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Alginate microbeads with internal microvoids for the sustained release of drugs
The process of Ca2+ mediated gelation of alginate and the fabrication of nanoengineered polyelectrolyte capsules were combined for the preparation of alginate microbeads characterized by the presence of well-defined drug loaded microvoids in their volume. The obtained engineered alginate microbeads...
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Published in: | International journal of biological macromolecules 2020-08, Vol.156, p.454-461 |
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container_title | International journal of biological macromolecules |
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creator | Boi, Stefania Rouatbi, Nadia Dellacasa, Elena Di Lisa, Donatella Bianchini, Paolo Monticelli, Orietta Pastorino, Laura |
description | The process of Ca2+ mediated gelation of alginate and the fabrication of nanoengineered polyelectrolyte capsules were combined for the preparation of alginate microbeads characterized by the presence of well-defined drug loaded microvoids in their volume.
The obtained engineered alginate microbeads are described in terms of their morphology, loading efficiency and release characteristics. It was found that the generation of microvoids in the volume of alginate microbeads could be a promising approach for the creation of microstructured and biocompatible hydrogels, prospectively having highly tunable properties in terms of loading and releasing characteristics. In particular, it was found that the developed system was able to limit drug leakage during the gelation process and to control the initial burst release of small hydrophilic drug molecules, such as doxorubicin hydrochloride. Finally, the cytocompatibility of the developed microhydrogels was assessed on MCF-7 human breast cancer cells as well as their ability to sustain the release of the model drug during time.
•Shell delimited microvoids are present into alginate microbead volume.•Release of small hydrophilic doxorubicin hydrochloride is sustained over time.•Fully cytocompatible microgel is developed. |
doi_str_mv | 10.1016/j.ijbiomac.2020.04.083 |
format | article |
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The obtained engineered alginate microbeads are described in terms of their morphology, loading efficiency and release characteristics. It was found that the generation of microvoids in the volume of alginate microbeads could be a promising approach for the creation of microstructured and biocompatible hydrogels, prospectively having highly tunable properties in terms of loading and releasing characteristics. In particular, it was found that the developed system was able to limit drug leakage during the gelation process and to control the initial burst release of small hydrophilic drug molecules, such as doxorubicin hydrochloride. Finally, the cytocompatibility of the developed microhydrogels was assessed on MCF-7 human breast cancer cells as well as their ability to sustain the release of the model drug during time.
•Shell delimited microvoids are present into alginate microbead volume.•Release of small hydrophilic doxorubicin hydrochloride is sustained over time.•Fully cytocompatible microgel is developed.</description><identifier>ISSN: 0141-8130</identifier><identifier>EISSN: 1879-0003</identifier><identifier>DOI: 10.1016/j.ijbiomac.2020.04.083</identifier><identifier>PMID: 32302635</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Alginate microbeads ; Alginates - chemistry ; Biopolymers ; Capsules ; Cell Line, Tumor ; Delayed-Action Preparations ; Drug Carriers ; Drug Delivery Systems ; Humans ; Microspheres ; Molecular Weight ; Nanoengineered polymeric capsules</subject><ispartof>International journal of biological macromolecules, 2020-08, Vol.156, p.454-461</ispartof><rights>2020 Elsevier B.V.</rights><rights>Copyright © 2020 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c368t-2543c3b88cf021c842e4f694baf05e50d80f5db678da45aa86ae1022a3e6d2f33</citedby><cites>FETCH-LOGICAL-c368t-2543c3b88cf021c842e4f694baf05e50d80f5db678da45aa86ae1022a3e6d2f33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32302635$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Boi, Stefania</creatorcontrib><creatorcontrib>Rouatbi, Nadia</creatorcontrib><creatorcontrib>Dellacasa, Elena</creatorcontrib><creatorcontrib>Di Lisa, Donatella</creatorcontrib><creatorcontrib>Bianchini, Paolo</creatorcontrib><creatorcontrib>Monticelli, Orietta</creatorcontrib><creatorcontrib>Pastorino, Laura</creatorcontrib><title>Alginate microbeads with internal microvoids for the sustained release of drugs</title><title>International journal of biological macromolecules</title><addtitle>Int J Biol Macromol</addtitle><description>The process of Ca2+ mediated gelation of alginate and the fabrication of nanoengineered polyelectrolyte capsules were combined for the preparation of alginate microbeads characterized by the presence of well-defined drug loaded microvoids in their volume.
The obtained engineered alginate microbeads are described in terms of their morphology, loading efficiency and release characteristics. It was found that the generation of microvoids in the volume of alginate microbeads could be a promising approach for the creation of microstructured and biocompatible hydrogels, prospectively having highly tunable properties in terms of loading and releasing characteristics. In particular, it was found that the developed system was able to limit drug leakage during the gelation process and to control the initial burst release of small hydrophilic drug molecules, such as doxorubicin hydrochloride. Finally, the cytocompatibility of the developed microhydrogels was assessed on MCF-7 human breast cancer cells as well as their ability to sustain the release of the model drug during time.
•Shell delimited microvoids are present into alginate microbead volume.•Release of small hydrophilic doxorubicin hydrochloride is sustained over time.•Fully cytocompatible microgel is developed.</description><subject>Alginate microbeads</subject><subject>Alginates - chemistry</subject><subject>Biopolymers</subject><subject>Capsules</subject><subject>Cell Line, Tumor</subject><subject>Delayed-Action Preparations</subject><subject>Drug Carriers</subject><subject>Drug Delivery Systems</subject><subject>Humans</subject><subject>Microspheres</subject><subject>Molecular Weight</subject><subject>Nanoengineered polymeric capsules</subject><issn>0141-8130</issn><issn>1879-0003</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNqFkEtPwzAQhC0EoqXwF6ocuSSs7cR1b1QVL6lSL3C2HHvdusqj2EkR_55UpVw5rbQzs6v5CJlSyChQ8bDL_K70ba1NxoBBBnkGkl-QMZWzeQoA_JKMgeY0lZTDiNzEuBu2oqDymow448AEL8Zkvag2vtEdJrU3oS1R25h8-W6b-KbD0OjqJBxaPwiuDUm3xST2sdO-QZsErFBHTFqX2NBv4i25crqKePc7J-Tj-el9-Zqu1i9vy8UqNVzILmVFzg0vpTQOGDUyZ5g7Mc9L7aDAAqwEV9hSzKTVeaG1FBopMKY5Cssc5xNyf7q7D-1nj7FTtY8Gq0o32PZRMT6nc8kEZYNVnKxDjRgDOrUPvtbhW1FQR5hqp84w1RGmglwNMIfg9PdHX9Zo_2JneoPh8WTAoenBY1DReGwMWh_QdMq2_r8fP67LiYU</recordid><startdate>20200801</startdate><enddate>20200801</enddate><creator>Boi, Stefania</creator><creator>Rouatbi, Nadia</creator><creator>Dellacasa, Elena</creator><creator>Di Lisa, Donatella</creator><creator>Bianchini, Paolo</creator><creator>Monticelli, Orietta</creator><creator>Pastorino, Laura</creator><general>Elsevier B.V</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>20200801</creationdate><title>Alginate microbeads with internal microvoids for the sustained release of drugs</title><author>Boi, Stefania ; Rouatbi, Nadia ; Dellacasa, Elena ; Di Lisa, Donatella ; Bianchini, Paolo ; Monticelli, Orietta ; Pastorino, Laura</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c368t-2543c3b88cf021c842e4f694baf05e50d80f5db678da45aa86ae1022a3e6d2f33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Alginate microbeads</topic><topic>Alginates - chemistry</topic><topic>Biopolymers</topic><topic>Capsules</topic><topic>Cell Line, Tumor</topic><topic>Delayed-Action Preparations</topic><topic>Drug Carriers</topic><topic>Drug Delivery Systems</topic><topic>Humans</topic><topic>Microspheres</topic><topic>Molecular Weight</topic><topic>Nanoengineered polymeric capsules</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Boi, Stefania</creatorcontrib><creatorcontrib>Rouatbi, Nadia</creatorcontrib><creatorcontrib>Dellacasa, Elena</creatorcontrib><creatorcontrib>Di Lisa, Donatella</creatorcontrib><creatorcontrib>Bianchini, Paolo</creatorcontrib><creatorcontrib>Monticelli, Orietta</creatorcontrib><creatorcontrib>Pastorino, Laura</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>International journal of biological macromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Boi, Stefania</au><au>Rouatbi, Nadia</au><au>Dellacasa, Elena</au><au>Di Lisa, Donatella</au><au>Bianchini, Paolo</au><au>Monticelli, Orietta</au><au>Pastorino, Laura</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Alginate microbeads with internal microvoids for the sustained release of drugs</atitle><jtitle>International journal of biological macromolecules</jtitle><addtitle>Int J Biol Macromol</addtitle><date>2020-08-01</date><risdate>2020</risdate><volume>156</volume><spage>454</spage><epage>461</epage><pages>454-461</pages><issn>0141-8130</issn><eissn>1879-0003</eissn><abstract>The process of Ca2+ mediated gelation of alginate and the fabrication of nanoengineered polyelectrolyte capsules were combined for the preparation of alginate microbeads characterized by the presence of well-defined drug loaded microvoids in their volume.
The obtained engineered alginate microbeads are described in terms of their morphology, loading efficiency and release characteristics. It was found that the generation of microvoids in the volume of alginate microbeads could be a promising approach for the creation of microstructured and biocompatible hydrogels, prospectively having highly tunable properties in terms of loading and releasing characteristics. In particular, it was found that the developed system was able to limit drug leakage during the gelation process and to control the initial burst release of small hydrophilic drug molecules, such as doxorubicin hydrochloride. Finally, the cytocompatibility of the developed microhydrogels was assessed on MCF-7 human breast cancer cells as well as their ability to sustain the release of the model drug during time.
•Shell delimited microvoids are present into alginate microbead volume.•Release of small hydrophilic doxorubicin hydrochloride is sustained over time.•Fully cytocompatible microgel is developed.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>32302635</pmid><doi>10.1016/j.ijbiomac.2020.04.083</doi><tpages>8</tpages></addata></record> |
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subjects | Alginate microbeads Alginates - chemistry Biopolymers Capsules Cell Line, Tumor Delayed-Action Preparations Drug Carriers Drug Delivery Systems Humans Microspheres Molecular Weight Nanoengineered polymeric capsules |
title | Alginate microbeads with internal microvoids for the sustained release of drugs |
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