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DBS-platform for biomonitoring and toxicokinetics of toxicants: proof of concept using LC-MS/MS analysis of fipronil and its metabolites in blood

A simple, sensitive and high throughput LC-MS/MS method was developed and validated for quantification of fipronil, fipronil sulfone and fipronil desulfinyl in rat and human dried blood spots (DBS). DBS samples were prepared by spiking 10 μl blood on DMPK-C cards followed by drying at room temperatu...

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Autores principales: Raju, Kanumuri Siva Rama, Taneja, Isha, Rashid, Mamunur, Sonkar, Ashish Kumar, Wahajuddin, Muhammad, Singh, Sheelendra Pratap
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4785372/
https://www.ncbi.nlm.nih.gov/pubmed/26960908
http://dx.doi.org/10.1038/srep22447
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author Raju, Kanumuri Siva Rama
Taneja, Isha
Rashid, Mamunur
Sonkar, Ashish Kumar
Wahajuddin, Muhammad
Singh, Sheelendra Pratap
author_facet Raju, Kanumuri Siva Rama
Taneja, Isha
Rashid, Mamunur
Sonkar, Ashish Kumar
Wahajuddin, Muhammad
Singh, Sheelendra Pratap
author_sort Raju, Kanumuri Siva Rama
collection PubMed
description A simple, sensitive and high throughput LC-MS/MS method was developed and validated for quantification of fipronil, fipronil sulfone and fipronil desulfinyl in rat and human dried blood spots (DBS). DBS samples were prepared by spiking 10 μl blood on DMPK-C cards followed by drying at room temperature. The whole blood spots were then punched from the card and extracted using acetonitrile. The total chromatographic run time of the method was only 2 min. The lower limit of quantification of the method was 0.1 ng/ml for all the analytes. The method was successfully applied to determine fipronil desulfinyl in DBS samples obtained from its toxicokinetic study in rats following intravenous dose (1 mg/kg). In conclusion, the proposed DBS methodology has significant potential in toxicokinetics and biomonitoring studies of environmental toxicants. This microvolume DBS technique will be an ideal tool for biomonitoring studies, particularly in paediatric population. Small volume requirements, minimally invasive blood sampling method, easier storage and shipping procedure make DBS a suitable technique for such studies. Further, DBS technique contributes towards the principles of 3Rs resulting in significant reduction in the number of rodents used and refinement in sample collection for toxicokinetic studies.
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spelling pubmed-47853722016-03-11 DBS-platform for biomonitoring and toxicokinetics of toxicants: proof of concept using LC-MS/MS analysis of fipronil and its metabolites in blood Raju, Kanumuri Siva Rama Taneja, Isha Rashid, Mamunur Sonkar, Ashish Kumar Wahajuddin, Muhammad Singh, Sheelendra Pratap Sci Rep Article A simple, sensitive and high throughput LC-MS/MS method was developed and validated for quantification of fipronil, fipronil sulfone and fipronil desulfinyl in rat and human dried blood spots (DBS). DBS samples were prepared by spiking 10 μl blood on DMPK-C cards followed by drying at room temperature. The whole blood spots were then punched from the card and extracted using acetonitrile. The total chromatographic run time of the method was only 2 min. The lower limit of quantification of the method was 0.1 ng/ml for all the analytes. The method was successfully applied to determine fipronil desulfinyl in DBS samples obtained from its toxicokinetic study in rats following intravenous dose (1 mg/kg). In conclusion, the proposed DBS methodology has significant potential in toxicokinetics and biomonitoring studies of environmental toxicants. This microvolume DBS technique will be an ideal tool for biomonitoring studies, particularly in paediatric population. Small volume requirements, minimally invasive blood sampling method, easier storage and shipping procedure make DBS a suitable technique for such studies. Further, DBS technique contributes towards the principles of 3Rs resulting in significant reduction in the number of rodents used and refinement in sample collection for toxicokinetic studies. Nature Publishing Group 2016-03-10 /pmc/articles/PMC4785372/ /pubmed/26960908 http://dx.doi.org/10.1038/srep22447 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Raju, Kanumuri Siva Rama
Taneja, Isha
Rashid, Mamunur
Sonkar, Ashish Kumar
Wahajuddin, Muhammad
Singh, Sheelendra Pratap
DBS-platform for biomonitoring and toxicokinetics of toxicants: proof of concept using LC-MS/MS analysis of fipronil and its metabolites in blood
title DBS-platform for biomonitoring and toxicokinetics of toxicants: proof of concept using LC-MS/MS analysis of fipronil and its metabolites in blood
title_full DBS-platform for biomonitoring and toxicokinetics of toxicants: proof of concept using LC-MS/MS analysis of fipronil and its metabolites in blood
title_fullStr DBS-platform for biomonitoring and toxicokinetics of toxicants: proof of concept using LC-MS/MS analysis of fipronil and its metabolites in blood
title_full_unstemmed DBS-platform for biomonitoring and toxicokinetics of toxicants: proof of concept using LC-MS/MS analysis of fipronil and its metabolites in blood
title_short DBS-platform for biomonitoring and toxicokinetics of toxicants: proof of concept using LC-MS/MS analysis of fipronil and its metabolites in blood
title_sort dbs-platform for biomonitoring and toxicokinetics of toxicants: proof of concept using lc-ms/ms analysis of fipronil and its metabolites in blood
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4785372/
https://www.ncbi.nlm.nih.gov/pubmed/26960908
http://dx.doi.org/10.1038/srep22447
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