Fabrication of PLA/PEG/MWCNT electrospun nanofibrous scaffolds for anticancer drug delivery
ABSTRACT In the present study, polylactic acid (PLA)/polyethylene glycol (PEG)/multiwalled carbon nanotube (MWCNT) electrospun nanofibrous scaffolds were prepared via electrospinning process and their applications for the anticancer drug delivery system were investigated. A response surface methodol...
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description | ABSTRACT
In the present study, polylactic acid (PLA)/polyethylene glycol (PEG)/multiwalled carbon nanotube (MWCNT) electrospun nanofibrous scaffolds were prepared via electrospinning process and their applications for the anticancer drug delivery system were investigated. A response surface methodology based on Box–Behnken design (BBD) was used to evaluate the effect of key parameters of electrospinning process including solution concentration, feeding rate, tip–collector distance (TCD) and applied voltage on the morphology of PLA/PEG/MWCNT nanofibrous scaffolds. In optimum conditions (concentration of 8.15%, feeding rate of 0.2 mL/h, voltage of 18.50 kV and TCD of 13.0 cm), the minimum experimental fiber diameter was found to be 225 nm which was in good agreement with the predicted value by the BBD analysis (228 nm). In vitro drug release study of doxorubicin (DOX)‐loaded nanofibrous scaffolds, higher drug content induced an extended release of drug. Also, drug release rate was not dependent on drug/polymer ratio in different electrospun nanofibrous formulations. The equation of Mt = c0 + kt0.5was used to describe the kinetic data of DOX release from electrospun nanofibers. The cell viability of DOX‐loaded nanofibrous scaffolds was evaluated using 3‐(4,5‐dimethylthiazol‐2‐yl)‐2,5‐diphenyltetrazolium bromide, a tetrazole assay on lung cancer A549 cell lines. We propose that DOX‐incorporated PLA/PEG/MWCNT nanofibrous scaffold could be used as a superior candidate for antitumor drug delivery. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015, 132, 41286. |
doi_str_mv | 10.1002/app.41286 |
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In the present study, polylactic acid (PLA)/polyethylene glycol (PEG)/multiwalled carbon nanotube (MWCNT) electrospun nanofibrous scaffolds were prepared via electrospinning process and their applications for the anticancer drug delivery system were investigated. A response surface methodology based on Box–Behnken design (BBD) was used to evaluate the effect of key parameters of electrospinning process including solution concentration, feeding rate, tip–collector distance (TCD) and applied voltage on the morphology of PLA/PEG/MWCNT nanofibrous scaffolds. In optimum conditions (concentration of 8.15%, feeding rate of 0.2 mL/h, voltage of 18.50 kV and TCD of 13.0 cm), the minimum experimental fiber diameter was found to be 225 nm which was in good agreement with the predicted value by the BBD analysis (228 nm). In vitro drug release study of doxorubicin (DOX)‐loaded nanofibrous scaffolds, higher drug content induced an extended release of drug. Also, drug release rate was not dependent on drug/polymer ratio in different electrospun nanofibrous formulations. The equation of Mt = c0 + kt0.5was used to describe the kinetic data of DOX release from electrospun nanofibers. The cell viability of DOX‐loaded nanofibrous scaffolds was evaluated using 3‐(4,5‐dimethylthiazol‐2‐yl)‐2,5‐diphenyltetrazolium bromide, a tetrazole assay on lung cancer A549 cell lines. We propose that DOX‐incorporated PLA/PEG/MWCNT nanofibrous scaffold could be used as a superior candidate for antitumor drug delivery. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015, 132, 41286.</description><identifier>ISSN: 0021-8995</identifier><identifier>EISSN: 1097-4628</identifier><identifier>DOI: 10.1002/app.41286</identifier><identifier>CODEN: JAPNAB</identifier><language>eng</language><publisher>Hoboken: Blackwell Publishing Ltd</publisher><subject>Drug delivery systems ; Drugs ; Electric potential ; Electrospinning ; fibers ; Materials science ; Mathematical analysis ; Nanostructure ; Polyethylene glycol ; Polymers ; Scaffolds ; Voltage</subject><ispartof>Journal of applied polymer science, 2015-01, Vol.132 (3), p.n/a</ispartof><rights>2014 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5706-449902e06f84960d9ad87f2c79fea67e7cd6e475cc2122d21488bf1a99726fc03</citedby><cites>FETCH-LOGICAL-c5706-449902e06f84960d9ad87f2c79fea67e7cd6e475cc2122d21488bf1a99726fc03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fapp.41286$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fapp.41286$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids></links><search><creatorcontrib>Aboutalebi Anaraki, Nadia</creatorcontrib><creatorcontrib>Roshanfekr Rad, Leila</creatorcontrib><creatorcontrib>Irani, Mohammad</creatorcontrib><creatorcontrib>Haririan, Ismaeil</creatorcontrib><title>Fabrication of PLA/PEG/MWCNT electrospun nanofibrous scaffolds for anticancer drug delivery</title><title>Journal of applied polymer science</title><addtitle>J. Appl. Polym. Sci</addtitle><description>ABSTRACT
In the present study, polylactic acid (PLA)/polyethylene glycol (PEG)/multiwalled carbon nanotube (MWCNT) electrospun nanofibrous scaffolds were prepared via electrospinning process and their applications for the anticancer drug delivery system were investigated. A response surface methodology based on Box–Behnken design (BBD) was used to evaluate the effect of key parameters of electrospinning process including solution concentration, feeding rate, tip–collector distance (TCD) and applied voltage on the morphology of PLA/PEG/MWCNT nanofibrous scaffolds. In optimum conditions (concentration of 8.15%, feeding rate of 0.2 mL/h, voltage of 18.50 kV and TCD of 13.0 cm), the minimum experimental fiber diameter was found to be 225 nm which was in good agreement with the predicted value by the BBD analysis (228 nm). In vitro drug release study of doxorubicin (DOX)‐loaded nanofibrous scaffolds, higher drug content induced an extended release of drug. Also, drug release rate was not dependent on drug/polymer ratio in different electrospun nanofibrous formulations. The equation of Mt = c0 + kt0.5was used to describe the kinetic data of DOX release from electrospun nanofibers. The cell viability of DOX‐loaded nanofibrous scaffolds was evaluated using 3‐(4,5‐dimethylthiazol‐2‐yl)‐2,5‐diphenyltetrazolium bromide, a tetrazole assay on lung cancer A549 cell lines. We propose that DOX‐incorporated PLA/PEG/MWCNT nanofibrous scaffold could be used as a superior candidate for antitumor drug delivery. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015, 132, 41286.</description><subject>Drug delivery systems</subject><subject>Drugs</subject><subject>Electric potential</subject><subject>Electrospinning</subject><subject>fibers</subject><subject>Materials science</subject><subject>Mathematical analysis</subject><subject>Nanostructure</subject><subject>Polyethylene glycol</subject><subject>Polymers</subject><subject>Scaffolds</subject><subject>Voltage</subject><issn>0021-8995</issn><issn>1097-4628</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNqN0U9P2zAYBnBrYtJKt8O-gSUucEhjO47_HKuKlk0dRFoZhx0s17GnQIiDnbD12-NR4ICExMkH_55X9vsA8BWjGUaI5LrvZxQTwT6ACUaSZ5QRcQAm6Q5nQsryEziM8RohjEvEJuD3Um9DY_TQ-A56B6v1PK9OV_mPq8X5BtrWmiH42I8d7HTnXbMNfowwGu2cb-sInQ9Qd0Oa0BkbYB3GP7C2bXNvw-4z-Oh0G-2Xp3MKLpenm8VZtr5YfVvM15kpOWIZpVIiYhFzgkqGaqlrwR0xXDqrGbfc1MxSXhpDMCE1wVSIrcNaSk6YM6iYguP93D74u9HGQd020di21Z1Nr1WYcVyWVNDiHZQQhjktWKJHr-i1H0OXPpJU2nDBGBdJneyVSWuKwTrVh-ZWh53CSP1vRKVG1GMjyeZ7-7dp7e5tqOZV9ZzI9okmDvbfS0KHG8V4wUt1db5S66VYfK9-_VS0eABsAZpQ</recordid><startdate>20150115</startdate><enddate>20150115</enddate><creator>Aboutalebi Anaraki, Nadia</creator><creator>Roshanfekr Rad, Leila</creator><creator>Irani, Mohammad</creator><creator>Haririan, Ismaeil</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>JG9</scope><scope>7QO</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>20150115</creationdate><title>Fabrication of PLA/PEG/MWCNT electrospun nanofibrous scaffolds for anticancer drug delivery</title><author>Aboutalebi Anaraki, Nadia ; Roshanfekr Rad, Leila ; Irani, Mohammad ; Haririan, Ismaeil</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5706-449902e06f84960d9ad87f2c79fea67e7cd6e475cc2122d21488bf1a99726fc03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Drug delivery systems</topic><topic>Drugs</topic><topic>Electric potential</topic><topic>Electrospinning</topic><topic>fibers</topic><topic>Materials science</topic><topic>Mathematical analysis</topic><topic>Nanostructure</topic><topic>Polyethylene glycol</topic><topic>Polymers</topic><topic>Scaffolds</topic><topic>Voltage</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Aboutalebi Anaraki, Nadia</creatorcontrib><creatorcontrib>Roshanfekr Rad, Leila</creatorcontrib><creatorcontrib>Irani, Mohammad</creatorcontrib><creatorcontrib>Haririan, Ismaeil</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Biotechnology Research Abstracts</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Journal of applied polymer science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Aboutalebi Anaraki, Nadia</au><au>Roshanfekr Rad, Leila</au><au>Irani, Mohammad</au><au>Haririan, Ismaeil</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fabrication of PLA/PEG/MWCNT electrospun nanofibrous scaffolds for anticancer drug delivery</atitle><jtitle>Journal of applied polymer science</jtitle><addtitle>J. Appl. Polym. Sci</addtitle><date>2015-01-15</date><risdate>2015</risdate><volume>132</volume><issue>3</issue><epage>n/a</epage><issn>0021-8995</issn><eissn>1097-4628</eissn><coden>JAPNAB</coden><abstract>ABSTRACT
In the present study, polylactic acid (PLA)/polyethylene glycol (PEG)/multiwalled carbon nanotube (MWCNT) electrospun nanofibrous scaffolds were prepared via electrospinning process and their applications for the anticancer drug delivery system were investigated. A response surface methodology based on Box–Behnken design (BBD) was used to evaluate the effect of key parameters of electrospinning process including solution concentration, feeding rate, tip–collector distance (TCD) and applied voltage on the morphology of PLA/PEG/MWCNT nanofibrous scaffolds. In optimum conditions (concentration of 8.15%, feeding rate of 0.2 mL/h, voltage of 18.50 kV and TCD of 13.0 cm), the minimum experimental fiber diameter was found to be 225 nm which was in good agreement with the predicted value by the BBD analysis (228 nm). In vitro drug release study of doxorubicin (DOX)‐loaded nanofibrous scaffolds, higher drug content induced an extended release of drug. Also, drug release rate was not dependent on drug/polymer ratio in different electrospun nanofibrous formulations. The equation of Mt = c0 + kt0.5was used to describe the kinetic data of DOX release from electrospun nanofibers. The cell viability of DOX‐loaded nanofibrous scaffolds was evaluated using 3‐(4,5‐dimethylthiazol‐2‐yl)‐2,5‐diphenyltetrazolium bromide, a tetrazole assay on lung cancer A549 cell lines. We propose that DOX‐incorporated PLA/PEG/MWCNT nanofibrous scaffold could be used as a superior candidate for antitumor drug delivery. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015, 132, 41286.</abstract><cop>Hoboken</cop><pub>Blackwell Publishing Ltd</pub><doi>10.1002/app.41286</doi><tpages>9</tpages></addata></record> |
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subjects | Drug delivery systems Drugs Electric potential Electrospinning fibers Materials science Mathematical analysis Nanostructure Polyethylene glycol Polymers Scaffolds Voltage |
title | Fabrication of PLA/PEG/MWCNT electrospun nanofibrous scaffolds for anticancer drug delivery |
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