Cargando…
Qualitative identification of growth hormone-releasing hormones in human plasma by means of immunoaffinity purification and LC-HRMS/MS
The use of growth hormone-releasing hormones (GHRHs) is prohibited in sports according to the regulations of the World Anti-Doping Agency (WADA). The aim of the present study was to develop a method for the simultaneous detection of four different GHRHs and respective metabolites from human plasma b...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4830873/ https://www.ncbi.nlm.nih.gov/pubmed/26879649 http://dx.doi.org/10.1007/s00216-016-9377-3 |
_version_ | 1782426965141094400 |
---|---|
author | Knoop, Andre Thomas, Andreas Fichant, Eric Delahaut, Philippe Schänzer, Wilhelm Thevis, Mario |
author_facet | Knoop, Andre Thomas, Andreas Fichant, Eric Delahaut, Philippe Schänzer, Wilhelm Thevis, Mario |
author_sort | Knoop, Andre |
collection | PubMed |
description | The use of growth hormone-releasing hormones (GHRHs) is prohibited in sports according to the regulations of the World Anti-Doping Agency (WADA). The aim of the present study was to develop a method for the simultaneous detection of four different GHRHs and respective metabolites from human plasma by means of immunoaffinity purification and subsequent nano-ultrahigh performance liquid chromatography-high resolution/high accuracy (tandem) mass spectrometry. The target analytes included Geref (Sermorelin), CJC-1293, CJC-1295, and Egrifta (Tesamorelin) as well as two metabolites of Geref and CJC-1293, which were captured from plasma samples using a polyclonal GHRH antibody in concert with protein A/G monolithic MSIA™ D.A.R.T.’S® (Disposable Automation Research Tips) prior to separation and detection. The method was fully validated and found to be fit for purpose considering the parameters specificity, linearity, recovery (19–37 %), lower limit of detection (<50 pg/mL), imprecision (<20 %), and ion suppression/enhancement effects. The analytes’ stability and metabolism were elucidated using in vitro and in vivo approaches. EDTA blood samples were collected from rats 2, 4, and 8 h after intravenous administration of GHRH (one compound per test animal). All intact substances were detected for at least 4 h but no anticipated metabolite was confirmed in laboratory rodents’ samples; conversely, a Geref metabolite (GHRH(3-29)) was found in a human plasma sample collected after subcutaneous injection of the drug to a healthy male volunteer. The obtained results demonstrate that GHRHs are successfully detected in plasma using an immunoaffinity-mass spectrometry-based method, which can be applied to sports drug testing samples. Further studies are however required and warranted to account for potential species-related differences in metabolism and elimination of the target analytes [Figure: see text] |
format | Online Article Text |
id | pubmed-4830873 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-48308732016-04-22 Qualitative identification of growth hormone-releasing hormones in human plasma by means of immunoaffinity purification and LC-HRMS/MS Knoop, Andre Thomas, Andreas Fichant, Eric Delahaut, Philippe Schänzer, Wilhelm Thevis, Mario Anal Bioanal Chem Research Paper The use of growth hormone-releasing hormones (GHRHs) is prohibited in sports according to the regulations of the World Anti-Doping Agency (WADA). The aim of the present study was to develop a method for the simultaneous detection of four different GHRHs and respective metabolites from human plasma by means of immunoaffinity purification and subsequent nano-ultrahigh performance liquid chromatography-high resolution/high accuracy (tandem) mass spectrometry. The target analytes included Geref (Sermorelin), CJC-1293, CJC-1295, and Egrifta (Tesamorelin) as well as two metabolites of Geref and CJC-1293, which were captured from plasma samples using a polyclonal GHRH antibody in concert with protein A/G monolithic MSIA™ D.A.R.T.’S® (Disposable Automation Research Tips) prior to separation and detection. The method was fully validated and found to be fit for purpose considering the parameters specificity, linearity, recovery (19–37 %), lower limit of detection (<50 pg/mL), imprecision (<20 %), and ion suppression/enhancement effects. The analytes’ stability and metabolism were elucidated using in vitro and in vivo approaches. EDTA blood samples were collected from rats 2, 4, and 8 h after intravenous administration of GHRH (one compound per test animal). All intact substances were detected for at least 4 h but no anticipated metabolite was confirmed in laboratory rodents’ samples; conversely, a Geref metabolite (GHRH(3-29)) was found in a human plasma sample collected after subcutaneous injection of the drug to a healthy male volunteer. The obtained results demonstrate that GHRHs are successfully detected in plasma using an immunoaffinity-mass spectrometry-based method, which can be applied to sports drug testing samples. Further studies are however required and warranted to account for potential species-related differences in metabolism and elimination of the target analytes [Figure: see text] Springer Berlin Heidelberg 2016-02-15 2016 /pmc/articles/PMC4830873/ /pubmed/26879649 http://dx.doi.org/10.1007/s00216-016-9377-3 Text en © The Author(s) 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Research Paper Knoop, Andre Thomas, Andreas Fichant, Eric Delahaut, Philippe Schänzer, Wilhelm Thevis, Mario Qualitative identification of growth hormone-releasing hormones in human plasma by means of immunoaffinity purification and LC-HRMS/MS |
title | Qualitative identification of growth hormone-releasing hormones in human plasma by means of immunoaffinity purification and LC-HRMS/MS |
title_full | Qualitative identification of growth hormone-releasing hormones in human plasma by means of immunoaffinity purification and LC-HRMS/MS |
title_fullStr | Qualitative identification of growth hormone-releasing hormones in human plasma by means of immunoaffinity purification and LC-HRMS/MS |
title_full_unstemmed | Qualitative identification of growth hormone-releasing hormones in human plasma by means of immunoaffinity purification and LC-HRMS/MS |
title_short | Qualitative identification of growth hormone-releasing hormones in human plasma by means of immunoaffinity purification and LC-HRMS/MS |
title_sort | qualitative identification of growth hormone-releasing hormones in human plasma by means of immunoaffinity purification and lc-hrms/ms |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4830873/ https://www.ncbi.nlm.nih.gov/pubmed/26879649 http://dx.doi.org/10.1007/s00216-016-9377-3 |
work_keys_str_mv | AT knoopandre qualitativeidentificationofgrowthhormonereleasinghormonesinhumanplasmabymeansofimmunoaffinitypurificationandlchrmsms AT thomasandreas qualitativeidentificationofgrowthhormonereleasinghormonesinhumanplasmabymeansofimmunoaffinitypurificationandlchrmsms AT fichanteric qualitativeidentificationofgrowthhormonereleasinghormonesinhumanplasmabymeansofimmunoaffinitypurificationandlchrmsms AT delahautphilippe qualitativeidentificationofgrowthhormonereleasinghormonesinhumanplasmabymeansofimmunoaffinitypurificationandlchrmsms AT schanzerwilhelm qualitativeidentificationofgrowthhormonereleasinghormonesinhumanplasmabymeansofimmunoaffinitypurificationandlchrmsms AT thevismario qualitativeidentificationofgrowthhormonereleasinghormonesinhumanplasmabymeansofimmunoaffinitypurificationandlchrmsms |