Fabrication and bioevaluation of a medicated electrospun mat based on azido-cellulose acetate via click chemistry
Cellulose acetate (CA) electrospun fibers have been used in different medical applications such as drug delivery systems to release various drugs. CA, usually available with a typical degree of substitution (DS) of 2.4–2.5, shows little control over the release rate of the incorporated substances, d...
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Veröffentlicht in: | Cellulose (London) 2019-12, Vol.26 (18), p.9721-9736 |
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description | Cellulose acetate (CA) electrospun fibers have been used in different medical applications such as drug delivery systems to release various drugs. CA, usually available with a typical degree of substitution (DS) of 2.4–2.5, shows little control over the release rate of the incorporated substances, due to the lack of active functional groups. In this work, click chemistry was used to activate CA and produce crosslinked electrospun mats to provide sustained release for topical administration. CA was activated by introducing azide functional groups on the residual hydroxyl groups of the polymer chains with a DS
Azido
of 0.24 by a coupling reaction. Azido-CA was then electrospun to produce nanofibers, in which capsaicin and sodium diclofenac, as pain-relieving drugs were encapsulated. Propargylated maltose was synthesized as a crosslinker to the Azido-CA via triazole chemistry. Spectral analysis was used to confirm the chemical structure of the new derivatives and the click-matrices. SEM morphological analysis of the Azido-CA electrospun fibers showed a range of diameters from 140 to 270 nm, with clear, smooth surfaces. Samples of the matrices were assessed for cytotoxicity and showed an acceptable cell viability. In a rat model, sodium diclofenac and capsaicin-loaded electrospun mats of Azido-CA showed superior closure rates over the untreated rats and those treated with a commercial cream. Rats treated with electrospun mat of CA, Azido-CA loaded with drugs showed normal intact histological structure of the epidermis and dermis. |
doi_str_mv | 10.1007/s10570-019-02739-9 |
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Azido
of 0.24 by a coupling reaction. Azido-CA was then electrospun to produce nanofibers, in which capsaicin and sodium diclofenac, as pain-relieving drugs were encapsulated. Propargylated maltose was synthesized as a crosslinker to the Azido-CA via triazole chemistry. Spectral analysis was used to confirm the chemical structure of the new derivatives and the click-matrices. SEM morphological analysis of the Azido-CA electrospun fibers showed a range of diameters from 140 to 270 nm, with clear, smooth surfaces. Samples of the matrices were assessed for cytotoxicity and showed an acceptable cell viability. In a rat model, sodium diclofenac and capsaicin-loaded electrospun mats of Azido-CA showed superior closure rates over the untreated rats and those treated with a commercial cream. Rats treated with electrospun mat of CA, Azido-CA loaded with drugs showed normal intact histological structure of the epidermis and dermis.</description><identifier>ISSN: 0969-0239</identifier><identifier>EISSN: 1572-882X</identifier><identifier>DOI: 10.1007/s10570-019-02739-9</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Bioorganic Chemistry ; Cellulose acetate ; Cellulose fibers ; Ceramics ; Chemical synthesis ; Chemistry ; Chemistry and Materials Science ; Composites ; Crosslinking ; Diclofenac ; Drug delivery systems ; Electrospinning ; Epidermis ; Functional groups ; Glass ; Hydroxyl groups ; Maltose ; Mats ; Nanofibers ; Natural Materials ; Nonsteroidal anti-inflammatory drugs ; Organic Chemistry ; Original Research ; Physical Chemistry ; Polymer Sciences ; Spectrum analysis ; Substitution reactions ; Sustainable Development ; Sustained release ; Toxicity ; Triazoles</subject><ispartof>Cellulose (London), 2019-12, Vol.26 (18), p.9721-9736</ispartof><rights>Springer Nature B.V. 2019</rights><rights>Cellulose is a copyright of Springer, (2019). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c356t-9d210c889c47b4450320cbf220e9068d09637f352ea756410580c2f6dc1ea8473</citedby><cites>FETCH-LOGICAL-c356t-9d210c889c47b4450320cbf220e9068d09637f352ea756410580c2f6dc1ea8473</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10570-019-02739-9$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10570-019-02739-9$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>315,781,785,27929,27930,41493,42562,51324</link.rule.ids></links><search><creatorcontrib>Nada, Ahmed A.</creatorcontrib><creatorcontrib>Abdellatif, Faten Hassan Hassan</creatorcontrib><creatorcontrib>Soliman, Ahmed A. F.</creatorcontrib><creatorcontrib>Shen, Jialong</creatorcontrib><creatorcontrib>Hudson, Samuel M.</creatorcontrib><creatorcontrib>Abou-Zeid, Nabil Y.</creatorcontrib><title>Fabrication and bioevaluation of a medicated electrospun mat based on azido-cellulose acetate via click chemistry</title><title>Cellulose (London)</title><addtitle>Cellulose</addtitle><description>Cellulose acetate (CA) electrospun fibers have been used in different medical applications such as drug delivery systems to release various drugs. CA, usually available with a typical degree of substitution (DS) of 2.4–2.5, shows little control over the release rate of the incorporated substances, due to the lack of active functional groups. In this work, click chemistry was used to activate CA and produce crosslinked electrospun mats to provide sustained release for topical administration. CA was activated by introducing azide functional groups on the residual hydroxyl groups of the polymer chains with a DS
Azido
of 0.24 by a coupling reaction. Azido-CA was then electrospun to produce nanofibers, in which capsaicin and sodium diclofenac, as pain-relieving drugs were encapsulated. Propargylated maltose was synthesized as a crosslinker to the Azido-CA via triazole chemistry. Spectral analysis was used to confirm the chemical structure of the new derivatives and the click-matrices. SEM morphological analysis of the Azido-CA electrospun fibers showed a range of diameters from 140 to 270 nm, with clear, smooth surfaces. Samples of the matrices were assessed for cytotoxicity and showed an acceptable cell viability. In a rat model, sodium diclofenac and capsaicin-loaded electrospun mats of Azido-CA showed superior closure rates over the untreated rats and those treated with a commercial cream. Rats treated with electrospun mat of CA, Azido-CA loaded with drugs showed normal intact histological structure of the epidermis and dermis.</description><subject>Bioorganic Chemistry</subject><subject>Cellulose acetate</subject><subject>Cellulose fibers</subject><subject>Ceramics</subject><subject>Chemical synthesis</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Composites</subject><subject>Crosslinking</subject><subject>Diclofenac</subject><subject>Drug delivery systems</subject><subject>Electrospinning</subject><subject>Epidermis</subject><subject>Functional groups</subject><subject>Glass</subject><subject>Hydroxyl groups</subject><subject>Maltose</subject><subject>Mats</subject><subject>Nanofibers</subject><subject>Natural Materials</subject><subject>Nonsteroidal anti-inflammatory drugs</subject><subject>Organic Chemistry</subject><subject>Original Research</subject><subject>Physical Chemistry</subject><subject>Polymer Sciences</subject><subject>Spectrum analysis</subject><subject>Substitution reactions</subject><subject>Sustainable Development</subject><subject>Sustained release</subject><subject>Toxicity</subject><subject>Triazoles</subject><issn>0969-0239</issn><issn>1572-882X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNp9kE9LxDAQxYMouK5-AU8Bz9FJ0jbJURZXhQUvCt5CmqaatX92k3ZBP72pFbx5GnjzfjO8h9AlhWsKIG4ihVwAAaoIMMEVUUdoQXPBiJTs9RgtQBXTiqtTdBbjFgCUYHSB9mtTBm_N4PsOm67Cpe_dwTTjrPQ1Nrh11eRwFXaNs0Po427scGsGXJqY1In88lVPrGuasemjw8a6IRH44A22jbcf2L671schfJ6jk9o00V38ziV6Wd89rx7I5un-cXW7IZbnxUBUxShYKZXNRJllOXAGtqwZA6egkFUKxEXNc-aMyIss5ZdgWV1UljojM8GX6Gq-uwv9fnRx0Nt-DF16qRmTSoqc8SK52OyyKVYMrta74FsTPjUFPVWr52p1qlb_VKtVgvgMxWTu3lz4O_0P9Q0mPnyw</recordid><startdate>20191201</startdate><enddate>20191201</enddate><creator>Nada, Ahmed A.</creator><creator>Abdellatif, Faten Hassan Hassan</creator><creator>Soliman, Ahmed A. F.</creator><creator>Shen, Jialong</creator><creator>Hudson, Samuel M.</creator><creator>Abou-Zeid, Nabil Y.</creator><general>Springer Netherlands</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>HCIFZ</scope><scope>KB.</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20191201</creationdate><title>Fabrication and bioevaluation of a medicated electrospun mat based on azido-cellulose acetate via click chemistry</title><author>Nada, Ahmed A. ; Abdellatif, Faten Hassan Hassan ; Soliman, Ahmed A. F. ; Shen, Jialong ; Hudson, Samuel M. ; Abou-Zeid, Nabil Y.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c356t-9d210c889c47b4450320cbf220e9068d09637f352ea756410580c2f6dc1ea8473</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Bioorganic Chemistry</topic><topic>Cellulose acetate</topic><topic>Cellulose fibers</topic><topic>Ceramics</topic><topic>Chemical synthesis</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Composites</topic><topic>Crosslinking</topic><topic>Diclofenac</topic><topic>Drug delivery systems</topic><topic>Electrospinning</topic><topic>Epidermis</topic><topic>Functional groups</topic><topic>Glass</topic><topic>Hydroxyl groups</topic><topic>Maltose</topic><topic>Mats</topic><topic>Nanofibers</topic><topic>Natural Materials</topic><topic>Nonsteroidal anti-inflammatory drugs</topic><topic>Organic Chemistry</topic><topic>Original Research</topic><topic>Physical Chemistry</topic><topic>Polymer Sciences</topic><topic>Spectrum analysis</topic><topic>Substitution reactions</topic><topic>Sustainable Development</topic><topic>Sustained release</topic><topic>Toxicity</topic><topic>Triazoles</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nada, Ahmed A.</creatorcontrib><creatorcontrib>Abdellatif, Faten Hassan Hassan</creatorcontrib><creatorcontrib>Soliman, Ahmed A. F.</creatorcontrib><creatorcontrib>Shen, Jialong</creatorcontrib><creatorcontrib>Hudson, Samuel M.</creatorcontrib><creatorcontrib>Abou-Zeid, Nabil Y.</creatorcontrib><collection>CrossRef</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>Technology Collection (ProQuest)</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>SciTech Premium Collection</collection><collection>Materials Science Database</collection><collection>Materials Science Collection</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>Cellulose (London)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nada, Ahmed A.</au><au>Abdellatif, Faten Hassan Hassan</au><au>Soliman, Ahmed A. F.</au><au>Shen, Jialong</au><au>Hudson, Samuel M.</au><au>Abou-Zeid, Nabil Y.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fabrication and bioevaluation of a medicated electrospun mat based on azido-cellulose acetate via click chemistry</atitle><jtitle>Cellulose (London)</jtitle><stitle>Cellulose</stitle><date>2019-12-01</date><risdate>2019</risdate><volume>26</volume><issue>18</issue><spage>9721</spage><epage>9736</epage><pages>9721-9736</pages><issn>0969-0239</issn><eissn>1572-882X</eissn><abstract>Cellulose acetate (CA) electrospun fibers have been used in different medical applications such as drug delivery systems to release various drugs. CA, usually available with a typical degree of substitution (DS) of 2.4–2.5, shows little control over the release rate of the incorporated substances, due to the lack of active functional groups. In this work, click chemistry was used to activate CA and produce crosslinked electrospun mats to provide sustained release for topical administration. CA was activated by introducing azide functional groups on the residual hydroxyl groups of the polymer chains with a DS
Azido
of 0.24 by a coupling reaction. Azido-CA was then electrospun to produce nanofibers, in which capsaicin and sodium diclofenac, as pain-relieving drugs were encapsulated. Propargylated maltose was synthesized as a crosslinker to the Azido-CA via triazole chemistry. Spectral analysis was used to confirm the chemical structure of the new derivatives and the click-matrices. SEM morphological analysis of the Azido-CA electrospun fibers showed a range of diameters from 140 to 270 nm, with clear, smooth surfaces. Samples of the matrices were assessed for cytotoxicity and showed an acceptable cell viability. In a rat model, sodium diclofenac and capsaicin-loaded electrospun mats of Azido-CA showed superior closure rates over the untreated rats and those treated with a commercial cream. Rats treated with electrospun mat of CA, Azido-CA loaded with drugs showed normal intact histological structure of the epidermis and dermis.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><doi>10.1007/s10570-019-02739-9</doi><tpages>16</tpages></addata></record> |
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subjects | Bioorganic Chemistry Cellulose acetate Cellulose fibers Ceramics Chemical synthesis Chemistry Chemistry and Materials Science Composites Crosslinking Diclofenac Drug delivery systems Electrospinning Epidermis Functional groups Glass Hydroxyl groups Maltose Mats Nanofibers Natural Materials Nonsteroidal anti-inflammatory drugs Organic Chemistry Original Research Physical Chemistry Polymer Sciences Spectrum analysis Substitution reactions Sustainable Development Sustained release Toxicity Triazoles |
title | Fabrication and bioevaluation of a medicated electrospun mat based on azido-cellulose acetate via click chemistry |
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