Matrices containing NaCMC and HPMC 1. Dissolution performance characterization
In this study hydroxypropylmethylcellulose (HPMC) and sodium carboxymethylcellulose (NaCMC) were used as polymeric carriers to improve controlled release performances of matrix tablets containing a soluble drug. The drug release behaviour of the systems containing these two polymers mixture and each...
Gespeichert in:
Veröffentlicht in: | International journal of pharmaceutics 2007-03, Vol.333 (1-2), p.136-142 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 142 |
---|---|
container_issue | 1-2 |
container_start_page | 136 |
container_title | International journal of pharmaceutics |
container_volume | 333 |
creator | CONTI, S MAGGI, L SEGALE, L OCHOA MACHISTE, E CENTE, U GRENIER, P VERGNAULT, G |
description | In this study hydroxypropylmethylcellulose (HPMC) and sodium carboxymethylcellulose (NaCMC) were used as polymeric carriers to improve controlled release performances of matrix tablets containing a soluble drug. The drug release behaviour of the systems containing these two polymers mixture and each material separately was investigated. To evaluate the effect of the dissolution medium pH, on the drug release performance, release tests were conducted at pH 1, 4.5 and 6.8. In vitro release studies demonstrated that the mixture of the two cellulose derivatives enables a better control of the drug release profiles at pH 4.5 and at 6.8 both in term of rate and mechanism. Texture analysis on the swollen tablets helps to understand drug release kinetic and mechanism. In fact, the results obtained confirm that a gel, which is characterized by high strength and consistence is less susceptible to erosion and chains disentanglement and the drug release mechanism is mainly governed by diffusion. On the contrary, gels, which show a low strength and texture, have low resistance to the fluid erosion action and the release of the active molecule is manly due to polymer relaxation and chains disentanglement moving the drug delivery kinetic towards an erosion/relaxation mechanism. |
doi_str_mv | 10.1016/j.ijpharm.2006.11.059 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_70207444</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>70207444</sourcerecordid><originalsourceid>FETCH-LOGICAL-p239t-161df2260e6b37ca4aa2267a285cdc23f41bd8dac890bd5bb6aa3aeaa8a88f113</originalsourceid><addsrcrecordid>eNpFkEtPwzAQhC0EoqXwE0C5wC3Bayexc0ThUaS2cIBztHEccJUXdnKAX48RQZx2R_tpNLOEnAONgEJ6vY_MfnhH20aM0jQCiGiSHZAlSMFDHov0kCwpFzJMQPAFOXFuTz3IgB-TBQhGRRbzJdltcbRGaReovhvRdKZ7C3aYb_MAuypYP_sFouDWONc302j6Lhi0rXvbYqd0oHwCVKO25gt_jqfkqMbG6bN5rsjr_d1Lvg43Tw-P-c0mHBjPxhBSqGrGUqrTkguFMaJXAplMVKUYr2MoK1mhkhktq6QsU0SOGlGilDUAX5GrX9_B9h-TdmPRGqd002Cn-8kVgvqCcRx78GIGp7LVVTFY06L9LP4-4IHLGUCnsKmt72XcPycTmYA3-gZEO20G</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>70207444</pqid></control><display><type>article</type><title>Matrices containing NaCMC and HPMC 1. Dissolution performance characterization</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>CONTI, S ; MAGGI, L ; SEGALE, L ; OCHOA MACHISTE, E ; CENTE, U ; GRENIER, P ; VERGNAULT, G</creator><creatorcontrib>CONTI, S ; MAGGI, L ; SEGALE, L ; OCHOA MACHISTE, E ; CENTE, U ; GRENIER, P ; VERGNAULT, G</creatorcontrib><description>In this study hydroxypropylmethylcellulose (HPMC) and sodium carboxymethylcellulose (NaCMC) were used as polymeric carriers to improve controlled release performances of matrix tablets containing a soluble drug. The drug release behaviour of the systems containing these two polymers mixture and each material separately was investigated. To evaluate the effect of the dissolution medium pH, on the drug release performance, release tests were conducted at pH 1, 4.5 and 6.8. In vitro release studies demonstrated that the mixture of the two cellulose derivatives enables a better control of the drug release profiles at pH 4.5 and at 6.8 both in term of rate and mechanism. Texture analysis on the swollen tablets helps to understand drug release kinetic and mechanism. In fact, the results obtained confirm that a gel, which is characterized by high strength and consistence is less susceptible to erosion and chains disentanglement and the drug release mechanism is mainly governed by diffusion. On the contrary, gels, which show a low strength and texture, have low resistance to the fluid erosion action and the release of the active molecule is manly due to polymer relaxation and chains disentanglement moving the drug delivery kinetic towards an erosion/relaxation mechanism.</description><identifier>ISSN: 0378-5173</identifier><identifier>EISSN: 1873-3476</identifier><identifier>DOI: 10.1016/j.ijpharm.2006.11.059</identifier><identifier>PMID: 17207943</identifier><identifier>CODEN: IJPHDE</identifier><language>eng</language><publisher>Amsterdam: Elsevier</publisher><subject>Biological and medical sciences ; Carboxymethylcellulose Sodium - chemistry ; Chemistry, Pharmaceutical ; Delayed-Action Preparations ; Diffusion ; Diltiazem - chemistry ; Drug Carriers ; General pharmacology ; Hydrogels ; Hydrogen-Ion Concentration ; Hypromellose Derivatives ; Kinetics ; Medical sciences ; Methylcellulose - analogs & derivatives ; Methylcellulose - chemistry ; Models, Chemical ; Pharmaceutical technology. Pharmaceutical industry ; Pharmacology. Drug treatments ; Solubility ; Tablets ; Technology, Pharmaceutical</subject><ispartof>International journal of pharmaceutics, 2007-03, Vol.333 (1-2), p.136-142</ispartof><rights>2007 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18585144$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17207943$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>CONTI, S</creatorcontrib><creatorcontrib>MAGGI, L</creatorcontrib><creatorcontrib>SEGALE, L</creatorcontrib><creatorcontrib>OCHOA MACHISTE, E</creatorcontrib><creatorcontrib>CENTE, U</creatorcontrib><creatorcontrib>GRENIER, P</creatorcontrib><creatorcontrib>VERGNAULT, G</creatorcontrib><title>Matrices containing NaCMC and HPMC 1. Dissolution performance characterization</title><title>International journal of pharmaceutics</title><addtitle>Int J Pharm</addtitle><description>In this study hydroxypropylmethylcellulose (HPMC) and sodium carboxymethylcellulose (NaCMC) were used as polymeric carriers to improve controlled release performances of matrix tablets containing a soluble drug. The drug release behaviour of the systems containing these two polymers mixture and each material separately was investigated. To evaluate the effect of the dissolution medium pH, on the drug release performance, release tests were conducted at pH 1, 4.5 and 6.8. In vitro release studies demonstrated that the mixture of the two cellulose derivatives enables a better control of the drug release profiles at pH 4.5 and at 6.8 both in term of rate and mechanism. Texture analysis on the swollen tablets helps to understand drug release kinetic and mechanism. In fact, the results obtained confirm that a gel, which is characterized by high strength and consistence is less susceptible to erosion and chains disentanglement and the drug release mechanism is mainly governed by diffusion. On the contrary, gels, which show a low strength and texture, have low resistance to the fluid erosion action and the release of the active molecule is manly due to polymer relaxation and chains disentanglement moving the drug delivery kinetic towards an erosion/relaxation mechanism.</description><subject>Biological and medical sciences</subject><subject>Carboxymethylcellulose Sodium - chemistry</subject><subject>Chemistry, Pharmaceutical</subject><subject>Delayed-Action Preparations</subject><subject>Diffusion</subject><subject>Diltiazem - chemistry</subject><subject>Drug Carriers</subject><subject>General pharmacology</subject><subject>Hydrogels</subject><subject>Hydrogen-Ion Concentration</subject><subject>Hypromellose Derivatives</subject><subject>Kinetics</subject><subject>Medical sciences</subject><subject>Methylcellulose - analogs & derivatives</subject><subject>Methylcellulose - chemistry</subject><subject>Models, Chemical</subject><subject>Pharmaceutical technology. Pharmaceutical industry</subject><subject>Pharmacology. Drug treatments</subject><subject>Solubility</subject><subject>Tablets</subject><subject>Technology, Pharmaceutical</subject><issn>0378-5173</issn><issn>1873-3476</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkEtPwzAQhC0EoqXwE0C5wC3Bayexc0ThUaS2cIBztHEccJUXdnKAX48RQZx2R_tpNLOEnAONgEJ6vY_MfnhH20aM0jQCiGiSHZAlSMFDHov0kCwpFzJMQPAFOXFuTz3IgB-TBQhGRRbzJdltcbRGaReovhvRdKZ7C3aYb_MAuypYP_sFouDWONc302j6Lhi0rXvbYqd0oHwCVKO25gt_jqfkqMbG6bN5rsjr_d1Lvg43Tw-P-c0mHBjPxhBSqGrGUqrTkguFMaJXAplMVKUYr2MoK1mhkhktq6QsU0SOGlGilDUAX5GrX9_B9h-TdmPRGqd002Cn-8kVgvqCcRx78GIGp7LVVTFY06L9LP4-4IHLGUCnsKmt72XcPycTmYA3-gZEO20G</recordid><startdate>20070321</startdate><enddate>20070321</enddate><creator>CONTI, S</creator><creator>MAGGI, L</creator><creator>SEGALE, L</creator><creator>OCHOA MACHISTE, E</creator><creator>CENTE, U</creator><creator>GRENIER, P</creator><creator>VERGNAULT, G</creator><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20070321</creationdate><title>Matrices containing NaCMC and HPMC 1. Dissolution performance characterization</title><author>CONTI, S ; MAGGI, L ; SEGALE, L ; OCHOA MACHISTE, E ; CENTE, U ; GRENIER, P ; VERGNAULT, G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p239t-161df2260e6b37ca4aa2267a285cdc23f41bd8dac890bd5bb6aa3aeaa8a88f113</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Biological and medical sciences</topic><topic>Carboxymethylcellulose Sodium - chemistry</topic><topic>Chemistry, Pharmaceutical</topic><topic>Delayed-Action Preparations</topic><topic>Diffusion</topic><topic>Diltiazem - chemistry</topic><topic>Drug Carriers</topic><topic>General pharmacology</topic><topic>Hydrogels</topic><topic>Hydrogen-Ion Concentration</topic><topic>Hypromellose Derivatives</topic><topic>Kinetics</topic><topic>Medical sciences</topic><topic>Methylcellulose - analogs & derivatives</topic><topic>Methylcellulose - chemistry</topic><topic>Models, Chemical</topic><topic>Pharmaceutical technology. Pharmaceutical industry</topic><topic>Pharmacology. Drug treatments</topic><topic>Solubility</topic><topic>Tablets</topic><topic>Technology, Pharmaceutical</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>CONTI, S</creatorcontrib><creatorcontrib>MAGGI, L</creatorcontrib><creatorcontrib>SEGALE, L</creatorcontrib><creatorcontrib>OCHOA MACHISTE, E</creatorcontrib><creatorcontrib>CENTE, U</creatorcontrib><creatorcontrib>GRENIER, P</creatorcontrib><creatorcontrib>VERGNAULT, G</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>International journal of pharmaceutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>CONTI, S</au><au>MAGGI, L</au><au>SEGALE, L</au><au>OCHOA MACHISTE, E</au><au>CENTE, U</au><au>GRENIER, P</au><au>VERGNAULT, G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Matrices containing NaCMC and HPMC 1. Dissolution performance characterization</atitle><jtitle>International journal of pharmaceutics</jtitle><addtitle>Int J Pharm</addtitle><date>2007-03-21</date><risdate>2007</risdate><volume>333</volume><issue>1-2</issue><spage>136</spage><epage>142</epage><pages>136-142</pages><issn>0378-5173</issn><eissn>1873-3476</eissn><coden>IJPHDE</coden><abstract>In this study hydroxypropylmethylcellulose (HPMC) and sodium carboxymethylcellulose (NaCMC) were used as polymeric carriers to improve controlled release performances of matrix tablets containing a soluble drug. The drug release behaviour of the systems containing these two polymers mixture and each material separately was investigated. To evaluate the effect of the dissolution medium pH, on the drug release performance, release tests were conducted at pH 1, 4.5 and 6.8. In vitro release studies demonstrated that the mixture of the two cellulose derivatives enables a better control of the drug release profiles at pH 4.5 and at 6.8 both in term of rate and mechanism. Texture analysis on the swollen tablets helps to understand drug release kinetic and mechanism. In fact, the results obtained confirm that a gel, which is characterized by high strength and consistence is less susceptible to erosion and chains disentanglement and the drug release mechanism is mainly governed by diffusion. On the contrary, gels, which show a low strength and texture, have low resistance to the fluid erosion action and the release of the active molecule is manly due to polymer relaxation and chains disentanglement moving the drug delivery kinetic towards an erosion/relaxation mechanism.</abstract><cop>Amsterdam</cop><pub>Elsevier</pub><pmid>17207943</pmid><doi>10.1016/j.ijpharm.2006.11.059</doi><tpages>7</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0378-5173 |
ispartof | International journal of pharmaceutics, 2007-03, Vol.333 (1-2), p.136-142 |
issn | 0378-5173 1873-3476 |
language | eng |
recordid | cdi_proquest_miscellaneous_70207444 |
source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | Biological and medical sciences Carboxymethylcellulose Sodium - chemistry Chemistry, Pharmaceutical Delayed-Action Preparations Diffusion Diltiazem - chemistry Drug Carriers General pharmacology Hydrogels Hydrogen-Ion Concentration Hypromellose Derivatives Kinetics Medical sciences Methylcellulose - analogs & derivatives Methylcellulose - chemistry Models, Chemical Pharmaceutical technology. Pharmaceutical industry Pharmacology. Drug treatments Solubility Tablets Technology, Pharmaceutical |
title | Matrices containing NaCMC and HPMC 1. Dissolution performance characterization |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-26T13%3A55%3A57IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Matrices%20containing%20NaCMC%20and%20HPMC%201.%20Dissolution%20performance%20characterization&rft.jtitle=International%20journal%20of%20pharmaceutics&rft.au=CONTI,%20S&rft.date=2007-03-21&rft.volume=333&rft.issue=1-2&rft.spage=136&rft.epage=142&rft.pages=136-142&rft.issn=0378-5173&rft.eissn=1873-3476&rft.coden=IJPHDE&rft_id=info:doi/10.1016/j.ijpharm.2006.11.059&rft_dat=%3Cproquest_pubme%3E70207444%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=70207444&rft_id=info:pmid/17207943&rfr_iscdi=true |