Suppr超能文献

高效液相色谱法分析生物材料中的氯碘羟喹

Analysis of iodochlorhydroxyquin in biological materials by high-performance liquid chromatography.

作者信息

Ezzedeen F W, Stohs S J, Stublar M

出版信息

J Chromatogr. 1983 Aug 12;276(1):121-8. doi: 10.1016/s0378-4347(00)85072-0.

Abstract

A reversed-phase high-performance liquid chromatographic system using a mobile phase of 0.05 M phosphoric acid--methanol (30:70) was developed for determination of iodochlorhydroxyquin (clioquinol, I) in biological material. I was extracted from samples with diethyl ether. Conjugates of I were hydrolyzed to free I and extracted by the same method. The ether phases were evaporated to dryness, reconstituted in the mobile phase and chromatographed using a microparticulate C18 column, a pre-column and a UV detector set at 256 nm. Quantitation of I in the range of 0.20-2.0 micrograms/ml of urine, 0.50-2.0 micrograms/g of liver, and 0.25-2.0 micrograms/g of feces was obtained with coefficients of variation of 0.02, 0.05, and 0.06, respectively. The detection limit of I was 0.2 micrograms. Extensive absorption of I upon topical application to dogs was also demonstrated.

摘要

建立了一种反相高效液相色谱系统,以0.05 M磷酸-甲醇(30:70)作为流动相,用于测定生物材料中的碘氯羟喹(氯碘喹啉,I)。I用乙醚从样品中萃取。I的共轭物水解为游离I,并采用相同方法萃取。将乙醚相蒸发至干,用流动相复溶,然后使用微粒C18柱、预柱和设定在256 nm的紫外检测器进行色谱分析。在0.20 - 2.0微克/毫升尿液、0.50 - 2.0微克/克肝脏和0.25 - 2.0微克/克粪便范围内对I进行定量,变异系数分别为0.02、0.05和0.06。I的检测限为0.2微克。还证明了I局部应用于犬时具有广泛的吸收。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验