Core–Shell Chitosan Microcapsules for Programmed Sequential Drug Release

A novel type of core–shell chitosan microcapsule with programmed sequential drug release is developed by the microfluidic technique for acute gastrosis therapy. The microcapsule is composed of a cross-linked chitosan hydrogel shell and an oily core containing both free drug molecules and drug-loaded...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:ACS applied materials & interfaces 2016-04, Vol.8 (16), p.10524-10534
Hauptverfasser: Yang, Xiu-Lan, Ju, Xiao-Jie, Mu, Xiao-Ting, Wang, Wei, Xie, Rui, Liu, Zhuang, Chu, Liang-Yin
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 10534
container_issue 16
container_start_page 10524
container_title ACS applied materials & interfaces
container_volume 8
creator Yang, Xiu-Lan
Ju, Xiao-Jie
Mu, Xiao-Ting
Wang, Wei
Xie, Rui
Liu, Zhuang
Chu, Liang-Yin
description A novel type of core–shell chitosan microcapsule with programmed sequential drug release is developed by the microfluidic technique for acute gastrosis therapy. The microcapsule is composed of a cross-linked chitosan hydrogel shell and an oily core containing both free drug molecules and drug-loaded poly­(lactic-co-glycolic acid) (PLGA) nanoparticles. Before exposure to acid stimulus, the resultant microcapsules can keep their structural integrity without leakage of the encapsulated substances. Upon acid-triggering, the microcapsules first achieve burst release due to the acid-induced decomposition of the chitosan shell. The encapsulated free drug molecules and drug-loaded PLGA nanoparticles are rapidly released within 60 s. Next, the drugs loaded in the PLGA nanoparticles are slowly released for several days to achieve sustained release based on the synergistic effect of drug diffusion and PLGA degradation. Such core–shell chitosan microcapsules with programmed sequential drug release are promising for rational drug delivery and controlled-release for the treatment of acute gastritis. In addition, the microcapsule systems with programmed sequential release provide more versatility for controlled release in biomedical applications.
doi_str_mv 10.1021/acsami.6b01277
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1785212374</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1785212374</sourcerecordid><originalsourceid>FETCH-LOGICAL-a330t-77470f420b9555603c080bca32c2cc8e8b0a4f6f4fa7e4ab9bd0ac23046e9cd13</originalsourceid><addsrcrecordid>eNp1kL1OwzAUhS0EoqWwMqKMCCnl2nHiZEThXyAQhdm6cZ02VRIXOxnYeAfekCfBKKUb073Dd47OOYQcU5hSYPQclcOmmiYFUCbEDhnTjPMwZTHb3f6cj8iBcyuAJGIQ75MRExCzlLIxuc-N1d-fX7OlrusgX1adcdgGj5WyRuHa9bV2QWls8GzNwmLT6Hkw0--9brsK6-DS9ovgRdcanT4keyXWTh9t7oS8XV-95rfhw9PNXX7xEGIUQRcKwQWUnEGRxXGcQKQghUJhxBRTKtVpAcjLpOQlCs2xyIo5oGIR8ERnak6jCTkdfNfW-CCuk03llI-PrTa9k1SkMaMsEtyj0wH1bZyzupRrWzVoPyQF-bufHPaTm_284GTj3Re-6hb_G8wDZwPghXJletv6qv-5_QCHmXuJ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1785212374</pqid></control><display><type>article</type><title>Core–Shell Chitosan Microcapsules for Programmed Sequential Drug Release</title><source>MEDLINE</source><source>American Chemical Society Journals</source><creator>Yang, Xiu-Lan ; Ju, Xiao-Jie ; Mu, Xiao-Ting ; Wang, Wei ; Xie, Rui ; Liu, Zhuang ; Chu, Liang-Yin</creator><creatorcontrib>Yang, Xiu-Lan ; Ju, Xiao-Jie ; Mu, Xiao-Ting ; Wang, Wei ; Xie, Rui ; Liu, Zhuang ; Chu, Liang-Yin</creatorcontrib><description>A novel type of core–shell chitosan microcapsule with programmed sequential drug release is developed by the microfluidic technique for acute gastrosis therapy. The microcapsule is composed of a cross-linked chitosan hydrogel shell and an oily core containing both free drug molecules and drug-loaded poly­(lactic-co-glycolic acid) (PLGA) nanoparticles. Before exposure to acid stimulus, the resultant microcapsules can keep their structural integrity without leakage of the encapsulated substances. Upon acid-triggering, the microcapsules first achieve burst release due to the acid-induced decomposition of the chitosan shell. The encapsulated free drug molecules and drug-loaded PLGA nanoparticles are rapidly released within 60 s. Next, the drugs loaded in the PLGA nanoparticles are slowly released for several days to achieve sustained release based on the synergistic effect of drug diffusion and PLGA degradation. Such core–shell chitosan microcapsules with programmed sequential drug release are promising for rational drug delivery and controlled-release for the treatment of acute gastritis. In addition, the microcapsule systems with programmed sequential release provide more versatility for controlled release in biomedical applications.</description><identifier>ISSN: 1944-8244</identifier><identifier>EISSN: 1944-8252</identifier><identifier>DOI: 10.1021/acsami.6b01277</identifier><identifier>PMID: 27052812</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Capsules ; Chitosan - chemistry ; Drug Liberation ; Lactic Acid ; Polyglycolic Acid</subject><ispartof>ACS applied materials &amp; interfaces, 2016-04, Vol.8 (16), p.10524-10534</ispartof><rights>Copyright © 2016 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a330t-77470f420b9555603c080bca32c2cc8e8b0a4f6f4fa7e4ab9bd0ac23046e9cd13</citedby><cites>FETCH-LOGICAL-a330t-77470f420b9555603c080bca32c2cc8e8b0a4f6f4fa7e4ab9bd0ac23046e9cd13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acsami.6b01277$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acsami.6b01277$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,776,780,2752,27053,27901,27902,56713,56763</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27052812$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yang, Xiu-Lan</creatorcontrib><creatorcontrib>Ju, Xiao-Jie</creatorcontrib><creatorcontrib>Mu, Xiao-Ting</creatorcontrib><creatorcontrib>Wang, Wei</creatorcontrib><creatorcontrib>Xie, Rui</creatorcontrib><creatorcontrib>Liu, Zhuang</creatorcontrib><creatorcontrib>Chu, Liang-Yin</creatorcontrib><title>Core–Shell Chitosan Microcapsules for Programmed Sequential Drug Release</title><title>ACS applied materials &amp; interfaces</title><addtitle>ACS Appl. Mater. Interfaces</addtitle><description>A novel type of core–shell chitosan microcapsule with programmed sequential drug release is developed by the microfluidic technique for acute gastrosis therapy. The microcapsule is composed of a cross-linked chitosan hydrogel shell and an oily core containing both free drug molecules and drug-loaded poly­(lactic-co-glycolic acid) (PLGA) nanoparticles. Before exposure to acid stimulus, the resultant microcapsules can keep their structural integrity without leakage of the encapsulated substances. Upon acid-triggering, the microcapsules first achieve burst release due to the acid-induced decomposition of the chitosan shell. The encapsulated free drug molecules and drug-loaded PLGA nanoparticles are rapidly released within 60 s. Next, the drugs loaded in the PLGA nanoparticles are slowly released for several days to achieve sustained release based on the synergistic effect of drug diffusion and PLGA degradation. Such core–shell chitosan microcapsules with programmed sequential drug release are promising for rational drug delivery and controlled-release for the treatment of acute gastritis. In addition, the microcapsule systems with programmed sequential release provide more versatility for controlled release in biomedical applications.</description><subject>Capsules</subject><subject>Chitosan - chemistry</subject><subject>Drug Liberation</subject><subject>Lactic Acid</subject><subject>Polyglycolic Acid</subject><issn>1944-8244</issn><issn>1944-8252</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kL1OwzAUhS0EoqWwMqKMCCnl2nHiZEThXyAQhdm6cZ02VRIXOxnYeAfekCfBKKUb073Dd47OOYQcU5hSYPQclcOmmiYFUCbEDhnTjPMwZTHb3f6cj8iBcyuAJGIQ75MRExCzlLIxuc-N1d-fX7OlrusgX1adcdgGj5WyRuHa9bV2QWls8GzNwmLT6Hkw0--9brsK6-DS9ovgRdcanT4keyXWTh9t7oS8XV-95rfhw9PNXX7xEGIUQRcKwQWUnEGRxXGcQKQghUJhxBRTKtVpAcjLpOQlCs2xyIo5oGIR8ERnak6jCTkdfNfW-CCuk03llI-PrTa9k1SkMaMsEtyj0wH1bZyzupRrWzVoPyQF-bufHPaTm_284GTj3Re-6hb_G8wDZwPghXJletv6qv-5_QCHmXuJ</recordid><startdate>20160427</startdate><enddate>20160427</enddate><creator>Yang, Xiu-Lan</creator><creator>Ju, Xiao-Jie</creator><creator>Mu, Xiao-Ting</creator><creator>Wang, Wei</creator><creator>Xie, Rui</creator><creator>Liu, Zhuang</creator><creator>Chu, Liang-Yin</creator><general>American Chemical Society</general><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>20160427</creationdate><title>Core–Shell Chitosan Microcapsules for Programmed Sequential Drug Release</title><author>Yang, Xiu-Lan ; Ju, Xiao-Jie ; Mu, Xiao-Ting ; Wang, Wei ; Xie, Rui ; Liu, Zhuang ; Chu, Liang-Yin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a330t-77470f420b9555603c080bca32c2cc8e8b0a4f6f4fa7e4ab9bd0ac23046e9cd13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Capsules</topic><topic>Chitosan - chemistry</topic><topic>Drug Liberation</topic><topic>Lactic Acid</topic><topic>Polyglycolic Acid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, Xiu-Lan</creatorcontrib><creatorcontrib>Ju, Xiao-Jie</creatorcontrib><creatorcontrib>Mu, Xiao-Ting</creatorcontrib><creatorcontrib>Wang, Wei</creatorcontrib><creatorcontrib>Xie, Rui</creatorcontrib><creatorcontrib>Liu, Zhuang</creatorcontrib><creatorcontrib>Chu, Liang-Yin</creatorcontrib><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>ACS applied materials &amp; interfaces</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, Xiu-Lan</au><au>Ju, Xiao-Jie</au><au>Mu, Xiao-Ting</au><au>Wang, Wei</au><au>Xie, Rui</au><au>Liu, Zhuang</au><au>Chu, Liang-Yin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Core–Shell Chitosan Microcapsules for Programmed Sequential Drug Release</atitle><jtitle>ACS applied materials &amp; interfaces</jtitle><addtitle>ACS Appl. Mater. Interfaces</addtitle><date>2016-04-27</date><risdate>2016</risdate><volume>8</volume><issue>16</issue><spage>10524</spage><epage>10534</epage><pages>10524-10534</pages><issn>1944-8244</issn><eissn>1944-8252</eissn><abstract>A novel type of core–shell chitosan microcapsule with programmed sequential drug release is developed by the microfluidic technique for acute gastrosis therapy. The microcapsule is composed of a cross-linked chitosan hydrogel shell and an oily core containing both free drug molecules and drug-loaded poly­(lactic-co-glycolic acid) (PLGA) nanoparticles. Before exposure to acid stimulus, the resultant microcapsules can keep their structural integrity without leakage of the encapsulated substances. Upon acid-triggering, the microcapsules first achieve burst release due to the acid-induced decomposition of the chitosan shell. The encapsulated free drug molecules and drug-loaded PLGA nanoparticles are rapidly released within 60 s. Next, the drugs loaded in the PLGA nanoparticles are slowly released for several days to achieve sustained release based on the synergistic effect of drug diffusion and PLGA degradation. Such core–shell chitosan microcapsules with programmed sequential drug release are promising for rational drug delivery and controlled-release for the treatment of acute gastritis. In addition, the microcapsule systems with programmed sequential release provide more versatility for controlled release in biomedical applications.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>27052812</pmid><doi>10.1021/acsami.6b01277</doi><tpages>11</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1944-8244
ispartof ACS applied materials & interfaces, 2016-04, Vol.8 (16), p.10524-10534
issn 1944-8244
1944-8252
language eng
recordid cdi_proquest_miscellaneous_1785212374
source MEDLINE; American Chemical Society Journals
subjects Capsules
Chitosan - chemistry
Drug Liberation
Lactic Acid
Polyglycolic Acid
title Core–Shell Chitosan Microcapsules for Programmed Sequential Drug Release
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-07T07%3A26%3A38IST&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=Core%E2%80%93Shell%20Chitosan%20Microcapsules%20for%20Programmed%20Sequential%20Drug%20Release&rft.jtitle=ACS%20applied%20materials%20&%20interfaces&rft.au=Yang,%20Xiu-Lan&rft.date=2016-04-27&rft.volume=8&rft.issue=16&rft.spage=10524&rft.epage=10534&rft.pages=10524-10534&rft.issn=1944-8244&rft.eissn=1944-8252&rft_id=info:doi/10.1021/acsami.6b01277&rft_dat=%3Cproquest_cross%3E1785212374%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=1785212374&rft_id=info:pmid/27052812&rfr_iscdi=true