Design of double-walled carbon nanotubes for biomedical applications
Double-walled carbon nanotubes (DWNTs) prepared by catalytic chemical vapour deposition were functionalized in such a way that they were optimally designed as a nano-vector for the delivery of small interfering RNA (siRNA), which is of great interest for biomedical research and drug development. DWN...
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Veröffentlicht in: | Nanotechnology 2012-09, Vol.23 (36), p.365102-365102 |
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container_title | Nanotechnology |
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creator | Neves, V Heister, E Costa, S Tîlmaciu, C Flahaut, E Soula, B Coley, H M McFadden, J Silva, S R P |
description | Double-walled carbon nanotubes (DWNTs) prepared by catalytic chemical vapour deposition were functionalized in such a way that they were optimally designed as a nano-vector for the delivery of small interfering RNA (siRNA), which is of great interest for biomedical research and drug development. DWNTs were initially oxidized and coated with a polypeptide (Poly(Lys:Phe)), which was then conjugated to thiol-modified siRNA using a heterobifunctional cross-linker. The obtained oxDWNT-siRNA was characterized by Raman spectroscopy inside and outside a biological environment (mammalian cells). Uptake of the custom-designed nanotubes was not associated with detectable biochemical perturbations in cultured cells, but transfection of cells with DWNTs loaded with siRNA targeting the green fluorescent protein (GFP) gene, serving as a model system, as well as with therapeutic siRNA targeting the survivin gene, led to a significant gene silencing effect, and in the latter case a resulting apoptotic effect in cancer cells. |
doi_str_mv | 10.1088/0957-4484/23/36/365102 |
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DWNTs were initially oxidized and coated with a polypeptide (Poly(Lys:Phe)), which was then conjugated to thiol-modified siRNA using a heterobifunctional cross-linker. The obtained oxDWNT-siRNA was characterized by Raman spectroscopy inside and outside a biological environment (mammalian cells). Uptake of the custom-designed nanotubes was not associated with detectable biochemical perturbations in cultured cells, but transfection of cells with DWNTs loaded with siRNA targeting the green fluorescent protein (GFP) gene, serving as a model system, as well as with therapeutic siRNA targeting the survivin gene, led to a significant gene silencing effect, and in the latter case a resulting apoptotic effect in cancer cells.</description><identifier>ISSN: 0957-4484</identifier><identifier>EISSN: 1361-6528</identifier><identifier>DOI: 10.1088/0957-4484/23/36/365102</identifier><identifier>PMID: 22914449</identifier><identifier>CODEN: NNOTER</identifier><language>eng</language><publisher>England: IOP Publishing</publisher><subject>Apoptosis ; Biochemistry, Molecular Biology ; Bioengineering ; Biomedical Research - methods ; Carbon nanotubes ; Cell Line, Tumor ; Chemical vapor deposition ; Crosslinking ; Engineering Sciences ; Flow Cytometry ; Gene Silencing ; Genes ; Green Fluorescent Proteins - metabolism ; Humans ; Life Sciences ; Micro and nanotechnologies ; Microelectronics ; Nanostructure ; Nanotechnology ; Nanotubes, Carbon - chemistry ; Polypeptides ; Ribonucleic acids ; RNA, Small Interfering - metabolism ; Spectrum Analysis, Raman ; Time Factors</subject><ispartof>Nanotechnology, 2012-09, Vol.23 (36), p.365102-365102</ispartof><rights>2012 IOP Publishing Ltd</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c506t-3054fb2b6efee97994c74c817798bf5a6a9c86956bd897917462065756299c73</citedby><orcidid>0000-0001-8344-6902</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://iopscience.iop.org/article/10.1088/0957-4484/23/36/365102/pdf$$EPDF$$P50$$Giop$$H</linktopdf><link.rule.ids>230,314,776,780,881,27901,27902,53821,53868</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22914449$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-00858588$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Neves, V</creatorcontrib><creatorcontrib>Heister, E</creatorcontrib><creatorcontrib>Costa, S</creatorcontrib><creatorcontrib>Tîlmaciu, C</creatorcontrib><creatorcontrib>Flahaut, E</creatorcontrib><creatorcontrib>Soula, B</creatorcontrib><creatorcontrib>Coley, H M</creatorcontrib><creatorcontrib>McFadden, J</creatorcontrib><creatorcontrib>Silva, S R P</creatorcontrib><title>Design of double-walled carbon nanotubes for biomedical applications</title><title>Nanotechnology</title><addtitle>Nano</addtitle><addtitle>Nanotechnology</addtitle><description>Double-walled carbon nanotubes (DWNTs) prepared by catalytic chemical vapour deposition were functionalized in such a way that they were optimally designed as a nano-vector for the delivery of small interfering RNA (siRNA), which is of great interest for biomedical research and drug development. DWNTs were initially oxidized and coated with a polypeptide (Poly(Lys:Phe)), which was then conjugated to thiol-modified siRNA using a heterobifunctional cross-linker. The obtained oxDWNT-siRNA was characterized by Raman spectroscopy inside and outside a biological environment (mammalian cells). Uptake of the custom-designed nanotubes was not associated with detectable biochemical perturbations in cultured cells, but transfection of cells with DWNTs loaded with siRNA targeting the green fluorescent protein (GFP) gene, serving as a model system, as well as with therapeutic siRNA targeting the survivin gene, led to a significant gene silencing effect, and in the latter case a resulting apoptotic effect in cancer cells.</description><subject>Apoptosis</subject><subject>Biochemistry, Molecular Biology</subject><subject>Bioengineering</subject><subject>Biomedical Research - methods</subject><subject>Carbon nanotubes</subject><subject>Cell Line, Tumor</subject><subject>Chemical vapor deposition</subject><subject>Crosslinking</subject><subject>Engineering Sciences</subject><subject>Flow Cytometry</subject><subject>Gene Silencing</subject><subject>Genes</subject><subject>Green Fluorescent Proteins - metabolism</subject><subject>Humans</subject><subject>Life Sciences</subject><subject>Micro and nanotechnologies</subject><subject>Microelectronics</subject><subject>Nanostructure</subject><subject>Nanotechnology</subject><subject>Nanotubes, Carbon - chemistry</subject><subject>Polypeptides</subject><subject>Ribonucleic acids</subject><subject>RNA, Small Interfering - metabolism</subject><subject>Spectrum Analysis, Raman</subject><subject>Time Factors</subject><issn>0957-4484</issn><issn>1361-6528</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU1LxDAQhoMoun78BelRD3Uz-c5R_IYFL3sPSTbVSrapzVbx35ululdlAhMmz0yG90XoHPAVYKXmWHNZM6bYnNA5FeVwwGQPzYAKqAUnah_NdtAROs75DWMAReAQHRGigTGmZ-j2NuT2patSU63S6GKoP22MYVV5O7jUVZ3t0mZ0IVdNGirXpnVYtd7GyvZ9LJdNm7p8ig4aG3M4-8knaHl_t7x5rBfPD08314vacyw2NcWcNY44EZoQtNSaecm8Aim1cg23wmqvhObCrVR5BskEwYJLLojWXtITdDmNfbXR9EO7tsOXSbY1j9cLs61hrHgJ9QGFvZjYfkjvY8gbs26zDzHaLqQxGyAElASK_4FiKoUAwWlBxYT6IeU8hGa3BmCz9cVsJTdbyQ2hhgoz-VIaz3_-GF1RcNf2a0QByAS0qTdvaRy6IuRfU78BseqUfg</recordid><startdate>20120914</startdate><enddate>20120914</enddate><creator>Neves, V</creator><creator>Heister, E</creator><creator>Costa, S</creator><creator>Tîlmaciu, C</creator><creator>Flahaut, E</creator><creator>Soula, B</creator><creator>Coley, H M</creator><creator>McFadden, J</creator><creator>Silva, S R P</creator><general>IOP Publishing</general><general>Institute of Physics</general><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>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope><scope>JG9</scope><scope>L7M</scope><scope>1XC</scope><scope>VOOES</scope><orcidid>https://orcid.org/0000-0001-8344-6902</orcidid></search><sort><creationdate>20120914</creationdate><title>Design of double-walled carbon nanotubes for biomedical applications</title><author>Neves, V ; Heister, E ; Costa, S ; Tîlmaciu, C ; Flahaut, E ; Soula, B ; Coley, H M ; McFadden, J ; Silva, S R P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c506t-3054fb2b6efee97994c74c817798bf5a6a9c86956bd897917462065756299c73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Apoptosis</topic><topic>Biochemistry, Molecular Biology</topic><topic>Bioengineering</topic><topic>Biomedical Research - methods</topic><topic>Carbon nanotubes</topic><topic>Cell Line, Tumor</topic><topic>Chemical vapor deposition</topic><topic>Crosslinking</topic><topic>Engineering Sciences</topic><topic>Flow Cytometry</topic><topic>Gene Silencing</topic><topic>Genes</topic><topic>Green Fluorescent Proteins - metabolism</topic><topic>Humans</topic><topic>Life Sciences</topic><topic>Micro and nanotechnologies</topic><topic>Microelectronics</topic><topic>Nanostructure</topic><topic>Nanotechnology</topic><topic>Nanotubes, Carbon - chemistry</topic><topic>Polypeptides</topic><topic>Ribonucleic acids</topic><topic>RNA, Small Interfering - metabolism</topic><topic>Spectrum Analysis, Raman</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Neves, V</creatorcontrib><creatorcontrib>Heister, E</creatorcontrib><creatorcontrib>Costa, S</creatorcontrib><creatorcontrib>Tîlmaciu, C</creatorcontrib><creatorcontrib>Flahaut, E</creatorcontrib><creatorcontrib>Soula, B</creatorcontrib><creatorcontrib>Coley, H M</creatorcontrib><creatorcontrib>McFadden, J</creatorcontrib><creatorcontrib>Silva, S R P</creatorcontrib><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>Engineered Materials 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>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><jtitle>Nanotechnology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Neves, V</au><au>Heister, E</au><au>Costa, S</au><au>Tîlmaciu, C</au><au>Flahaut, E</au><au>Soula, B</au><au>Coley, H M</au><au>McFadden, J</au><au>Silva, S R P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Design of double-walled carbon nanotubes for biomedical applications</atitle><jtitle>Nanotechnology</jtitle><stitle>Nano</stitle><addtitle>Nanotechnology</addtitle><date>2012-09-14</date><risdate>2012</risdate><volume>23</volume><issue>36</issue><spage>365102</spage><epage>365102</epage><pages>365102-365102</pages><issn>0957-4484</issn><eissn>1361-6528</eissn><coden>NNOTER</coden><abstract>Double-walled carbon nanotubes (DWNTs) prepared by catalytic chemical vapour deposition were functionalized in such a way that they were optimally designed as a nano-vector for the delivery of small interfering RNA (siRNA), which is of great interest for biomedical research and drug development. DWNTs were initially oxidized and coated with a polypeptide (Poly(Lys:Phe)), which was then conjugated to thiol-modified siRNA using a heterobifunctional cross-linker. The obtained oxDWNT-siRNA was characterized by Raman spectroscopy inside and outside a biological environment (mammalian cells). Uptake of the custom-designed nanotubes was not associated with detectable biochemical perturbations in cultured cells, but transfection of cells with DWNTs loaded with siRNA targeting the green fluorescent protein (GFP) gene, serving as a model system, as well as with therapeutic siRNA targeting the survivin gene, led to a significant gene silencing effect, and in the latter case a resulting apoptotic effect in cancer cells.</abstract><cop>England</cop><pub>IOP Publishing</pub><pmid>22914449</pmid><doi>10.1088/0957-4484/23/36/365102</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0001-8344-6902</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Apoptosis Biochemistry, Molecular Biology Bioengineering Biomedical Research - methods Carbon nanotubes Cell Line, Tumor Chemical vapor deposition Crosslinking Engineering Sciences Flow Cytometry Gene Silencing Genes Green Fluorescent Proteins - metabolism Humans Life Sciences Micro and nanotechnologies Microelectronics Nanostructure Nanotechnology Nanotubes, Carbon - chemistry Polypeptides Ribonucleic acids RNA, Small Interfering - metabolism Spectrum Analysis, Raman Time Factors |
title | Design of double-walled carbon nanotubes for biomedical applications |
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