Stabilized Amorphous State of Ibuprofen by Co‐Spray Drying With Mesoporous SBA‐15 to Enhance Dissolution Properties
A novel formulation process via co‐spray drying ibuprofen (IBU) with mesoporous SBA‐15 submicron particles exhibited excellence in production of stable amorphous IBU with significantly enhanced dissolution rate. With drug loading of IBU/SBA‐15 ratio being 50:50 (w/w) or below, most drug molecules we...
Gespeichert in:
Veröffentlicht in: | Journal of pharmaceutical sciences 2010-04, Vol.99 (4), p.1997-2007 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 2007 |
---|---|
container_issue | 4 |
container_start_page | 1997 |
container_title | Journal of pharmaceutical sciences |
container_volume | 99 |
creator | Shen, Shou‐Cang Ng, Wai Kiong Chia, Leonard Dong, Yuan‐Cai Tan, Reginald B.H. |
description | A novel formulation process via co‐spray drying ibuprofen (IBU) with mesoporous SBA‐15 submicron particles exhibited excellence in production of stable amorphous IBU with significantly enhanced dissolution rate. With drug loading of IBU/SBA‐15 ratio being 50:50 (w/w) or below, most drug molecules were entrapped inside the straight mesoporous channels via the co‐spray drying and the morphology of SBA‐15 submicron particles remained unchanged. IBU confined inside the mesoporous structure was in the amorphous state shown by PXRD and DSC measurements. The amorphous state of IBU in the solid dispersion showed remarkable stability when subject to stress test condition of 40°C/75% RH in open pans for 12 months. The uniform pore walls were believed to prevent the re‐crystallization of the homogeneously dispersed drug molecules inside the mesoporous channels with confined nanospace. The dissolution rate of IBU from the co‐spray‐dried solid dispersion was significantly enhanced to achieve a rapid release. Even after the accelerated stability test, the rapid drug release property was well preserved. © 2009 Wiley‐Liss, Inc. and the American Pharmacists Association J Pharm Sci 99: 1997–2007, 2010 |
doi_str_mv | 10.1002/jps.21967 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_734022471</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0022354916304713</els_id><sourcerecordid>734022471</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4367-ef2e01dc5f6f453bca2ac9cdd395e1ec16cb57b0947a198d5a7fa25cf08542873</originalsourceid><addsrcrecordid>eNp1kc9u1DAQhy0EotvCgRdAviDEIa3t2PHmuGz_UFSgYkGVuFiOM2ZdsnGwE0o48Qg8I0-C2SzlAidLnm9m_PuM0CNKDikh7Oi6i4eMloW8g2ZUMJIVhMq7aJZqLMsFL_fQfozXhJCCCHEf7dFyTotSiBm6WfW6co37BjVebHzo1n6IOF32gL3F59XQBW-hxdWIl_7n9x-rLugRH4fRtR_xlevX-BVE3_mw7Xu-SAgVuPf4pF3r1gA-djH6Zuidb_Fl8B2E3kF8gO5Z3UR4uDsP0PvTk3fLF9nFm7Pz5eIiMzwvZAaWAaG1EbawXOSV0Uyb0tR1XgqgYGhhKiErUnKpU6haaGk1E8aSueBsLvMD9HSam2J8HiD2auOigabRLaQXK5nzJIlLmshnE2mCjzGAVV1wGx1GRYn6rVklzWqrObGPd1OHagP1X3LnNQFPdoCORjc2JBUu3nKMCSnJljuauBvXwPj_jerl5erP6mzqcLGHr7cdOnxSqSqFunp9pvhbXvDVh1yVic8nHpLlLw6CisZB-pjaBTC9qr37R8BfqKO3jg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>734022471</pqid></control><display><type>article</type><title>Stabilized Amorphous State of Ibuprofen by Co‐Spray Drying With Mesoporous SBA‐15 to Enhance Dissolution Properties</title><source>MEDLINE</source><source>Access via Wiley Online Library</source><source>Alma/SFX Local Collection</source><creator>Shen, Shou‐Cang ; Ng, Wai Kiong ; Chia, Leonard ; Dong, Yuan‐Cai ; Tan, Reginald B.H.</creator><creatorcontrib>Shen, Shou‐Cang ; Ng, Wai Kiong ; Chia, Leonard ; Dong, Yuan‐Cai ; Tan, Reginald B.H.</creatorcontrib><description>A novel formulation process via co‐spray drying ibuprofen (IBU) with mesoporous SBA‐15 submicron particles exhibited excellence in production of stable amorphous IBU with significantly enhanced dissolution rate. With drug loading of IBU/SBA‐15 ratio being 50:50 (w/w) or below, most drug molecules were entrapped inside the straight mesoporous channels via the co‐spray drying and the morphology of SBA‐15 submicron particles remained unchanged. IBU confined inside the mesoporous structure was in the amorphous state shown by PXRD and DSC measurements. The amorphous state of IBU in the solid dispersion showed remarkable stability when subject to stress test condition of 40°C/75% RH in open pans for 12 months. The uniform pore walls were believed to prevent the re‐crystallization of the homogeneously dispersed drug molecules inside the mesoporous channels with confined nanospace. The dissolution rate of IBU from the co‐spray‐dried solid dispersion was significantly enhanced to achieve a rapid release. Even after the accelerated stability test, the rapid drug release property was well preserved. © 2009 Wiley‐Liss, Inc. and the American Pharmacists Association J Pharm Sci 99: 1997–2007, 2010</description><identifier>ISSN: 0022-3549</identifier><identifier>EISSN: 1520-6017</identifier><identifier>DOI: 10.1002/jps.21967</identifier><identifier>PMID: 19816955</identifier><identifier>CODEN: JPMSAE</identifier><language>eng</language><publisher>Hoboken: Elsevier Inc</publisher><subject>amorphous ; Anti-Inflammatory Agents, Non-Steroidal - chemistry ; Biological and medical sciences ; co-spray drying ; Crystallization ; Drug Compounding - methods ; Drug Stability ; General pharmacology ; Ibuprofen - chemistry ; Medical sciences ; Particle Size ; Pharmaceutical technology. Pharmaceutical industry ; Pharmacology. Drug treatments ; poorly soluble drugs ; Porosity ; rapid release ; SBA-15 ; Silicon Dioxide - chemistry ; Solubility ; stability</subject><ispartof>Journal of pharmaceutical sciences, 2010-04, Vol.99 (4), p.1997-2007</ispartof><rights>2010 Wiley-Liss, Inc.</rights><rights>Copyright © 2009 Wiley‐Liss, Inc.</rights><rights>2015 INIST-CNRS</rights><rights>2009 Wiley-Liss, Inc. and the American Pharmacists Association</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4367-ef2e01dc5f6f453bca2ac9cdd395e1ec16cb57b0947a198d5a7fa25cf08542873</citedby><cites>FETCH-LOGICAL-c4367-ef2e01dc5f6f453bca2ac9cdd395e1ec16cb57b0947a198d5a7fa25cf08542873</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjps.21967$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjps.21967$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22577055$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19816955$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shen, Shou‐Cang</creatorcontrib><creatorcontrib>Ng, Wai Kiong</creatorcontrib><creatorcontrib>Chia, Leonard</creatorcontrib><creatorcontrib>Dong, Yuan‐Cai</creatorcontrib><creatorcontrib>Tan, Reginald B.H.</creatorcontrib><title>Stabilized Amorphous State of Ibuprofen by Co‐Spray Drying With Mesoporous SBA‐15 to Enhance Dissolution Properties</title><title>Journal of pharmaceutical sciences</title><addtitle>J. Pharm. Sci</addtitle><description>A novel formulation process via co‐spray drying ibuprofen (IBU) with mesoporous SBA‐15 submicron particles exhibited excellence in production of stable amorphous IBU with significantly enhanced dissolution rate. With drug loading of IBU/SBA‐15 ratio being 50:50 (w/w) or below, most drug molecules were entrapped inside the straight mesoporous channels via the co‐spray drying and the morphology of SBA‐15 submicron particles remained unchanged. IBU confined inside the mesoporous structure was in the amorphous state shown by PXRD and DSC measurements. The amorphous state of IBU in the solid dispersion showed remarkable stability when subject to stress test condition of 40°C/75% RH in open pans for 12 months. The uniform pore walls were believed to prevent the re‐crystallization of the homogeneously dispersed drug molecules inside the mesoporous channels with confined nanospace. The dissolution rate of IBU from the co‐spray‐dried solid dispersion was significantly enhanced to achieve a rapid release. Even after the accelerated stability test, the rapid drug release property was well preserved. © 2009 Wiley‐Liss, Inc. and the American Pharmacists Association J Pharm Sci 99: 1997–2007, 2010</description><subject>amorphous</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - chemistry</subject><subject>Biological and medical sciences</subject><subject>co-spray drying</subject><subject>Crystallization</subject><subject>Drug Compounding - methods</subject><subject>Drug Stability</subject><subject>General pharmacology</subject><subject>Ibuprofen - chemistry</subject><subject>Medical sciences</subject><subject>Particle Size</subject><subject>Pharmaceutical technology. Pharmaceutical industry</subject><subject>Pharmacology. Drug treatments</subject><subject>poorly soluble drugs</subject><subject>Porosity</subject><subject>rapid release</subject><subject>SBA-15</subject><subject>Silicon Dioxide - chemistry</subject><subject>Solubility</subject><subject>stability</subject><issn>0022-3549</issn><issn>1520-6017</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kc9u1DAQhy0EotvCgRdAviDEIa3t2PHmuGz_UFSgYkGVuFiOM2ZdsnGwE0o48Qg8I0-C2SzlAidLnm9m_PuM0CNKDikh7Oi6i4eMloW8g2ZUMJIVhMq7aJZqLMsFL_fQfozXhJCCCHEf7dFyTotSiBm6WfW6co37BjVebHzo1n6IOF32gL3F59XQBW-hxdWIl_7n9x-rLugRH4fRtR_xlevX-BVE3_mw7Xu-SAgVuPf4pF3r1gA-djH6Zuidb_Fl8B2E3kF8gO5Z3UR4uDsP0PvTk3fLF9nFm7Pz5eIiMzwvZAaWAaG1EbawXOSV0Uyb0tR1XgqgYGhhKiErUnKpU6haaGk1E8aSueBsLvMD9HSam2J8HiD2auOigabRLaQXK5nzJIlLmshnE2mCjzGAVV1wGx1GRYn6rVklzWqrObGPd1OHagP1X3LnNQFPdoCORjc2JBUu3nKMCSnJljuauBvXwPj_jerl5erP6mzqcLGHr7cdOnxSqSqFunp9pvhbXvDVh1yVic8nHpLlLw6CisZB-pjaBTC9qr37R8BfqKO3jg</recordid><startdate>201004</startdate><enddate>201004</enddate><creator>Shen, Shou‐Cang</creator><creator>Ng, Wai Kiong</creator><creator>Chia, Leonard</creator><creator>Dong, Yuan‐Cai</creator><creator>Tan, Reginald B.H.</creator><general>Elsevier Inc</general><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley</general><general>American Pharmaceutical Association</general><scope>BSCLL</scope><scope>IQODW</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><scope>7X8</scope></search><sort><creationdate>201004</creationdate><title>Stabilized Amorphous State of Ibuprofen by Co‐Spray Drying With Mesoporous SBA‐15 to Enhance Dissolution Properties</title><author>Shen, Shou‐Cang ; Ng, Wai Kiong ; Chia, Leonard ; Dong, Yuan‐Cai ; Tan, Reginald B.H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4367-ef2e01dc5f6f453bca2ac9cdd395e1ec16cb57b0947a198d5a7fa25cf08542873</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>amorphous</topic><topic>Anti-Inflammatory Agents, Non-Steroidal - chemistry</topic><topic>Biological and medical sciences</topic><topic>co-spray drying</topic><topic>Crystallization</topic><topic>Drug Compounding - methods</topic><topic>Drug Stability</topic><topic>General pharmacology</topic><topic>Ibuprofen - chemistry</topic><topic>Medical sciences</topic><topic>Particle Size</topic><topic>Pharmaceutical technology. Pharmaceutical industry</topic><topic>Pharmacology. Drug treatments</topic><topic>poorly soluble drugs</topic><topic>Porosity</topic><topic>rapid release</topic><topic>SBA-15</topic><topic>Silicon Dioxide - chemistry</topic><topic>Solubility</topic><topic>stability</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shen, Shou‐Cang</creatorcontrib><creatorcontrib>Ng, Wai Kiong</creatorcontrib><creatorcontrib>Chia, Leonard</creatorcontrib><creatorcontrib>Dong, Yuan‐Cai</creatorcontrib><creatorcontrib>Tan, Reginald B.H.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of pharmaceutical sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shen, Shou‐Cang</au><au>Ng, Wai Kiong</au><au>Chia, Leonard</au><au>Dong, Yuan‐Cai</au><au>Tan, Reginald B.H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Stabilized Amorphous State of Ibuprofen by Co‐Spray Drying With Mesoporous SBA‐15 to Enhance Dissolution Properties</atitle><jtitle>Journal of pharmaceutical sciences</jtitle><addtitle>J. Pharm. Sci</addtitle><date>2010-04</date><risdate>2010</risdate><volume>99</volume><issue>4</issue><spage>1997</spage><epage>2007</epage><pages>1997-2007</pages><issn>0022-3549</issn><eissn>1520-6017</eissn><coden>JPMSAE</coden><abstract>A novel formulation process via co‐spray drying ibuprofen (IBU) with mesoporous SBA‐15 submicron particles exhibited excellence in production of stable amorphous IBU with significantly enhanced dissolution rate. With drug loading of IBU/SBA‐15 ratio being 50:50 (w/w) or below, most drug molecules were entrapped inside the straight mesoporous channels via the co‐spray drying and the morphology of SBA‐15 submicron particles remained unchanged. IBU confined inside the mesoporous structure was in the amorphous state shown by PXRD and DSC measurements. The amorphous state of IBU in the solid dispersion showed remarkable stability when subject to stress test condition of 40°C/75% RH in open pans for 12 months. The uniform pore walls were believed to prevent the re‐crystallization of the homogeneously dispersed drug molecules inside the mesoporous channels with confined nanospace. The dissolution rate of IBU from the co‐spray‐dried solid dispersion was significantly enhanced to achieve a rapid release. Even after the accelerated stability test, the rapid drug release property was well preserved. © 2009 Wiley‐Liss, Inc. and the American Pharmacists Association J Pharm Sci 99: 1997–2007, 2010</abstract><cop>Hoboken</cop><pub>Elsevier Inc</pub><pmid>19816955</pmid><doi>10.1002/jps.21967</doi><tpages>11</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0022-3549 |
ispartof | Journal of pharmaceutical sciences, 2010-04, Vol.99 (4), p.1997-2007 |
issn | 0022-3549 1520-6017 |
language | eng |
recordid | cdi_proquest_miscellaneous_734022471 |
source | MEDLINE; Access via Wiley Online Library; Alma/SFX Local Collection |
subjects | amorphous Anti-Inflammatory Agents, Non-Steroidal - chemistry Biological and medical sciences co-spray drying Crystallization Drug Compounding - methods Drug Stability General pharmacology Ibuprofen - chemistry Medical sciences Particle Size Pharmaceutical technology. Pharmaceutical industry Pharmacology. Drug treatments poorly soluble drugs Porosity rapid release SBA-15 Silicon Dioxide - chemistry Solubility stability |
title | Stabilized Amorphous State of Ibuprofen by Co‐Spray Drying With Mesoporous SBA‐15 to Enhance Dissolution Properties |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T16%3A38%3A27IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Stabilized%20Amorphous%20State%20of%20Ibuprofen%20by%20Co%E2%80%90Spray%20Drying%20With%20Mesoporous%20SBA%E2%80%9015%20to%20Enhance%20Dissolution%20Properties&rft.jtitle=Journal%20of%20pharmaceutical%20sciences&rft.au=Shen,%20Shou%E2%80%90Cang&rft.date=2010-04&rft.volume=99&rft.issue=4&rft.spage=1997&rft.epage=2007&rft.pages=1997-2007&rft.issn=0022-3549&rft.eissn=1520-6017&rft.coden=JPMSAE&rft_id=info:doi/10.1002/jps.21967&rft_dat=%3Cproquest_cross%3E734022471%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=734022471&rft_id=info:pmid/19816955&rft_els_id=S0022354916304713&rfr_iscdi=true |