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Screening of Phosphodiesterase-5 Inhibitors and Their Analogs in Dietary Supplements by Liquid Chromatography–Hybrid Ion Trap–Time of Flight Mass Spectrometry
An accurate and reliable method based on ion trap–time of flight mass spectrometry (IT–TOF MS) was developed for screening phosphodiesterase-5 inhibitors, including sildenafil, vardenafil, and tadalafil, and their analogs in dietary supplements. Various parameters affecting liquid chromatographic se...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7355528/ https://www.ncbi.nlm.nih.gov/pubmed/32545673 http://dx.doi.org/10.3390/molecules25122734 |
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author | Kim, Unyong Cho, Hyun-Deok Kang, Myung Hee Suh, Joon Hyuk Eom, Han Young Kim, Junghyun Seo, Sumin Kim, Gunwoo Koo, Hye Ryoung Ha, Nary Song, Un Tak Han, Sang Beom |
author_facet | Kim, Unyong Cho, Hyun-Deok Kang, Myung Hee Suh, Joon Hyuk Eom, Han Young Kim, Junghyun Seo, Sumin Kim, Gunwoo Koo, Hye Ryoung Ha, Nary Song, Un Tak Han, Sang Beom |
author_sort | Kim, Unyong |
collection | PubMed |
description | An accurate and reliable method based on ion trap–time of flight mass spectrometry (IT–TOF MS) was developed for screening phosphodiesterase-5 inhibitors, including sildenafil, vardenafil, and tadalafil, and their analogs in dietary supplements. Various parameters affecting liquid chromatographic separation and IT–TOF detection were investigated, and the optimal conditions were determined. The separation was achieved on a reversed-phase column under gradient elution using acetonitrile and water containing 0.2% acetic acid at a flow rate of 0.2 mL/min. The chromatographic eluents were directly ionized in the IT–TOF system equipped with an electrospray ion source operating in the positive ion mode. The proposed screening method was validated by assessing its linearity, precision, and accuracy. Sequential tandem MS was conducted to obtain structural information of the references, and the fragmentation mechanism of each reference was proposed for providing spectral insight for newly synthesized analogs. Structural information, including accurate masses of both parent and fragment ions, was incorporated into the MS(n) spectral library. The developed method was successfully applied for screening adulterated dietary supplement samples. |
format | Online Article Text |
id | pubmed-7355528 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-73555282020-07-23 Screening of Phosphodiesterase-5 Inhibitors and Their Analogs in Dietary Supplements by Liquid Chromatography–Hybrid Ion Trap–Time of Flight Mass Spectrometry Kim, Unyong Cho, Hyun-Deok Kang, Myung Hee Suh, Joon Hyuk Eom, Han Young Kim, Junghyun Seo, Sumin Kim, Gunwoo Koo, Hye Ryoung Ha, Nary Song, Un Tak Han, Sang Beom Molecules Article An accurate and reliable method based on ion trap–time of flight mass spectrometry (IT–TOF MS) was developed for screening phosphodiesterase-5 inhibitors, including sildenafil, vardenafil, and tadalafil, and their analogs in dietary supplements. Various parameters affecting liquid chromatographic separation and IT–TOF detection were investigated, and the optimal conditions were determined. The separation was achieved on a reversed-phase column under gradient elution using acetonitrile and water containing 0.2% acetic acid at a flow rate of 0.2 mL/min. The chromatographic eluents were directly ionized in the IT–TOF system equipped with an electrospray ion source operating in the positive ion mode. The proposed screening method was validated by assessing its linearity, precision, and accuracy. Sequential tandem MS was conducted to obtain structural information of the references, and the fragmentation mechanism of each reference was proposed for providing spectral insight for newly synthesized analogs. Structural information, including accurate masses of both parent and fragment ions, was incorporated into the MS(n) spectral library. The developed method was successfully applied for screening adulterated dietary supplement samples. MDPI 2020-06-12 /pmc/articles/PMC7355528/ /pubmed/32545673 http://dx.doi.org/10.3390/molecules25122734 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Kim, Unyong Cho, Hyun-Deok Kang, Myung Hee Suh, Joon Hyuk Eom, Han Young Kim, Junghyun Seo, Sumin Kim, Gunwoo Koo, Hye Ryoung Ha, Nary Song, Un Tak Han, Sang Beom Screening of Phosphodiesterase-5 Inhibitors and Their Analogs in Dietary Supplements by Liquid Chromatography–Hybrid Ion Trap–Time of Flight Mass Spectrometry |
title | Screening of Phosphodiesterase-5 Inhibitors and Their Analogs in Dietary Supplements by Liquid Chromatography–Hybrid Ion Trap–Time of Flight Mass Spectrometry |
title_full | Screening of Phosphodiesterase-5 Inhibitors and Their Analogs in Dietary Supplements by Liquid Chromatography–Hybrid Ion Trap–Time of Flight Mass Spectrometry |
title_fullStr | Screening of Phosphodiesterase-5 Inhibitors and Their Analogs in Dietary Supplements by Liquid Chromatography–Hybrid Ion Trap–Time of Flight Mass Spectrometry |
title_full_unstemmed | Screening of Phosphodiesterase-5 Inhibitors and Their Analogs in Dietary Supplements by Liquid Chromatography–Hybrid Ion Trap–Time of Flight Mass Spectrometry |
title_short | Screening of Phosphodiesterase-5 Inhibitors and Their Analogs in Dietary Supplements by Liquid Chromatography–Hybrid Ion Trap–Time of Flight Mass Spectrometry |
title_sort | screening of phosphodiesterase-5 inhibitors and their analogs in dietary supplements by liquid chromatography–hybrid ion trap–time of flight mass spectrometry |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7355528/ https://www.ncbi.nlm.nih.gov/pubmed/32545673 http://dx.doi.org/10.3390/molecules25122734 |
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