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建立一种简单的净化程序和生物测定法,用于测定环境样品中2,3,7,8-四氯二苯并对二恶英的毒性当量。

Establishment of a simple cleanup procedure and bioassay for determining 2,3,7,8-tetrachlorodibenzo-p-dioxin toxicity equivalents of environmental samples.

作者信息

Schwirzer S M, Hofmaier A M, Kettrup A, Nerdinger P E, Schramm K W, Thoma H, Wegenke M, Wiebel F J

机构信息

Institute of Toxicology, Institute of Ecological Chemistry, GSF-National Research Center for Environment and Health, Ingolstädter Landstrasse 1, Neuherberg, D-85764, Germany.

出版信息

Ecotoxicol Environ Saf. 1998 Sep;41(1):77-82. doi: 10.1006/eesa.1998.1670.

Abstract

The study was aimed at establishing a bioassay for the determination of 2,3,7,8-tetrachlorodibenzo-p-dioxin toxicity equivalents (TEQs) in environmental samples. Specifically, development of a rapid cleanup procedure adapted to the needs of the bioassay and simplification of the measurement of its endpoint, the induction of 7-ethoxyresorufin O-deethylase (EROD) in rat H4IIEC3/T hepatoma cells, were desired. The results indicate that a single "sandwich" column suffices to remove substances that may interfere with the bioassay from extracts of various environmental matrices such as sewage sludge, compost, soil, sediment, fly ash, tissue filter dust, and fire residue. The cumbersome conventional in vitro assay for EROD activity on cells exposed to the test material in culture plates could readily be replaced by a simple assay on intact cells grown and treated in 96-well microtiter plates. TEQ values obtained from the bioassays were consistently higher than those derived from chemical analysis of dibenzo-p-dioxins/furans and biphenyls by a factor of 1.5-3.0 depending on the matrix used. The results indicate that this bioassay, which combines a simple cleanup and a rapid procedure for measuring biological effects, offers a cost- and time-effective alternative to chemical analysis when screening large numbers of samples from complex environmental matrices.

摘要

本研究旨在建立一种生物测定方法,用于测定环境样品中2,3,7,8-四氯二苯并对二恶英毒性当量(TEQ)。具体而言,需要开发一种适应生物测定需求的快速净化程序,并简化其终点测量方法,即大鼠H4IIEC3/T肝癌细胞中7-乙氧基异吩恶唑酮O-脱乙基酶(EROD)的诱导。结果表明,单个“夹心”柱足以从各种环境基质(如污水污泥、堆肥、土壤、沉积物、飞灰、组织滤尘和火灾残留物)的提取物中去除可能干扰生物测定的物质。在培养板中对暴露于测试材料的细胞进行EROD活性的繁琐传统体外测定,可以很容易地被在96孔微量滴定板中生长和处理的完整细胞的简单测定所取代。根据所使用的基质,从生物测定中获得的TEQ值始终比通过化学分析二苯并对二恶英/呋喃和联苯得出的值高1.5至3.0倍。结果表明,如果要从复杂环境基质中筛选大量样品,这种结合了简单净化和快速生物效应测量程序的生物测定方法,提供了一种比化学分析更具成本效益和时间效益的替代方法。

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