Optimization, synthesis, and characterization of coaxial electrospun sodium carboxymethyl cellulose-graft-methyl acrylate/poly(ethylene oxide) nanofibers for potential drug-delivery applications

•Nanofibers for drug delivery were synthesized using thermoplastic carboxymethyl cellulose.•Nanofiber mats were fabricated via coaxial electrospinning.•The in vitro sustained drug release of the anti-infection drugs has been investigated.•Drug loaded nanofibers were effective against S. aureus and E...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Carbohydrate polymers 2017-10, Vol.173, p.645-653
Hauptverfasser: Esmaeili, Akbar, Haseli, Mahsa
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 653
container_issue
container_start_page 645
container_title Carbohydrate polymers
container_volume 173
creator Esmaeili, Akbar
Haseli, Mahsa
description •Nanofibers for drug delivery were synthesized using thermoplastic carboxymethyl cellulose.•Nanofiber mats were fabricated via coaxial electrospinning.•The in vitro sustained drug release of the anti-infection drugs has been investigated.•Drug loaded nanofibers were effective against S. aureus and E. coli bacteria.•The nanofibers were non-toxic. In this study, nanofiber drug carriers were fabricated via coaxial electrospinning, using a new, degradable core–shell nanofiber drug carrier fabricated via coaxial electrospinning. Fabrication of the shell was carried out by graft polymerization of sodium carboxymethyl cellulose (NaCMC) with methyl acrylate (TCMC) and poly(ethylene oxide) (PEO). Tetracycline hydrochloride (TCH) was used as a drug model incorporated within the nanofibers as the core, and their performance as a drug carrier scaffold was evaluated. The loading of TCH within PEO nanofibers and the loading of TCH within the TCMC nanofibers were characterized via different techniques. The structure morphology of the obtained nanofibers was viewed under scanning electron microscope (SEM). The changes in the polymer structure before and after grafting and confirmation of incorporation of the drug in the fibers were characterized by Fourier transform infrared spectroscopy (FT-IR). Response surface methodology (RSM) was applied to predict the optimum conditions for fabrication of the nanofibers. The cell viability of the optimized samples was assessed with 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. The TCH loaded into the optimized core–shell sample of TCMC 3% (w/v)/PEO 1% (w/v) had a smooth and beadless morphology with a diameter of 86.12nm, slow and sustained drug release, and excellent bactericidal activity against a wide range of bacteria. This shows promise for use as an antibacterial material in such applications as tissue engineering and pharmaceutical science.
doi_str_mv 10.1016/j.carbpol.2017.06.037
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1922508443</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0144861717306744</els_id><sourcerecordid>1922508443</sourcerecordid><originalsourceid>FETCH-LOGICAL-c365t-8361d41ff0779c85f2b893b58053aa33e313ac2f31c026c3a5d3087f2513f1383</originalsourceid><addsrcrecordid>eNqFkc1u1TAQhS0EopfCI4C8LFJza8f5cVYIVfxJlbqBteXY415fOXawneqGx-PJSHoDW2ZjaXRmzhl_CL2lZE8JbW6OeyVjPwa3Lwlt96TZE9Y-QzvK266grKqeox2hVVXwhrYX6FVKR7JUQ8lLdFHylpUd6Xbo9_2Y7WB_yWyDv8Zp9vkAyaZrLL3G6iCjVBniJsDBYBXkyUqHwYHKMaRx8jgFbacBr4nCaR4gH2aHFTg3uZCgeIjS5GJrSxVnJzPcLNnnq6ceeMDhZDW8x176YGwPMWETIh5DBp9XOx2nh0KDs48QZyzH0Vn1lCm9Ri-MdAnebO8l-vH50_fbr8Xd_Zdvtx_vCsWaOhecNVRX1BjStp3itSl73rG-5qRmUjIGjDKpSsOoImWjmKw1I7w1ZU2ZoYyzS3R13jvG8HOClMVg03qk9BCmJGhXljXhVcUWaX2WquWDUgQjxmgHGWdBiVjxiaPY8IkVnyCNWPAtc-82i6kfQP-b-strEXw4C2A59NFCFElZ8Aq0jQsOoYP9j8UfKxG1AA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1922508443</pqid></control><display><type>article</type><title>Optimization, synthesis, and characterization of coaxial electrospun sodium carboxymethyl cellulose-graft-methyl acrylate/poly(ethylene oxide) nanofibers for potential drug-delivery applications</title><source>Access via ScienceDirect (Elsevier)</source><creator>Esmaeili, Akbar ; Haseli, Mahsa</creator><creatorcontrib>Esmaeili, Akbar ; Haseli, Mahsa</creatorcontrib><description>•Nanofibers for drug delivery were synthesized using thermoplastic carboxymethyl cellulose.•Nanofiber mats were fabricated via coaxial electrospinning.•The in vitro sustained drug release of the anti-infection drugs has been investigated.•Drug loaded nanofibers were effective against S. aureus and E. coli bacteria.•The nanofibers were non-toxic. In this study, nanofiber drug carriers were fabricated via coaxial electrospinning, using a new, degradable core–shell nanofiber drug carrier fabricated via coaxial electrospinning. Fabrication of the shell was carried out by graft polymerization of sodium carboxymethyl cellulose (NaCMC) with methyl acrylate (TCMC) and poly(ethylene oxide) (PEO). Tetracycline hydrochloride (TCH) was used as a drug model incorporated within the nanofibers as the core, and their performance as a drug carrier scaffold was evaluated. The loading of TCH within PEO nanofibers and the loading of TCH within the TCMC nanofibers were characterized via different techniques. The structure morphology of the obtained nanofibers was viewed under scanning electron microscope (SEM). The changes in the polymer structure before and after grafting and confirmation of incorporation of the drug in the fibers were characterized by Fourier transform infrared spectroscopy (FT-IR). Response surface methodology (RSM) was applied to predict the optimum conditions for fabrication of the nanofibers. The cell viability of the optimized samples was assessed with 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. The TCH loaded into the optimized core–shell sample of TCMC 3% (w/v)/PEO 1% (w/v) had a smooth and beadless morphology with a diameter of 86.12nm, slow and sustained drug release, and excellent bactericidal activity against a wide range of bacteria. This shows promise for use as an antibacterial material in such applications as tissue engineering and pharmaceutical science.</description><identifier>ISSN: 0144-8617</identifier><identifier>EISSN: 1879-1344</identifier><identifier>DOI: 10.1016/j.carbpol.2017.06.037</identifier><identifier>PMID: 28732909</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Coaxial electrospinning ; Drug release ; Poly(ethylene oxide) ; Sodium carboxymethyl cellulose ; Tetracycline hydrochloride</subject><ispartof>Carbohydrate polymers, 2017-10, Vol.173, p.645-653</ispartof><rights>2017 Elsevier Ltd</rights><rights>Copyright © 2017 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c365t-8361d41ff0779c85f2b893b58053aa33e313ac2f31c026c3a5d3087f2513f1383</citedby><cites>FETCH-LOGICAL-c365t-8361d41ff0779c85f2b893b58053aa33e313ac2f31c026c3a5d3087f2513f1383</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.carbpol.2017.06.037$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,782,786,3552,27931,27932,46002</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28732909$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Esmaeili, Akbar</creatorcontrib><creatorcontrib>Haseli, Mahsa</creatorcontrib><title>Optimization, synthesis, and characterization of coaxial electrospun sodium carboxymethyl cellulose-graft-methyl acrylate/poly(ethylene oxide) nanofibers for potential drug-delivery applications</title><title>Carbohydrate polymers</title><addtitle>Carbohydr Polym</addtitle><description>•Nanofibers for drug delivery were synthesized using thermoplastic carboxymethyl cellulose.•Nanofiber mats were fabricated via coaxial electrospinning.•The in vitro sustained drug release of the anti-infection drugs has been investigated.•Drug loaded nanofibers were effective against S. aureus and E. coli bacteria.•The nanofibers were non-toxic. In this study, nanofiber drug carriers were fabricated via coaxial electrospinning, using a new, degradable core–shell nanofiber drug carrier fabricated via coaxial electrospinning. Fabrication of the shell was carried out by graft polymerization of sodium carboxymethyl cellulose (NaCMC) with methyl acrylate (TCMC) and poly(ethylene oxide) (PEO). Tetracycline hydrochloride (TCH) was used as a drug model incorporated within the nanofibers as the core, and their performance as a drug carrier scaffold was evaluated. The loading of TCH within PEO nanofibers and the loading of TCH within the TCMC nanofibers were characterized via different techniques. The structure morphology of the obtained nanofibers was viewed under scanning electron microscope (SEM). The changes in the polymer structure before and after grafting and confirmation of incorporation of the drug in the fibers were characterized by Fourier transform infrared spectroscopy (FT-IR). Response surface methodology (RSM) was applied to predict the optimum conditions for fabrication of the nanofibers. The cell viability of the optimized samples was assessed with 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. The TCH loaded into the optimized core–shell sample of TCMC 3% (w/v)/PEO 1% (w/v) had a smooth and beadless morphology with a diameter of 86.12nm, slow and sustained drug release, and excellent bactericidal activity against a wide range of bacteria. This shows promise for use as an antibacterial material in such applications as tissue engineering and pharmaceutical science.</description><subject>Coaxial electrospinning</subject><subject>Drug release</subject><subject>Poly(ethylene oxide)</subject><subject>Sodium carboxymethyl cellulose</subject><subject>Tetracycline hydrochloride</subject><issn>0144-8617</issn><issn>1879-1344</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNqFkc1u1TAQhS0EopfCI4C8LFJza8f5cVYIVfxJlbqBteXY415fOXawneqGx-PJSHoDW2ZjaXRmzhl_CL2lZE8JbW6OeyVjPwa3Lwlt96TZE9Y-QzvK266grKqeox2hVVXwhrYX6FVKR7JUQ8lLdFHylpUd6Xbo9_2Y7WB_yWyDv8Zp9vkAyaZrLL3G6iCjVBniJsDBYBXkyUqHwYHKMaRx8jgFbacBr4nCaR4gH2aHFTg3uZCgeIjS5GJrSxVnJzPcLNnnq6ceeMDhZDW8x176YGwPMWETIh5DBp9XOx2nh0KDs48QZyzH0Vn1lCm9Ri-MdAnebO8l-vH50_fbr8Xd_Zdvtx_vCsWaOhecNVRX1BjStp3itSl73rG-5qRmUjIGjDKpSsOoImWjmKw1I7w1ZU2ZoYyzS3R13jvG8HOClMVg03qk9BCmJGhXljXhVcUWaX2WquWDUgQjxmgHGWdBiVjxiaPY8IkVnyCNWPAtc-82i6kfQP-b-strEXw4C2A59NFCFElZ8Aq0jQsOoYP9j8UfKxG1AA</recordid><startdate>20171001</startdate><enddate>20171001</enddate><creator>Esmaeili, Akbar</creator><creator>Haseli, Mahsa</creator><general>Elsevier Ltd</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20171001</creationdate><title>Optimization, synthesis, and characterization of coaxial electrospun sodium carboxymethyl cellulose-graft-methyl acrylate/poly(ethylene oxide) nanofibers for potential drug-delivery applications</title><author>Esmaeili, Akbar ; Haseli, Mahsa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c365t-8361d41ff0779c85f2b893b58053aa33e313ac2f31c026c3a5d3087f2513f1383</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Coaxial electrospinning</topic><topic>Drug release</topic><topic>Poly(ethylene oxide)</topic><topic>Sodium carboxymethyl cellulose</topic><topic>Tetracycline hydrochloride</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Esmaeili, Akbar</creatorcontrib><creatorcontrib>Haseli, Mahsa</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Carbohydrate polymers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Esmaeili, Akbar</au><au>Haseli, Mahsa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Optimization, synthesis, and characterization of coaxial electrospun sodium carboxymethyl cellulose-graft-methyl acrylate/poly(ethylene oxide) nanofibers for potential drug-delivery applications</atitle><jtitle>Carbohydrate polymers</jtitle><addtitle>Carbohydr Polym</addtitle><date>2017-10-01</date><risdate>2017</risdate><volume>173</volume><spage>645</spage><epage>653</epage><pages>645-653</pages><issn>0144-8617</issn><eissn>1879-1344</eissn><abstract>•Nanofibers for drug delivery were synthesized using thermoplastic carboxymethyl cellulose.•Nanofiber mats were fabricated via coaxial electrospinning.•The in vitro sustained drug release of the anti-infection drugs has been investigated.•Drug loaded nanofibers were effective against S. aureus and E. coli bacteria.•The nanofibers were non-toxic. In this study, nanofiber drug carriers were fabricated via coaxial electrospinning, using a new, degradable core–shell nanofiber drug carrier fabricated via coaxial electrospinning. Fabrication of the shell was carried out by graft polymerization of sodium carboxymethyl cellulose (NaCMC) with methyl acrylate (TCMC) and poly(ethylene oxide) (PEO). Tetracycline hydrochloride (TCH) was used as a drug model incorporated within the nanofibers as the core, and their performance as a drug carrier scaffold was evaluated. The loading of TCH within PEO nanofibers and the loading of TCH within the TCMC nanofibers were characterized via different techniques. The structure morphology of the obtained nanofibers was viewed under scanning electron microscope (SEM). The changes in the polymer structure before and after grafting and confirmation of incorporation of the drug in the fibers were characterized by Fourier transform infrared spectroscopy (FT-IR). Response surface methodology (RSM) was applied to predict the optimum conditions for fabrication of the nanofibers. The cell viability of the optimized samples was assessed with 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. The TCH loaded into the optimized core–shell sample of TCMC 3% (w/v)/PEO 1% (w/v) had a smooth and beadless morphology with a diameter of 86.12nm, slow and sustained drug release, and excellent bactericidal activity against a wide range of bacteria. This shows promise for use as an antibacterial material in such applications as tissue engineering and pharmaceutical science.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>28732909</pmid><doi>10.1016/j.carbpol.2017.06.037</doi><tpages>9</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0144-8617
ispartof Carbohydrate polymers, 2017-10, Vol.173, p.645-653
issn 0144-8617
1879-1344
language eng
recordid cdi_proquest_miscellaneous_1922508443
source Access via ScienceDirect (Elsevier)
subjects Coaxial electrospinning
Drug release
Poly(ethylene oxide)
Sodium carboxymethyl cellulose
Tetracycline hydrochloride
title Optimization, synthesis, and characterization of coaxial electrospun sodium carboxymethyl cellulose-graft-methyl acrylate/poly(ethylene oxide) nanofibers for potential drug-delivery applications
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-07T15%3A53%3A00IST&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=Optimization,%20synthesis,%20and%20characterization%20of%20coaxial%20electrospun%20sodium%20carboxymethyl%20cellulose-graft-methyl%20acrylate/poly(ethylene%20oxide)%20nanofibers%20for%20potential%20drug-delivery%20applications&rft.jtitle=Carbohydrate%20polymers&rft.au=Esmaeili,%20Akbar&rft.date=2017-10-01&rft.volume=173&rft.spage=645&rft.epage=653&rft.pages=645-653&rft.issn=0144-8617&rft.eissn=1879-1344&rft_id=info:doi/10.1016/j.carbpol.2017.06.037&rft_dat=%3Cproquest_cross%3E1922508443%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=1922508443&rft_id=info:pmid/28732909&rft_els_id=S0144861717306744&rfr_iscdi=true