Preparation and characterization of metformin hydrochloride controlled-release tablet using fatty acid coated granules
Metformin hydrochloride (MFM) is often used as a controlled-release (CR) tablet to reduce dosing frequency. However, the MFM CR tablet contains significant amounts of excipients and the tablet size is also large. Dosing convenience and patient compliance can be increased by reducing the size of the...
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Veröffentlicht in: | Drug development and industrial pharmacy 2020-05, Vol.46 (5), p.852-860 |
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creator | Kang, Ji-Hyun Chun, Myung-Hee Cho, Mi-Seo Kwon, Yong-Bin Choi, Jae-Cheol Kim, Dong-Wook Park, Chun-Woong Park, Eun-Seok |
description | Metformin hydrochloride (MFM) is often used as a controlled-release (CR) tablet to reduce dosing frequency. However, the MFM CR tablet contains significant amounts of excipients and the tablet size is also large. Dosing convenience and patient compliance can be increased by reducing the size of the CR tablets. The aim of this study was to prepare and evaluate the MFM controlled-release tablet (MFM-CRT) using two types of release modulators, inner and outer. The MFM-CRT was prepared by coating the MFM granules using a binder solution containing aluminum stearate (ALS) as the inner release-modulator, and polyethylene oxide (PEO) as the outer release-modulator. The dispersion stability of the binder solution was optimized by the dispersion analyzer. The MFM-CRT was evaluated for dissolution rate and tablet volume. Additionally, dissolution behavior and dissolution kinetics of the MFM-CRT were analyzed using micro-computed tomography (micro-CT). Although the optimal MFM-CRT showed no difference in the release rate as compared to the commercially available product of Glucophage
®
XR 500 mg (f
2
value: 72), the length of the long axis was reduced by 6 mm and the weight was reduced by about 27%. We expect patient compliance to improve because of effective sustained release and volume reduction of MFM-CRT. |
doi_str_mv | 10.1080/03639045.2020.1762198 |
format | Article |
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®
XR 500 mg (f
2
value: 72), the length of the long axis was reduced by 6 mm and the weight was reduced by about 27%. We expect patient compliance to improve because of effective sustained release and volume reduction of MFM-CRT.</description><identifier>ISSN: 0363-9045</identifier><identifier>EISSN: 1520-5762</identifier><identifier>DOI: 10.1080/03639045.2020.1762198</identifier><identifier>PMID: 32338551</identifier><language>eng</language><publisher>ABINGDON: Taylor & Francis</publisher><subject>aluminum stearate ; Chemistry, Medicinal ; Delayed-Action Preparations - chemical synthesis ; Delayed-Action Preparations - metabolism ; dispersion analyzer ; Drug Carriers - chemical synthesis ; Drug Carriers - metabolism ; Drug Liberation ; Fatty Acids - chemical synthesis ; Fatty Acids - metabolism ; Hypoglycemic Agents - chemical synthesis ; Hypoglycemic Agents - metabolism ; Life Sciences & Biomedicine ; Metformin - chemical synthesis ; Metformin - metabolism ; Metformin hydrochloride ; micro-computed tomography ; Pharmacology & Pharmacy ; polyethylene oxide ; Science & Technology ; Spectrometry, X-Ray Emission - methods ; X-Ray Microtomography - methods</subject><ispartof>Drug development and industrial pharmacy, 2020-05, Vol.46 (5), p.852-860</ispartof><rights>2020 Informa UK Limited, trading as Taylor & Francis Group 2020</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>true</woscitedreferencessubscribed><woscitedreferencescount>7</woscitedreferencescount><woscitedreferencesoriginalsourcerecordid>wos000533693100001</woscitedreferencesoriginalsourcerecordid><citedby>FETCH-LOGICAL-c432t-3a01d194b05bd6658a0d4bc7c477dc0b549c9b68d75115cab1365709793a0cfe3</citedby><cites>FETCH-LOGICAL-c432t-3a01d194b05bd6658a0d4bc7c477dc0b549c9b68d75115cab1365709793a0cfe3</cites><orcidid>0000-0003-1294-9160 ; 0000-0001-5329-8443</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,782,786,27931,27932,28255</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32338551$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kang, Ji-Hyun</creatorcontrib><creatorcontrib>Chun, Myung-Hee</creatorcontrib><creatorcontrib>Cho, Mi-Seo</creatorcontrib><creatorcontrib>Kwon, Yong-Bin</creatorcontrib><creatorcontrib>Choi, Jae-Cheol</creatorcontrib><creatorcontrib>Kim, Dong-Wook</creatorcontrib><creatorcontrib>Park, Chun-Woong</creatorcontrib><creatorcontrib>Park, Eun-Seok</creatorcontrib><title>Preparation and characterization of metformin hydrochloride controlled-release tablet using fatty acid coated granules</title><title>Drug development and industrial pharmacy</title><addtitle>DRUG DEV IND PHARM</addtitle><addtitle>Drug Dev Ind Pharm</addtitle><description>Metformin hydrochloride (MFM) is often used as a controlled-release (CR) tablet to reduce dosing frequency. However, the MFM CR tablet contains significant amounts of excipients and the tablet size is also large. Dosing convenience and patient compliance can be increased by reducing the size of the CR tablets. The aim of this study was to prepare and evaluate the MFM controlled-release tablet (MFM-CRT) using two types of release modulators, inner and outer. The MFM-CRT was prepared by coating the MFM granules using a binder solution containing aluminum stearate (ALS) as the inner release-modulator, and polyethylene oxide (PEO) as the outer release-modulator. The dispersion stability of the binder solution was optimized by the dispersion analyzer. The MFM-CRT was evaluated for dissolution rate and tablet volume. Additionally, dissolution behavior and dissolution kinetics of the MFM-CRT were analyzed using micro-computed tomography (micro-CT). Although the optimal MFM-CRT showed no difference in the release rate as compared to the commercially available product of Glucophage
®
XR 500 mg (f
2
value: 72), the length of the long axis was reduced by 6 mm and the weight was reduced by about 27%. We expect patient compliance to improve because of effective sustained release and volume reduction of MFM-CRT.</description><subject>aluminum stearate</subject><subject>Chemistry, Medicinal</subject><subject>Delayed-Action Preparations - chemical synthesis</subject><subject>Delayed-Action Preparations - metabolism</subject><subject>dispersion analyzer</subject><subject>Drug Carriers - chemical synthesis</subject><subject>Drug Carriers - metabolism</subject><subject>Drug Liberation</subject><subject>Fatty Acids - chemical synthesis</subject><subject>Fatty Acids - metabolism</subject><subject>Hypoglycemic Agents - chemical synthesis</subject><subject>Hypoglycemic Agents - metabolism</subject><subject>Life Sciences & Biomedicine</subject><subject>Metformin - chemical synthesis</subject><subject>Metformin - metabolism</subject><subject>Metformin hydrochloride</subject><subject>micro-computed tomography</subject><subject>Pharmacology & Pharmacy</subject><subject>polyethylene oxide</subject><subject>Science & Technology</subject><subject>Spectrometry, X-Ray Emission - methods</subject><subject>X-Ray Microtomography - methods</subject><issn>0363-9045</issn><issn>1520-5762</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>AOWDO</sourceid><sourceid>EIF</sourceid><recordid>eNqNkU1P3DAQhq0KVLbQn9DKdxQ6juMkvoFW0FZCKgc4R_6YsK6y9sr2Fm1_PQ4BjlVP9oyed6R5hpAvDC4Y9PANeMslNOKihrq0urZmsv9AVkzUUIlSHpHVzFQzdEI-pfQbgNVSiI_khNec90KwFflzF3GnosoueKq8pWZTKpMxur9LM4x0i3kMces83RxsDGYzhegsUhN8jmGa0FYRJ1QJaVZ6wkz3yflHOqqcD1QZV8YGldHSx6j8fsJ0Ro5HNSX8_Pqekoeb6_v1j-r21_ef66vbyjS8zhVXwCyTjQahbduKXoFttOlM03XWgBaNNFK3ve0EY8IozXgrOpCdLEkzIj8lYplrYkgp4jjsotuqeBgYDLPH4c3jMHscXj2W3Nclt9vrLdr31Ju4ApwvwBPqMCbj0Bt8xwBAcN5KzsoPZrr_f3rt8ov5ddj7XKKXS9T5-QbqKcTJDlkdyg3GYtO4NPB_L_MMMhGlcQ</recordid><startdate>20200503</startdate><enddate>20200503</enddate><creator>Kang, Ji-Hyun</creator><creator>Chun, Myung-Hee</creator><creator>Cho, Mi-Seo</creator><creator>Kwon, Yong-Bin</creator><creator>Choi, Jae-Cheol</creator><creator>Kim, Dong-Wook</creator><creator>Park, Chun-Woong</creator><creator>Park, Eun-Seok</creator><general>Taylor & Francis</general><scope>AOWDO</scope><scope>BLEPL</scope><scope>DTL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0003-1294-9160</orcidid><orcidid>https://orcid.org/0000-0001-5329-8443</orcidid></search><sort><creationdate>20200503</creationdate><title>Preparation and characterization of metformin hydrochloride controlled-release tablet using fatty acid coated granules</title><author>Kang, Ji-Hyun ; Chun, Myung-Hee ; Cho, Mi-Seo ; Kwon, Yong-Bin ; Choi, Jae-Cheol ; Kim, Dong-Wook ; Park, Chun-Woong ; Park, Eun-Seok</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c432t-3a01d194b05bd6658a0d4bc7c477dc0b549c9b68d75115cab1365709793a0cfe3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>aluminum stearate</topic><topic>Chemistry, Medicinal</topic><topic>Delayed-Action Preparations - chemical synthesis</topic><topic>Delayed-Action Preparations - metabolism</topic><topic>dispersion analyzer</topic><topic>Drug Carriers - chemical synthesis</topic><topic>Drug Carriers - metabolism</topic><topic>Drug Liberation</topic><topic>Fatty Acids - chemical synthesis</topic><topic>Fatty Acids - metabolism</topic><topic>Hypoglycemic Agents - chemical synthesis</topic><topic>Hypoglycemic Agents - metabolism</topic><topic>Life Sciences & Biomedicine</topic><topic>Metformin - chemical synthesis</topic><topic>Metformin - metabolism</topic><topic>Metformin hydrochloride</topic><topic>micro-computed tomography</topic><topic>Pharmacology & Pharmacy</topic><topic>polyethylene oxide</topic><topic>Science & Technology</topic><topic>Spectrometry, X-Ray Emission - methods</topic><topic>X-Ray Microtomography - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kang, Ji-Hyun</creatorcontrib><creatorcontrib>Chun, Myung-Hee</creatorcontrib><creatorcontrib>Cho, Mi-Seo</creatorcontrib><creatorcontrib>Kwon, Yong-Bin</creatorcontrib><creatorcontrib>Choi, Jae-Cheol</creatorcontrib><creatorcontrib>Kim, Dong-Wook</creatorcontrib><creatorcontrib>Park, Chun-Woong</creatorcontrib><creatorcontrib>Park, Eun-Seok</creatorcontrib><collection>Web of Science - Science Citation Index Expanded - 2020</collection><collection>Web of Science Core Collection</collection><collection>Science Citation Index Expanded</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Drug development and industrial pharmacy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kang, Ji-Hyun</au><au>Chun, Myung-Hee</au><au>Cho, Mi-Seo</au><au>Kwon, Yong-Bin</au><au>Choi, Jae-Cheol</au><au>Kim, Dong-Wook</au><au>Park, Chun-Woong</au><au>Park, Eun-Seok</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preparation and characterization of metformin hydrochloride controlled-release tablet using fatty acid coated granules</atitle><jtitle>Drug development and industrial pharmacy</jtitle><stitle>DRUG DEV IND PHARM</stitle><addtitle>Drug Dev Ind Pharm</addtitle><date>2020-05-03</date><risdate>2020</risdate><volume>46</volume><issue>5</issue><spage>852</spage><epage>860</epage><pages>852-860</pages><issn>0363-9045</issn><eissn>1520-5762</eissn><abstract>Metformin hydrochloride (MFM) is often used as a controlled-release (CR) tablet to reduce dosing frequency. However, the MFM CR tablet contains significant amounts of excipients and the tablet size is also large. Dosing convenience and patient compliance can be increased by reducing the size of the CR tablets. The aim of this study was to prepare and evaluate the MFM controlled-release tablet (MFM-CRT) using two types of release modulators, inner and outer. The MFM-CRT was prepared by coating the MFM granules using a binder solution containing aluminum stearate (ALS) as the inner release-modulator, and polyethylene oxide (PEO) as the outer release-modulator. The dispersion stability of the binder solution was optimized by the dispersion analyzer. The MFM-CRT was evaluated for dissolution rate and tablet volume. Additionally, dissolution behavior and dissolution kinetics of the MFM-CRT were analyzed using micro-computed tomography (micro-CT). Although the optimal MFM-CRT showed no difference in the release rate as compared to the commercially available product of Glucophage
®
XR 500 mg (f
2
value: 72), the length of the long axis was reduced by 6 mm and the weight was reduced by about 27%. We expect patient compliance to improve because of effective sustained release and volume reduction of MFM-CRT.</abstract><cop>ABINGDON</cop><pub>Taylor & Francis</pub><pmid>32338551</pmid><doi>10.1080/03639045.2020.1762198</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0003-1294-9160</orcidid><orcidid>https://orcid.org/0000-0001-5329-8443</orcidid></addata></record> |
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subjects | aluminum stearate Chemistry, Medicinal Delayed-Action Preparations - chemical synthesis Delayed-Action Preparations - metabolism dispersion analyzer Drug Carriers - chemical synthesis Drug Carriers - metabolism Drug Liberation Fatty Acids - chemical synthesis Fatty Acids - metabolism Hypoglycemic Agents - chemical synthesis Hypoglycemic Agents - metabolism Life Sciences & Biomedicine Metformin - chemical synthesis Metformin - metabolism Metformin hydrochloride micro-computed tomography Pharmacology & Pharmacy polyethylene oxide Science & Technology Spectrometry, X-Ray Emission - methods X-Ray Microtomography - methods |
title | Preparation and characterization of metformin hydrochloride controlled-release tablet using fatty acid coated granules |
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