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高效液相色谱法同时测定大鼠血浆和尿液中溴吡斯的明、N,N-二乙基间甲苯酰胺、氯菊酯及其代谢物

Simultaneous determination of pyridostigmine bromide, N,N-diethyl-m-toluamide, permethrin, and their metabolites in rat plasma and urine by high-performance liquid chromatography.

作者信息

Abu-Qare A W, Abou-Donia M B

机构信息

Department of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, NC 27710, USA.

出版信息

J Chromatogr B Biomed Sci Appl. 2000 Dec 1;749(2):171-8. doi: 10.1016/s0378-4347(00)00407-2.

Abstract

A rapid and simple method was developed for the separation and quantification of the anti nerve agent drug pyridostignmine bromide (PB; 3-dimethylaminocarbonyloxy-N-methyl pyridinium bromide) its metabolite N-methyl-3-hydroxypyridinium bromide, the insect repellent DEET (N,N-diethyl-m-toluamide), its metabolites m-toluamide and m-toluic acid, the insecticide permethrin (3-(2,2-dichloro-ethenyl)-2,2-dimethylcyclopropanecarboxylic acid(3-phenoxyphenyl)methylester), and two of its metabolites m-phenoxybenzyl alcohol, and m-phenoxybenzoic acid in rat plasma and urine. The method is based on using C18 Sep-Pak cartridges for solid-phase extraction (SPE) and high-performance liquid chromatography (HPLC) with reversed-phase C18 column, and gradient UV detection ranging between 208 and 230 nm. The compounds were separated using gradient of 1 to 99% acetonitrile in water (pH 3.20) at a flow-rate ranging between 0.5 and 1.7 ml/min in a period of 17 min. The retention times ranged from 5.7 to 14.5 min. The limits of detection were ranged between 20 and 100 ng/ml, while limits of quantitation were 150-200 ng/ml. Average percentage recovery of five spiked plasma samples were 51.4+/-10.6, 71.1+/-11.0, 82.3+/-6.7, 60.4+/-11.8, 63.6+/-10.1, 69.3+/-8.5, 68.3+/-12.0, 82.6+/-8.1, and from urine 55.9+/-9.8, 60.3+/-7.4, 77.9+/-9.1, 61.7+/-13.5, 68.6+/-8.9, 62.0+/-9.5, 72.9+/-9.1, and 72.1+/-8.0, for pyridostigmine bromide, DEET, permethrin, N-methyl-3-hydroxypyridinium bromide, m-toluamide, m-toluic acid, m-phenoxybenzyl alcohol and m-phenoxybenzoic acid, respectively. The relationship between peak areas and concentration was linear over the range between 100 and 5000 ng/ml. This method was applied to analyze the above chemicals and metabolites following their administration in rats.

摘要

已开发出一种快速简便的方法,用于分离和定量大鼠血浆及尿液中的抗神经毒剂药物溴化吡啶斯的明(PB;3 - 二甲基氨基甲酰氧基 - N - 甲基吡啶溴化物)及其代谢物N - 甲基 - 3 - 羟基吡啶溴化物、驱虫剂避蚊胺(N,N - 二乙基 - m - 甲苯酰胺)及其代谢物m - 甲苯酰胺和m - 甲苯酸、杀虫剂氯菊酯(3 - (2,2 - 二氯乙烯基)-2,2 - 二甲基环丙烷羧酸(3 - 苯氧基苯基)甲酯)及其两种代谢物m - 苯氧基苄醇和m - 苯氧基苯甲酸。该方法基于使用C18 Sep - Pak柱进行固相萃取(SPE),以及采用反相C18柱的高效液相色谱(HPLC),并在208至230 nm范围内进行梯度紫外检测。使用水(pH 3.20)中1%至99%的乙腈梯度,以0.5至1.7 ml/min的流速在17分钟内分离化合物。保留时间范围为5.7至14.5分钟。检测限在20至100 ng/ml之间,定量限为150 - 200 ng/ml。五个加标血浆样品中溴化吡啶斯的明、避蚊胺、氯菊酯、N - 甲基 - 3 - 羟基吡啶溴化物、m - 甲苯酰胺、m - 甲苯酸、m - 苯氧基苄醇和m - 苯氧基苯甲酸的平均回收率分别为51.4±10.6、71.1±11.0、82.3±6.7、60.4±11.8、63.6±10.1、69.3±8.5、68.3±12.0、82.6±8.1,尿液中的平均回收率分别为55.9±9.8、60.3±7.4、77.9±9.1、61.7±13.5、68.6±8.9、62.0±9.5、72.9±9.1和72.1±8.0。峰面积与浓度之间的关系在100至5000 ng/ml范围内呈线性。该方法用于分析大鼠给药后上述化学物质及其代谢物。

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