High-throughput analysis of 19 endogenous androgenic steroids by ultra-performance convergence chromatography tandem mass spectrometry
•A high throughput UPC2-MS/MS method for the analysis of 19 steroids is described.•UPC2-MS/MS offers superior selectivity and increased chromatographic efficiency.•Significant improvements in sensitivity were achieved by UPC2-MS/MS.•UPC2-MS/MS is a SFC based technology which is ideal for steroid ana...
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Veröffentlicht in: | Journal of chromatography. B, Analytical technologies in the biomedical and life sciences Analytical technologies in the biomedical and life sciences, 2016-09, Vol.1031, p.131-138 |
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container_title | Journal of chromatography. B, Analytical technologies in the biomedical and life sciences |
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creator | Quanson, Jonathan L. Stander, Marietjie A. Pretorius, Elzette Jenkinson, Carl Taylor, Angela E. Storbeck, Karl-Heinz |
description | •A high throughput UPC2-MS/MS method for the analysis of 19 steroids is described.•UPC2-MS/MS offers superior selectivity and increased chromatographic efficiency.•Significant improvements in sensitivity were achieved by UPC2-MS/MS.•UPC2-MS/MS is a SFC based technology which is ideal for steroid analysis.
11-Oxygenated steroids such as 11-ketotestosterone and 11-ketodihydrotestosterone have recently been shown to play a putative role in the development and progression of castration resistant prostate cancer. In this study we report on the development of a high throughput ultra-performance convergence chromatography tandem mass spectrometry (UPC2-MS/MS) method for the analysis of thirteen 11-oxygenated and six canonical C19 steroids isolated from a cell culture matrix. Using an Acquity UPC2 BEH 2-EP column we found that UPC2 resulted in superior selectivity, increased chromatographic efficiency and a scattered elution order when compared to conventional reverse phase ultra-performance liquid chromatography (UPLC). Furthermore, there was a significant improvement in sensitivity (5–50 times). The lower limits of quantification ranged between 0.01–10ngmL−1, while the upper limit of quantification was 100ngmL−1 for all steroids. Accuracy, precision, intra-day variation, recovery, matrix effects and process efficiency were all evaluated and found to be within acceptable limits. Taken together we show that the increased power of UPC2-MS/MS allows the analyst to complete in vitro assays at biologically relevant concentrations for the first time and in so doing determine the routes of steroid metabolism which is vital for studies of androgen responsive cancers, such as prostate cancer, and could highlight new mechanisms of disease progression and new targets for cancer therapy. |
doi_str_mv | 10.1016/j.jchromb.2016.07.024 |
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11-Oxygenated steroids such as 11-ketotestosterone and 11-ketodihydrotestosterone have recently been shown to play a putative role in the development and progression of castration resistant prostate cancer. In this study we report on the development of a high throughput ultra-performance convergence chromatography tandem mass spectrometry (UPC2-MS/MS) method for the analysis of thirteen 11-oxygenated and six canonical C19 steroids isolated from a cell culture matrix. Using an Acquity UPC2 BEH 2-EP column we found that UPC2 resulted in superior selectivity, increased chromatographic efficiency and a scattered elution order when compared to conventional reverse phase ultra-performance liquid chromatography (UPLC). Furthermore, there was a significant improvement in sensitivity (5–50 times). The lower limits of quantification ranged between 0.01–10ngmL−1, while the upper limit of quantification was 100ngmL−1 for all steroids. Accuracy, precision, intra-day variation, recovery, matrix effects and process efficiency were all evaluated and found to be within acceptable limits. Taken together we show that the increased power of UPC2-MS/MS allows the analyst to complete in vitro assays at biologically relevant concentrations for the first time and in so doing determine the routes of steroid metabolism which is vital for studies of androgen responsive cancers, such as prostate cancer, and could highlight new mechanisms of disease progression and new targets for cancer therapy.</description><identifier>ISSN: 1570-0232</identifier><identifier>EISSN: 1873-376X</identifier><identifier>DOI: 10.1016/j.jchromb.2016.07.024</identifier><identifier>PMID: 27479683</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Adrenal androgens ; Androgens - analysis ; Chromatography, Liquid - methods ; Chromatography, Supercritical Fluid - methods ; Gas chromatography ; High-Throughput Screening Assays ; Humans ; Reference Standards ; Reproducibility of Results ; Steroids ; Supercritical fluid chromatography ; Tandem Mass Spectrometry - methods ; Ultra performance convergence chromatography ; Ultra performance liquid chromatography</subject><ispartof>Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 2016-09, Vol.1031, p.131-138</ispartof><rights>2016 Elsevier B.V.</rights><rights>Copyright © 2016 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c412t-44cc6a2ef95d999321b69a37ee642eb62a86a4b2f1c9471cedb05c7257017d273</citedby><cites>FETCH-LOGICAL-c412t-44cc6a2ef95d999321b69a37ee642eb62a86a4b2f1c9471cedb05c7257017d273</cites><orcidid>0000-0003-1669-6383</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S157002321630486X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27903,27904,65309</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27479683$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Quanson, Jonathan L.</creatorcontrib><creatorcontrib>Stander, Marietjie A.</creatorcontrib><creatorcontrib>Pretorius, Elzette</creatorcontrib><creatorcontrib>Jenkinson, Carl</creatorcontrib><creatorcontrib>Taylor, Angela E.</creatorcontrib><creatorcontrib>Storbeck, Karl-Heinz</creatorcontrib><title>High-throughput analysis of 19 endogenous androgenic steroids by ultra-performance convergence chromatography tandem mass spectrometry</title><title>Journal of chromatography. B, Analytical technologies in the biomedical and life sciences</title><addtitle>J Chromatogr B Analyt Technol Biomed Life Sci</addtitle><description>•A high throughput UPC2-MS/MS method for the analysis of 19 steroids is described.•UPC2-MS/MS offers superior selectivity and increased chromatographic efficiency.•Significant improvements in sensitivity were achieved by UPC2-MS/MS.•UPC2-MS/MS is a SFC based technology which is ideal for steroid analysis.
11-Oxygenated steroids such as 11-ketotestosterone and 11-ketodihydrotestosterone have recently been shown to play a putative role in the development and progression of castration resistant prostate cancer. In this study we report on the development of a high throughput ultra-performance convergence chromatography tandem mass spectrometry (UPC2-MS/MS) method for the analysis of thirteen 11-oxygenated and six canonical C19 steroids isolated from a cell culture matrix. Using an Acquity UPC2 BEH 2-EP column we found that UPC2 resulted in superior selectivity, increased chromatographic efficiency and a scattered elution order when compared to conventional reverse phase ultra-performance liquid chromatography (UPLC). Furthermore, there was a significant improvement in sensitivity (5–50 times). The lower limits of quantification ranged between 0.01–10ngmL−1, while the upper limit of quantification was 100ngmL−1 for all steroids. Accuracy, precision, intra-day variation, recovery, matrix effects and process efficiency were all evaluated and found to be within acceptable limits. Taken together we show that the increased power of UPC2-MS/MS allows the analyst to complete in vitro assays at biologically relevant concentrations for the first time and in so doing determine the routes of steroid metabolism which is vital for studies of androgen responsive cancers, such as prostate cancer, and could highlight new mechanisms of disease progression and new targets for cancer therapy.</description><subject>Adrenal androgens</subject><subject>Androgens - analysis</subject><subject>Chromatography, Liquid - methods</subject><subject>Chromatography, Supercritical Fluid - methods</subject><subject>Gas chromatography</subject><subject>High-Throughput Screening Assays</subject><subject>Humans</subject><subject>Reference Standards</subject><subject>Reproducibility of Results</subject><subject>Steroids</subject><subject>Supercritical fluid chromatography</subject><subject>Tandem Mass Spectrometry - methods</subject><subject>Ultra performance convergence chromatography</subject><subject>Ultra performance liquid chromatography</subject><issn>1570-0232</issn><issn>1873-376X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUU1v3SAQRFGqfDU_IRXHXuwCxmCfoihKm0iRemml3hCG9Xs82cYFHMl_oL-7WO-115wYtLOzuzMI3VFSUkLFl0N5MPvgx65k-VsSWRLGz9AVbWRVVFL8Os-4lqQgrGKX6DrGAyFUElldoEsmuWxFU12hP89uty9SVlp2-3lJWE96WKOL2PeYthgm63cw-SXmig0bdgbHBME7G3G34mVIQRczhN6HUU8GsPHTG4TM3PC2o05-F_S8X3HKIjDiUceI4wwm5SqksH5EH3o9RLg9vTfo59enH4_Pxev3by-PD6-F4ZSlgnNjhGbQt7Vt27ZitBOtriSA4Aw6wXQjNO9YT03LJTVgO1IbybIPVFomqxv0-ag7B_97gZjU6KKBYdAT5BsVbSgXNWlYk6n1kWqCjzFAr-bgRh1WRYnaIlAHdYpAbREoIlWOIPd9Oo1YuhHs_65_nmfC_ZEA-dA3B0FF4zazrAvZEWW9e2fEXzkNnlU</recordid><startdate>20160915</startdate><enddate>20160915</enddate><creator>Quanson, Jonathan L.</creator><creator>Stander, Marietjie A.</creator><creator>Pretorius, Elzette</creator><creator>Jenkinson, Carl</creator><creator>Taylor, Angela E.</creator><creator>Storbeck, Karl-Heinz</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-1669-6383</orcidid></search><sort><creationdate>20160915</creationdate><title>High-throughput analysis of 19 endogenous androgenic steroids by ultra-performance convergence chromatography tandem mass spectrometry</title><author>Quanson, Jonathan L. ; Stander, Marietjie A. ; Pretorius, Elzette ; Jenkinson, Carl ; Taylor, Angela E. ; Storbeck, Karl-Heinz</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c412t-44cc6a2ef95d999321b69a37ee642eb62a86a4b2f1c9471cedb05c7257017d273</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adrenal androgens</topic><topic>Androgens - analysis</topic><topic>Chromatography, Liquid - methods</topic><topic>Chromatography, Supercritical Fluid - methods</topic><topic>Gas chromatography</topic><topic>High-Throughput Screening Assays</topic><topic>Humans</topic><topic>Reference Standards</topic><topic>Reproducibility of Results</topic><topic>Steroids</topic><topic>Supercritical fluid chromatography</topic><topic>Tandem Mass Spectrometry - methods</topic><topic>Ultra performance convergence chromatography</topic><topic>Ultra performance liquid chromatography</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Quanson, Jonathan L.</creatorcontrib><creatorcontrib>Stander, Marietjie A.</creatorcontrib><creatorcontrib>Pretorius, Elzette</creatorcontrib><creatorcontrib>Jenkinson, Carl</creatorcontrib><creatorcontrib>Taylor, Angela E.</creatorcontrib><creatorcontrib>Storbeck, Karl-Heinz</creatorcontrib><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>Journal of chromatography. 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B, Analytical technologies in the biomedical and life sciences</jtitle><addtitle>J Chromatogr B Analyt Technol Biomed Life Sci</addtitle><date>2016-09-15</date><risdate>2016</risdate><volume>1031</volume><spage>131</spage><epage>138</epage><pages>131-138</pages><issn>1570-0232</issn><eissn>1873-376X</eissn><abstract>•A high throughput UPC2-MS/MS method for the analysis of 19 steroids is described.•UPC2-MS/MS offers superior selectivity and increased chromatographic efficiency.•Significant improvements in sensitivity were achieved by UPC2-MS/MS.•UPC2-MS/MS is a SFC based technology which is ideal for steroid analysis.
11-Oxygenated steroids such as 11-ketotestosterone and 11-ketodihydrotestosterone have recently been shown to play a putative role in the development and progression of castration resistant prostate cancer. In this study we report on the development of a high throughput ultra-performance convergence chromatography tandem mass spectrometry (UPC2-MS/MS) method for the analysis of thirteen 11-oxygenated and six canonical C19 steroids isolated from a cell culture matrix. Using an Acquity UPC2 BEH 2-EP column we found that UPC2 resulted in superior selectivity, increased chromatographic efficiency and a scattered elution order when compared to conventional reverse phase ultra-performance liquid chromatography (UPLC). Furthermore, there was a significant improvement in sensitivity (5–50 times). The lower limits of quantification ranged between 0.01–10ngmL−1, while the upper limit of quantification was 100ngmL−1 for all steroids. Accuracy, precision, intra-day variation, recovery, matrix effects and process efficiency were all evaluated and found to be within acceptable limits. Taken together we show that the increased power of UPC2-MS/MS allows the analyst to complete in vitro assays at biologically relevant concentrations for the first time and in so doing determine the routes of steroid metabolism which is vital for studies of androgen responsive cancers, such as prostate cancer, and could highlight new mechanisms of disease progression and new targets for cancer therapy.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>27479683</pmid><doi>10.1016/j.jchromb.2016.07.024</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-1669-6383</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adrenal androgens Androgens - analysis Chromatography, Liquid - methods Chromatography, Supercritical Fluid - methods Gas chromatography High-Throughput Screening Assays Humans Reference Standards Reproducibility of Results Steroids Supercritical fluid chromatography Tandem Mass Spectrometry - methods Ultra performance convergence chromatography Ultra performance liquid chromatography |
title | High-throughput analysis of 19 endogenous androgenic steroids by ultra-performance convergence chromatography tandem mass spectrometry |
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