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用甲烷化学电离质谱碎片分析法检测和测定食鸦片者尿液中的鸦片生物碱及其代谢物。

Detection and measurement of opium alkaloids and metabolites in urine of opium eaters by methane chemical ionization mass fragmentography.

作者信息

Cone E J, Gorodetzky C W, Yeh S Y, Darwin W D, Buchwald W F

出版信息

J Chromatogr. 1982 Jun 11;230(1):57-67. doi: 10.1016/s0378-4347(00)81430-9.

Abstract

A gas chromatographic-mass spectrometric assay for eight opium alkaloids in human urine following opium ingestion is described. The compounds were extracted from urine with methylene chloride-isopropanol (7:3, v/v) at pH 9.5, evaporated, derivatized with Tri-Sil Z and analyzed by methane chemical ionization mass fragmentography. The method in sensitive to ca. 0.01 microgram/ml for morphine and codeine and ca. 0.05 microgram/ml for the other compounds. Adsorption problems on the gas chromatography column prevented obtaining reproducible results for the measurement of noscapine. Extraction efficiencies over the pH range of 8-11 for the eight compounds are reported. Retention times of the opium alkaloids were determined using five different liquid phases (3%) on Gas-Chrom Q (100-120 mesh) and two column lengths (36 cm and 183 cm). The 36-cm column packed with OV-210 was selected for use in the assay. Ions were selected for monitoring for each component from their methane chemical ionization spectrum to provide the needed sensitivity and specificity for analysis of a multi-component mixture. The assay was used for the analysis of an "opium eater's" urine. Morphine, codeine, nomorphine, norcodeine and noscapine were detected; however, no evidence was obtained for thebaine, papaverine or oripavine. Unconjugated morphine (0.64 microgram/ml) was present at nearly twice the concentration of codeine (0.37 microgram/ml) and normorphine and norcodeine were present in equal amounts (ca. 0.15 microgram/ml).

摘要

本文描述了一种气相色谱 - 质谱分析法,用于检测人体摄入鸦片后尿液中的八种鸦片生物碱。这些化合物在pH 9.5条件下用二氯甲烷 - 异丙醇(7:3,v/v)从尿液中萃取,蒸发后用Tri - Sil Z进行衍生化,然后通过甲烷化学电离质谱碎片分析法进行分析。该方法对吗啡和可待因的检测灵敏度约为0.01微克/毫升,对其他化合物的检测灵敏度约为0.05微克/毫升。气相色谱柱上的吸附问题导致在测定那可丁时无法获得可重复的结果。报告了这八种化合物在pH 8 - 11范围内的萃取效率。使用五种不同的液相(3%)涂覆在Gas - Chrom Q(100 - 120目)上,并采用两种柱长(36厘米和183厘米)来测定鸦片生物碱的保留时间。选择填充有OV - 210的36厘米柱用于该分析方法。从每种成分的甲烷化学电离谱中选择离子进行监测,以便为多组分混合物的分析提供所需的灵敏度和特异性。该分析方法用于分析一位“食鸦片者”的尿液。检测到了吗啡、可待因、去甲吗啡、去甲可待因和那可丁;然而,未获得有关蒂巴因、罂粟碱或阿片碱的证据。未结合的吗啡(0.64微克/毫升)的浓度几乎是可待因(0.37微克/毫升)的两倍,而去甲吗啡和去甲可待因的含量相等(约0.15微克/毫升)。

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