Functionalizing Electrospun Fibers with Biologically Relevant Macromolecules

The development of functionalized polymers that can elicit specific biological responses is of great interest in the biomedical community, as well as the development of methods to fabricate these biologically functionalized polymers. For example, the generation of fibrous matrices with biological pr...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Biomacromolecules 2005-07, Vol.6 (4), p.1998-2007
Hauptverfasser: Casper, Cheryl L, Yamaguchi, Nori, Kiick, Kristi L, Rabolt, John F
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 2007
container_issue 4
container_start_page 1998
container_title Biomacromolecules
container_volume 6
creator Casper, Cheryl L
Yamaguchi, Nori
Kiick, Kristi L
Rabolt, John F
description The development of functionalized polymers that can elicit specific biological responses is of great interest in the biomedical community, as well as the development of methods to fabricate these biologically functionalized polymers. For example, the generation of fibrous matrices with biological properties and fiber diameters commensurate with those of the natural extracellular matrix (ECM) may permit the development of novel materials for use in wound healing or tissue engineering. The goal of this work is, therefore, to create a biologically active functionalized electrospun matrix to permit immobilization and long-term delivery of growth factors. In this work, poly(ethylene glycol) functionalized with low molecular weight heparin (PEG-LMWH) was fabricated into fibers for possible use in drug delivery, tissue engineering, or wound repair applications. Electrospinning was chosen to process the LMWH into fiber form due to the small fiber diameters and high degree of porosity that can be obtained relatively quickly and using small amounts of starting material. Both free LMWH and PEG-LMWH were investigated for their ability to be incorporated into electrospun fibers. Each of the samples were mixed with a carrier polymer consisting of either a 10 wt % poly(ethylene oxide) (PEO) or 45 wt % poly(lactide-co-glycolide) (PLGA). Field emission scanning electron microscopy (FESEM), energy-dispersive X-ray analysis (EDX), UV−vis spectroscopy, and multiphoton microscopy were used to characterize the electrospun matrices. The incorporation of heparin into the electrospun PEO and PLGA fibers did not affect the surface morphology or fiber diameters. The fibers produced had diameters ranging from approximately 100 to 400 nm. Toluidine blue assays of heparin suggest that it can be incorporated into an electrospun matrix at concentrations ranging from 3.5 to 85 μg per milligram of electrospun fibers. Multiphoton microscopy confirmed that incorporation of PEG-LMWH into the matrix permits retention of the heparin for at least 14 days. Improvements in the binding of basic fibroblast growth factor to the electrospun fibers were also observed for fibers functionalized with PEG-LMWH over those functionalized with LMWH alone. The combination of these results suggests the utility for producing electrospun fibers that are appropriately functionalized for use in biomaterials applications.
doi_str_mv 10.1021/bm050007e
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2744094</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>68014801</sourcerecordid><originalsourceid>FETCH-LOGICAL-a433t-8dcbb7337e7629d9e22e53510b81bbed071f54cab77eae3896ea01a354b86c613</originalsourceid><addsrcrecordid>eNptkd9LHDEQx0NR6q8-9B-QfbHgw9pkk012XwpWvCqcFKR9DpPc3BnJJmeya7F_faMeasGHMAPzme_MfEPIZ0ZPGG3YVzPQllKq8APZZW0jayFps_WUt7VSvdoheznfFqTnov1IdpikVAje7ZL5bAp2dDGAd39dWFXnHu2YYl5PoZo5gylXf9x4U3130ceVs-D9Q3WNHu8hjNUV2BSHWHomj_mAbC_BZ_y0ifvk9-z819lFPf_54_LsdF6D4Hysu4U1RnGuUMmmX_TYNNjyllHTMWNwQRVbtsKCUQoBeddLBMqAt8J00krG98m3Z931ZAZcWAxjAq_XyQ2QHnQEp_-vBHejV_FeN0oI2osi8GUjkOLdhHnUg8sWvYeAccpadpSJ8gp4_AyWM3NOuHwZwqh-9F6_eF_Yw7dbvZIbswtwtAEgFx-XCYJ1-Q3XSyokf-XAZn0bp1Q-J78z8B8w2pnp</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>68014801</pqid></control><display><type>article</type><title>Functionalizing Electrospun Fibers with Biologically Relevant Macromolecules</title><source>MEDLINE</source><source>American Chemical Society Journals</source><creator>Casper, Cheryl L ; Yamaguchi, Nori ; Kiick, Kristi L ; Rabolt, John F</creator><creatorcontrib>Casper, Cheryl L ; Yamaguchi, Nori ; Kiick, Kristi L ; Rabolt, John F</creatorcontrib><description>The development of functionalized polymers that can elicit specific biological responses is of great interest in the biomedical community, as well as the development of methods to fabricate these biologically functionalized polymers. For example, the generation of fibrous matrices with biological properties and fiber diameters commensurate with those of the natural extracellular matrix (ECM) may permit the development of novel materials for use in wound healing or tissue engineering. The goal of this work is, therefore, to create a biologically active functionalized electrospun matrix to permit immobilization and long-term delivery of growth factors. In this work, poly(ethylene glycol) functionalized with low molecular weight heparin (PEG-LMWH) was fabricated into fibers for possible use in drug delivery, tissue engineering, or wound repair applications. Electrospinning was chosen to process the LMWH into fiber form due to the small fiber diameters and high degree of porosity that can be obtained relatively quickly and using small amounts of starting material. Both free LMWH and PEG-LMWH were investigated for their ability to be incorporated into electrospun fibers. Each of the samples were mixed with a carrier polymer consisting of either a 10 wt % poly(ethylene oxide) (PEO) or 45 wt % poly(lactide-co-glycolide) (PLGA). Field emission scanning electron microscopy (FESEM), energy-dispersive X-ray analysis (EDX), UV−vis spectroscopy, and multiphoton microscopy were used to characterize the electrospun matrices. The incorporation of heparin into the electrospun PEO and PLGA fibers did not affect the surface morphology or fiber diameters. The fibers produced had diameters ranging from approximately 100 to 400 nm. Toluidine blue assays of heparin suggest that it can be incorporated into an electrospun matrix at concentrations ranging from 3.5 to 85 μg per milligram of electrospun fibers. Multiphoton microscopy confirmed that incorporation of PEG-LMWH into the matrix permits retention of the heparin for at least 14 days. Improvements in the binding of basic fibroblast growth factor to the electrospun fibers were also observed for fibers functionalized with PEG-LMWH over those functionalized with LMWH alone. The combination of these results suggests the utility for producing electrospun fibers that are appropriately functionalized for use in biomaterials applications.</description><identifier>ISSN: 1525-7797</identifier><identifier>EISSN: 1526-4602</identifier><identifier>DOI: 10.1021/bm050007e</identifier><identifier>PMID: 16004438</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Applied sciences ; Coloring Agents ; Exact sciences and technology ; Heparin, Low-Molecular-Weight - chemistry ; Machinery and processing ; Microscopy, Electron, Scanning ; Plastics ; Polyethylene Glycols - chemistry ; Polymer industry, paints, wood ; Polymers - chemistry ; Spectrum Analysis - methods ; Spinning ; Technology of polymers</subject><ispartof>Biomacromolecules, 2005-07, Vol.6 (4), p.1998-2007</ispartof><rights>Copyright © 2005 American Chemical Society</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a433t-8dcbb7337e7629d9e22e53510b81bbed071f54cab77eae3896ea01a354b86c613</citedby><cites>FETCH-LOGICAL-a433t-8dcbb7337e7629d9e22e53510b81bbed071f54cab77eae3896ea01a354b86c613</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/bm050007e$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/bm050007e$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>230,314,780,784,885,2765,27076,27924,27925,56738,56788</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=16960463$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16004438$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Casper, Cheryl L</creatorcontrib><creatorcontrib>Yamaguchi, Nori</creatorcontrib><creatorcontrib>Kiick, Kristi L</creatorcontrib><creatorcontrib>Rabolt, John F</creatorcontrib><title>Functionalizing Electrospun Fibers with Biologically Relevant Macromolecules</title><title>Biomacromolecules</title><addtitle>Biomacromolecules</addtitle><description>The development of functionalized polymers that can elicit specific biological responses is of great interest in the biomedical community, as well as the development of methods to fabricate these biologically functionalized polymers. For example, the generation of fibrous matrices with biological properties and fiber diameters commensurate with those of the natural extracellular matrix (ECM) may permit the development of novel materials for use in wound healing or tissue engineering. The goal of this work is, therefore, to create a biologically active functionalized electrospun matrix to permit immobilization and long-term delivery of growth factors. In this work, poly(ethylene glycol) functionalized with low molecular weight heparin (PEG-LMWH) was fabricated into fibers for possible use in drug delivery, tissue engineering, or wound repair applications. Electrospinning was chosen to process the LMWH into fiber form due to the small fiber diameters and high degree of porosity that can be obtained relatively quickly and using small amounts of starting material. Both free LMWH and PEG-LMWH were investigated for their ability to be incorporated into electrospun fibers. Each of the samples were mixed with a carrier polymer consisting of either a 10 wt % poly(ethylene oxide) (PEO) or 45 wt % poly(lactide-co-glycolide) (PLGA). Field emission scanning electron microscopy (FESEM), energy-dispersive X-ray analysis (EDX), UV−vis spectroscopy, and multiphoton microscopy were used to characterize the electrospun matrices. The incorporation of heparin into the electrospun PEO and PLGA fibers did not affect the surface morphology or fiber diameters. The fibers produced had diameters ranging from approximately 100 to 400 nm. Toluidine blue assays of heparin suggest that it can be incorporated into an electrospun matrix at concentrations ranging from 3.5 to 85 μg per milligram of electrospun fibers. Multiphoton microscopy confirmed that incorporation of PEG-LMWH into the matrix permits retention of the heparin for at least 14 days. Improvements in the binding of basic fibroblast growth factor to the electrospun fibers were also observed for fibers functionalized with PEG-LMWH over those functionalized with LMWH alone. The combination of these results suggests the utility for producing electrospun fibers that are appropriately functionalized for use in biomaterials applications.</description><subject>Applied sciences</subject><subject>Coloring Agents</subject><subject>Exact sciences and technology</subject><subject>Heparin, Low-Molecular-Weight - chemistry</subject><subject>Machinery and processing</subject><subject>Microscopy, Electron, Scanning</subject><subject>Plastics</subject><subject>Polyethylene Glycols - chemistry</subject><subject>Polymer industry, paints, wood</subject><subject>Polymers - chemistry</subject><subject>Spectrum Analysis - methods</subject><subject>Spinning</subject><subject>Technology of polymers</subject><issn>1525-7797</issn><issn>1526-4602</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkd9LHDEQx0NR6q8-9B-QfbHgw9pkk012XwpWvCqcFKR9DpPc3BnJJmeya7F_faMeasGHMAPzme_MfEPIZ0ZPGG3YVzPQllKq8APZZW0jayFps_WUt7VSvdoheznfFqTnov1IdpikVAje7ZL5bAp2dDGAd39dWFXnHu2YYl5PoZo5gylXf9x4U3130ceVs-D9Q3WNHu8hjNUV2BSHWHomj_mAbC_BZ_y0ifvk9-z819lFPf_54_LsdF6D4Hysu4U1RnGuUMmmX_TYNNjyllHTMWNwQRVbtsKCUQoBeddLBMqAt8J00krG98m3Z931ZAZcWAxjAq_XyQ2QHnQEp_-vBHejV_FeN0oI2osi8GUjkOLdhHnUg8sWvYeAccpadpSJ8gp4_AyWM3NOuHwZwqh-9F6_eF_Yw7dbvZIbswtwtAEgFx-XCYJ1-Q3XSyokf-XAZn0bp1Q-J78z8B8w2pnp</recordid><startdate>20050701</startdate><enddate>20050701</enddate><creator>Casper, Cheryl L</creator><creator>Yamaguchi, Nori</creator><creator>Kiick, Kristi L</creator><creator>Rabolt, John F</creator><general>American Chemical Society</general><scope>IQODW</scope><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>5PM</scope></search><sort><creationdate>20050701</creationdate><title>Functionalizing Electrospun Fibers with Biologically Relevant Macromolecules</title><author>Casper, Cheryl L ; Yamaguchi, Nori ; Kiick, Kristi L ; Rabolt, John F</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a433t-8dcbb7337e7629d9e22e53510b81bbed071f54cab77eae3896ea01a354b86c613</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Applied sciences</topic><topic>Coloring Agents</topic><topic>Exact sciences and technology</topic><topic>Heparin, Low-Molecular-Weight - chemistry</topic><topic>Machinery and processing</topic><topic>Microscopy, Electron, Scanning</topic><topic>Plastics</topic><topic>Polyethylene Glycols - chemistry</topic><topic>Polymer industry, paints, wood</topic><topic>Polymers - chemistry</topic><topic>Spectrum Analysis - methods</topic><topic>Spinning</topic><topic>Technology of polymers</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Casper, Cheryl L</creatorcontrib><creatorcontrib>Yamaguchi, Nori</creatorcontrib><creatorcontrib>Kiick, Kristi L</creatorcontrib><creatorcontrib>Rabolt, John F</creatorcontrib><collection>Pascal-Francis</collection><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>PubMed Central (Full Participant titles)</collection><jtitle>Biomacromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Casper, Cheryl L</au><au>Yamaguchi, Nori</au><au>Kiick, Kristi L</au><au>Rabolt, John F</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Functionalizing Electrospun Fibers with Biologically Relevant Macromolecules</atitle><jtitle>Biomacromolecules</jtitle><addtitle>Biomacromolecules</addtitle><date>2005-07-01</date><risdate>2005</risdate><volume>6</volume><issue>4</issue><spage>1998</spage><epage>2007</epage><pages>1998-2007</pages><issn>1525-7797</issn><eissn>1526-4602</eissn><abstract>The development of functionalized polymers that can elicit specific biological responses is of great interest in the biomedical community, as well as the development of methods to fabricate these biologically functionalized polymers. For example, the generation of fibrous matrices with biological properties and fiber diameters commensurate with those of the natural extracellular matrix (ECM) may permit the development of novel materials for use in wound healing or tissue engineering. The goal of this work is, therefore, to create a biologically active functionalized electrospun matrix to permit immobilization and long-term delivery of growth factors. In this work, poly(ethylene glycol) functionalized with low molecular weight heparin (PEG-LMWH) was fabricated into fibers for possible use in drug delivery, tissue engineering, or wound repair applications. Electrospinning was chosen to process the LMWH into fiber form due to the small fiber diameters and high degree of porosity that can be obtained relatively quickly and using small amounts of starting material. Both free LMWH and PEG-LMWH were investigated for their ability to be incorporated into electrospun fibers. Each of the samples were mixed with a carrier polymer consisting of either a 10 wt % poly(ethylene oxide) (PEO) or 45 wt % poly(lactide-co-glycolide) (PLGA). Field emission scanning electron microscopy (FESEM), energy-dispersive X-ray analysis (EDX), UV−vis spectroscopy, and multiphoton microscopy were used to characterize the electrospun matrices. The incorporation of heparin into the electrospun PEO and PLGA fibers did not affect the surface morphology or fiber diameters. The fibers produced had diameters ranging from approximately 100 to 400 nm. Toluidine blue assays of heparin suggest that it can be incorporated into an electrospun matrix at concentrations ranging from 3.5 to 85 μg per milligram of electrospun fibers. Multiphoton microscopy confirmed that incorporation of PEG-LMWH into the matrix permits retention of the heparin for at least 14 days. Improvements in the binding of basic fibroblast growth factor to the electrospun fibers were also observed for fibers functionalized with PEG-LMWH over those functionalized with LMWH alone. The combination of these results suggests the utility for producing electrospun fibers that are appropriately functionalized for use in biomaterials applications.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>16004438</pmid><doi>10.1021/bm050007e</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1525-7797
ispartof Biomacromolecules, 2005-07, Vol.6 (4), p.1998-2007
issn 1525-7797
1526-4602
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2744094
source MEDLINE; American Chemical Society Journals
subjects Applied sciences
Coloring Agents
Exact sciences and technology
Heparin, Low-Molecular-Weight - chemistry
Machinery and processing
Microscopy, Electron, Scanning
Plastics
Polyethylene Glycols - chemistry
Polymer industry, paints, wood
Polymers - chemistry
Spectrum Analysis - methods
Spinning
Technology of polymers
title Functionalizing Electrospun Fibers with Biologically Relevant Macromolecules
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-18T20%3A56%3A04IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Functionalizing%20Electrospun%20Fibers%20with%20Biologically%20Relevant%20Macromolecules&rft.jtitle=Biomacromolecules&rft.au=Casper,%20Cheryl%20L&rft.date=2005-07-01&rft.volume=6&rft.issue=4&rft.spage=1998&rft.epage=2007&rft.pages=1998-2007&rft.issn=1525-7797&rft.eissn=1526-4602&rft_id=info:doi/10.1021/bm050007e&rft_dat=%3Cproquest_pubme%3E68014801%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=68014801&rft_id=info:pmid/16004438&rfr_iscdi=true