B(12)-mediated, long wavelength photopolymerization of hydrogels
Medical hydrogel applications have expanded rapidly over the past decade. Implantation in patients by noninvasive injection is preferred, but this requires hydrogel solidification from a low viscosity solution to occur in vivo via an applied stimuli. Transdermal photo-cross-linking of acrylated biop...
Gespeichert in:
Veröffentlicht in: | Journal of the American Chemical Society 2015-03, Vol.137 (9), p.3372-3378 |
---|---|
Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 3378 |
---|---|
container_issue | 9 |
container_start_page | 3372 |
container_title | Journal of the American Chemical Society |
container_volume | 137 |
creator | Rodgers, Zachary L Hughes, Robert M Doherty, Laura M Shell, Jennifer R Molesky, Brian P Brugh, Alexander M Forbes, Malcolm D E Moran, Andrew M Lawrence, David S |
description | Medical hydrogel applications have expanded rapidly over the past decade. Implantation in patients by noninvasive injection is preferred, but this requires hydrogel solidification from a low viscosity solution to occur in vivo via an applied stimuli. Transdermal photo-cross-linking of acrylated biopolymers with photoinitiators and lights offers a mild, spatiotemporally controlled solidification trigger. However, the current short wavelength initiators limit curing depth and efficacy because they do not absorb within the optical window of tissue (600-900 nm). As a solution to the current wavelength limitations, we report the development of a red light responsive initiator capable of polymerizing a range of acrylated monomers. Photoactivation occurs within a range of skin type models containing high biochromophore concentrations. |
doi_str_mv | 10.1021/jacs.5b00182 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_1662638452</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1662638452</sourcerecordid><originalsourceid>FETCH-LOGICAL-p568-94fa2efb20dc3b9324d92312ea49ca1b752cfc4526e31c51e4d1f662a1f157e63</originalsourceid><addsrcrecordid>eNo1j89LwzAYQIMgbk5vnqXHCXbm-9Jk7U03_AUDL7uXNP2ydaRNbTql_vUWnKd3eTx4jN0AXwBHeDhoExay4BxSPGNTkMhjCagm7DKEA-c8wRQu2ASlypaSp1P2uJoD3sU1lZXuqbyPnG920bf-IkfNrt9H7d73vvVuqKmrfnRf-SbyNtoPZed35MIVO7faBbo-cca2L8_b9Vu8-Xh9Xz9t4laqNM4Sq5Fsgbw0osgEJmWGApB0khkNxVKisSaRqEiAkUBJCVYp1GBBLkmJGZv_ZdvOfx4p9HldBUPO6Yb8MeQwykqkY2FUb0_qsRi_8rarat0N-f-0-AU7qFZ0</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1662638452</pqid></control><display><type>article</type><title>B(12)-mediated, long wavelength photopolymerization of hydrogels</title><source>ACS Publications</source><source>MEDLINE</source><creator>Rodgers, Zachary L ; Hughes, Robert M ; Doherty, Laura M ; Shell, Jennifer R ; Molesky, Brian P ; Brugh, Alexander M ; Forbes, Malcolm D E ; Moran, Andrew M ; Lawrence, David S</creator><creatorcontrib>Rodgers, Zachary L ; Hughes, Robert M ; Doherty, Laura M ; Shell, Jennifer R ; Molesky, Brian P ; Brugh, Alexander M ; Forbes, Malcolm D E ; Moran, Andrew M ; Lawrence, David S</creatorcontrib><description>Medical hydrogel applications have expanded rapidly over the past decade. Implantation in patients by noninvasive injection is preferred, but this requires hydrogel solidification from a low viscosity solution to occur in vivo via an applied stimuli. Transdermal photo-cross-linking of acrylated biopolymers with photoinitiators and lights offers a mild, spatiotemporally controlled solidification trigger. However, the current short wavelength initiators limit curing depth and efficacy because they do not absorb within the optical window of tissue (600-900 nm). As a solution to the current wavelength limitations, we report the development of a red light responsive initiator capable of polymerizing a range of acrylated monomers. Photoactivation occurs within a range of skin type models containing high biochromophore concentrations.</description><identifier>EISSN: 1520-5126</identifier><identifier>DOI: 10.1021/jacs.5b00182</identifier><identifier>PMID: 25697508</identifier><language>eng</language><publisher>United States</publisher><subject>Acrylates - chemistry ; Cell Survival ; Hep G2 Cells ; Humans ; Hydrogels - chemistry ; Light ; Materials Testing - methods ; Melanins - chemistry ; Photochemistry - methods ; Photolysis ; Polyethylene Glycols - chemistry ; Polymerization ; Propane - analogs & derivatives ; Propane - chemistry ; Skin ; Vitamin B 12 - chemistry</subject><ispartof>Journal of the American Chemical Society, 2015-03, Vol.137 (9), p.3372-3378</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25697508$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rodgers, Zachary L</creatorcontrib><creatorcontrib>Hughes, Robert M</creatorcontrib><creatorcontrib>Doherty, Laura M</creatorcontrib><creatorcontrib>Shell, Jennifer R</creatorcontrib><creatorcontrib>Molesky, Brian P</creatorcontrib><creatorcontrib>Brugh, Alexander M</creatorcontrib><creatorcontrib>Forbes, Malcolm D E</creatorcontrib><creatorcontrib>Moran, Andrew M</creatorcontrib><creatorcontrib>Lawrence, David S</creatorcontrib><title>B(12)-mediated, long wavelength photopolymerization of hydrogels</title><title>Journal of the American Chemical Society</title><addtitle>J Am Chem Soc</addtitle><description>Medical hydrogel applications have expanded rapidly over the past decade. Implantation in patients by noninvasive injection is preferred, but this requires hydrogel solidification from a low viscosity solution to occur in vivo via an applied stimuli. Transdermal photo-cross-linking of acrylated biopolymers with photoinitiators and lights offers a mild, spatiotemporally controlled solidification trigger. However, the current short wavelength initiators limit curing depth and efficacy because they do not absorb within the optical window of tissue (600-900 nm). As a solution to the current wavelength limitations, we report the development of a red light responsive initiator capable of polymerizing a range of acrylated monomers. Photoactivation occurs within a range of skin type models containing high biochromophore concentrations.</description><subject>Acrylates - chemistry</subject><subject>Cell Survival</subject><subject>Hep G2 Cells</subject><subject>Humans</subject><subject>Hydrogels - chemistry</subject><subject>Light</subject><subject>Materials Testing - methods</subject><subject>Melanins - chemistry</subject><subject>Photochemistry - methods</subject><subject>Photolysis</subject><subject>Polyethylene Glycols - chemistry</subject><subject>Polymerization</subject><subject>Propane - analogs & derivatives</subject><subject>Propane - chemistry</subject><subject>Skin</subject><subject>Vitamin B 12 - chemistry</subject><issn>1520-5126</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1j89LwzAYQIMgbk5vnqXHCXbm-9Jk7U03_AUDL7uXNP2ydaRNbTql_vUWnKd3eTx4jN0AXwBHeDhoExay4BxSPGNTkMhjCagm7DKEA-c8wRQu2ASlypaSp1P2uJoD3sU1lZXuqbyPnG920bf-IkfNrt9H7d73vvVuqKmrfnRf-SbyNtoPZed35MIVO7faBbo-cca2L8_b9Vu8-Xh9Xz9t4laqNM4Sq5Fsgbw0osgEJmWGApB0khkNxVKisSaRqEiAkUBJCVYp1GBBLkmJGZv_ZdvOfx4p9HldBUPO6Yb8MeQwykqkY2FUb0_qsRi_8rarat0N-f-0-AU7qFZ0</recordid><startdate>20150311</startdate><enddate>20150311</enddate><creator>Rodgers, Zachary L</creator><creator>Hughes, Robert M</creator><creator>Doherty, Laura M</creator><creator>Shell, Jennifer R</creator><creator>Molesky, Brian P</creator><creator>Brugh, Alexander M</creator><creator>Forbes, Malcolm D E</creator><creator>Moran, Andrew M</creator><creator>Lawrence, David S</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20150311</creationdate><title>B(12)-mediated, long wavelength photopolymerization of hydrogels</title><author>Rodgers, Zachary L ; Hughes, Robert M ; Doherty, Laura M ; Shell, Jennifer R ; Molesky, Brian P ; Brugh, Alexander M ; Forbes, Malcolm D E ; Moran, Andrew M ; Lawrence, David S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p568-94fa2efb20dc3b9324d92312ea49ca1b752cfc4526e31c51e4d1f662a1f157e63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Acrylates - chemistry</topic><topic>Cell Survival</topic><topic>Hep G2 Cells</topic><topic>Humans</topic><topic>Hydrogels - chemistry</topic><topic>Light</topic><topic>Materials Testing - methods</topic><topic>Melanins - chemistry</topic><topic>Photochemistry - methods</topic><topic>Photolysis</topic><topic>Polyethylene Glycols - chemistry</topic><topic>Polymerization</topic><topic>Propane - analogs & derivatives</topic><topic>Propane - chemistry</topic><topic>Skin</topic><topic>Vitamin B 12 - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rodgers, Zachary L</creatorcontrib><creatorcontrib>Hughes, Robert M</creatorcontrib><creatorcontrib>Doherty, Laura M</creatorcontrib><creatorcontrib>Shell, Jennifer R</creatorcontrib><creatorcontrib>Molesky, Brian P</creatorcontrib><creatorcontrib>Brugh, Alexander M</creatorcontrib><creatorcontrib>Forbes, Malcolm D E</creatorcontrib><creatorcontrib>Moran, Andrew M</creatorcontrib><creatorcontrib>Lawrence, David S</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of the American Chemical Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rodgers, Zachary L</au><au>Hughes, Robert M</au><au>Doherty, Laura M</au><au>Shell, Jennifer R</au><au>Molesky, Brian P</au><au>Brugh, Alexander M</au><au>Forbes, Malcolm D E</au><au>Moran, Andrew M</au><au>Lawrence, David S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>B(12)-mediated, long wavelength photopolymerization of hydrogels</atitle><jtitle>Journal of the American Chemical Society</jtitle><addtitle>J Am Chem Soc</addtitle><date>2015-03-11</date><risdate>2015</risdate><volume>137</volume><issue>9</issue><spage>3372</spage><epage>3378</epage><pages>3372-3378</pages><eissn>1520-5126</eissn><abstract>Medical hydrogel applications have expanded rapidly over the past decade. Implantation in patients by noninvasive injection is preferred, but this requires hydrogel solidification from a low viscosity solution to occur in vivo via an applied stimuli. Transdermal photo-cross-linking of acrylated biopolymers with photoinitiators and lights offers a mild, spatiotemporally controlled solidification trigger. However, the current short wavelength initiators limit curing depth and efficacy because they do not absorb within the optical window of tissue (600-900 nm). As a solution to the current wavelength limitations, we report the development of a red light responsive initiator capable of polymerizing a range of acrylated monomers. Photoactivation occurs within a range of skin type models containing high biochromophore concentrations.</abstract><cop>United States</cop><pmid>25697508</pmid><doi>10.1021/jacs.5b00182</doi><tpages>7</tpages></addata></record> |
fulltext | fulltext |
identifier | EISSN: 1520-5126 |
ispartof | Journal of the American Chemical Society, 2015-03, Vol.137 (9), p.3372-3378 |
issn | 1520-5126 |
language | eng |
recordid | cdi_proquest_miscellaneous_1662638452 |
source | ACS Publications; MEDLINE |
subjects | Acrylates - chemistry Cell Survival Hep G2 Cells Humans Hydrogels - chemistry Light Materials Testing - methods Melanins - chemistry Photochemistry - methods Photolysis Polyethylene Glycols - chemistry Polymerization Propane - analogs & derivatives Propane - chemistry Skin Vitamin B 12 - chemistry |
title | B(12)-mediated, long wavelength photopolymerization of hydrogels |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-28T20%3A51%3A50IST&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=B(12)-mediated,%20long%20wavelength%20photopolymerization%20of%20hydrogels&rft.jtitle=Journal%20of%20the%20American%20Chemical%20Society&rft.au=Rodgers,%20Zachary%20L&rft.date=2015-03-11&rft.volume=137&rft.issue=9&rft.spage=3372&rft.epage=3378&rft.pages=3372-3378&rft.eissn=1520-5126&rft_id=info:doi/10.1021/jacs.5b00182&rft_dat=%3Cproquest_pubme%3E1662638452%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=1662638452&rft_id=info:pmid/25697508&rfr_iscdi=true |