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Quantification of dehydroepiandrosterone in human serum on a routine basis: development and validation of a tandem mass spectrometry method based on a surrogate analyte
In the clinical laboratories, dehydroepiandrostenedione (DHEA) is usually quantified by immunoassay-based methods, which are often affected by cross-reactivity with endogenous interferences, such as 4-androsten-3β-ol-17-one. The interfering compounds lead to a poor accuracy of the measurements, main...
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Published in: | Analytical and bioanalytical chemistry 2018, Vol.410 (2), p.407-416 |
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creator | Campi, Beatrice Frascarelli, Sabina Pietri, Elisabetta Massa, Ilaria Donati, Caterina Bozic, Roberto Bertelloni, Silvano Paolicchi, Aldo Zucchi, Riccardo Saba, Alessandro |
description | In the clinical laboratories, dehydroepiandrostenedione (DHEA) is usually quantified by immunoassay-based methods, which are often affected by cross-reactivity with endogenous interferences, such as 4-androsten-3β-ol-17-one. The interfering compounds lead to a poor accuracy of the measurements, mainly at a low concentration level. The present paper describes a validated method based on tandem mass spectrometry coupled to liquid chromatography, for the accurate quantification of DHEA in serum. The peculiarity of this method is the use of calibrators and quality controls prepared by adding measured amounts of DHEA-D
5
, a stable isotope-labeled analogue of DHEA, to real serum from healthy subjects. DHEA-D
5
is used in place of DHEA, which is usually present in unstripped serum at physiological levels, as it has the same basic structure, provides an equivalent instrumental response, and can be easily distinguish by DHEA by mass spectrometry due to its different
m
/
z
value. The method proved to be sensitive, with a LLOD of 0.09 ng/mL and a LLOQ of 0.23 ng/mL, and selective, with overall performances that allow its use on a routine basis. |
doi_str_mv | 10.1007/s00216-017-0731-x |
format | article |
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5
, a stable isotope-labeled analogue of DHEA, to real serum from healthy subjects. DHEA-D
5
is used in place of DHEA, which is usually present in unstripped serum at physiological levels, as it has the same basic structure, provides an equivalent instrumental response, and can be easily distinguish by DHEA by mass spectrometry due to its different
m
/
z
value. The method proved to be sensitive, with a LLOD of 0.09 ng/mL and a LLOQ of 0.23 ng/mL, and selective, with overall performances that allow its use on a routine basis.</description><identifier>ISSN: 1618-2642</identifier><identifier>EISSN: 1618-2650</identifier><identifier>DOI: 10.1007/s00216-017-0731-x</identifier><identifier>PMID: 29110028</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Analytical Chemistry ; Biochemistry ; Calibration ; Characterization and Evaluation of Materials ; Chemistry ; Chemistry and Materials Science ; Chromatography, High Pressure Liquid - methods ; Cross-reactivity ; Dehydroepiandrosterone ; Dehydroepiandrosterone - analogs & derivatives ; Dehydroepiandrosterone - blood ; Deuterium - analysis ; Deuterium - blood ; Food Science ; Humans ; Immunoassay ; Ions ; Kinetics ; Laboratory Medicine ; Limit of Detection ; Liquid chromatography ; Mass spectrometry ; Mass spectroscopy ; Monitoring/Environmental Analysis ; Research Paper ; Scientific imaging ; Spectroscopy ; Stable isotopes ; Tandem Mass Spectrometry - methods</subject><ispartof>Analytical and bioanalytical chemistry, 2018, Vol.410 (2), p.407-416</ispartof><rights>Springer-Verlag GmbH Germany 2017</rights><rights>Analytical and Bioanalytical Chemistry is a copyright of Springer, (2017). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c452t-138c5b3ae171b80e49a7ba209a0dd7b75429cbc6e403a49c5afb776885b87b1c3</citedby><cites>FETCH-LOGICAL-c452t-138c5b3ae171b80e49a7ba209a0dd7b75429cbc6e403a49c5afb776885b87b1c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27900,27901</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29110028$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Campi, Beatrice</creatorcontrib><creatorcontrib>Frascarelli, Sabina</creatorcontrib><creatorcontrib>Pietri, Elisabetta</creatorcontrib><creatorcontrib>Massa, Ilaria</creatorcontrib><creatorcontrib>Donati, Caterina</creatorcontrib><creatorcontrib>Bozic, Roberto</creatorcontrib><creatorcontrib>Bertelloni, Silvano</creatorcontrib><creatorcontrib>Paolicchi, Aldo</creatorcontrib><creatorcontrib>Zucchi, Riccardo</creatorcontrib><creatorcontrib>Saba, Alessandro</creatorcontrib><title>Quantification of dehydroepiandrosterone in human serum on a routine basis: development and validation of a tandem mass spectrometry method based on a surrogate analyte</title><title>Analytical and bioanalytical chemistry</title><addtitle>Anal Bioanal Chem</addtitle><addtitle>Anal Bioanal Chem</addtitle><description>In the clinical laboratories, dehydroepiandrostenedione (DHEA) is usually quantified by immunoassay-based methods, which are often affected by cross-reactivity with endogenous interferences, such as 4-androsten-3β-ol-17-one. The interfering compounds lead to a poor accuracy of the measurements, mainly at a low concentration level. The present paper describes a validated method based on tandem mass spectrometry coupled to liquid chromatography, for the accurate quantification of DHEA in serum. The peculiarity of this method is the use of calibrators and quality controls prepared by adding measured amounts of DHEA-D
5
, a stable isotope-labeled analogue of DHEA, to real serum from healthy subjects. DHEA-D
5
is used in place of DHEA, which is usually present in unstripped serum at physiological levels, as it has the same basic structure, provides an equivalent instrumental response, and can be easily distinguish by DHEA by mass spectrometry due to its different
m
/
z
value. The method proved to be sensitive, with a LLOD of 0.09 ng/mL and a LLOQ of 0.23 ng/mL, and selective, with overall performances that allow its use on a routine basis.</description><subject>Analytical Chemistry</subject><subject>Biochemistry</subject><subject>Calibration</subject><subject>Characterization and Evaluation of Materials</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Chromatography, High Pressure Liquid - methods</subject><subject>Cross-reactivity</subject><subject>Dehydroepiandrosterone</subject><subject>Dehydroepiandrosterone - analogs & derivatives</subject><subject>Dehydroepiandrosterone - blood</subject><subject>Deuterium - analysis</subject><subject>Deuterium - blood</subject><subject>Food Science</subject><subject>Humans</subject><subject>Immunoassay</subject><subject>Ions</subject><subject>Kinetics</subject><subject>Laboratory Medicine</subject><subject>Limit of Detection</subject><subject>Liquid 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Alessandro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Quantification of dehydroepiandrosterone in human serum on a routine basis: development and validation of a tandem mass spectrometry method based on a surrogate analyte</atitle><jtitle>Analytical and bioanalytical chemistry</jtitle><stitle>Anal Bioanal Chem</stitle><addtitle>Anal Bioanal Chem</addtitle><date>2018</date><risdate>2018</risdate><volume>410</volume><issue>2</issue><spage>407</spage><epage>416</epage><pages>407-416</pages><issn>1618-2642</issn><eissn>1618-2650</eissn><abstract>In the clinical laboratories, dehydroepiandrostenedione (DHEA) is usually quantified by immunoassay-based methods, which are often affected by cross-reactivity with endogenous interferences, such as 4-androsten-3β-ol-17-one. The interfering compounds lead to a poor accuracy of the measurements, mainly at a low concentration level. The present paper describes a validated method based on tandem mass spectrometry coupled to liquid chromatography, for the accurate quantification of DHEA in serum. The peculiarity of this method is the use of calibrators and quality controls prepared by adding measured amounts of DHEA-D
5
, a stable isotope-labeled analogue of DHEA, to real serum from healthy subjects. DHEA-D
5
is used in place of DHEA, which is usually present in unstripped serum at physiological levels, as it has the same basic structure, provides an equivalent instrumental response, and can be easily distinguish by DHEA by mass spectrometry due to its different
m
/
z
value. The method proved to be sensitive, with a LLOD of 0.09 ng/mL and a LLOQ of 0.23 ng/mL, and selective, with overall performances that allow its use on a routine basis.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>29110028</pmid><doi>10.1007/s00216-017-0731-x</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Analytical Chemistry Biochemistry Calibration Characterization and Evaluation of Materials Chemistry Chemistry and Materials Science Chromatography, High Pressure Liquid - methods Cross-reactivity Dehydroepiandrosterone Dehydroepiandrosterone - analogs & derivatives Dehydroepiandrosterone - blood Deuterium - analysis Deuterium - blood Food Science Humans Immunoassay Ions Kinetics Laboratory Medicine Limit of Detection Liquid chromatography Mass spectrometry Mass spectroscopy Monitoring/Environmental Analysis Research Paper Scientific imaging Spectroscopy Stable isotopes Tandem Mass Spectrometry - methods |
title | Quantification of dehydroepiandrosterone in human serum on a routine basis: development and validation of a tandem mass spectrometry method based on a surrogate analyte |
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