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
Hauptverfasser: Kang, Ji-Hyun, Chun, Myung-Hee, Cho, Mi-Seo, Kwon, Yong-Bin, Choi, Jae-Cheol, Kim, Dong-Wook, Park, Chun-Woong, Park, Eun-Seok
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container_issue 5
container_start_page 852
container_title Drug development and industrial pharmacy
container_volume 46
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
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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><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 &amp; 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 &amp; Biomedicine ; Metformin - chemical synthesis ; Metformin - metabolism ; Metformin hydrochloride ; micro-computed tomography ; Pharmacology &amp; Pharmacy ; polyethylene oxide ; Science &amp; 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 &amp; 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%. 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Biomedicine</topic><topic>Metformin - chemical synthesis</topic><topic>Metformin - metabolism</topic><topic>Metformin hydrochloride</topic><topic>micro-computed tomography</topic><topic>Pharmacology &amp; Pharmacy</topic><topic>polyethylene oxide</topic><topic>Science &amp; 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 &amp; 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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