Stanazolol derived ELISA as a sensitive forensic tool for the detection of multiple 17α-methylated anabolics

[Display omitted] •Stanazolol antigens and polyclonal rabbit antibodies (RAbs) were produced.•Biotinylated antigens were synthesized.•Two highly stable ELISA methods were developed.•Sensitivity towards multiple 17α-methylated anabolics was identified.•Developed methods were applied for real samples...

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Veröffentlicht in:Steroids 2020-03, Vol.155, p.108550-108550, Article 108550
Hauptverfasser: Huml, Lukáš, Havlová, Dominika, Longin, Ondřej, Staňková, Eliška, Holubová, Barbora, Kuchař, Martin, Prokudina, Elena, Rottnerová, Zdeňka, Zimmermann, Tomáš, Drašar, Pavel, Lapčík, Oldřich, Jurášek, Michal
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container_issue
container_start_page 108550
container_title Steroids
container_volume 155
creator Huml, Lukáš
Havlová, Dominika
Longin, Ondřej
Staňková, Eliška
Holubová, Barbora
Kuchař, Martin
Prokudina, Elena
Rottnerová, Zdeňka
Zimmermann, Tomáš
Drašar, Pavel
Lapčík, Oldřich
Jurášek, Michal
description [Display omitted] •Stanazolol antigens and polyclonal rabbit antibodies (RAbs) were produced.•Biotinylated antigens were synthesized.•Two highly stable ELISA methods were developed.•Sensitivity towards multiple 17α-methylated anabolics was identified.•Developed methods were applied for real samples analyses. Two valuable forensic tools based on enzyme-linked immunoassays (ELISAs) for the analysis of 17α-methylated steroids were developed using haptens of stanazolol and its conjugates with biotin. Haptens containing terminal carboxylic group were conjugated to bovine serum albumin (BSA), rabbit serum albumin (RSA) or ovalbumin (OVA). Eight batches of antisera (RAbs) obtained by immunization of rabbits were tested in an indirect competitive ELISA system using immobilization of RSA conjugate (RSA/hapten) and competitor immobilization of the biotinylated conjugate (AB-ELISA) to avidin (avidin/hapten). The best results were achieved with the RAb 212 antibodies in RSA/ST-3 and avidin/ST-10 assembled variants. For the RSA/ST-3 system, an IC50 of 0.3 ng/mL and a detection limit of 0.02 ng/mL were measured. In case of avidin/ST-10 variant, IC50 was of 3.9 ng/mL and a detection limit of 0.57 ng/mL were obtained. The effect of solvent was tested as well as the stability of coated microtiter plates over four-month period. The cross-reactivity of the developed assays with other anabolic steroids was tested and high sensitivity towards 17α-methylated steroids was observed. RSA/ST-3 assay showed significant cross-reactivity with 17α-methyltestosterone (81.2%), oxymetholone (30.4%), methandienone (10.0%) and methyl dihydrotestosterone (7.7%). Similarly, in the avidin/ST-10 assay, 17α-methyltestosterone (34.5%), mestanolone (32.1%), oxymetholone (22.7%), methandienone (14.2%), 9-dehydromethyltestosterone (12.5%) and oxandrolone (1.2%) exhibited high cross-reactivity. The functionality of the developed systems was verified by the successful identification of a series of 17α-methylated anabolic steroids in a set of real samples including pharmaceutical preparations seized by the Police of the Czech Republic on the black market.
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Two valuable forensic tools based on enzyme-linked immunoassays (ELISAs) for the analysis of 17α-methylated steroids were developed using haptens of stanazolol and its conjugates with biotin. Haptens containing terminal carboxylic group were conjugated to bovine serum albumin (BSA), rabbit serum albumin (RSA) or ovalbumin (OVA). Eight batches of antisera (RAbs) obtained by immunization of rabbits were tested in an indirect competitive ELISA system using immobilization of RSA conjugate (RSA/hapten) and competitor immobilization of the biotinylated conjugate (AB-ELISA) to avidin (avidin/hapten). The best results were achieved with the RAb 212 antibodies in RSA/ST-3 and avidin/ST-10 assembled variants. For the RSA/ST-3 system, an IC50 of 0.3 ng/mL and a detection limit of 0.02 ng/mL were measured. In case of avidin/ST-10 variant, IC50 was of 3.9 ng/mL and a detection limit of 0.57 ng/mL were obtained. The effect of solvent was tested as well as the stability of coated microtiter plates over four-month period. The cross-reactivity of the developed assays with other anabolic steroids was tested and high sensitivity towards 17α-methylated steroids was observed. RSA/ST-3 assay showed significant cross-reactivity with 17α-methyltestosterone (81.2%), oxymetholone (30.4%), methandienone (10.0%) and methyl dihydrotestosterone (7.7%). Similarly, in the avidin/ST-10 assay, 17α-methyltestosterone (34.5%), mestanolone (32.1%), oxymetholone (22.7%), methandienone (14.2%), 9-dehydromethyltestosterone (12.5%) and oxandrolone (1.2%) exhibited high cross-reactivity. 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Two valuable forensic tools based on enzyme-linked immunoassays (ELISAs) for the analysis of 17α-methylated steroids were developed using haptens of stanazolol and its conjugates with biotin. Haptens containing terminal carboxylic group were conjugated to bovine serum albumin (BSA), rabbit serum albumin (RSA) or ovalbumin (OVA). Eight batches of antisera (RAbs) obtained by immunization of rabbits were tested in an indirect competitive ELISA system using immobilization of RSA conjugate (RSA/hapten) and competitor immobilization of the biotinylated conjugate (AB-ELISA) to avidin (avidin/hapten). The best results were achieved with the RAb 212 antibodies in RSA/ST-3 and avidin/ST-10 assembled variants. For the RSA/ST-3 system, an IC50 of 0.3 ng/mL and a detection limit of 0.02 ng/mL were measured. In case of avidin/ST-10 variant, IC50 was of 3.9 ng/mL and a detection limit of 0.57 ng/mL were obtained. The effect of solvent was tested as well as the stability of coated microtiter plates over four-month period. The cross-reactivity of the developed assays with other anabolic steroids was tested and high sensitivity towards 17α-methylated steroids was observed. RSA/ST-3 assay showed significant cross-reactivity with 17α-methyltestosterone (81.2%), oxymetholone (30.4%), methandienone (10.0%) and methyl dihydrotestosterone (7.7%). Similarly, in the avidin/ST-10 assay, 17α-methyltestosterone (34.5%), mestanolone (32.1%), oxymetholone (22.7%), methandienone (14.2%), 9-dehydromethyltestosterone (12.5%) and oxandrolone (1.2%) exhibited high cross-reactivity. 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Havlová, Dominika ; Longin, Ondřej ; Staňková, Eliška ; Holubová, Barbora ; Kuchař, Martin ; Prokudina, Elena ; Rottnerová, Zdeňka ; Zimmermann, Tomáš ; Drašar, Pavel ; Lapčík, Oldřich ; Jurášek, Michal</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c368t-c106086d2398e11c354743ec97cd55513deedda92f58b58520b2270eff41413a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>17α-methylated anabolics</topic><topic>Animals</topic><topic>Biochemistry &amp; Molecular Biology</topic><topic>Calibration</topic><topic>Cattle</topic><topic>ELISA</topic><topic>Endocrinology &amp; Metabolism</topic><topic>Enzyme-Linked Immunosorbent Assay</topic><topic>Forensic Medicine</topic><topic>Immune Sera</topic><topic>Life Sciences &amp; Biomedicine</topic><topic>Methylation</topic><topic>Molecular Conformation</topic><topic>Rabbits</topic><topic>Science &amp; Technology</topic><topic>Serum Albumin - chemistry</topic><topic>Stanazolol</topic><topic>Stanozolol - chemistry</topic><topic>Stereoisomerism</topic><topic>Testosterone Congeners - analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Huml, Lukáš</creatorcontrib><creatorcontrib>Havlová, Dominika</creatorcontrib><creatorcontrib>Longin, Ondřej</creatorcontrib><creatorcontrib>Staňková, Eliška</creatorcontrib><creatorcontrib>Holubová, Barbora</creatorcontrib><creatorcontrib>Kuchař, Martin</creatorcontrib><creatorcontrib>Prokudina, Elena</creatorcontrib><creatorcontrib>Rottnerová, Zdeňka</creatorcontrib><creatorcontrib>Zimmermann, Tomáš</creatorcontrib><creatorcontrib>Drašar, Pavel</creatorcontrib><creatorcontrib>Lapčík, Oldřich</creatorcontrib><creatorcontrib>Jurášek, Michal</creatorcontrib><collection>Index Chemicus</collection><collection>Web of Science - Science Citation Index Expanded - 2020</collection><collection>Web of Science Core Collection</collection><collection>Science Citation Index Expanded</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Steroids</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Huml, Lukáš</au><au>Havlová, Dominika</au><au>Longin, Ondřej</au><au>Staňková, Eliška</au><au>Holubová, Barbora</au><au>Kuchař, Martin</au><au>Prokudina, Elena</au><au>Rottnerová, Zdeňka</au><au>Zimmermann, Tomáš</au><au>Drašar, Pavel</au><au>Lapčík, Oldřich</au><au>Jurášek, Michal</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Stanazolol derived ELISA as a sensitive forensic tool for the detection of multiple 17α-methylated anabolics</atitle><jtitle>Steroids</jtitle><stitle>STEROIDS</stitle><addtitle>Steroids</addtitle><date>2020-03</date><risdate>2020</risdate><volume>155</volume><spage>108550</spage><epage>108550</epage><pages>108550-108550</pages><artnum>108550</artnum><issn>0039-128X</issn><eissn>1878-5867</eissn><abstract>[Display omitted] •Stanazolol antigens and polyclonal rabbit antibodies (RAbs) were produced.•Biotinylated antigens were synthesized.•Two highly stable ELISA methods were developed.•Sensitivity towards multiple 17α-methylated anabolics was identified.•Developed methods were applied for real samples analyses. Two valuable forensic tools based on enzyme-linked immunoassays (ELISAs) for the analysis of 17α-methylated steroids were developed using haptens of stanazolol and its conjugates with biotin. Haptens containing terminal carboxylic group were conjugated to bovine serum albumin (BSA), rabbit serum albumin (RSA) or ovalbumin (OVA). Eight batches of antisera (RAbs) obtained by immunization of rabbits were tested in an indirect competitive ELISA system using immobilization of RSA conjugate (RSA/hapten) and competitor immobilization of the biotinylated conjugate (AB-ELISA) to avidin (avidin/hapten). The best results were achieved with the RAb 212 antibodies in RSA/ST-3 and avidin/ST-10 assembled variants. For the RSA/ST-3 system, an IC50 of 0.3 ng/mL and a detection limit of 0.02 ng/mL were measured. In case of avidin/ST-10 variant, IC50 was of 3.9 ng/mL and a detection limit of 0.57 ng/mL were obtained. 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subjects 17α-methylated anabolics
Animals
Biochemistry & Molecular Biology
Calibration
Cattle
ELISA
Endocrinology & Metabolism
Enzyme-Linked Immunosorbent Assay
Forensic Medicine
Immune Sera
Life Sciences & Biomedicine
Methylation
Molecular Conformation
Rabbits
Science & Technology
Serum Albumin - chemistry
Stanazolol
Stanozolol - chemistry
Stereoisomerism
Testosterone Congeners - analysis
title Stanazolol derived ELISA as a sensitive forensic tool for the detection of multiple 17α-methylated anabolics
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