<?xml version="1.0" encoding="UTF-8"?>
<xml>
<records>
<record>
	<source-app name="Actavia">Actavia</source-app>
	<ref-type name="Journal Article">0</ref-type>
	<contributors>
		<authors>
			<author>HOLUBOVÁ, Barbora</author>
			<author>GÖSELOVÁ, Sandra</author>
			<author>ŠEVČÍKOVÁ, Ludmila</author>
			<author>VLACH, Miroslav</author>
			<author>BLAŽKOVÁ, Martina</author>
			<author>LAPČÍK, Oldřich</author>
			<author>FUKAL, Ladislav</author>
		</authors>
		<secondary-authors></secondary-authors>
	</contributors>
	<titles><title>Rapid immunoassays for detection of anabolic nortestosterone in dietary supplements</title></titles>
	<dates>
		<year>2013</year>
		<pub-dates><date>2013-10-31</date></pub-dates>
	</dates>
	<pages>514-519</pages>
	<abstract>An enzyme immunoassay (ELISA) and an immunochromatographic strip were designed for a rapid detection of nortestosterone in dietary supplements. Two polyclonal antibodies and two types of nortestosterone-protein coating conjugates were tested to develop the most appropriate method. Under optimal experimental conditions, the most sensitive ELISA achieved the IC&lt;sub&gt;50 &lt;/sub&gt;and the limit of detection values of 6.41 and 0.09 ng/ml, respectively. The assay specificity was tested measuring cross-reactivity of several steroids. The interference with the assay was negligible (&amp;lt; 0.1%), except for cross-reactivity with another frequently abused steroid testosterone (23%). The optimised gold particle-based immunochromatographic strip provided in semi-quantitative test a visual detection limit of 1 ng/ml. None of these methods showed the interference using a filtrate of the suspension of non-contaminated sample. After the validation for particular matrices, the ELISA and the strip test could be useful tools for a rapid analysis of nortestosterone in crude extracts of dietary supplements.</abstract>
	<number>5</number>
	<volume>31</volume>
</record>
</records>
</xml>
