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
Hauptverfasser: Yang, Yichen, Gengji, Jiajia, Gong, Tao, Zhang, Zhirong, Deng, Li
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container_title Pharmaceutical research
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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.
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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. 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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 &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; 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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