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采用毛细管气相色谱-质谱联用法同时测定小牛尿液中作为七氟丁酰衍生物的12种同化激素。

Simultaneous determination, in calf urine, of twelve anabolic agents as heptafluorobutyryl derivatives by capillary gas chromatography-mass spectrometry.

作者信息

Casademont G, Pérez B, García Regueiro J A

机构信息

IRTA, Unitat Tecnologia Analítica, Centre de Tecnologia de la Carn, Monells (Girona), Spain.

出版信息

J Chromatogr B Biomed Appl. 1996 Nov 15;686(2):189-98. doi: 10.1016/s0378-4347(96)00211-3.

DOI:10.1016/s0378-4347(96)00211-3
PMID:8971599
Abstract

A method to determine twelve anabolic hormones (diethylstilbestrol, hexestrol, dienestrol, 17 beta-estradiol, 19-nortestosterone, testosterone, 1-dehydrotestosterone, 17 alpha-methyltestosterone, progesterone, estrone, 17 alpha-ethynilestradiol, and trenbolone) is presented. Urine samples were extracted with octadecylsilica columns and clean-up was performed in two steps with basic alumina and silica solid-phase extraction cartridges. The extracts obtained were derivatized with heptafluorobutyric anhydride and analyzed by GC-MS. Stability of derivatives was good and compounds having keto groups produced enol derivatives that were stable also. SIM mode was applied to increase the sensitivity and, when possible, the higher m/z ions were selected to improve identification. Repeatability of the chromatographic analysis was evaluated on the basis of area repeatability, and the coefficient of variation obtained was lower than 13%. Absolute recoveries were in the range 35-60% (dehydrotestosterone and estrone < 20%) with coefficients of variation between 14 and 37% for the whole procedure. [2H3]Testosterone and [2H8]diethylstilbestrol were evaluated to improve quantitative data. The recovery of [2H3]testosterone was found to be equal to or slightly higher than that of the other hormones, but the recovery of [2H8]diethylstilbestrol was lower than any other. [2H3]Testosterone was the most suitable for use as an internal standard, as its addition at the beginning of analytical procedure, corrected recovery results and greatly improved precision. Corrected recoveries from urine ranged from 72-110%, and coefficients of variation ranged from 6-15%, except for testosterone which yielded slightly higher values. The limit of detection was 0.5 ng/ml for all the compounds studied.

摘要

本文介绍了一种测定十二种同化激素(己烯雌酚、己烷雌酚、二乙雌酚、17β-雌二醇、19-去甲睾酮、睾酮、1-脱氢睾酮、17α-甲基睾酮、孕酮、雌酮、17α-乙炔雌二醇和群勃龙)的方法。尿样用十八烷基硅柱萃取,并分两步用碱性氧化铝和硅胶固相萃取柱进行净化。所得萃取物用七氟丁酸酐衍生化,然后通过气相色谱-质谱联用仪进行分析。衍生物的稳定性良好,具有酮基的化合物生成的烯醇衍生物也很稳定。采用选择离子监测模式提高灵敏度,并尽可能选择较高的m/z离子以改善鉴定效果。根据面积重复性评估色谱分析的重复性,所得变异系数低于13%。整个过程的绝对回收率在35%-60%之间(脱氢睾酮和雌酮<20%),变异系数在14%-37%之间。对[2H3]睾酮和[2H8]己烯雌酚进行了评估以改善定量数据。发现[2H3]睾酮的回收率等于或略高于其他激素,但[2H8]己烯雌酚的回收率低于其他任何一种。[2H3]睾酮最适合用作内标,因为在分析过程开始时加入该内标可校正回收率结果并大大提高精密度。尿样的校正回收率在72%-110%之间,变异系数在6%-15%之间,睾酮的变异系数略高。所有研究化合物的检测限均为0.5 ng/ml。

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