Shopping Cart

No products in the cart.

ASTM-E1853M:2004 Edition(Redline)

$26.65

E1853M-04 Standard Guide for Measuring the Presence of Planar Organic Compounds Which Induce CYP1A, Using Reporter Gene Test Systems (Redline)

Published By Publication Date Number of Pages
ASTM 2004 12
Guaranteed Safe Checkout
Category:

If you have any questions, feel free to reach out to our online customer service team by clicking on the bottom right corner. We’re here to assist you 24/7.
Email:[email protected]

Significance and Use

The compounds that bind to the Ah-receptor and induce CYP1A have often been shown to be either more toxic or carcinogenic, or both, than other organic compounds. Dioxins, furans, and PCBs have been shown to bioconcentrate in exposed organisms and biomagnify in the food web (see Guide E 1023). Testing with birds, mammals, and fish species has shown that exposure to these compounds can produce physiological, reproductive and histopathological effects (12, 13) . Concern for the possible contamination of water, food, wildlife, soil, and aquatic sediment from these compounds has led to the requirement for analytical chemical analyses of a great many environmental samples. Use of a screening tool such as this Human Reporter Gene System (HRGS) will allow identification of significantly contaminated samples. These methods will aid in the cost-effective separation of high priority samples from those that do not require further costly chemical characterization.

1. Scope

1.1 This guide covers the recommended guidelines for performing a test for presence of organic compounds that bind to the Ah Receptor and induce the CYP1A locus on the vertebrate chromosome. Under appropriate test conditions, induction of CYP1A is evidence that the cells have been exposed to one or more of these xenobiotic organic compounds that include dioxins, furans, coplanar PCBs, and several polycyclic aromatic hydrocarbons (PAHs). Detection of induction has been made simple and rapid by the stable integration of the firefly plasmid such that Ah-receptor binding results in the production of luciferase. Luciferase production is a function of both the potency of the compound(s) and the concentration. This type of Human Reporter Gene System (HRGS) has shown concentration-response relationships using 2,3,7,8-TCDD, 5 coplanar PCBs, and several polycyclic aromatic hydrocarbons (PAHs) (1-3) . This guide describes test conditions under which solvent extracts of environmental samples (water, tissue, soil, or sediments) may be tested for the presence of CYP1A-inducing organic compounds.

1.2 The test procedures presented in this guide have been published previously (4, 5 ) and established as EPA Method 4425 (6) . These references should be consulted to obtain details regarding the construction and maintenance of the cell line, and the response of the

ASTM-E1853M
$26.65