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	<titleInfo><title>Rapid immunoassays for detection of anabolic nortestosterone in dietary supplements</title></titleInfo>
	<name type="personal">
		<namePart type="family">HOLUBOVÁ</namePart>
		<namePart type="given">Barbora</namePart>
		<role><roleTerm type="text">author</roleTerm></role>
	</name>
	<name type="personal">
		<namePart type="family">GÖSELOVÁ</namePart>
		<namePart type="given">Sandra</namePart>
		<role><roleTerm type="text">author</roleTerm></role>
	</name>
	<name type="personal">
		<namePart type="family">ŠEVČÍKOVÁ</namePart>
		<namePart type="given">Ludmila</namePart>
		<role><roleTerm type="text">author</roleTerm></role>
	</name>
	<name type="personal">
		<namePart type="family">VLACH</namePart>
		<namePart type="given">Miroslav</namePart>
		<role><roleTerm type="text">author</roleTerm></role>
	</name>
	<name type="personal">
		<namePart type="family">BLAŽKOVÁ</namePart>
		<namePart type="given">Martina</namePart>
		<role><roleTerm type="text">author</roleTerm></role>
	</name>
	<name type="personal">
		<namePart type="family">LAPČÍK</namePart>
		<namePart type="given">Oldřich</namePart>
		<role><roleTerm type="text">author</roleTerm></role>
	</name>
	<name type="personal">
		<namePart type="family">FUKAL</namePart>
		<namePart type="given">Ladislav</namePart>
		<role><roleTerm type="text">author</roleTerm></role>
	</name>
	<typeOfResource>text</typeOfResource>
	<genre>journal article</genre>
	<originInfo><dateIssued>2013</dateIssued></originInfo>
	<language></language>
	<abstract lang="English">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>
	<subject><topic>19-nortestosterone; ELISA; colloidal gold immunoassay; strip test</topic></subject>
	<identifier type="doi">10.17221/507/2012-CJFS</identifier>
	<identifier type="uri">https://cjfs.agriculturejournals.cz/artkey/cjf-201305-0013.php</identifier>
	<location><url>https://cjfs.agriculturejournals.cz/artkey/cjf-201305-0013.php</url></location>
	<relatedItem type="host">
		<titleInfo><title>Czech Journal of Food Sciences</title></titleInfo>
		<originInfo><issuance>continuing</issuance></originInfo>
		<part>
			<detail type="volume"><number>31</number></detail>
			<detail type="issue"><number>5</number></detail>
			<extent unit="pages">
				<start>514</start>
				<end>519</end>
			</extent>
			<date>2013</date>
		</part>
		<identifier type="issn">12121800</identifier>
		<genre authority="marc">periodical</genre>
		<genre>academic journal</genre>
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