Loading…
Structure Determination of Felodipine Photoproducts in UV-Irradiated Medicines Using ESI-LC/MS/MS
Dihydropyridine drugs are well known as photodegradable pharmaceuticals. Herein, we evaluate the photostability of felodipine (FL) medicine (Splendil (SPL) tablets) and its altered forms (powders and suspensions). FL is a type of dihydropyridine drug, but its photochemical behavior is unknown. FL co...
Saved in:
Published in: | Pharmaceutics 2023-02, Vol.15 (2), p.697 |
---|---|
Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c638t-23d49750481a029ab0125025eeda32281619f9d47bd4715d401b646316b833293 |
---|---|
cites | cdi_FETCH-LOGICAL-c638t-23d49750481a029ab0125025eeda32281619f9d47bd4715d401b646316b833293 |
container_end_page | |
container_issue | 2 |
container_start_page | 697 |
container_title | Pharmaceutics |
container_volume | 15 |
creator | Kawabata, Kohei Kohashi, Miya Akimoto, Shiori Nishi, Hiroyuki |
description | Dihydropyridine drugs are well known as photodegradable pharmaceuticals. Herein, we evaluate the photostability of felodipine (FL) medicine (Splendil
(SPL) tablets) and its altered forms (powders and suspensions). FL is a type of dihydropyridine drug, but its photochemical behavior is unknown. FL contents after ultraviolet light (UV) irradiation for 24 h were monitored using high-performance liquid chromatography (HPLC). Values of the residual amounts of FL in UV-irradiated SPL powders and suspensions were 32.76 ± 4.88% and 0.79 ± 0.74%, respectively, with the generation of two photoproducts (FL photoproduct 1 and 2). To identify the chemical structures of these photoproducts, electrospray ionization liquid chromatography mass spectrometry (ESI-LC/MS/MS) analysis was performed. Based on their mass-to-charge ratio values and fragment patterns, it was proposed that FL photoproduct 1 was a pyridine derivative and FL photoproduct 2 was an FL dimer. Interestingly, generation rates of FL photoproduct 1 and 2 were dependent on the presence of the aqueous media. The photodimerization of FL was induced in UV-irradiated SPL suspensions. This is the first report evaluating the photostability of SPL tablets and its altered forms and estimating FL photoproducts induced by UV irradiation in the formulation of SPL. |
doi_str_mv | 10.3390/pharmaceutics15020697 |
format | article |
fullrecord | <record><control><sourceid>gale_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_80fa3766f8284bd7be0b82c6ebc2749f</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A743329688</galeid><doaj_id>oai_doaj_org_article_80fa3766f8284bd7be0b82c6ebc2749f</doaj_id><sourcerecordid>A743329688</sourcerecordid><originalsourceid>FETCH-LOGICAL-c638t-23d49750481a029ab0125025eeda32281619f9d47bd4715d401b646316b833293</originalsourceid><addsrcrecordid>eNptkl1r2zAUhs3YWEvXn7Bh2M1u3OrLsnQzKGm7BlI2yLJbIUvHiYItZZI92L-f0nRdM6oPJI7e9xHncIriPUYXlEp0udvoOGgD0-hMwjUiiMvmVXGKpZQVk4S-fnY_Kc5T2qI8KMWCyrfFCeWCIYTlaaGXY5zMOEUor2GEODivRxd8GbryFvpg3c55KL9twhh2MdisTaXz5epHNY9RW6dHsOU9WGeyLpWr5Py6vFnOq8Xs8n6Z17viTaf7BOeP51mxur35PrurFl-_zGdXi8pwKsaKUMtkUyMmsEZE6hZhkhOrAaymhAjMseykZU2bN64tQ7jljFPMW0EpkfSsmB-4Nuit2kU36PhbBe3UQyDEtdIx16sHJVCnacN5J4hgrW1aQK0ghkNrSMNkl1mfD6zd1A5gDfgx6v4Ievzi3Uatwy8lJWc15xnw6REQw88J0qgGlwz0vfYQpqRIIxDiXJC99ON_0m2Yos-lyqom8zCS7J9qrXMCznch_2v2UHXVsH0BuBBZdfGCKk8LgzPBQ-dy_MhQHwwmhpQidE85YqT2raZebLXs-_C8QE-uv41F_wBoDdAU</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2779641094</pqid></control><display><type>article</type><title>Structure Determination of Felodipine Photoproducts in UV-Irradiated Medicines Using ESI-LC/MS/MS</title><source>PubMed (Medline)</source><source>Access via ProQuest (Open Access)</source><creator>Kawabata, Kohei ; Kohashi, Miya ; Akimoto, Shiori ; Nishi, Hiroyuki</creator><creatorcontrib>Kawabata, Kohei ; Kohashi, Miya ; Akimoto, Shiori ; Nishi, Hiroyuki</creatorcontrib><description>Dihydropyridine drugs are well known as photodegradable pharmaceuticals. Herein, we evaluate the photostability of felodipine (FL) medicine (Splendil
(SPL) tablets) and its altered forms (powders and suspensions). FL is a type of dihydropyridine drug, but its photochemical behavior is unknown. FL contents after ultraviolet light (UV) irradiation for 24 h were monitored using high-performance liquid chromatography (HPLC). Values of the residual amounts of FL in UV-irradiated SPL powders and suspensions were 32.76 ± 4.88% and 0.79 ± 0.74%, respectively, with the generation of two photoproducts (FL photoproduct 1 and 2). To identify the chemical structures of these photoproducts, electrospray ionization liquid chromatography mass spectrometry (ESI-LC/MS/MS) analysis was performed. Based on their mass-to-charge ratio values and fragment patterns, it was proposed that FL photoproduct 1 was a pyridine derivative and FL photoproduct 2 was an FL dimer. Interestingly, generation rates of FL photoproduct 1 and 2 were dependent on the presence of the aqueous media. The photodimerization of FL was induced in UV-irradiated SPL suspensions. This is the first report evaluating the photostability of SPL tablets and its altered forms and estimating FL photoproducts induced by UV irradiation in the formulation of SPL.</description><identifier>ISSN: 1999-4923</identifier><identifier>EISSN: 1999-4923</identifier><identifier>DOI: 10.3390/pharmaceutics15020697</identifier><identifier>PMID: 36840019</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Blood pressure ; Chemical properties ; Drug dosages ; Experiments ; Felodipine ; High performance liquid chromatography ; HPLC ; Humidity ; Light ; Mass spectrometry ; Medical research ; Optical properties ; Pharmaceuticals ; Photodegradation ; photodimerization ; photooxidation ; photoproduct ; Sensors ; Structure</subject><ispartof>Pharmaceutics, 2023-02, Vol.15 (2), p.697</ispartof><rights>COPYRIGHT 2023 MDPI AG</rights><rights>2023 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 (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2023 by the authors. 2023</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c638t-23d49750481a029ab0125025eeda32281619f9d47bd4715d401b646316b833293</citedby><cites>FETCH-LOGICAL-c638t-23d49750481a029ab0125025eeda32281619f9d47bd4715d401b646316b833293</cites><orcidid>0000-0003-1760-2422</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2779641094/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2779641094?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36840019$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kawabata, Kohei</creatorcontrib><creatorcontrib>Kohashi, Miya</creatorcontrib><creatorcontrib>Akimoto, Shiori</creatorcontrib><creatorcontrib>Nishi, Hiroyuki</creatorcontrib><title>Structure Determination of Felodipine Photoproducts in UV-Irradiated Medicines Using ESI-LC/MS/MS</title><title>Pharmaceutics</title><addtitle>Pharmaceutics</addtitle><description>Dihydropyridine drugs are well known as photodegradable pharmaceuticals. Herein, we evaluate the photostability of felodipine (FL) medicine (Splendil
(SPL) tablets) and its altered forms (powders and suspensions). FL is a type of dihydropyridine drug, but its photochemical behavior is unknown. FL contents after ultraviolet light (UV) irradiation for 24 h were monitored using high-performance liquid chromatography (HPLC). Values of the residual amounts of FL in UV-irradiated SPL powders and suspensions were 32.76 ± 4.88% and 0.79 ± 0.74%, respectively, with the generation of two photoproducts (FL photoproduct 1 and 2). To identify the chemical structures of these photoproducts, electrospray ionization liquid chromatography mass spectrometry (ESI-LC/MS/MS) analysis was performed. Based on their mass-to-charge ratio values and fragment patterns, it was proposed that FL photoproduct 1 was a pyridine derivative and FL photoproduct 2 was an FL dimer. Interestingly, generation rates of FL photoproduct 1 and 2 were dependent on the presence of the aqueous media. The photodimerization of FL was induced in UV-irradiated SPL suspensions. This is the first report evaluating the photostability of SPL tablets and its altered forms and estimating FL photoproducts induced by UV irradiation in the formulation of SPL.</description><subject>Blood pressure</subject><subject>Chemical properties</subject><subject>Drug dosages</subject><subject>Experiments</subject><subject>Felodipine</subject><subject>High performance liquid chromatography</subject><subject>HPLC</subject><subject>Humidity</subject><subject>Light</subject><subject>Mass spectrometry</subject><subject>Medical research</subject><subject>Optical properties</subject><subject>Pharmaceuticals</subject><subject>Photodegradation</subject><subject>photodimerization</subject><subject>photooxidation</subject><subject>photoproduct</subject><subject>Sensors</subject><subject>Structure</subject><issn>1999-4923</issn><issn>1999-4923</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkl1r2zAUhs3YWEvXn7Bh2M1u3OrLsnQzKGm7BlI2yLJbIUvHiYItZZI92L-f0nRdM6oPJI7e9xHncIriPUYXlEp0udvoOGgD0-hMwjUiiMvmVXGKpZQVk4S-fnY_Kc5T2qI8KMWCyrfFCeWCIYTlaaGXY5zMOEUor2GEODivRxd8GbryFvpg3c55KL9twhh2MdisTaXz5epHNY9RW6dHsOU9WGeyLpWr5Py6vFnOq8Xs8n6Z17viTaf7BOeP51mxur35PrurFl-_zGdXi8pwKsaKUMtkUyMmsEZE6hZhkhOrAaymhAjMseykZU2bN64tQ7jljFPMW0EpkfSsmB-4Nuit2kU36PhbBe3UQyDEtdIx16sHJVCnacN5J4hgrW1aQK0ghkNrSMNkl1mfD6zd1A5gDfgx6v4Ievzi3Uatwy8lJWc15xnw6REQw88J0qgGlwz0vfYQpqRIIxDiXJC99ON_0m2Yos-lyqom8zCS7J9qrXMCznch_2v2UHXVsH0BuBBZdfGCKk8LgzPBQ-dy_MhQHwwmhpQidE85YqT2raZebLXs-_C8QE-uv41F_wBoDdAU</recordid><startdate>20230219</startdate><enddate>20230219</enddate><creator>Kawabata, Kohei</creator><creator>Kohashi, Miya</creator><creator>Akimoto, Shiori</creator><creator>Nishi, Hiroyuki</creator><general>MDPI AG</general><general>MDPI</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7XB</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-1760-2422</orcidid></search><sort><creationdate>20230219</creationdate><title>Structure Determination of Felodipine Photoproducts in UV-Irradiated Medicines Using ESI-LC/MS/MS</title><author>Kawabata, Kohei ; Kohashi, Miya ; Akimoto, Shiori ; Nishi, Hiroyuki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c638t-23d49750481a029ab0125025eeda32281619f9d47bd4715d401b646316b833293</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Blood pressure</topic><topic>Chemical properties</topic><topic>Drug dosages</topic><topic>Experiments</topic><topic>Felodipine</topic><topic>High performance liquid chromatography</topic><topic>HPLC</topic><topic>Humidity</topic><topic>Light</topic><topic>Mass spectrometry</topic><topic>Medical research</topic><topic>Optical properties</topic><topic>Pharmaceuticals</topic><topic>Photodegradation</topic><topic>photodimerization</topic><topic>photooxidation</topic><topic>photoproduct</topic><topic>Sensors</topic><topic>Structure</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kawabata, Kohei</creatorcontrib><creatorcontrib>Kohashi, Miya</creatorcontrib><creatorcontrib>Akimoto, Shiori</creatorcontrib><creatorcontrib>Nishi, Hiroyuki</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest research library</collection><collection>Research Library (Corporate)</collection><collection>Access via ProQuest (Open Access)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Directory of Open Access Journals (DOAJ)</collection><jtitle>Pharmaceutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kawabata, Kohei</au><au>Kohashi, Miya</au><au>Akimoto, Shiori</au><au>Nishi, Hiroyuki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Structure Determination of Felodipine Photoproducts in UV-Irradiated Medicines Using ESI-LC/MS/MS</atitle><jtitle>Pharmaceutics</jtitle><addtitle>Pharmaceutics</addtitle><date>2023-02-19</date><risdate>2023</risdate><volume>15</volume><issue>2</issue><spage>697</spage><pages>697-</pages><issn>1999-4923</issn><eissn>1999-4923</eissn><abstract>Dihydropyridine drugs are well known as photodegradable pharmaceuticals. Herein, we evaluate the photostability of felodipine (FL) medicine (Splendil
(SPL) tablets) and its altered forms (powders and suspensions). FL is a type of dihydropyridine drug, but its photochemical behavior is unknown. FL contents after ultraviolet light (UV) irradiation for 24 h were monitored using high-performance liquid chromatography (HPLC). Values of the residual amounts of FL in UV-irradiated SPL powders and suspensions were 32.76 ± 4.88% and 0.79 ± 0.74%, respectively, with the generation of two photoproducts (FL photoproduct 1 and 2). To identify the chemical structures of these photoproducts, electrospray ionization liquid chromatography mass spectrometry (ESI-LC/MS/MS) analysis was performed. Based on their mass-to-charge ratio values and fragment patterns, it was proposed that FL photoproduct 1 was a pyridine derivative and FL photoproduct 2 was an FL dimer. Interestingly, generation rates of FL photoproduct 1 and 2 were dependent on the presence of the aqueous media. The photodimerization of FL was induced in UV-irradiated SPL suspensions. This is the first report evaluating the photostability of SPL tablets and its altered forms and estimating FL photoproducts induced by UV irradiation in the formulation of SPL.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>36840019</pmid><doi>10.3390/pharmaceutics15020697</doi><orcidid>https://orcid.org/0000-0003-1760-2422</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1999-4923 |
ispartof | Pharmaceutics, 2023-02, Vol.15 (2), p.697 |
issn | 1999-4923 1999-4923 |
language | eng |
recordid | cdi_doaj_primary_oai_doaj_org_article_80fa3766f8284bd7be0b82c6ebc2749f |
source | PubMed (Medline); Access via ProQuest (Open Access) |
subjects | Blood pressure Chemical properties Drug dosages Experiments Felodipine High performance liquid chromatography HPLC Humidity Light Mass spectrometry Medical research Optical properties Pharmaceuticals Photodegradation photodimerization photooxidation photoproduct Sensors Structure |
title | Structure Determination of Felodipine Photoproducts in UV-Irradiated Medicines Using ESI-LC/MS/MS |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-01T13%3A31%3A48IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Structure%20Determination%20of%20Felodipine%20Photoproducts%20in%20UV-Irradiated%20Medicines%20Using%20ESI-LC/MS/MS&rft.jtitle=Pharmaceutics&rft.au=Kawabata,%20Kohei&rft.date=2023-02-19&rft.volume=15&rft.issue=2&rft.spage=697&rft.pages=697-&rft.issn=1999-4923&rft.eissn=1999-4923&rft_id=info:doi/10.3390/pharmaceutics15020697&rft_dat=%3Cgale_doaj_%3EA743329688%3C/gale_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c638t-23d49750481a029ab0125025eeda32281619f9d47bd4715d401b646316b833293%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2779641094&rft_id=info:pmid/36840019&rft_galeid=A743329688&rfr_iscdi=true |