离10分钟后,于240 nm处测量吸光度。只有氯米帕明、多塞平、普鲁卡因胺和N - 乙酰普鲁卡因胺可能干扰对可能具有治疗相关性的化合物(阿米替林、去甲替林和E - 10 - 羟基去甲替林)的测定。尿毒症、脂血症和黄疸也不影响分析。

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