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Influence of the formulation components on the properties of the system SLN-dextran hydrogel for the modified release of drugs
A system composed by solid lipid nanoparticles (SLN) entrapped into a chemical hydrogel of dextran was recently proposed for the controlled release of lipophilic drugs in oral formulations. This study reports now an extension of such study focused on the investigation of how the nature and the amoun...
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Published in: | Journal of microencapsulation 2009-06, Vol.26 (4), p.355-364 |
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creator | Paolicelli, Patrizia Cerreto, Felice Cesa, Stefania Feeney, Michelle Corrente, Federica Marianecci, Carlotta Casadei, Maria Antonietta |
description | A system composed by solid lipid nanoparticles (SLN) entrapped into a chemical hydrogel of dextran was recently proposed for the controlled release of lipophilic drugs in oral formulations. This study reports now an extension of such study focused on the investigation of how the nature and the amount of the formulation components are able to modify the properties of the system. In particular the concentration of the two surfactants used for the nanosuspension stabilization, the nature of the lipid phase used for the nanoparticles preparation, as well as the concentration and the derivatization degree of the polymer employed for the gel preparation were investigated. The effects of these variables on the physicochemical properties of the nanoparticles and/or on the release profiles of the model drug (S)-(+)-2-(4-isobutylphenyl)-propionic acid (ibuprofen) were reported and discussed. Rheological experiments on samples of SLN, dextran hydrogel, and SLN-dextran hydrogel were also performed. |
doi_str_mv | 10.1080/02652040802372899 |
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This study reports now an extension of such study focused on the investigation of how the nature and the amount of the formulation components are able to modify the properties of the system. In particular the concentration of the two surfactants used for the nanosuspension stabilization, the nature of the lipid phase used for the nanoparticles preparation, as well as the concentration and the derivatization degree of the polymer employed for the gel preparation were investigated. The effects of these variables on the physicochemical properties of the nanoparticles and/or on the release profiles of the model drug (S)-(+)-2-(4-isobutylphenyl)-propionic acid (ibuprofen) were reported and discussed. Rheological experiments on samples of SLN, dextran hydrogel, and SLN-dextran hydrogel were also performed.</description><identifier>ISSN: 0265-2048</identifier><identifier>EISSN: 1464-5246</identifier><identifier>DOI: 10.1080/02652040802372899</identifier><identifier>PMID: 18785054</identifier><identifier>CODEN: JOMIEF</identifier><language>eng</language><publisher>Colchester: Informa UK Ltd</publisher><subject>Anti-Inflammatory Agents, Non-Steroidal - administration & dosage ; Biological and medical sciences ; dextran methacrylate ; Dextrans - chemistry ; General pharmacology ; hydrogel ; Hydrogel, Polyethylene Glycol Dimethacrylate - chemistry ; ibuprofen ; Ibuprofen - administration & dosage ; Lipids - chemistry ; Medical sciences ; Methacrylates - chemistry ; modified release ; Nanoparticles - chemistry ; Pharmaceutical technology. Pharmaceutical industry ; Pharmacology. Drug treatments ; photochemical cross-linking reaction ; Rheology ; Solid lipid nanoparticles ; Surface-Active Agents - chemistry</subject><ispartof>Journal of microencapsulation, 2009-06, Vol.26 (4), p.355-364</ispartof><rights>2009 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 2009</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c466t-c44ab3e1221eebe63f07f51d58fd8471661e55a7756623a69b6e5790fceb8b7d3</citedby><cites>FETCH-LOGICAL-c466t-c44ab3e1221eebe63f07f51d58fd8471661e55a7756623a69b6e5790fceb8b7d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21646855$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18785054$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Paolicelli, Patrizia</creatorcontrib><creatorcontrib>Cerreto, Felice</creatorcontrib><creatorcontrib>Cesa, Stefania</creatorcontrib><creatorcontrib>Feeney, Michelle</creatorcontrib><creatorcontrib>Corrente, Federica</creatorcontrib><creatorcontrib>Marianecci, Carlotta</creatorcontrib><creatorcontrib>Casadei, Maria Antonietta</creatorcontrib><title>Influence of the formulation components on the properties of the system SLN-dextran hydrogel for the modified release of drugs</title><title>Journal of microencapsulation</title><addtitle>J Microencapsul</addtitle><description>A system composed by solid lipid nanoparticles (SLN) entrapped into a chemical hydrogel of dextran was recently proposed for the controlled release of lipophilic drugs in oral formulations. This study reports now an extension of such study focused on the investigation of how the nature and the amount of the formulation components are able to modify the properties of the system. In particular the concentration of the two surfactants used for the nanosuspension stabilization, the nature of the lipid phase used for the nanoparticles preparation, as well as the concentration and the derivatization degree of the polymer employed for the gel preparation were investigated. The effects of these variables on the physicochemical properties of the nanoparticles and/or on the release profiles of the model drug (S)-(+)-2-(4-isobutylphenyl)-propionic acid (ibuprofen) were reported and discussed. Rheological experiments on samples of SLN, dextran hydrogel, and SLN-dextran hydrogel were also performed.</description><subject>Anti-Inflammatory Agents, Non-Steroidal - administration & dosage</subject><subject>Biological and medical sciences</subject><subject>dextran methacrylate</subject><subject>Dextrans - chemistry</subject><subject>General pharmacology</subject><subject>hydrogel</subject><subject>Hydrogel, Polyethylene Glycol Dimethacrylate - chemistry</subject><subject>ibuprofen</subject><subject>Ibuprofen - administration & dosage</subject><subject>Lipids - chemistry</subject><subject>Medical sciences</subject><subject>Methacrylates - chemistry</subject><subject>modified release</subject><subject>Nanoparticles - chemistry</subject><subject>Pharmaceutical technology. Pharmaceutical industry</subject><subject>Pharmacology. Drug treatments</subject><subject>photochemical cross-linking reaction</subject><subject>Rheology</subject><subject>Solid lipid nanoparticles</subject><subject>Surface-Active Agents - chemistry</subject><issn>0265-2048</issn><issn>1464-5246</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNp9kUtv1DAUhS1ERYfCD2CDsqGsUmzHr4huUMWj0ggWwDpy7OtOKicebEd0Nvx2nM4UhJBm44fud8699kHoBcEXBCv8BlPBKWblSBtJVds-QivCBKs5ZeIxWi31ugDqFD1N6RZjzFtFn6BToqTimLMV-nU9OT_DZKAKrsobqFyI4-x1HsJUmTBuwwRTTlW5LdVtDFuIeYD0wKddyjBWX9efawt3Oeqp2uxsDDfgF697Zgx2cAPYKoIHne572TjfpGfoxGmf4PlhP0PfP7z_dvWpXn_5eH31bl0bJkQuK9N9A4RSAtCDaByWjhPLlbOKSSIEAc61lFwI2mjR9gK4bLEz0Kte2uYMvd77lvl_zJByNw7JgPd6gjCnTnEiOVGtKuT5UZJiiiXlC0j2oIkhpQiu28Zh1HHXEdwt8XT_xVM0Lw_mcz-C_as45FGAVwdAJ6O9K79phvSHo0QwoTgv3OWeG6YlL_0zRG-7rHc-xAdRc2yOt__IN6B93hgdobsNc5xKFEde8RumPr4r</recordid><startdate>200906</startdate><enddate>200906</enddate><creator>Paolicelli, Patrizia</creator><creator>Cerreto, Felice</creator><creator>Cesa, Stefania</creator><creator>Feeney, Michelle</creator><creator>Corrente, Federica</creator><creator>Marianecci, Carlotta</creator><creator>Casadei, Maria Antonietta</creator><general>Informa UK Ltd</general><general>Taylor & Francis</general><general>Informa</general><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>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>200906</creationdate><title>Influence of the formulation components on the properties of the system SLN-dextran hydrogel for the modified release of drugs</title><author>Paolicelli, Patrizia ; Cerreto, Felice ; Cesa, Stefania ; Feeney, Michelle ; Corrente, Federica ; Marianecci, Carlotta ; Casadei, Maria Antonietta</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c466t-c44ab3e1221eebe63f07f51d58fd8471661e55a7756623a69b6e5790fceb8b7d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Anti-Inflammatory Agents, Non-Steroidal - administration & dosage</topic><topic>Biological and medical sciences</topic><topic>dextran methacrylate</topic><topic>Dextrans - chemistry</topic><topic>General pharmacology</topic><topic>hydrogel</topic><topic>Hydrogel, Polyethylene Glycol Dimethacrylate - chemistry</topic><topic>ibuprofen</topic><topic>Ibuprofen - administration & dosage</topic><topic>Lipids - chemistry</topic><topic>Medical sciences</topic><topic>Methacrylates - chemistry</topic><topic>modified release</topic><topic>Nanoparticles - chemistry</topic><topic>Pharmaceutical technology. 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Drug treatments</topic><topic>photochemical cross-linking reaction</topic><topic>Rheology</topic><topic>Solid lipid nanoparticles</topic><topic>Surface-Active Agents - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Paolicelli, Patrizia</creatorcontrib><creatorcontrib>Cerreto, Felice</creatorcontrib><creatorcontrib>Cesa, Stefania</creatorcontrib><creatorcontrib>Feeney, Michelle</creatorcontrib><creatorcontrib>Corrente, Federica</creatorcontrib><creatorcontrib>Marianecci, Carlotta</creatorcontrib><creatorcontrib>Casadei, Maria Antonietta</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>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of microencapsulation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Paolicelli, Patrizia</au><au>Cerreto, Felice</au><au>Cesa, Stefania</au><au>Feeney, Michelle</au><au>Corrente, Federica</au><au>Marianecci, Carlotta</au><au>Casadei, Maria Antonietta</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Influence of the formulation components on the properties of the system SLN-dextran hydrogel for the modified release of drugs</atitle><jtitle>Journal of microencapsulation</jtitle><addtitle>J Microencapsul</addtitle><date>2009-06</date><risdate>2009</risdate><volume>26</volume><issue>4</issue><spage>355</spage><epage>364</epage><pages>355-364</pages><issn>0265-2048</issn><eissn>1464-5246</eissn><coden>JOMIEF</coden><abstract>A system composed by solid lipid nanoparticles (SLN) entrapped into a chemical hydrogel of dextran was recently proposed for the controlled release of lipophilic drugs in oral formulations. This study reports now an extension of such study focused on the investigation of how the nature and the amount of the formulation components are able to modify the properties of the system. In particular the concentration of the two surfactants used for the nanosuspension stabilization, the nature of the lipid phase used for the nanoparticles preparation, as well as the concentration and the derivatization degree of the polymer employed for the gel preparation were investigated. The effects of these variables on the physicochemical properties of the nanoparticles and/or on the release profiles of the model drug (S)-(+)-2-(4-isobutylphenyl)-propionic acid (ibuprofen) were reported and discussed. Rheological experiments on samples of SLN, dextran hydrogel, and SLN-dextran hydrogel were also performed.</abstract><cop>Colchester</cop><pub>Informa UK Ltd</pub><pmid>18785054</pmid><doi>10.1080/02652040802372899</doi><tpages>10</tpages></addata></record> |
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subjects | Anti-Inflammatory Agents, Non-Steroidal - administration & dosage Biological and medical sciences dextran methacrylate Dextrans - chemistry General pharmacology hydrogel Hydrogel, Polyethylene Glycol Dimethacrylate - chemistry ibuprofen Ibuprofen - administration & dosage Lipids - chemistry Medical sciences Methacrylates - chemistry modified release Nanoparticles - chemistry Pharmaceutical technology. Pharmaceutical industry Pharmacology. Drug treatments photochemical cross-linking reaction Rheology Solid lipid nanoparticles Surface-Active Agents - chemistry |
title | Influence of the formulation components on the properties of the system SLN-dextran hydrogel for the modified release of drugs |
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