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An immunochromatographic dipstick as an alternate for monitoring of heroin metabolites in urine samples
Heroin use and addiction pose serious risks and side effects due to overdose. Quantification of heroin in biological samples is challenging due to rapid deacetylation of heroin to its active metabolites. In this study, we report the quantification of metabolic degradation of heroin by-products in bi...
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Published in: | RSC advances 2018-01, Vol.8 (41), p.23163-2317 |
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container_title | RSC advances |
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creator | Mishra, Priya Banga, Ivneet Tyagi, Roshika Munjal, Tanya Goel, Aditya Capalash, Neena Sharma, Prince Suri, C. R Gandhi, Sonu |
description | Heroin use and addiction pose serious risks and side effects due to overdose. Quantification of heroin in biological samples is challenging due to rapid deacetylation of heroin to its active metabolites. In this study, we report the quantification of metabolic degradation of heroin by-products in biological urine samples. The presence of the drug was monitored after oral administration of heroin at different time intervals. Various biophysical techniques, such as high performance liquid chromatography (HPLC) and mass spectrometry (MS) were used to evaluate the presence of the drug. A competitive fluorescence based immunoassay was developed with a limit of detection (LOD) up to 0.01 ng mL
−1
and the IC
50
value was 0.1 ng mL
−1
, while the dipstick assay shows a LOD up to 5 ng mL
−1
. Rapid detection of narcotic drugs was carried out for biological urine samples collected at various time points. Validation of the developed dipstick was carried out for the standard as well as the spiked urine samples by fluorescence based immunoassay (FIA), using anti-morphine antibodies. A strong correlation (
R
= 0.94) was obtained between the developed dipstick and FIA assay for biological urine samples collected at various time points. The developed immunochromatographic dipstick is highly sensitive, field applicable and cost effective, and can serve as a first choice for the monitoring of narcotic drugs in blood, urine and saliva in drug addicts and athletes.
Pathway of heroin degradation post oral administration in mice. |
doi_str_mv | 10.1039/c8ra02018c |
format | article |
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−1
and the IC
50
value was 0.1 ng mL
−1
, while the dipstick assay shows a LOD up to 5 ng mL
−1
. Rapid detection of narcotic drugs was carried out for biological urine samples collected at various time points. Validation of the developed dipstick was carried out for the standard as well as the spiked urine samples by fluorescence based immunoassay (FIA), using anti-morphine antibodies. A strong correlation (
R
= 0.94) was obtained between the developed dipstick and FIA assay for biological urine samples collected at various time points. The developed immunochromatographic dipstick is highly sensitive, field applicable and cost effective, and can serve as a first choice for the monitoring of narcotic drugs in blood, urine and saliva in drug addicts and athletes.
Pathway of heroin degradation post oral administration in mice.</description><identifier>ISSN: 2046-2069</identifier><identifier>EISSN: 2046-2069</identifier><identifier>DOI: 10.1039/c8ra02018c</identifier><identifier>PMID: 35540121</identifier><language>eng</language><publisher>England: Royal Society of Chemistry</publisher><subject>Antibodies ; Athletes ; Biological properties ; Chemistry ; Drug abuse ; Fluorescence ; High performance liquid chromatography ; Immunoassay ; Mass spectrometry ; Metabolites ; Morphine ; Narcotics ; Saliva ; Side effects ; Urine</subject><ispartof>RSC advances, 2018-01, Vol.8 (41), p.23163-2317</ispartof><rights>This journal is © The Royal Society of Chemistry.</rights><rights>Copyright Royal Society of Chemistry 2018</rights><rights>This journal is © The Royal Society of Chemistry 2018 The Royal Society of Chemistry</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c428t-a5ea6731792f4aca6b0909352588aec7bedf2b8d0e4bfeb6600db44a2ae963a63</citedby><cites>FETCH-LOGICAL-c428t-a5ea6731792f4aca6b0909352588aec7bedf2b8d0e4bfeb6600db44a2ae963a63</cites><orcidid>0000-0003-0960-2780</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9081577/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9081577/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35540121$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mishra, Priya</creatorcontrib><creatorcontrib>Banga, Ivneet</creatorcontrib><creatorcontrib>Tyagi, Roshika</creatorcontrib><creatorcontrib>Munjal, Tanya</creatorcontrib><creatorcontrib>Goel, Aditya</creatorcontrib><creatorcontrib>Capalash, Neena</creatorcontrib><creatorcontrib>Sharma, Prince</creatorcontrib><creatorcontrib>Suri, C. R</creatorcontrib><creatorcontrib>Gandhi, Sonu</creatorcontrib><title>An immunochromatographic dipstick as an alternate for monitoring of heroin metabolites in urine samples</title><title>RSC advances</title><addtitle>RSC Adv</addtitle><description>Heroin use and addiction pose serious risks and side effects due to overdose. Quantification of heroin in biological samples is challenging due to rapid deacetylation of heroin to its active metabolites. In this study, we report the quantification of metabolic degradation of heroin by-products in biological urine samples. The presence of the drug was monitored after oral administration of heroin at different time intervals. Various biophysical techniques, such as high performance liquid chromatography (HPLC) and mass spectrometry (MS) were used to evaluate the presence of the drug. A competitive fluorescence based immunoassay was developed with a limit of detection (LOD) up to 0.01 ng mL
−1
and the IC
50
value was 0.1 ng mL
−1
, while the dipstick assay shows a LOD up to 5 ng mL
−1
. Rapid detection of narcotic drugs was carried out for biological urine samples collected at various time points. Validation of the developed dipstick was carried out for the standard as well as the spiked urine samples by fluorescence based immunoassay (FIA), using anti-morphine antibodies. A strong correlation (
R
= 0.94) was obtained between the developed dipstick and FIA assay for biological urine samples collected at various time points. The developed immunochromatographic dipstick is highly sensitive, field applicable and cost effective, and can serve as a first choice for the monitoring of narcotic drugs in blood, urine and saliva in drug addicts and athletes.
Pathway of heroin degradation post oral administration in mice.</description><subject>Antibodies</subject><subject>Athletes</subject><subject>Biological properties</subject><subject>Chemistry</subject><subject>Drug abuse</subject><subject>Fluorescence</subject><subject>High performance liquid chromatography</subject><subject>Immunoassay</subject><subject>Mass spectrometry</subject><subject>Metabolites</subject><subject>Morphine</subject><subject>Narcotics</subject><subject>Saliva</subject><subject>Side effects</subject><subject>Urine</subject><issn>2046-2069</issn><issn>2046-2069</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNpdks2LFDEQxYMo7rLuxbsS8CLCaCXdne6-CMPgFywIoudQna6eydpJ2iQt7H9v1lnH1VwqxfvxKOoVY08FvBZQ9W9MFxEkiM48YOcSarWRoPqH9_5n7DKlayhPNUIq8ZidVU1Tg5DinO23nlvnVh_MIQaHOewjLgdr-GiXlK35zjFx9BznTNFjJj6FyF3wNodo_Z6HiR8oBuu5o4xDmG2mxEu7Fpl4QrfMlJ6wRxPOiS7v6gX79v7d193HzdXnD59226uNqWWXN9gQqrYSbS-nGg2qAXroq0Y2XYdk2oHGSQ7dCFQPEw1KAYxDXaNE6lWFqrpgb4--yzo4Gg35HHHWS7QO440OaPW_ircHvQ8_dQ-daNq2GLy8M4jhx0opa2eToXlGT2FNWioly_IqqAv64j_0OqxlR3OhQMlWQdvdUq-OlIkhpUjTaRgB-jZCveu-bH9HuCvw8_vjn9A_gRXg2RGIyZzUvzdQ_QJaO6Lh</recordid><startdate>20180101</startdate><enddate>20180101</enddate><creator>Mishra, Priya</creator><creator>Banga, Ivneet</creator><creator>Tyagi, Roshika</creator><creator>Munjal, Tanya</creator><creator>Goel, Aditya</creator><creator>Capalash, Neena</creator><creator>Sharma, Prince</creator><creator>Suri, C. R</creator><creator>Gandhi, Sonu</creator><general>Royal Society of Chemistry</general><general>The Royal Society of Chemistry</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-0960-2780</orcidid></search><sort><creationdate>20180101</creationdate><title>An immunochromatographic dipstick as an alternate for monitoring of heroin metabolites in urine samples</title><author>Mishra, Priya ; Banga, Ivneet ; Tyagi, Roshika ; Munjal, Tanya ; Goel, Aditya ; Capalash, Neena ; Sharma, Prince ; Suri, C. R ; Gandhi, Sonu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c428t-a5ea6731792f4aca6b0909352588aec7bedf2b8d0e4bfeb6600db44a2ae963a63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Antibodies</topic><topic>Athletes</topic><topic>Biological properties</topic><topic>Chemistry</topic><topic>Drug abuse</topic><topic>Fluorescence</topic><topic>High performance liquid chromatography</topic><topic>Immunoassay</topic><topic>Mass spectrometry</topic><topic>Metabolites</topic><topic>Morphine</topic><topic>Narcotics</topic><topic>Saliva</topic><topic>Side effects</topic><topic>Urine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mishra, Priya</creatorcontrib><creatorcontrib>Banga, Ivneet</creatorcontrib><creatorcontrib>Tyagi, Roshika</creatorcontrib><creatorcontrib>Munjal, Tanya</creatorcontrib><creatorcontrib>Goel, Aditya</creatorcontrib><creatorcontrib>Capalash, Neena</creatorcontrib><creatorcontrib>Sharma, Prince</creatorcontrib><creatorcontrib>Suri, C. R</creatorcontrib><creatorcontrib>Gandhi, Sonu</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>RSC advances</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mishra, Priya</au><au>Banga, Ivneet</au><au>Tyagi, Roshika</au><au>Munjal, Tanya</au><au>Goel, Aditya</au><au>Capalash, Neena</au><au>Sharma, Prince</au><au>Suri, C. R</au><au>Gandhi, Sonu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An immunochromatographic dipstick as an alternate for monitoring of heroin metabolites in urine samples</atitle><jtitle>RSC advances</jtitle><addtitle>RSC Adv</addtitle><date>2018-01-01</date><risdate>2018</risdate><volume>8</volume><issue>41</issue><spage>23163</spage><epage>2317</epage><pages>23163-2317</pages><issn>2046-2069</issn><eissn>2046-2069</eissn><abstract>Heroin use and addiction pose serious risks and side effects due to overdose. Quantification of heroin in biological samples is challenging due to rapid deacetylation of heroin to its active metabolites. In this study, we report the quantification of metabolic degradation of heroin by-products in biological urine samples. The presence of the drug was monitored after oral administration of heroin at different time intervals. Various biophysical techniques, such as high performance liquid chromatography (HPLC) and mass spectrometry (MS) were used to evaluate the presence of the drug. A competitive fluorescence based immunoassay was developed with a limit of detection (LOD) up to 0.01 ng mL
−1
and the IC
50
value was 0.1 ng mL
−1
, while the dipstick assay shows a LOD up to 5 ng mL
−1
. Rapid detection of narcotic drugs was carried out for biological urine samples collected at various time points. Validation of the developed dipstick was carried out for the standard as well as the spiked urine samples by fluorescence based immunoassay (FIA), using anti-morphine antibodies. A strong correlation (
R
= 0.94) was obtained between the developed dipstick and FIA assay for biological urine samples collected at various time points. The developed immunochromatographic dipstick is highly sensitive, field applicable and cost effective, and can serve as a first choice for the monitoring of narcotic drugs in blood, urine and saliva in drug addicts and athletes.
Pathway of heroin degradation post oral administration in mice.</abstract><cop>England</cop><pub>Royal Society of Chemistry</pub><pmid>35540121</pmid><doi>10.1039/c8ra02018c</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-0960-2780</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Antibodies Athletes Biological properties Chemistry Drug abuse Fluorescence High performance liquid chromatography Immunoassay Mass spectrometry Metabolites Morphine Narcotics Saliva Side effects Urine |
title | An immunochromatographic dipstick as an alternate for monitoring of heroin metabolites in urine samples |
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