Time-programmed release of fluoroscein isocyanate dextran from micro-pattern-designed polymer scrolls
In this article we present a relevant strategy for a non-trivial time-programmed release of water-soluble macromolecules from biocompatible μ-containers. The system is based on self-scrolled chitosan acetate (CA) fibers, encapsulated in a poly(dimethylsiloxane) matrix. Mass transfer between a fiber...
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Veröffentlicht in: | Journal of controlled release 2016-07, Vol.233, p.39-47 |
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description | In this article we present a relevant strategy for a non-trivial time-programmed release of water-soluble macromolecules from biocompatible μ-containers. The system is based on self-scrolled chitosan acetate (CA) fibers, encapsulated in a poly(dimethylsiloxane) matrix. Mass transfer between a fiber and the external environment takes place via the only opened extremity of the fiber. Fluoroscein isocyanate dextran (FID) is initially deposited at the inner surface of the CA fiber according to a programmed pattern. The FID molecules became mobile after the arriving of the swelling front, which propagates along the fiber's axis upon the immersion of the system in aqueous solution. Diffusion of the macromolecules into the environment is enabled by the open-tube geometry of the swollen part of the fiber, while a programmed kinetics of the drug release is due to patterning of the polymer film prior to rolling. The release of the macromolecules can be retarded by a few hours according to the placement of the FID spot with respect to the fibers orifice. A pulsatile release kinetics is demonstrated for a discrete pattern. A few millimeter spacing of the FID spots results in a few hours time interval between the release impulses. Random walk model is plugged in the effective diffusion coefficient for Fick's law and the release kinetics are simulated.
Programmable release kinetics of a fluorescein isocyanate dextran (FID) is achieved via its nonuniform distribution in a biopolymer self-rolled fiber, and directional swelling of the fiber. [Display omitted] |
doi_str_mv | 10.1016/j.jconrel.2016.05.022 |
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Programmable release kinetics of a fluorescein isocyanate dextran (FID) is achieved via its nonuniform distribution in a biopolymer self-rolled fiber, and directional swelling of the fiber. [Display omitted]</description><identifier>ISSN: 0168-3659</identifier><identifier>EISSN: 1873-4995</identifier><identifier>DOI: 10.1016/j.jconrel.2016.05.022</identifier><identifier>PMID: 27179634</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Acetates - chemistry ; ATR FTIR spectroscopy ; Chemical Sciences ; Chitosan ; Chitosan - chemistry ; Chronopharmacology ; Controlled release ; Delayed-Action Preparations - chemistry ; Dextrans - chemistry ; Drug Delivery Systems ; Drug Liberation ; Fluorescein-5-isothiocyanate - analogs & derivatives ; Fluorescein-5-isothiocyanate - chemistry ; Fluorescent Dyes - chemistry ; Fluoroscein isocyanate dextran ; Kinetics ; Macromolecule ; Medicinal Chemistry ; Model drug ; Models, Theoretical</subject><ispartof>Journal of controlled release, 2016-07, Vol.233, p.39-47</ispartof><rights>2016 Elsevier B.V.</rights><rights>Copyright © 2016 Elsevier B.V. All rights reserved.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c479t-ac5e5fbb945e13cca3370994fb44103e6d5593bc520aa5d4ef6e2e3cf09a67c93</citedby><cites>FETCH-LOGICAL-c479t-ac5e5fbb945e13cca3370994fb44103e6d5593bc520aa5d4ef6e2e3cf09a67c93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jconrel.2016.05.022$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,780,784,885,3549,27923,27924,45994</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27179634$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-03940037$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Egunov, Aleksandr I.</creatorcontrib><creatorcontrib>Inaba, Ayano</creatorcontrib><creatorcontrib>Gree, Simon</creatorcontrib><creatorcontrib>Malval, Jean-Pierre</creatorcontrib><creatorcontrib>Tamura, Katsuhiro</creatorcontrib><creatorcontrib>Saito, Yukie</creatorcontrib><creatorcontrib>Luchnikov, Valeriy A.</creatorcontrib><title>Time-programmed release of fluoroscein isocyanate dextran from micro-pattern-designed polymer scrolls</title><title>Journal of controlled release</title><addtitle>J Control Release</addtitle><description>In this article we present a relevant strategy for a non-trivial time-programmed release of water-soluble macromolecules from biocompatible μ-containers. The system is based on self-scrolled chitosan acetate (CA) fibers, encapsulated in a poly(dimethylsiloxane) matrix. Mass transfer between a fiber and the external environment takes place via the only opened extremity of the fiber. Fluoroscein isocyanate dextran (FID) is initially deposited at the inner surface of the CA fiber according to a programmed pattern. The FID molecules became mobile after the arriving of the swelling front, which propagates along the fiber's axis upon the immersion of the system in aqueous solution. Diffusion of the macromolecules into the environment is enabled by the open-tube geometry of the swollen part of the fiber, while a programmed kinetics of the drug release is due to patterning of the polymer film prior to rolling. The release of the macromolecules can be retarded by a few hours according to the placement of the FID spot with respect to the fibers orifice. A pulsatile release kinetics is demonstrated for a discrete pattern. A few millimeter spacing of the FID spots results in a few hours time interval between the release impulses. Random walk model is plugged in the effective diffusion coefficient for Fick's law and the release kinetics are simulated.
Programmable release kinetics of a fluorescein isocyanate dextran (FID) is achieved via its nonuniform distribution in a biopolymer self-rolled fiber, and directional swelling of the fiber. [Display omitted]</description><subject>Acetates - chemistry</subject><subject>ATR FTIR spectroscopy</subject><subject>Chemical Sciences</subject><subject>Chitosan</subject><subject>Chitosan - chemistry</subject><subject>Chronopharmacology</subject><subject>Controlled release</subject><subject>Delayed-Action Preparations - chemistry</subject><subject>Dextrans - chemistry</subject><subject>Drug Delivery Systems</subject><subject>Drug Liberation</subject><subject>Fluorescein-5-isothiocyanate - analogs & derivatives</subject><subject>Fluorescein-5-isothiocyanate - chemistry</subject><subject>Fluorescent Dyes - chemistry</subject><subject>Fluoroscein isocyanate dextran</subject><subject>Kinetics</subject><subject>Macromolecule</subject><subject>Medicinal Chemistry</subject><subject>Model drug</subject><subject>Models, Theoretical</subject><issn>0168-3659</issn><issn>1873-4995</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkUFv3CAQhVGVqtmm_QmJfEwPdgcDxpyqaJU2lVbqJT0jjIeUFTZb8EbZf19Wu821PSGYb97M4xFyTaGhQLvP22Zr45wwNG25NiAaaNs3ZEV7yWqulLggq1Loa9YJdUne57wFAMG4fEcuW0ml6hhfEXz0E9a7FJ-SmSYcq6KIJmMVXeXCPqaYLfq58jnag5nNgtWIL0syc-VSnKrJ2xTrnVkWTHM9YvZPc1HZxXCYMFW5VEPIH8hbZ0LGj-fzivz8ev-4fqg3P759X99tasulWmpjBQo3DIoLpMxaw5gEpbgbOKfAsBuFUGywogVjxMjRddgisw6U6aRV7Ip8Oun-MkHvkp9MOuhovH642-jjGzDFAZh8poW9PbHF_O895kVPvngNwcwY91nTHnrZcs7-A5WqbztOFSuoOKHFeM4J3esaFPQxOL3V5-D0MTgNQpfgSt_NecR-KDG8dv1NqgBfTgCW_3v2mHS2HmeLo09oFz1G_48RfwAVka2i</recordid><startdate>20160710</startdate><enddate>20160710</enddate><creator>Egunov, Aleksandr I.</creator><creator>Inaba, Ayano</creator><creator>Gree, Simon</creator><creator>Malval, Jean-Pierre</creator><creator>Tamura, Katsuhiro</creator><creator>Saito, Yukie</creator><creator>Luchnikov, Valeriy A.</creator><general>Elsevier B.V</general><general>Elsevier</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><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>1XC</scope><scope>VOOES</scope></search><sort><creationdate>20160710</creationdate><title>Time-programmed release of fluoroscein isocyanate dextran from micro-pattern-designed polymer scrolls</title><author>Egunov, Aleksandr I. ; Inaba, Ayano ; Gree, Simon ; Malval, Jean-Pierre ; Tamura, Katsuhiro ; Saito, Yukie ; Luchnikov, Valeriy A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c479t-ac5e5fbb945e13cca3370994fb44103e6d5593bc520aa5d4ef6e2e3cf09a67c93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Acetates - chemistry</topic><topic>ATR FTIR spectroscopy</topic><topic>Chemical Sciences</topic><topic>Chitosan</topic><topic>Chitosan - chemistry</topic><topic>Chronopharmacology</topic><topic>Controlled release</topic><topic>Delayed-Action Preparations - chemistry</topic><topic>Dextrans - chemistry</topic><topic>Drug Delivery Systems</topic><topic>Drug Liberation</topic><topic>Fluorescein-5-isothiocyanate - analogs & derivatives</topic><topic>Fluorescein-5-isothiocyanate - chemistry</topic><topic>Fluorescent Dyes - chemistry</topic><topic>Fluoroscein isocyanate dextran</topic><topic>Kinetics</topic><topic>Macromolecule</topic><topic>Medicinal Chemistry</topic><topic>Model drug</topic><topic>Models, Theoretical</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Egunov, Aleksandr I.</creatorcontrib><creatorcontrib>Inaba, Ayano</creatorcontrib><creatorcontrib>Gree, Simon</creatorcontrib><creatorcontrib>Malval, Jean-Pierre</creatorcontrib><creatorcontrib>Tamura, Katsuhiro</creatorcontrib><creatorcontrib>Saito, Yukie</creatorcontrib><creatorcontrib>Luchnikov, Valeriy A.</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><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>Journal of controlled release</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Egunov, Aleksandr I.</au><au>Inaba, Ayano</au><au>Gree, Simon</au><au>Malval, Jean-Pierre</au><au>Tamura, Katsuhiro</au><au>Saito, Yukie</au><au>Luchnikov, Valeriy A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Time-programmed release of fluoroscein isocyanate dextran from micro-pattern-designed polymer scrolls</atitle><jtitle>Journal of controlled release</jtitle><addtitle>J Control Release</addtitle><date>2016-07-10</date><risdate>2016</risdate><volume>233</volume><spage>39</spage><epage>47</epage><pages>39-47</pages><issn>0168-3659</issn><eissn>1873-4995</eissn><abstract>In this article we present a relevant strategy for a non-trivial time-programmed release of water-soluble macromolecules from biocompatible μ-containers. The system is based on self-scrolled chitosan acetate (CA) fibers, encapsulated in a poly(dimethylsiloxane) matrix. Mass transfer between a fiber and the external environment takes place via the only opened extremity of the fiber. Fluoroscein isocyanate dextran (FID) is initially deposited at the inner surface of the CA fiber according to a programmed pattern. The FID molecules became mobile after the arriving of the swelling front, which propagates along the fiber's axis upon the immersion of the system in aqueous solution. Diffusion of the macromolecules into the environment is enabled by the open-tube geometry of the swollen part of the fiber, while a programmed kinetics of the drug release is due to patterning of the polymer film prior to rolling. The release of the macromolecules can be retarded by a few hours according to the placement of the FID spot with respect to the fibers orifice. A pulsatile release kinetics is demonstrated for a discrete pattern. A few millimeter spacing of the FID spots results in a few hours time interval between the release impulses. Random walk model is plugged in the effective diffusion coefficient for Fick's law and the release kinetics are simulated.
Programmable release kinetics of a fluorescein isocyanate dextran (FID) is achieved via its nonuniform distribution in a biopolymer self-rolled fiber, and directional swelling of the fiber. [Display omitted]</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>27179634</pmid><doi>10.1016/j.jconrel.2016.05.022</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Acetates - chemistry ATR FTIR spectroscopy Chemical Sciences Chitosan Chitosan - chemistry Chronopharmacology Controlled release Delayed-Action Preparations - chemistry Dextrans - chemistry Drug Delivery Systems Drug Liberation Fluorescein-5-isothiocyanate - analogs & derivatives Fluorescein-5-isothiocyanate - chemistry Fluorescent Dyes - chemistry Fluoroscein isocyanate dextran Kinetics Macromolecule Medicinal Chemistry Model drug Models, Theoretical |
title | Time-programmed release of fluoroscein isocyanate dextran from micro-pattern-designed polymer scrolls |
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