Differential fine-tuning of cochlear implant material-cell interactions by femtosecond laser microstructuring
Cochlear implants (CIs) can restore hearing in deaf patients by electrical stimulation of the auditory nerve. To optimize the electrical stimulation, the number of independent channels must be increased by reduction of connective tissue growth on the electrode surface and selective neuronal cell con...
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Veröffentlicht in: | Journal of biomedical materials research. Part B, Applied biomaterials Applied biomaterials, 2008-10, Vol.87B (1), p.146-153 |
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creator | Reich, Uta Mueller, Peter P. Fadeeva, Elena Chichkov, Boris N. Stoever, Timo Fabian, Tilman Lenarz, Thomas Reuter, Guenter |
description | Cochlear implants (CIs) can restore hearing in deaf patients by electrical stimulation of the auditory nerve. To optimize the electrical stimulation, the number of independent channels must be increased by reduction of connective tissue growth on the electrode surface and selective neuronal cell contact. The femtosecond laser microstructuring of the electrode surfaces was performed to investigate the effect of fibroblast growth on the implant material. A cell culture model system was established to evaluate cell–material interactions on these microstructured CI‐electrode materials. Fibroblasts were used as a cell culture model for connective tissue formation, and differentiating neuronal‐like cells were employed to represent neuronal cells. For nondestructive microscopic examination of living cells on the structured surfaces, the cells were genetically modified to express green fluorescent protein. To investigate the special interaction between the electrode material and the tissue we used electrode material which is originally used for manufacturing CI for human applications, namely platinum (contact material) and silicone carrier material (LSR 30, HCRP 50). Microstructures of various dimensions (groove width 1–10 μm) were generated by using femtosecond laser ablation. The highest fibroblast growth rate was observed on platinum, but cell growth rates on the silicone carrier material were lower. Microstructuring reduced fibroblast cell growth on platinum significantly. On the microstructured silicone, a trend to lower cell growth rates was observed. In addition, microgrooves on platinum surfaces can direct neurite outgrowth parallel to the grooves. The implications of the results are discussed with respect to the design of a microstructured CI surface. © 2008 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater 2008 |
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To optimize the electrical stimulation, the number of independent channels must be increased by reduction of connective tissue growth on the electrode surface and selective neuronal cell contact. The femtosecond laser microstructuring of the electrode surfaces was performed to investigate the effect of fibroblast growth on the implant material. A cell culture model system was established to evaluate cell–material interactions on these microstructured CI‐electrode materials. Fibroblasts were used as a cell culture model for connective tissue formation, and differentiating neuronal‐like cells were employed to represent neuronal cells. For nondestructive microscopic examination of living cells on the structured surfaces, the cells were genetically modified to express green fluorescent protein. To investigate the special interaction between the electrode material and the tissue we used electrode material which is originally used for manufacturing CI for human applications, namely platinum (contact material) and silicone carrier material (LSR 30, HCRP 50). Microstructures of various dimensions (groove width 1–10 μm) were generated by using femtosecond laser ablation. The highest fibroblast growth rate was observed on platinum, but cell growth rates on the silicone carrier material were lower. Microstructuring reduced fibroblast cell growth on platinum significantly. On the microstructured silicone, a trend to lower cell growth rates was observed. In addition, microgrooves on platinum surfaces can direct neurite outgrowth parallel to the grooves. The implications of the results are discussed with respect to the design of a microstructured CI surface. © 2008 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater 2008</description><identifier>ISSN: 1552-4973</identifier><identifier>EISSN: 1552-4981</identifier><identifier>DOI: 10.1002/jbm.b.31084</identifier><identifier>PMID: 18437711</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Animals ; Cell Differentiation ; Cell Proliferation ; Cells, Cultured ; cochlear implant electrode ; Cochlear Implants ; Electrodes ; femtosecond laser technology ; Fibroblasts - cytology ; Lasers ; Mice ; microstructured surface ; Neurons - cytology ; Platinum ; Rats ; Silicones ; transgenic cells</subject><ispartof>Journal of biomedical materials research. Part B, Applied biomaterials, 2008-10, Vol.87B (1), p.146-153</ispartof><rights>Copyright © 2008 Wiley Periodicals, Inc.</rights><rights>(c) 2008 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3984-f601247b2b708cc9023ce31d25450ab04df7579dd49ad99a87084e84122d75933</citedby><cites>FETCH-LOGICAL-c3984-f601247b2b708cc9023ce31d25450ab04df7579dd49ad99a87084e84122d75933</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%2Fjbm.b.31084$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjbm.b.31084$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18437711$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Reich, Uta</creatorcontrib><creatorcontrib>Mueller, Peter P.</creatorcontrib><creatorcontrib>Fadeeva, Elena</creatorcontrib><creatorcontrib>Chichkov, Boris N.</creatorcontrib><creatorcontrib>Stoever, Timo</creatorcontrib><creatorcontrib>Fabian, Tilman</creatorcontrib><creatorcontrib>Lenarz, Thomas</creatorcontrib><creatorcontrib>Reuter, Guenter</creatorcontrib><title>Differential fine-tuning of cochlear implant material-cell interactions by femtosecond laser microstructuring</title><title>Journal of biomedical materials research. Part B, Applied biomaterials</title><addtitle>J. Biomed. Mater. Res</addtitle><description>Cochlear implants (CIs) can restore hearing in deaf patients by electrical stimulation of the auditory nerve. To optimize the electrical stimulation, the number of independent channels must be increased by reduction of connective tissue growth on the electrode surface and selective neuronal cell contact. The femtosecond laser microstructuring of the electrode surfaces was performed to investigate the effect of fibroblast growth on the implant material. A cell culture model system was established to evaluate cell–material interactions on these microstructured CI‐electrode materials. Fibroblasts were used as a cell culture model for connective tissue formation, and differentiating neuronal‐like cells were employed to represent neuronal cells. For nondestructive microscopic examination of living cells on the structured surfaces, the cells were genetically modified to express green fluorescent protein. To investigate the special interaction between the electrode material and the tissue we used electrode material which is originally used for manufacturing CI for human applications, namely platinum (contact material) and silicone carrier material (LSR 30, HCRP 50). Microstructures of various dimensions (groove width 1–10 μm) were generated by using femtosecond laser ablation. The highest fibroblast growth rate was observed on platinum, but cell growth rates on the silicone carrier material were lower. Microstructuring reduced fibroblast cell growth on platinum significantly. On the microstructured silicone, a trend to lower cell growth rates was observed. In addition, microgrooves on platinum surfaces can direct neurite outgrowth parallel to the grooves. The implications of the results are discussed with respect to the design of a microstructured CI surface. © 2008 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater 2008</description><subject>Animals</subject><subject>Cell Differentiation</subject><subject>Cell Proliferation</subject><subject>Cells, Cultured</subject><subject>cochlear implant electrode</subject><subject>Cochlear Implants</subject><subject>Electrodes</subject><subject>femtosecond laser technology</subject><subject>Fibroblasts - cytology</subject><subject>Lasers</subject><subject>Mice</subject><subject>microstructured surface</subject><subject>Neurons - cytology</subject><subject>Platinum</subject><subject>Rats</subject><subject>Silicones</subject><subject>transgenic cells</subject><issn>1552-4973</issn><issn>1552-4981</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0c1vFCEYBvCJsbG1evJuOHlpZuVzGI5a26ppaxo1HgnDvCh1YFZgovvfy7rbetMTkPzeJ8DTNM8IXhGM6cvbIayGFSO45w-aIyIEbbnqycP7vWSHzeOcbyvusGCPmkPScyYlIUdNeOOdgwSxeDMh5yO0ZYk-fkWzQ3a23yYwCfmwnkwsKJgCqcLWwjQhH-vJ2OLnmNGwQQ5CmTPYOY5oMhkSCt6mOZe02LKkGvqkOXBmyvB0vx43n8_PPp2-bS8_XLw7fXXZWqZ63roOE8rlQAeJe2sVpswCIyMVXGAzYD46KaQaR67MqJTpK-PQc0LpKIVi7Lh5sctdp_nHArno4PP2zibCvGTdKSFw14v_QsYJJ1jSCk92cPugnMDpdfLBpI0mWG9r0LUGPeg_NVT9fB-7DAHGv3b_7xWQHfjpJ9j8K0u_f311F9ruZnwu8Ot-xqTvupNMCv3l-kJ_vGHXpDu_0VfsN_AHoyE</recordid><startdate>200810</startdate><enddate>200810</enddate><creator>Reich, Uta</creator><creator>Mueller, Peter P.</creator><creator>Fadeeva, Elena</creator><creator>Chichkov, Boris N.</creator><creator>Stoever, Timo</creator><creator>Fabian, Tilman</creator><creator>Lenarz, Thomas</creator><creator>Reuter, Guenter</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</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>7SR</scope><scope>7TB</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope><scope>JG9</scope><scope>L7M</scope><scope>7X8</scope></search><sort><creationdate>200810</creationdate><title>Differential fine-tuning of cochlear implant material-cell interactions by femtosecond laser microstructuring</title><author>Reich, Uta ; Mueller, Peter P. ; Fadeeva, Elena ; Chichkov, Boris N. ; Stoever, Timo ; Fabian, Tilman ; Lenarz, Thomas ; Reuter, Guenter</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3984-f601247b2b708cc9023ce31d25450ab04df7579dd49ad99a87084e84122d75933</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Animals</topic><topic>Cell Differentiation</topic><topic>Cell Proliferation</topic><topic>Cells, Cultured</topic><topic>cochlear implant electrode</topic><topic>Cochlear Implants</topic><topic>Electrodes</topic><topic>femtosecond laser technology</topic><topic>Fibroblasts - cytology</topic><topic>Lasers</topic><topic>Mice</topic><topic>microstructured surface</topic><topic>Neurons - cytology</topic><topic>Platinum</topic><topic>Rats</topic><topic>Silicones</topic><topic>transgenic cells</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Reich, Uta</creatorcontrib><creatorcontrib>Mueller, Peter P.</creatorcontrib><creatorcontrib>Fadeeva, Elena</creatorcontrib><creatorcontrib>Chichkov, Boris N.</creatorcontrib><creatorcontrib>Stoever, Timo</creatorcontrib><creatorcontrib>Fabian, Tilman</creatorcontrib><creatorcontrib>Lenarz, Thomas</creatorcontrib><creatorcontrib>Reuter, Guenter</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of biomedical materials research. Part B, Applied biomaterials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Reich, Uta</au><au>Mueller, Peter P.</au><au>Fadeeva, Elena</au><au>Chichkov, Boris N.</au><au>Stoever, Timo</au><au>Fabian, Tilman</au><au>Lenarz, Thomas</au><au>Reuter, Guenter</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differential fine-tuning of cochlear implant material-cell interactions by femtosecond laser microstructuring</atitle><jtitle>Journal of biomedical materials research. Part B, Applied biomaterials</jtitle><addtitle>J. Biomed. Mater. Res</addtitle><date>2008-10</date><risdate>2008</risdate><volume>87B</volume><issue>1</issue><spage>146</spage><epage>153</epage><pages>146-153</pages><issn>1552-4973</issn><eissn>1552-4981</eissn><abstract>Cochlear implants (CIs) can restore hearing in deaf patients by electrical stimulation of the auditory nerve. To optimize the electrical stimulation, the number of independent channels must be increased by reduction of connective tissue growth on the electrode surface and selective neuronal cell contact. The femtosecond laser microstructuring of the electrode surfaces was performed to investigate the effect of fibroblast growth on the implant material. A cell culture model system was established to evaluate cell–material interactions on these microstructured CI‐electrode materials. Fibroblasts were used as a cell culture model for connective tissue formation, and differentiating neuronal‐like cells were employed to represent neuronal cells. For nondestructive microscopic examination of living cells on the structured surfaces, the cells were genetically modified to express green fluorescent protein. To investigate the special interaction between the electrode material and the tissue we used electrode material which is originally used for manufacturing CI for human applications, namely platinum (contact material) and silicone carrier material (LSR 30, HCRP 50). Microstructures of various dimensions (groove width 1–10 μm) were generated by using femtosecond laser ablation. The highest fibroblast growth rate was observed on platinum, but cell growth rates on the silicone carrier material were lower. Microstructuring reduced fibroblast cell growth on platinum significantly. On the microstructured silicone, a trend to lower cell growth rates was observed. In addition, microgrooves on platinum surfaces can direct neurite outgrowth parallel to the grooves. The implications of the results are discussed with respect to the design of a microstructured CI surface. © 2008 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater 2008</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>18437711</pmid><doi>10.1002/jbm.b.31084</doi><tpages>8</tpages></addata></record> |
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subjects | Animals Cell Differentiation Cell Proliferation Cells, Cultured cochlear implant electrode Cochlear Implants Electrodes femtosecond laser technology Fibroblasts - cytology Lasers Mice microstructured surface Neurons - cytology Platinum Rats Silicones transgenic cells |
title | Differential fine-tuning of cochlear implant material-cell interactions by femtosecond laser microstructuring |
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