Multi-mycotoxin analysis using dried blood spots and dried serum spots

Detalhes bibliográficos
Autor(a) principal: Osteresch, Bernd
Data de Publicação: 2017
Outros Autores: Viegas , Susana, Cramer, Benedikt, Humpf, Hans Ulrich
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://doi.org/10.1007/s00216-017-0279-9
Resumo: In this study, a rapid multi-mycotoxin approach was developed for biomonitoring and quantification of 27 important mycotoxins and mycotoxin metabolites in human blood samples. HPLC-MS/MS detection was used for the analysis of dried serum spots (DSS) and dried blood spots (DBS). Detection of aflatoxins (AFB1, AFB2, AFG1, AFG2, AFM1), trichothecenes (deoxynivalenol, DON; DON-3-glucoronic acid, DON-3-GlcA; T-2; HT-2; and HT-2-4-GlcA), fumonisin B1 (FB1), ochratoxins (OTA and its thermal degradation product 2’R-OTA; OTα; 10-hydroxychratoxin A, 10-OH-OTA), citrinin (CIT and its urinary metabolite dihydrocitrinone, DH-CIT), zearalenone and zearalanone (ZEN, ZAN), altenuene (ALT), alternariols (AOH; alternariol monomethyl ether, AME), enniatins (EnA, EnA1, EnB, EnB1) and beauvericin (Bea) was validated for two matrices, serum (DSS), and whole blood (DBS). HPLC-MS/MS analysis showed signal suppression as well as signal enhancement due to matrix effects. However, for most analytes LOQs in the lower pg/mL range and excellent recovery rate were achieved using matrix-matched calibration. Besides validation of the method, the analyte stability in DBS and DSS was also investigated. Stability is a main issue for some analytes when the dried samples are stored under common conditions at room temperature. Nevertheless, the developed method was applied to DBS samples of a German cohort (n = 50). Besides positive findings of OTA and 2’R-OTA, all samples were positive for EnB. This methodical study establishes a validated multi-mycotoxin approach for the detection of 27 mycotoxins and metabolites in dried blood/serum spots based on a fast sample preparation followed by sensitive HPLC-MS/MS analysis. [Figure not available: see fulltext.]
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spelling Multi-mycotoxin analysis using dried blood spots and dried serum spotsBiomonitoringDried blood spotDried serum spotHPLC-MS/MSMass spectrometryMycotoxinAnalytical ChemistryBiochemistryIn this study, a rapid multi-mycotoxin approach was developed for biomonitoring and quantification of 27 important mycotoxins and mycotoxin metabolites in human blood samples. HPLC-MS/MS detection was used for the analysis of dried serum spots (DSS) and dried blood spots (DBS). Detection of aflatoxins (AFB1, AFB2, AFG1, AFG2, AFM1), trichothecenes (deoxynivalenol, DON; DON-3-glucoronic acid, DON-3-GlcA; T-2; HT-2; and HT-2-4-GlcA), fumonisin B1 (FB1), ochratoxins (OTA and its thermal degradation product 2’R-OTA; OTα; 10-hydroxychratoxin A, 10-OH-OTA), citrinin (CIT and its urinary metabolite dihydrocitrinone, DH-CIT), zearalenone and zearalanone (ZEN, ZAN), altenuene (ALT), alternariols (AOH; alternariol monomethyl ether, AME), enniatins (EnA, EnA1, EnB, EnB1) and beauvericin (Bea) was validated for two matrices, serum (DSS), and whole blood (DBS). HPLC-MS/MS analysis showed signal suppression as well as signal enhancement due to matrix effects. However, for most analytes LOQs in the lower pg/mL range and excellent recovery rate were achieved using matrix-matched calibration. Besides validation of the method, the analyte stability in DBS and DSS was also investigated. Stability is a main issue for some analytes when the dried samples are stored under common conditions at room temperature. Nevertheless, the developed method was applied to DBS samples of a German cohort (n = 50). Besides positive findings of OTA and 2’R-OTA, all samples were positive for EnB. This methodical study establishes a validated multi-mycotoxin approach for the detection of 27 mycotoxins and metabolites in dried blood/serum spots based on a fast sample preparation followed by sensitive HPLC-MS/MS analysis. [Figure not available: see fulltext.]Centro de Investigação em Saúde Pública (CISP/PHRC)RUNOsteresch, BerndViegas , SusanaCramer, BenediktHumpf, Hans Ulrich2018-02-14T23:10:09Z2017-05-012017-05-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article14application/pdfhttps://doi.org/10.1007/s00216-017-0279-9eng1618-2642PURE: 2987803http://www.scopus.com/inward/record.url?scp=85015230050&partnerID=8YFLogxKhttps://doi.org/10.1007/s00216-017-0279-9info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-03-11T04:16:46Zoai:run.unl.pt:10362/30504Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T03:29:28.224746Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Multi-mycotoxin analysis using dried blood spots and dried serum spots
title Multi-mycotoxin analysis using dried blood spots and dried serum spots
spellingShingle Multi-mycotoxin analysis using dried blood spots and dried serum spots
Osteresch, Bernd
Biomonitoring
Dried blood spot
Dried serum spot
HPLC-MS/MS
Mass spectrometry
Mycotoxin
Analytical Chemistry
Biochemistry
title_short Multi-mycotoxin analysis using dried blood spots and dried serum spots
title_full Multi-mycotoxin analysis using dried blood spots and dried serum spots
title_fullStr Multi-mycotoxin analysis using dried blood spots and dried serum spots
title_full_unstemmed Multi-mycotoxin analysis using dried blood spots and dried serum spots
title_sort Multi-mycotoxin analysis using dried blood spots and dried serum spots
author Osteresch, Bernd
author_facet Osteresch, Bernd
Viegas , Susana
Cramer, Benedikt
Humpf, Hans Ulrich
author_role author
author2 Viegas , Susana
Cramer, Benedikt
Humpf, Hans Ulrich
author2_role author
author
author
dc.contributor.none.fl_str_mv Centro de Investigação em Saúde Pública (CISP/PHRC)
RUN
dc.contributor.author.fl_str_mv Osteresch, Bernd
Viegas , Susana
Cramer, Benedikt
Humpf, Hans Ulrich
dc.subject.por.fl_str_mv Biomonitoring
Dried blood spot
Dried serum spot
HPLC-MS/MS
Mass spectrometry
Mycotoxin
Analytical Chemistry
Biochemistry
topic Biomonitoring
Dried blood spot
Dried serum spot
HPLC-MS/MS
Mass spectrometry
Mycotoxin
Analytical Chemistry
Biochemistry
description In this study, a rapid multi-mycotoxin approach was developed for biomonitoring and quantification of 27 important mycotoxins and mycotoxin metabolites in human blood samples. HPLC-MS/MS detection was used for the analysis of dried serum spots (DSS) and dried blood spots (DBS). Detection of aflatoxins (AFB1, AFB2, AFG1, AFG2, AFM1), trichothecenes (deoxynivalenol, DON; DON-3-glucoronic acid, DON-3-GlcA; T-2; HT-2; and HT-2-4-GlcA), fumonisin B1 (FB1), ochratoxins (OTA and its thermal degradation product 2’R-OTA; OTα; 10-hydroxychratoxin A, 10-OH-OTA), citrinin (CIT and its urinary metabolite dihydrocitrinone, DH-CIT), zearalenone and zearalanone (ZEN, ZAN), altenuene (ALT), alternariols (AOH; alternariol monomethyl ether, AME), enniatins (EnA, EnA1, EnB, EnB1) and beauvericin (Bea) was validated for two matrices, serum (DSS), and whole blood (DBS). HPLC-MS/MS analysis showed signal suppression as well as signal enhancement due to matrix effects. However, for most analytes LOQs in the lower pg/mL range and excellent recovery rate were achieved using matrix-matched calibration. Besides validation of the method, the analyte stability in DBS and DSS was also investigated. Stability is a main issue for some analytes when the dried samples are stored under common conditions at room temperature. Nevertheless, the developed method was applied to DBS samples of a German cohort (n = 50). Besides positive findings of OTA and 2’R-OTA, all samples were positive for EnB. This methodical study establishes a validated multi-mycotoxin approach for the detection of 27 mycotoxins and metabolites in dried blood/serum spots based on a fast sample preparation followed by sensitive HPLC-MS/MS analysis. [Figure not available: see fulltext.]
publishDate 2017
dc.date.none.fl_str_mv 2017-05-01
2017-05-01T00:00:00Z
2018-02-14T23:10:09Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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url https://doi.org/10.1007/s00216-017-0279-9
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 1618-2642
PURE: 2987803
http://www.scopus.com/inward/record.url?scp=85015230050&partnerID=8YFLogxK
https://doi.org/10.1007/s00216-017-0279-9
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eu_rights_str_mv openAccess
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instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
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reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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