The Finding of New In Vivo Metabolite Triptorelin (5-10) in Human Urine Using Liquid Chromatography Coupled with Ion Trap/Time-of-Flight Mass Spectrometry with Dimethyl Sulfoxide Additives in the Mobile Phase
Triptorelin and leuprorelin are synthetic gonadotrophin-releasing hormones (GnRH) that are on the World Anti-Doping Agency (WADA) list of prohibited substances. To investigate the possible in vivo metabolites of triptorelin and leuprorelin in humans compared to previously reported in vitro metabolit...
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Published in | Molecules (Basel, Switzerland) Vol. 28; no. 12; p. 4572 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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Abstract | Triptorelin and leuprorelin are synthetic gonadotrophin-releasing hormones (GnRH) that are on the World Anti-Doping Agency (WADA) list of prohibited substances. To investigate the possible in vivo metabolites of triptorelin and leuprorelin in humans compared to previously reported in vitro metabolites, excreted urine from five patients treated with either triptorelin or leuprorelin was analyzed by liquid chromatography coupled with ion trap/time-of-flight mass spectrometry (LC/MS-IT-TOF). The addition of dimethyl sulfoxide (DMSO) to the mobile phase was found to enhance the detection sensitivity of certain GnRH analogs. The method was validated, and the limit of detection (LOD) was found at 0.02−0.08 ng/mL. Using this method, a novel new metabolite of triptorelin was discovered in the urine of all subjects up to 1 month after triptorelin administration, but it was not observed in the urine of subjects before drug administration. The limit of detection was estimated to be 0.05 ng/mL. The structure of the metabolite, triptorelin (5-10), is proposed from bottom-up mass spectrometry analysis. The discovery of in vivo triptorelin (5-10) can possibly be used as supporting evidence of triptorelin misuse in athletes. |
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AbstractList | Triptorelin and leuprorelin are synthetic gonadotrophin-releasing hormones (GnRH) that are on the World Anti-Doping Agency (WADA) list of prohibited substances. To investigate the possible in vivo metabolites of triptorelin and leuprorelin in humans compared to previously reported in vitro metabolites, excreted urine from five patients treated with either triptorelin or leuprorelin was analyzed by liquid chromatography coupled with ion trap/time-of-flight mass spectrometry (LC/MS-IT-TOF). The addition of dimethyl sulfoxide (DMSO) to the mobile phase was found to enhance the detection sensitivity of certain GnRH analogs. The method was validated, and the limit of detection (LOD) was found at 0.02−0.08 ng/mL. Using this method, a novel new metabolite of triptorelin was discovered in the urine of all subjects up to 1 month after triptorelin administration, but it was not observed in the urine of subjects before drug administration. The limit of detection was estimated to be 0.05 ng/mL. The structure of the metabolite, triptorelin (5-10), is proposed from bottom-up mass spectrometry analysis. The discovery of in vivo triptorelin (5-10) can possibly be used as supporting evidence of triptorelin misuse in athletes. Triptorelin and leuprorelin are synthetic gonadotrophin-releasing hormones (GnRH) that are on the World Anti-Doping Agency (WADA) list of prohibited substances. To investigate the possible in vivo metabolites of triptorelin and leuprorelin in humans compared to previously reported in vitro metabolites, excreted urine from five patients treated with either triptorelin or leuprorelin was analyzed by liquid chromatography coupled with ion trap/time-of-flight mass spectrometry (LC/MS-IT-TOF). The addition of dimethyl sulfoxide (DMSO) to the mobile phase was found to enhance the detection sensitivity of certain GnRH analogs. The method was validated, and the limit of detection (LOD) was found at 0.02-0.08 ng/mL. Using this method, a novel new metabolite of triptorelin was discovered in the urine of all subjects up to 1 month after triptorelin administration, but it was not observed in the urine of subjects before drug administration. The limit of detection was estimated to be 0.05 ng/mL. The structure of the metabolite, triptorelin (5-10), is proposed from bottom-up mass spectrometry analysis. The discovery of in vivo triptorelin (5-10) can possibly be used as supporting evidence of triptorelin misuse in athletes.Triptorelin and leuprorelin are synthetic gonadotrophin-releasing hormones (GnRH) that are on the World Anti-Doping Agency (WADA) list of prohibited substances. To investigate the possible in vivo metabolites of triptorelin and leuprorelin in humans compared to previously reported in vitro metabolites, excreted urine from five patients treated with either triptorelin or leuprorelin was analyzed by liquid chromatography coupled with ion trap/time-of-flight mass spectrometry (LC/MS-IT-TOF). The addition of dimethyl sulfoxide (DMSO) to the mobile phase was found to enhance the detection sensitivity of certain GnRH analogs. The method was validated, and the limit of detection (LOD) was found at 0.02-0.08 ng/mL. Using this method, a novel new metabolite of triptorelin was discovered in the urine of all subjects up to 1 month after triptorelin administration, but it was not observed in the urine of subjects before drug administration. The limit of detection was estimated to be 0.05 ng/mL. The structure of the metabolite, triptorelin (5-10), is proposed from bottom-up mass spectrometry analysis. The discovery of in vivo triptorelin (5-10) can possibly be used as supporting evidence of triptorelin misuse in athletes. Triptorelin and leuprorelin are synthetic gonadotrophin-releasing hormones (GnRH) that are on the World Anti-Doping Agency (WADA) list of prohibited substances. To investigate the possible in vivo metabolites of triptorelin and leuprorelin in humans compared to previously reported in vitro metabolites, excreted urine from five patients treated with either triptorelin or leuprorelin was analyzed by liquid chromatography coupled with ion trap/time-of-flight mass spectrometry (LC/MS-IT-TOF). The addition of dimethyl sulfoxide (DMSO) to the mobile phase was found to enhance the detection sensitivity of certain GnRH analogs. The method was validated, and the limit of detection (LOD) was found at 0.02-0.08 ng/mL. Using this method, a novel new metabolite of triptorelin was discovered in the urine of all subjects up to 1 month after triptorelin administration, but it was not observed in the urine of subjects before drug administration. The limit of detection was estimated to be 0.05 ng/mL. The structure of the metabolite, triptorelin (5-10), is proposed from bottom-up mass spectrometry analysis. The discovery of in vivo triptorelin (5-10) can possibly be used as supporting evidence of triptorelin misuse in athletes. |
Audience | Academic |
Author | Kusamran, Thanit Songsaeng, Ruamsiri Pinthong, Darawan Saardpun, Navaporn Tanratana, Pansakorn |
AuthorAffiliation | 2 Analytical Science and National Doping Test Institute (ASNDTI), Mahidol University, Bangkok 10400, Thailand; ruamsiri.son@mahidol.ac.th (R.S.); thanit.kus@mahidol.ac.th (T.K.) 1 Department of Pharmacology, Faculty of Science, Mahidol University, Bangkok 10400, Thailand; navaporn.saa@mahidol.ac.th (N.S.); pansakorn.tan@mahidol.ac.th (P.T.) |
AuthorAffiliation_xml | – name: 2 Analytical Science and National Doping Test Institute (ASNDTI), Mahidol University, Bangkok 10400, Thailand; ruamsiri.son@mahidol.ac.th (R.S.); thanit.kus@mahidol.ac.th (T.K.) – name: 1 Department of Pharmacology, Faculty of Science, Mahidol University, Bangkok 10400, Thailand; navaporn.saa@mahidol.ac.th (N.S.); pansakorn.tan@mahidol.ac.th (P.T.) |
Author_xml | – sequence: 1 givenname: Navaporn surname: Saardpun fullname: Saardpun, Navaporn – sequence: 2 givenname: Ruamsiri surname: Songsaeng fullname: Songsaeng, Ruamsiri – sequence: 3 givenname: Pansakorn surname: Tanratana fullname: Tanratana, Pansakorn – sequence: 4 givenname: Thanit surname: Kusamran fullname: Kusamran, Thanit – sequence: 5 givenname: Darawan surname: Pinthong fullname: Pinthong, Darawan |
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Cites_doi | 10.1016/j.jpha.2011.09.008 10.1016/S0006-291X(71)80019-0 10.1016/j.ijms.2007.06.017 10.1002/jms.4049 10.1097/GCO.0b013e3281338874 10.1042/BIO20200057 10.1007/s10989-021-10177-0 10.2174/1389200219666180628171531 10.1002/jms.1453 10.1016/j.chroma.2009.05.054 10.1002/dta.2256 10.1002/rcm.526 10.1021/jasms.1c00280 10.1002/dta.1787 10.1038/nmeth.2610 10.1039/B618748J 10.1016/j.mce.2017.10.015 10.1002/jso.2930490109 10.1210/er.2004-0017 10.1007/s13361-017-1670-7 10.1016/j.jsbmb.2014.01.011 10.1016/j.ijms.2015.07.004 10.1021/ja00017a044 10.1006/abio.1996.9877 10.4103/0974-1208.142476 |
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SubjectTerms | Antimitotic agents Antineoplastic agents Chromatography Chromatography, Liquid - methods Comparative analysis Dimethyl Sulfoxide doping GnRH analogs Gonadotropin-Releasing Hormone Humans Ions LC/MS-IT-TOF Leuprolide leuprorelin detection Liquid chromatography Mass spectrometry Metabolites Peptides Pituitary hormones Prostate cancer Scientific imaging Tandem Mass Spectrometry - methods triptorelin detection triptorelin metabolite Triptorelin Pamoate Urine |
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Title | The Finding of New In Vivo Metabolite Triptorelin (5-10) in Human Urine Using Liquid Chromatography Coupled with Ion Trap/Time-of-Flight Mass Spectrometry with Dimethyl Sulfoxide Additives in the Mobile Phase |
URI | https://www.ncbi.nlm.nih.gov/pubmed/37375127 https://www.proquest.com/docview/2829853339 https://www.proquest.com/docview/2830671099 https://pubmed.ncbi.nlm.nih.gov/PMC10302202 https://doaj.org/article/77cf73008a3e4e3b81e278c07fc0a6d4 |
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