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Alginate encapsulated mesoporous silica nanospheres as a sustained drug delivery system for the poorly water-soluble drug indomethacin
We applied a combination of inorganic mesoporous silica material, frequently used as drug carriers, and a natural organic polymer alginate (ALG), to establish a sustained drug delivery system for the poorly water-soluble drug Indomethacin (IND). Mesoporous silica nanospheres (MSNs) were synthesized...
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Published in: | Asian journal of pharmceutical sciences 2014-08, Vol.9 (4), p.183-190 |
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container_title | Asian journal of pharmceutical sciences |
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creator | Hu, Liang Sun, Changshan Song, Aihua Chang, Di Zheng, Xin Gao, Yikun Jiang, Tongying Wang, Siling |
description | We applied a combination of inorganic mesoporous silica material, frequently used as drug carriers, and a natural organic polymer alginate (ALG), to establish a sustained drug delivery system for the poorly water-soluble drug Indomethacin (IND). Mesoporous silica nanospheres (MSNs) were synthesized using an organic template method and then functionalized with aminopropyl groups through postsynthesis. After drug loading into the pores of aninopropyl functionalized MSNs (AP-MSNs), IND loaded AP-MSNs (IND-AP-MSNs) were encapsulated by ALG through the ionic interaction. The effects of surface chemical groups and ALG layer on IND release were systematically studied using scanning electron microscopy (SEM), transmission electron microscopy (TEM), nitrogen adsorption, zeta-potential analysis and TGA analysis. The surface structure and surface charge changes of the ALG encapsulated AP-MSNs (ALG-AP-MSNs) were also investigated. The results showed that sustained release of IND from the designed drug delivery system was mainly due to the blockage effect from the coated ALG. We believe that this combination will help designing oral sustained drug delivery systems for poorly water-soluble drugs. |
doi_str_mv | 10.1016/j.ajps.2014.05.004 |
format | article |
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Mesoporous silica nanospheres (MSNs) were synthesized using an organic template method and then functionalized with aminopropyl groups through postsynthesis. After drug loading into the pores of aninopropyl functionalized MSNs (AP-MSNs), IND loaded AP-MSNs (IND-AP-MSNs) were encapsulated by ALG through the ionic interaction. The effects of surface chemical groups and ALG layer on IND release were systematically studied using scanning electron microscopy (SEM), transmission electron microscopy (TEM), nitrogen adsorption, zeta-potential analysis and TGA analysis. The surface structure and surface charge changes of the ALG encapsulated AP-MSNs (ALG-AP-MSNs) were also investigated. The results showed that sustained release of IND from the designed drug delivery system was mainly due to the blockage effect from the coated ALG. We believe that this combination will help designing oral sustained drug delivery systems for poorly water-soluble drugs.</description><identifier>ISSN: 1818-0876</identifier><identifier>EISSN: 2221-285X</identifier><identifier>DOI: 10.1016/j.ajps.2014.05.004</identifier><language>eng</language><publisher>Elsevier B.V</publisher><subject>Alginate ; Aminepropyl group ; Indomethacin ; Mesoporous silica nanospheres ; Poorly water-soluble drug ; Sustained release</subject><ispartof>Asian journal of pharmceutical sciences, 2014-08, Vol.9 (4), p.183-190</ispartof><rights>2014 Shenyang Pharmaceutical University</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c410t-cf7f9355b7cfb3c736de4ac22506a4a908acc96c1c0f3608fb93aa3a5a5ddcdd3</citedby><cites>FETCH-LOGICAL-c410t-cf7f9355b7cfb3c736de4ac22506a4a908acc96c1c0f3608fb93aa3a5a5ddcdd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1818087614000324$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,3536,27901,27902,45756</link.rule.ids></links><search><creatorcontrib>Hu, Liang</creatorcontrib><creatorcontrib>Sun, Changshan</creatorcontrib><creatorcontrib>Song, Aihua</creatorcontrib><creatorcontrib>Chang, Di</creatorcontrib><creatorcontrib>Zheng, Xin</creatorcontrib><creatorcontrib>Gao, Yikun</creatorcontrib><creatorcontrib>Jiang, Tongying</creatorcontrib><creatorcontrib>Wang, Siling</creatorcontrib><title>Alginate encapsulated mesoporous silica nanospheres as a sustained drug delivery system for the poorly water-soluble drug indomethacin</title><title>Asian journal of pharmceutical sciences</title><description>We applied a combination of inorganic mesoporous silica material, frequently used as drug carriers, and a natural organic polymer alginate (ALG), to establish a sustained drug delivery system for the poorly water-soluble drug Indomethacin (IND). Mesoporous silica nanospheres (MSNs) were synthesized using an organic template method and then functionalized with aminopropyl groups through postsynthesis. After drug loading into the pores of aninopropyl functionalized MSNs (AP-MSNs), IND loaded AP-MSNs (IND-AP-MSNs) were encapsulated by ALG through the ionic interaction. The effects of surface chemical groups and ALG layer on IND release were systematically studied using scanning electron microscopy (SEM), transmission electron microscopy (TEM), nitrogen adsorption, zeta-potential analysis and TGA analysis. The surface structure and surface charge changes of the ALG encapsulated AP-MSNs (ALG-AP-MSNs) were also investigated. The results showed that sustained release of IND from the designed drug delivery system was mainly due to the blockage effect from the coated ALG. We believe that this combination will help designing oral sustained drug delivery systems for poorly water-soluble drugs.</description><subject>Alginate</subject><subject>Aminepropyl group</subject><subject>Indomethacin</subject><subject>Mesoporous silica nanospheres</subject><subject>Poorly water-soluble drug</subject><subject>Sustained release</subject><issn>1818-0876</issn><issn>2221-285X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNp9kcFq3DAQhk1poUuaF-hJL2B3JFuyDLmEkLSBQC8N5CbG0nhXxmsZyU7YF-hzV5stPRYGZhjm_5iZvyi-cqg4cPVtrHBcUiWANxXICqD5UOyEELwUWr58LHZcc12CbtXn4jqlEQB43bZcN7vi9-209zOuxGi2uKRtyrVjR0phCTFsiSU_eYtsxjmk5UCREsMcLG1pRT_nYRe3PXM0-VeKJ5ZOaaUjG0Jk64HYEkKcTuwtY2OZwrT1E10UfnbhSOsBrZ-_FJ8GnBJd_81XxfPD_a-7H-XTz--Pd7dPpW04rKUd2qGrpexbO_S1bWvlqEErhASFDXag0dpOWW5hqBXooe9qxBolSuesc_VV8XjhuoCjWaI_YjyZgN68N0LcG4yrtxOZDpGE073Tqm5cD71UTjinQXdC5b9nlriwbAwpRRr-8TiYszFmNGdjzNkYA9JkY7Lo5iKifOWrp2iS9fn15Hwku-Y1_P_kfwBzqpvT</recordid><startdate>20140801</startdate><enddate>20140801</enddate><creator>Hu, Liang</creator><creator>Sun, Changshan</creator><creator>Song, Aihua</creator><creator>Chang, Di</creator><creator>Zheng, Xin</creator><creator>Gao, Yikun</creator><creator>Jiang, Tongying</creator><creator>Wang, Siling</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>DOA</scope></search><sort><creationdate>20140801</creationdate><title>Alginate encapsulated mesoporous silica nanospheres as a sustained drug delivery system for the poorly water-soluble drug indomethacin</title><author>Hu, Liang ; Sun, Changshan ; Song, Aihua ; Chang, Di ; Zheng, Xin ; Gao, Yikun ; Jiang, Tongying ; Wang, Siling</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c410t-cf7f9355b7cfb3c736de4ac22506a4a908acc96c1c0f3608fb93aa3a5a5ddcdd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Alginate</topic><topic>Aminepropyl group</topic><topic>Indomethacin</topic><topic>Mesoporous silica nanospheres</topic><topic>Poorly water-soluble drug</topic><topic>Sustained release</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hu, Liang</creatorcontrib><creatorcontrib>Sun, Changshan</creatorcontrib><creatorcontrib>Song, Aihua</creatorcontrib><creatorcontrib>Chang, Di</creatorcontrib><creatorcontrib>Zheng, Xin</creatorcontrib><creatorcontrib>Gao, Yikun</creatorcontrib><creatorcontrib>Jiang, Tongying</creatorcontrib><creatorcontrib>Wang, Siling</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>CrossRef</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Asian journal of pharmceutical sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hu, Liang</au><au>Sun, Changshan</au><au>Song, Aihua</au><au>Chang, Di</au><au>Zheng, Xin</au><au>Gao, Yikun</au><au>Jiang, Tongying</au><au>Wang, Siling</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Alginate encapsulated mesoporous silica nanospheres as a sustained drug delivery system for the poorly water-soluble drug indomethacin</atitle><jtitle>Asian journal of pharmceutical sciences</jtitle><date>2014-08-01</date><risdate>2014</risdate><volume>9</volume><issue>4</issue><spage>183</spage><epage>190</epage><pages>183-190</pages><issn>1818-0876</issn><eissn>2221-285X</eissn><abstract>We applied a combination of inorganic mesoporous silica material, frequently used as drug carriers, and a natural organic polymer alginate (ALG), to establish a sustained drug delivery system for the poorly water-soluble drug Indomethacin (IND). Mesoporous silica nanospheres (MSNs) were synthesized using an organic template method and then functionalized with aminopropyl groups through postsynthesis. After drug loading into the pores of aninopropyl functionalized MSNs (AP-MSNs), IND loaded AP-MSNs (IND-AP-MSNs) were encapsulated by ALG through the ionic interaction. The effects of surface chemical groups and ALG layer on IND release were systematically studied using scanning electron microscopy (SEM), transmission electron microscopy (TEM), nitrogen adsorption, zeta-potential analysis and TGA analysis. The surface structure and surface charge changes of the ALG encapsulated AP-MSNs (ALG-AP-MSNs) were also investigated. The results showed that sustained release of IND from the designed drug delivery system was mainly due to the blockage effect from the coated ALG. We believe that this combination will help designing oral sustained drug delivery systems for poorly water-soluble drugs.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.ajps.2014.05.004</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Alginate Aminepropyl group Indomethacin Mesoporous silica nanospheres Poorly water-soluble drug Sustained release |
title | Alginate encapsulated mesoporous silica nanospheres as a sustained drug delivery system for the poorly water-soluble drug indomethacin |
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