Time-Lapse Macro Imaging with Dissolution Tests for Exploring the Interrelationship Between Disintegration and Dissolution Behaviors of Solid Dosages
Objective This study aims to establish a Flow-through Visualization Dissolution System (FVDS) that combines time-lapse macro-imaging and a flow-through cell to simultaneously elucidate dissolution and disintegration profiles. Methods Three cefaclor extended-release tablets (CEC-1, CEC-2, CEC-3) from...
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Veröffentlicht in: | Pharmaceutical research 2024-02, Vol.41 (2), p.387-400 |
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creator | Yang, Yichen Gengji, Jiajia Gong, Tao Zhang, Zhirong Deng, Li |
description | Objective
This study aims to establish a Flow-through Visualization Dissolution System (FVDS) that combines time-lapse macro-imaging and a flow-through cell to simultaneously elucidate dissolution and disintegration profiles.
Methods
Three cefaclor extended-release tablets (CEC-1, CEC-2, CEC-3) from different manufacturers were subjected to dissolution tests using both the US Pharmacopeia basket method and the FVDS method. Two dissolution media plans were implemented in FVDS: i) Plan I involved dissolution in pH1.0 medium for 12 h; ii) Plan II initiated dissolution in pH1.0 medium for 1 h, followed by pH6.8 phosphate buffer for 11 h. The resulting dissolution data were fitted using classic mathematical models. Pixel information was further extracted from images obtained using FVDS and plotted over time.
Results
The basket method showed the cumulative dissolution of all three tablets in pH1.0, pH4.0 and water reached 80% within 6 h, but remained below 60% in the pH6.8 medium. The
f
2
values indicated CEC-2 was similar to CEC-1 in the pH4.0 medium, pH6.8 medium and water. Using FVDS with medium plan II, the cumulative dissolution of CEC-1 and CEC-2 reached about 80% showing similarity, while no similarity was observed between CEC-3 and CEC-1. The
f
2
factor of the percentage area change profiles also showed consistent results in the dissolution profile of medium plan II. However, FVDS with medium plan I cannot distinguish between CEC-2 and CEC-3.
Conclusion
FVDS offers an alternative to traditional dissolution methods by integrating imaging analysis as a complementary tool to disintegration and dissolution testing methods. |
doi_str_mv | 10.1007/s11095-024-03655-9 |
format | Article |
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This study aims to establish a Flow-through Visualization Dissolution System (FVDS) that combines time-lapse macro-imaging and a flow-through cell to simultaneously elucidate dissolution and disintegration profiles.
Methods
Three cefaclor extended-release tablets (CEC-1, CEC-2, CEC-3) from different manufacturers were subjected to dissolution tests using both the US Pharmacopeia basket method and the FVDS method. Two dissolution media plans were implemented in FVDS: i) Plan I involved dissolution in pH1.0 medium for 12 h; ii) Plan II initiated dissolution in pH1.0 medium for 1 h, followed by pH6.8 phosphate buffer for 11 h. The resulting dissolution data were fitted using classic mathematical models. Pixel information was further extracted from images obtained using FVDS and plotted over time.
Results
The basket method showed the cumulative dissolution of all three tablets in pH1.0, pH4.0 and water reached 80% within 6 h, but remained below 60% in the pH6.8 medium. The
f
2
values indicated CEC-2 was similar to CEC-1 in the pH4.0 medium, pH6.8 medium and water. Using FVDS with medium plan II, the cumulative dissolution of CEC-1 and CEC-2 reached about 80% showing similarity, while no similarity was observed between CEC-3 and CEC-1. The
f
2
factor of the percentage area change profiles also showed consistent results in the dissolution profile of medium plan II. However, FVDS with medium plan I cannot distinguish between CEC-2 and CEC-3.
Conclusion
FVDS offers an alternative to traditional dissolution methods by integrating imaging analysis as a complementary tool to disintegration and dissolution testing methods.</description><identifier>ISSN: 0724-8741</identifier><identifier>EISSN: 1573-904X</identifier><identifier>DOI: 10.1007/s11095-024-03655-9</identifier><identifier>PMID: 38243127</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Behavior ; Biochemistry ; Biomedical and Life Sciences ; Biomedical Engineering and Bioengineering ; Biomedicine ; Cefaclor ; Dissolution ; Drug dosages ; Hydrochloric acid ; Magnetic resonance imaging ; Manufacturing ; Mathematical models ; Medical Law ; Morphology ; Original Research Article ; Pharmaceutical industry ; Pharmacology/Toxicology ; Pharmacy ; Phosphates ; Proteins ; Tablets</subject><ispartof>Pharmaceutical research, 2024-02, Vol.41 (2), p.387-400</ispartof><rights>The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2024. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>2024. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.</rights><rights>COPYRIGHT 2024 Springer</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c393t-b6bc72cc94ea6412f5da41b3a9f7c8a457f4db1e656fef6e66e5791742e6d6db3</cites><orcidid>0000-0002-9606-4409</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s11095-024-03655-9$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s11095-024-03655-9$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38243127$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yang, Yichen</creatorcontrib><creatorcontrib>Gengji, Jiajia</creatorcontrib><creatorcontrib>Gong, Tao</creatorcontrib><creatorcontrib>Zhang, Zhirong</creatorcontrib><creatorcontrib>Deng, Li</creatorcontrib><title>Time-Lapse Macro Imaging with Dissolution Tests for Exploring the Interrelationship Between Disintegration and Dissolution Behaviors of Solid Dosages</title><title>Pharmaceutical research</title><addtitle>Pharm Res</addtitle><addtitle>Pharm Res</addtitle><description>Objective
This study aims to establish a Flow-through Visualization Dissolution System (FVDS) that combines time-lapse macro-imaging and a flow-through cell to simultaneously elucidate dissolution and disintegration profiles.
Methods
Three cefaclor extended-release tablets (CEC-1, CEC-2, CEC-3) from different manufacturers were subjected to dissolution tests using both the US Pharmacopeia basket method and the FVDS method. Two dissolution media plans were implemented in FVDS: i) Plan I involved dissolution in pH1.0 medium for 12 h; ii) Plan II initiated dissolution in pH1.0 medium for 1 h, followed by pH6.8 phosphate buffer for 11 h. The resulting dissolution data were fitted using classic mathematical models. Pixel information was further extracted from images obtained using FVDS and plotted over time.
Results
The basket method showed the cumulative dissolution of all three tablets in pH1.0, pH4.0 and water reached 80% within 6 h, but remained below 60% in the pH6.8 medium. The
f
2
values indicated CEC-2 was similar to CEC-1 in the pH4.0 medium, pH6.8 medium and water. Using FVDS with medium plan II, the cumulative dissolution of CEC-1 and CEC-2 reached about 80% showing similarity, while no similarity was observed between CEC-3 and CEC-1. The
f
2
factor of the percentage area change profiles also showed consistent results in the dissolution profile of medium plan II. However, FVDS with medium plan I cannot distinguish between CEC-2 and CEC-3.
Conclusion
FVDS offers an alternative to traditional dissolution methods by integrating imaging analysis as a complementary tool to disintegration and dissolution testing methods.</description><subject>Behavior</subject><subject>Biochemistry</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedical Engineering and Bioengineering</subject><subject>Biomedicine</subject><subject>Cefaclor</subject><subject>Dissolution</subject><subject>Drug dosages</subject><subject>Hydrochloric acid</subject><subject>Magnetic resonance imaging</subject><subject>Manufacturing</subject><subject>Mathematical models</subject><subject>Medical Law</subject><subject>Morphology</subject><subject>Original Research Article</subject><subject>Pharmaceutical industry</subject><subject>Pharmacology/Toxicology</subject><subject>Pharmacy</subject><subject>Phosphates</subject><subject>Proteins</subject><subject>Tablets</subject><issn>0724-8741</issn><issn>1573-904X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNp9ksFu1DAURS1ERYfCD7BAltiwSWvHjh0v21JgpKlYMEjsLCd5zrhK4mAnFD6E_8WZKa2KEPLCku-5V896F6FXlJxSQuRZpJSoIiM5zwgTRZGpJ2hFC8kyRfjXp2hFZJJKyekxeh7jDSGkpIo_Q8eszDmjuVyhX1vXQ7YxYwR8berg8bo3rRtafOumHX7nYvTdPDk_4C3EKWLrA776MXY-LNC0A7weJggBOrNQcedGfAHTLcCwuF0S27CXsBmaR4EXsDPfnQ8Re4s_-84l2UfTQnyBjqzpIry8u0_Ql_dX28uP2ebTh_Xl-SarmWJTVomqlnldKw5GcJrbojGcVswoK-vS8EJa3lQURCEsWAFCQCEVlTwH0YimYifo7SF3DP7bnP6nexdr6DozgJ-jzlVeloUQVCb0zV_ojZ_DkKbbU5JRyukD1ZoOtBusn4Kpl1B9LkvGSsEYSdTpP6h0Guhd7QewLr0_MuQHQ1pQjAGsHoPrTfipKdFLF_ShCzp1Qe-7oFUyvb6beK56aO4tf5afAHYA4rgsE8LDl_4T-xuRTMCa</recordid><startdate>20240201</startdate><enddate>20240201</enddate><creator>Yang, Yichen</creator><creator>Gengji, Jiajia</creator><creator>Gong, Tao</creator><creator>Zhang, Zhirong</creator><creator>Deng, Li</creator><general>Springer US</general><general>Springer</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-9606-4409</orcidid></search><sort><creationdate>20240201</creationdate><title>Time-Lapse Macro Imaging with Dissolution Tests for Exploring the Interrelationship Between Disintegration and Dissolution Behaviors of Solid Dosages</title><author>Yang, Yichen ; Gengji, Jiajia ; Gong, Tao ; Zhang, Zhirong ; Deng, Li</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c393t-b6bc72cc94ea6412f5da41b3a9f7c8a457f4db1e656fef6e66e5791742e6d6db3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Behavior</topic><topic>Biochemistry</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedical Engineering and Bioengineering</topic><topic>Biomedicine</topic><topic>Cefaclor</topic><topic>Dissolution</topic><topic>Drug dosages</topic><topic>Hydrochloric acid</topic><topic>Magnetic resonance imaging</topic><topic>Manufacturing</topic><topic>Mathematical models</topic><topic>Medical Law</topic><topic>Morphology</topic><topic>Original Research Article</topic><topic>Pharmaceutical industry</topic><topic>Pharmacology/Toxicology</topic><topic>Pharmacy</topic><topic>Phosphates</topic><topic>Proteins</topic><topic>Tablets</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, Yichen</creatorcontrib><creatorcontrib>Gengji, Jiajia</creatorcontrib><creatorcontrib>Gong, Tao</creatorcontrib><creatorcontrib>Zhang, Zhirong</creatorcontrib><creatorcontrib>Deng, Li</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Pharmaceutical research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, Yichen</au><au>Gengji, Jiajia</au><au>Gong, Tao</au><au>Zhang, Zhirong</au><au>Deng, Li</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Time-Lapse Macro Imaging with Dissolution Tests for Exploring the Interrelationship Between Disintegration and Dissolution Behaviors of Solid Dosages</atitle><jtitle>Pharmaceutical research</jtitle><stitle>Pharm Res</stitle><addtitle>Pharm Res</addtitle><date>2024-02-01</date><risdate>2024</risdate><volume>41</volume><issue>2</issue><spage>387</spage><epage>400</epage><pages>387-400</pages><issn>0724-8741</issn><eissn>1573-904X</eissn><abstract>Objective
This study aims to establish a Flow-through Visualization Dissolution System (FVDS) that combines time-lapse macro-imaging and a flow-through cell to simultaneously elucidate dissolution and disintegration profiles.
Methods
Three cefaclor extended-release tablets (CEC-1, CEC-2, CEC-3) from different manufacturers were subjected to dissolution tests using both the US Pharmacopeia basket method and the FVDS method. Two dissolution media plans were implemented in FVDS: i) Plan I involved dissolution in pH1.0 medium for 12 h; ii) Plan II initiated dissolution in pH1.0 medium for 1 h, followed by pH6.8 phosphate buffer for 11 h. The resulting dissolution data were fitted using classic mathematical models. Pixel information was further extracted from images obtained using FVDS and plotted over time.
Results
The basket method showed the cumulative dissolution of all three tablets in pH1.0, pH4.0 and water reached 80% within 6 h, but remained below 60% in the pH6.8 medium. The
f
2
values indicated CEC-2 was similar to CEC-1 in the pH4.0 medium, pH6.8 medium and water. Using FVDS with medium plan II, the cumulative dissolution of CEC-1 and CEC-2 reached about 80% showing similarity, while no similarity was observed between CEC-3 and CEC-1. The
f
2
factor of the percentage area change profiles also showed consistent results in the dissolution profile of medium plan II. However, FVDS with medium plan I cannot distinguish between CEC-2 and CEC-3.
Conclusion
FVDS offers an alternative to traditional dissolution methods by integrating imaging analysis as a complementary tool to disintegration and dissolution testing methods.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>38243127</pmid><doi>10.1007/s11095-024-03655-9</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0002-9606-4409</orcidid></addata></record> |
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subjects | Behavior Biochemistry Biomedical and Life Sciences Biomedical Engineering and Bioengineering Biomedicine Cefaclor Dissolution Drug dosages Hydrochloric acid Magnetic resonance imaging Manufacturing Mathematical models Medical Law Morphology Original Research Article Pharmaceutical industry Pharmacology/Toxicology Pharmacy Phosphates Proteins Tablets |
title | Time-Lapse Macro Imaging with Dissolution Tests for Exploring the Interrelationship Between Disintegration and Dissolution Behaviors of Solid Dosages |
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