Direct compression properties of melt-extruded isomalt

Isomalt, a sugar alcohol, was melt-extruded prior to compression in order to improve its tabletting properties. After fusion, crystalline isomalt was transformed into an amorphous form as shown by X-ray diffraction and differential scanning calorimetry (DSC). The tabletting properties of amorphous i...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:International journal of pharmaceutics 2002-03, Vol.235 (1), p.149-157
Hauptverfasser: Ndindayino, F, Henrist, D, Kiekens, F, Van den Mooter, Guy, Vervaet, C, Remon, J.P
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 157
container_issue 1
container_start_page 149
container_title International journal of pharmaceutics
container_volume 235
creator Ndindayino, F
Henrist, D
Kiekens, F
Van den Mooter, Guy
Vervaet, C
Remon, J.P
description Isomalt, a sugar alcohol, was melt-extruded prior to compression in order to improve its tabletting properties. After fusion, crystalline isomalt was transformed into an amorphous form as shown by X-ray diffraction and differential scanning calorimetry (DSC). The tabletting properties of amorphous isomalt were dramatically improved. Mixtures formulated with paracetamol (50%) and extruded isomalt yielded hard tablets. However, extruded isomalt powder showed agglomeration problems due to recrystallization of the amorphous phase into a stable crystalline form in the presence of atmospheric moisture. The evolution of the moisture content correlated well with the compressibility data. The tablets made of extruded isomalt powder had a lower friability in comparison to the tablets formulated with non-extruded isomalt powder. Their disintegration was fast and a rapid dissolution rate was recorded. Extruded isomalt displayed excellent tabletting properties; however, further experiments should be conducted to delay or even prevent recrystallization of amorphous isomalt.
format Article
fullrecord <record><control><sourceid>kuleuven</sourceid><recordid>TN_cdi_kuleuven_dspace_123456789_20336</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>123456789_20336</sourcerecordid><originalsourceid>FETCH-kuleuven_dspace_123456789_203363</originalsourceid><addsrcrecordid>eNqVyksOgjAQANAuNBE_d-jKhQlJYaTg2k88gPuGlCGpFtp0BsPx3XgAXb3NW4hMQd3kVVHDSqyJnkopXRaQCX1xCS1LG4aYkMiFUcYUIiZ2SDL0ckDPOc6cpg476SgMreetWPatJ9x93Yj97fo43_PX5HF642g6iq1FU5RwrHTdnEypADT8EQ8_RcMzwwd6p0NY</addsrcrecordid><sourcetype>Institutional Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Direct compression properties of melt-extruded isomalt</title><source>Lirias (KU Leuven Association)</source><source>Elsevier ScienceDirect Journals</source><creator>Ndindayino, F ; Henrist, D ; Kiekens, F ; Van den Mooter, Guy ; Vervaet, C ; Remon, J.P</creator><creatorcontrib>Ndindayino, F ; Henrist, D ; Kiekens, F ; Van den Mooter, Guy ; Vervaet, C ; Remon, J.P</creatorcontrib><description>Isomalt, a sugar alcohol, was melt-extruded prior to compression in order to improve its tabletting properties. After fusion, crystalline isomalt was transformed into an amorphous form as shown by X-ray diffraction and differential scanning calorimetry (DSC). The tabletting properties of amorphous isomalt were dramatically improved. Mixtures formulated with paracetamol (50%) and extruded isomalt yielded hard tablets. However, extruded isomalt powder showed agglomeration problems due to recrystallization of the amorphous phase into a stable crystalline form in the presence of atmospheric moisture. The evolution of the moisture content correlated well with the compressibility data. The tablets made of extruded isomalt powder had a lower friability in comparison to the tablets formulated with non-extruded isomalt powder. Their disintegration was fast and a rapid dissolution rate was recorded. Extruded isomalt displayed excellent tabletting properties; however, further experiments should be conducted to delay or even prevent recrystallization of amorphous isomalt.</description><identifier>ISSN: 0378-5173</identifier><language>eng</language><publisher>ELSEVIER SCIENCE BV</publisher><ispartof>International journal of pharmaceutics, 2002-03, Vol.235 (1), p.149-157</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,315,776,780,27837</link.rule.ids></links><search><creatorcontrib>Ndindayino, F</creatorcontrib><creatorcontrib>Henrist, D</creatorcontrib><creatorcontrib>Kiekens, F</creatorcontrib><creatorcontrib>Van den Mooter, Guy</creatorcontrib><creatorcontrib>Vervaet, C</creatorcontrib><creatorcontrib>Remon, J.P</creatorcontrib><title>Direct compression properties of melt-extruded isomalt</title><title>International journal of pharmaceutics</title><description>Isomalt, a sugar alcohol, was melt-extruded prior to compression in order to improve its tabletting properties. After fusion, crystalline isomalt was transformed into an amorphous form as shown by X-ray diffraction and differential scanning calorimetry (DSC). The tabletting properties of amorphous isomalt were dramatically improved. Mixtures formulated with paracetamol (50%) and extruded isomalt yielded hard tablets. However, extruded isomalt powder showed agglomeration problems due to recrystallization of the amorphous phase into a stable crystalline form in the presence of atmospheric moisture. The evolution of the moisture content correlated well with the compressibility data. The tablets made of extruded isomalt powder had a lower friability in comparison to the tablets formulated with non-extruded isomalt powder. Their disintegration was fast and a rapid dissolution rate was recorded. Extruded isomalt displayed excellent tabletting properties; however, further experiments should be conducted to delay or even prevent recrystallization of amorphous isomalt.</description><issn>0378-5173</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>FZOIL</sourceid><recordid>eNqVyksOgjAQANAuNBE_d-jKhQlJYaTg2k88gPuGlCGpFtp0BsPx3XgAXb3NW4hMQd3kVVHDSqyJnkopXRaQCX1xCS1LG4aYkMiFUcYUIiZ2SDL0ckDPOc6cpg476SgMreetWPatJ9x93Yj97fo43_PX5HF642g6iq1FU5RwrHTdnEypADT8EQ8_RcMzwwd6p0NY</recordid><startdate>200203</startdate><enddate>200203</enddate><creator>Ndindayino, F</creator><creator>Henrist, D</creator><creator>Kiekens, F</creator><creator>Van den Mooter, Guy</creator><creator>Vervaet, C</creator><creator>Remon, J.P</creator><general>ELSEVIER SCIENCE BV</general><scope>FZOIL</scope></search><sort><creationdate>200203</creationdate><title>Direct compression properties of melt-extruded isomalt</title><author>Ndindayino, F ; Henrist, D ; Kiekens, F ; Van den Mooter, Guy ; Vervaet, C ; Remon, J.P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-kuleuven_dspace_123456789_203363</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ndindayino, F</creatorcontrib><creatorcontrib>Henrist, D</creatorcontrib><creatorcontrib>Kiekens, F</creatorcontrib><creatorcontrib>Van den Mooter, Guy</creatorcontrib><creatorcontrib>Vervaet, C</creatorcontrib><creatorcontrib>Remon, J.P</creatorcontrib><collection>Lirias (KU Leuven Association)</collection><jtitle>International journal of pharmaceutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ndindayino, F</au><au>Henrist, D</au><au>Kiekens, F</au><au>Van den Mooter, Guy</au><au>Vervaet, C</au><au>Remon, J.P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Direct compression properties of melt-extruded isomalt</atitle><jtitle>International journal of pharmaceutics</jtitle><date>2002-03</date><risdate>2002</risdate><volume>235</volume><issue>1</issue><spage>149</spage><epage>157</epage><pages>149-157</pages><issn>0378-5173</issn><abstract>Isomalt, a sugar alcohol, was melt-extruded prior to compression in order to improve its tabletting properties. After fusion, crystalline isomalt was transformed into an amorphous form as shown by X-ray diffraction and differential scanning calorimetry (DSC). The tabletting properties of amorphous isomalt were dramatically improved. Mixtures formulated with paracetamol (50%) and extruded isomalt yielded hard tablets. However, extruded isomalt powder showed agglomeration problems due to recrystallization of the amorphous phase into a stable crystalline form in the presence of atmospheric moisture. The evolution of the moisture content correlated well with the compressibility data. The tablets made of extruded isomalt powder had a lower friability in comparison to the tablets formulated with non-extruded isomalt powder. Their disintegration was fast and a rapid dissolution rate was recorded. Extruded isomalt displayed excellent tabletting properties; however, further experiments should be conducted to delay or even prevent recrystallization of amorphous isomalt.</abstract><pub>ELSEVIER SCIENCE BV</pub></addata></record>
fulltext fulltext
identifier ISSN: 0378-5173
ispartof International journal of pharmaceutics, 2002-03, Vol.235 (1), p.149-157
issn 0378-5173
language eng
recordid cdi_kuleuven_dspace_123456789_20336
source Lirias (KU Leuven Association); Elsevier ScienceDirect Journals
title Direct compression properties of melt-extruded isomalt
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-29T01%3A25%3A21IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-kuleuven&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Direct%20compression%20properties%20of%20melt-extruded%20isomalt&rft.jtitle=International%20journal%20of%20pharmaceutics&rft.au=Ndindayino,%20F&rft.date=2002-03&rft.volume=235&rft.issue=1&rft.spage=149&rft.epage=157&rft.pages=149-157&rft.issn=0378-5173&rft_id=info:doi/&rft_dat=%3Ckuleuven%3E123456789_20336%3C/kuleuven%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true