Preparation and characterization of the electrospun nanofibers loaded with clarithromycin
Electrospinning was applied to prepare the drug-loaded nanofibers for potential use in drug delivery and wound healing. Clarithromycin (CLM) was selected as the model drug, whereas poly(l-lactic acid) (PLLA) was used as the biodegradable and biocompatible polymer carrier. The low toxicity solvents w...
Gespeichert in:
Veröffentlicht in: | Journal of applied polymer science 2010-10, Vol.118 (1), p.346-352 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 352 |
---|---|
container_issue | 1 |
container_start_page | 346 |
container_title | Journal of applied polymer science |
container_volume | 118 |
creator | Wei, Anfang Wang, Juan Wang, Xueqian Wei, Qufu Ge, Mingqiao Hou, Dayin |
description | Electrospinning was applied to prepare the drug-loaded nanofibers for potential use in drug delivery and wound healing. Clarithromycin (CLM) was selected as the model drug, whereas poly(l-lactic acid) (PLLA) was used as the biodegradable and biocompatible polymer carrier. The low toxicity solvents were tested, and the morphology and structures of the nanofibers were investigated by scanning electron microscopy (SEM), Fourier transform infrared spectrometer (FTIR), and X-ray diffraction (XRD). PLLA and its composite of CLM were electrospun using the solvents of dichloromethane and acetone. SEM images showed that the diameters of the electrospun PLLA fibers were about 1000 nm, decreased to about 400 nm when 5 wt % CLM was loaded. With the increase of the amount the drug loaded, the diameters of the fibers gradually decreased and their distributions varied. The drug aggregates of any kind were not observed on the surfaces of the fibers. FTIR spectra revealed that CLM was incorporated into the macromolecular carrier of PLLA by formation of the hydrogen bonds but no new functional groups in the structure of the composite nanofibers were formed. XRD patterns indicated that the drug distributed in the composite nanofibers existed in the noncrystalline form. |
doi_str_mv | 10.1002/app.32363 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_901664240</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>901664240</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4343-51185ad23018829eacdd4cf5b19d3d71c20859fe5c25a0862428a0ac0ec9457a3</originalsourceid><addsrcrecordid>eNp1kE1v1DAQhi0EEkvhwC8gF4Q4pPV37GNV0Q-ptFuxFeJkTZ0Ja8jGwc6qbH99XVJ662k0M8_7auYl5D2j-4xSfgDjuC-40OIFWTBqm1pqbl6SRdmx2lirXpM3Of-ilDFF9YL8WCYcIcEU4lDB0FZ-XTo_YQp38zB21bTGCnv0U4p53A7VAEPswg2mXPURWmyr2zCtK99DKjXFzc6H4S151UGf8d1j3SPXx19WR6f1-eXJ2dHhee2lkKJWjBkFLReUGcMtgm9b6Tt1w2wr2oZ5To2yHSrPFVCjueQGKHiK3krVgNgjn2bfMcU_W8yT24Tsse9hwLjNzlKmteSSFvLzTPryR07YuTGFDaSdY9Q9pOdKeu5feoX9-OgK2UPfJRh8yE-Ccq7lisvCHczcbehx97yhO1wu_zvXsyLkCf8-KSD9droRjXLfL07cxdVK2tXpsfta-A8z30F08DOVK66_ccoeAtNGaCbuAeRYl10</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>901664240</pqid></control><display><type>article</type><title>Preparation and characterization of the electrospun nanofibers loaded with clarithromycin</title><source>Wiley Online Library Journals Frontfile Complete</source><creator>Wei, Anfang ; Wang, Juan ; Wang, Xueqian ; Wei, Qufu ; Ge, Mingqiao ; Hou, Dayin</creator><creatorcontrib>Wei, Anfang ; Wang, Juan ; Wang, Xueqian ; Wei, Qufu ; Ge, Mingqiao ; Hou, Dayin</creatorcontrib><description>Electrospinning was applied to prepare the drug-loaded nanofibers for potential use in drug delivery and wound healing. Clarithromycin (CLM) was selected as the model drug, whereas poly(l-lactic acid) (PLLA) was used as the biodegradable and biocompatible polymer carrier. The low toxicity solvents were tested, and the morphology and structures of the nanofibers were investigated by scanning electron microscopy (SEM), Fourier transform infrared spectrometer (FTIR), and X-ray diffraction (XRD). PLLA and its composite of CLM were electrospun using the solvents of dichloromethane and acetone. SEM images showed that the diameters of the electrospun PLLA fibers were about 1000 nm, decreased to about 400 nm when 5 wt % CLM was loaded. With the increase of the amount the drug loaded, the diameters of the fibers gradually decreased and their distributions varied. The drug aggregates of any kind were not observed on the surfaces of the fibers. FTIR spectra revealed that CLM was incorporated into the macromolecular carrier of PLLA by formation of the hydrogen bonds but no new functional groups in the structure of the composite nanofibers were formed. XRD patterns indicated that the drug distributed in the composite nanofibers existed in the noncrystalline form.</description><identifier>ISSN: 0021-8995</identifier><identifier>ISSN: 1097-4628</identifier><identifier>EISSN: 1097-4628</identifier><identifier>DOI: 10.1002/app.32363</identifier><identifier>CODEN: JAPNAB</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Applied sciences ; Biological and medical sciences ; Carriers ; drug delivery ; Drugs ; elctrospinning ; Electrospinning ; Exact sciences and technology ; Fibers ; Fibers and threads ; Forms of application and semi-finished materials ; FTIR ; General pharmacology ; Medical sciences ; morphology ; Nanofibers ; Pharmaceutical technology. Pharmaceutical industry ; Pharmacology. Drug treatments ; Polymer industry, paints, wood ; Scanning electron microscopy ; Solvents ; Technology of polymers ; X-ray diffraction</subject><ispartof>Journal of applied polymer science, 2010-10, Vol.118 (1), p.346-352</ispartof><rights>Copyright © 2010 Wiley Periodicals, Inc.</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4343-51185ad23018829eacdd4cf5b19d3d71c20859fe5c25a0862428a0ac0ec9457a3</citedby><cites>FETCH-LOGICAL-c4343-51185ad23018829eacdd4cf5b19d3d71c20859fe5c25a0862428a0ac0ec9457a3</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.32363$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fapp.32363$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=23092524$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Wei, Anfang</creatorcontrib><creatorcontrib>Wang, Juan</creatorcontrib><creatorcontrib>Wang, Xueqian</creatorcontrib><creatorcontrib>Wei, Qufu</creatorcontrib><creatorcontrib>Ge, Mingqiao</creatorcontrib><creatorcontrib>Hou, Dayin</creatorcontrib><title>Preparation and characterization of the electrospun nanofibers loaded with clarithromycin</title><title>Journal of applied polymer science</title><addtitle>J. Appl. Polym. Sci</addtitle><description>Electrospinning was applied to prepare the drug-loaded nanofibers for potential use in drug delivery and wound healing. Clarithromycin (CLM) was selected as the model drug, whereas poly(l-lactic acid) (PLLA) was used as the biodegradable and biocompatible polymer carrier. The low toxicity solvents were tested, and the morphology and structures of the nanofibers were investigated by scanning electron microscopy (SEM), Fourier transform infrared spectrometer (FTIR), and X-ray diffraction (XRD). PLLA and its composite of CLM were electrospun using the solvents of dichloromethane and acetone. SEM images showed that the diameters of the electrospun PLLA fibers were about 1000 nm, decreased to about 400 nm when 5 wt % CLM was loaded. With the increase of the amount the drug loaded, the diameters of the fibers gradually decreased and their distributions varied. The drug aggregates of any kind were not observed on the surfaces of the fibers. FTIR spectra revealed that CLM was incorporated into the macromolecular carrier of PLLA by formation of the hydrogen bonds but no new functional groups in the structure of the composite nanofibers were formed. XRD patterns indicated that the drug distributed in the composite nanofibers existed in the noncrystalline form.</description><subject>Applied sciences</subject><subject>Biological and medical sciences</subject><subject>Carriers</subject><subject>drug delivery</subject><subject>Drugs</subject><subject>elctrospinning</subject><subject>Electrospinning</subject><subject>Exact sciences and technology</subject><subject>Fibers</subject><subject>Fibers and threads</subject><subject>Forms of application and semi-finished materials</subject><subject>FTIR</subject><subject>General pharmacology</subject><subject>Medical sciences</subject><subject>morphology</subject><subject>Nanofibers</subject><subject>Pharmaceutical technology. Pharmaceutical industry</subject><subject>Pharmacology. Drug treatments</subject><subject>Polymer industry, paints, wood</subject><subject>Scanning electron microscopy</subject><subject>Solvents</subject><subject>Technology of polymers</subject><subject>X-ray diffraction</subject><issn>0021-8995</issn><issn>1097-4628</issn><issn>1097-4628</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNp1kE1v1DAQhi0EEkvhwC8gF4Q4pPV37GNV0Q-ptFuxFeJkTZ0Ja8jGwc6qbH99XVJ662k0M8_7auYl5D2j-4xSfgDjuC-40OIFWTBqm1pqbl6SRdmx2lirXpM3Of-ilDFF9YL8WCYcIcEU4lDB0FZ-XTo_YQp38zB21bTGCnv0U4p53A7VAEPswg2mXPURWmyr2zCtK99DKjXFzc6H4S151UGf8d1j3SPXx19WR6f1-eXJ2dHhee2lkKJWjBkFLReUGcMtgm9b6Tt1w2wr2oZ5To2yHSrPFVCjueQGKHiK3krVgNgjn2bfMcU_W8yT24Tsse9hwLjNzlKmteSSFvLzTPryR07YuTGFDaSdY9Q9pOdKeu5feoX9-OgK2UPfJRh8yE-Ccq7lisvCHczcbehx97yhO1wu_zvXsyLkCf8-KSD9droRjXLfL07cxdVK2tXpsfta-A8z30F08DOVK66_ccoeAtNGaCbuAeRYl10</recordid><startdate>20101005</startdate><enddate>20101005</enddate><creator>Wei, Anfang</creator><creator>Wang, Juan</creator><creator>Wang, Xueqian</creator><creator>Wei, Qufu</creator><creator>Ge, Mingqiao</creator><creator>Hou, Dayin</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley</general><scope>FBQ</scope><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>20101005</creationdate><title>Preparation and characterization of the electrospun nanofibers loaded with clarithromycin</title><author>Wei, Anfang ; Wang, Juan ; Wang, Xueqian ; Wei, Qufu ; Ge, Mingqiao ; Hou, Dayin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4343-51185ad23018829eacdd4cf5b19d3d71c20859fe5c25a0862428a0ac0ec9457a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Applied sciences</topic><topic>Biological and medical sciences</topic><topic>Carriers</topic><topic>drug delivery</topic><topic>Drugs</topic><topic>elctrospinning</topic><topic>Electrospinning</topic><topic>Exact sciences and technology</topic><topic>Fibers</topic><topic>Fibers and threads</topic><topic>Forms of application and semi-finished materials</topic><topic>FTIR</topic><topic>General pharmacology</topic><topic>Medical sciences</topic><topic>morphology</topic><topic>Nanofibers</topic><topic>Pharmaceutical technology. Pharmaceutical industry</topic><topic>Pharmacology. Drug treatments</topic><topic>Polymer industry, paints, wood</topic><topic>Scanning electron microscopy</topic><topic>Solvents</topic><topic>Technology of polymers</topic><topic>X-ray diffraction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wei, Anfang</creatorcontrib><creatorcontrib>Wang, Juan</creatorcontrib><creatorcontrib>Wang, Xueqian</creatorcontrib><creatorcontrib>Wei, Qufu</creatorcontrib><creatorcontrib>Ge, Mingqiao</creatorcontrib><creatorcontrib>Hou, Dayin</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Journal of applied polymer science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wei, Anfang</au><au>Wang, Juan</au><au>Wang, Xueqian</au><au>Wei, Qufu</au><au>Ge, Mingqiao</au><au>Hou, Dayin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Preparation and characterization of the electrospun nanofibers loaded with clarithromycin</atitle><jtitle>Journal of applied polymer science</jtitle><addtitle>J. Appl. Polym. Sci</addtitle><date>2010-10-05</date><risdate>2010</risdate><volume>118</volume><issue>1</issue><spage>346</spage><epage>352</epage><pages>346-352</pages><issn>0021-8995</issn><issn>1097-4628</issn><eissn>1097-4628</eissn><coden>JAPNAB</coden><abstract>Electrospinning was applied to prepare the drug-loaded nanofibers for potential use in drug delivery and wound healing. Clarithromycin (CLM) was selected as the model drug, whereas poly(l-lactic acid) (PLLA) was used as the biodegradable and biocompatible polymer carrier. The low toxicity solvents were tested, and the morphology and structures of the nanofibers were investigated by scanning electron microscopy (SEM), Fourier transform infrared spectrometer (FTIR), and X-ray diffraction (XRD). PLLA and its composite of CLM were electrospun using the solvents of dichloromethane and acetone. SEM images showed that the diameters of the electrospun PLLA fibers were about 1000 nm, decreased to about 400 nm when 5 wt % CLM was loaded. With the increase of the amount the drug loaded, the diameters of the fibers gradually decreased and their distributions varied. The drug aggregates of any kind were not observed on the surfaces of the fibers. FTIR spectra revealed that CLM was incorporated into the macromolecular carrier of PLLA by formation of the hydrogen bonds but no new functional groups in the structure of the composite nanofibers were formed. XRD patterns indicated that the drug distributed in the composite nanofibers existed in the noncrystalline form.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><doi>10.1002/app.32363</doi><tpages>7</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0021-8995 |
ispartof | Journal of applied polymer science, 2010-10, Vol.118 (1), p.346-352 |
issn | 0021-8995 1097-4628 1097-4628 |
language | eng |
recordid | cdi_proquest_miscellaneous_901664240 |
source | Wiley Online Library Journals Frontfile Complete |
subjects | Applied sciences Biological and medical sciences Carriers drug delivery Drugs elctrospinning Electrospinning Exact sciences and technology Fibers Fibers and threads Forms of application and semi-finished materials FTIR General pharmacology Medical sciences morphology Nanofibers Pharmaceutical technology. Pharmaceutical industry Pharmacology. Drug treatments Polymer industry, paints, wood Scanning electron microscopy Solvents Technology of polymers X-ray diffraction |
title | Preparation and characterization of the electrospun nanofibers loaded with clarithromycin |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-31T06%3A36%3A07IST&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=Preparation%20and%20characterization%20of%20the%20electrospun%20nanofibers%20loaded%20with%20clarithromycin&rft.jtitle=Journal%20of%20applied%20polymer%20science&rft.au=Wei,%20Anfang&rft.date=2010-10-05&rft.volume=118&rft.issue=1&rft.spage=346&rft.epage=352&rft.pages=346-352&rft.issn=0021-8995&rft.eissn=1097-4628&rft.coden=JAPNAB&rft_id=info:doi/10.1002/app.32363&rft_dat=%3Cproquest_cross%3E901664240%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=901664240&rft_id=info:pmid/&rfr_iscdi=true |