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一种改进的尿液致突变性检测标准化程序。

An improved standardized procedure for urine mutagenicity testing.

作者信息

Rannug A, Olsson M, Aringer L, Brunius G

机构信息

Department of Toxicology, National Institute of Occupational Health, Solna, Sweden.

出版信息

IARC Sci Publ. 1988(89):396-400.

PMID:3198227
Abstract

The aim of the present study was to optimize the procedures for urinary mutagenicity testing in order to lower the baseline variation in mutagenic activity found in urine from unexposed subjects and to increase the sensitivity of the method. This was accomplished by using urine from nonsmokers and smokers as well as chemically spiked nonsmokers' urine. Diet was standardized. The number of mutants per ml of urine calculated from the linear portion of the dose-response curve was used as a measure of mutagenicity. The parameters investigated were (i) the total volume of urine per resin volume, (ii) the flow rate, (iii) the pH, (iv) the ionic strength of the urine, and (v) elimination of histidine. XAD-2 and C18 Sep-Pak resins recovered mutagens in smokers' urine and in chemically spiked urine with the same efficiency when an optimized procedure was adopted. The optimized procedure using a maximum volume of 50 ml acidified urine per Sep-Pak cartridge, or equal amount of XAD-2 resin, gave well over ten times greater recovery of mutagens from smokers' urine than in earlier reports. Histidine was effectively eliminated, and the background variation was also lowered.

摘要

本研究的目的是优化尿致突变性检测程序,以降低未接触者尿液中发现的诱变活性的基线变异,并提高该方法的灵敏度。这通过使用非吸烟者和吸烟者的尿液以及化学加标的非吸烟者尿液来实现。饮食进行了标准化。从剂量反应曲线的线性部分计算出的每毫升尿液中的突变体数量用作诱变活性的度量。研究的参数包括:(i)每树脂体积的尿液总体积;(ii)流速;(iii)pH值;(iv)尿液的离子强度;(v)组氨酸的去除。当采用优化程序时,XAD - 2和C18 Sep - Pak树脂从吸烟者尿液和化学加标尿液中回收诱变剂的效率相同。使用每个Sep - Pak柱最大50毫升酸化尿液或等量XAD - 2树脂的优化程序,从吸烟者尿液中回收的诱变剂比早期报告高出十倍以上。组氨酸被有效去除,背景变异也降低了。

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