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Article: Carbon nanotubes as multifunctional biological transporters and near-infrared agents for selective cancer cell destruction

TitleCarbon nanotubes as multifunctional biological transporters and near-infrared agents for selective cancer cell destruction
Authors
KeywordsCancer cells
Drug delivery nanobiotechnology
Optical excitation
Radiation therapy
Issue Date2005
Citation
Proceedings of the National Academy of Sciences of the United States of America, 2005, v. 102, n. 33, p. 11600-11605 How to Cite?
AbstractBiological systems are known to be highly transparent to 700- to 1,100-nm near-infrared (NIR) light. It is shown here that the strong optical absorbance of single-walled carbon nanotubes (SWNTs) in this special spectral window, an intrinsic property of SWNTs, can be used for optical stimulation of nanotubes inside living cells to afford multifunctional nanotube biological transporters. For oligonucleotides transported inside living cells by nanotubes, the oligos can translocate into cell nucleus upon endosomal rupture triggered by NIR laser pulses. Continuous NIR radiation can cause cell death because of excessive local heating of SWNT in vitro. Selective cancer cell destruction can be achieved by functionalization of SWNT with a folate moiety, selective internalization of SWNTs inside cells labeled with folate receptor tumor markers, and NIR-triggered cell death, without harming receptor-free normal cells. Thus, the transporting capabilities of carbon nanotubes combined with suitable functionalization chemistry and their intrinsic optical properties can lead to new classes of novel nanomaterials for drug delivery and cancer therapy. © 2005 by The National Academy of Sciences of the USA.
Persistent Identifierhttp://hdl.handle.net/10722/334112
ISSN
2023 Impact Factor: 9.4
2023 SCImago Journal Rankings: 3.737
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorKam, Nadine Wong Shi-
dc.contributor.authorO'Connell, Michael-
dc.contributor.authorWisdom, Jeffrey A.-
dc.contributor.authorDai, Hongjie-
dc.date.accessioned2023-10-20T06:45:43Z-
dc.date.available2023-10-20T06:45:43Z-
dc.date.issued2005-
dc.identifier.citationProceedings of the National Academy of Sciences of the United States of America, 2005, v. 102, n. 33, p. 11600-11605-
dc.identifier.issn0027-8424-
dc.identifier.urihttp://hdl.handle.net/10722/334112-
dc.description.abstractBiological systems are known to be highly transparent to 700- to 1,100-nm near-infrared (NIR) light. It is shown here that the strong optical absorbance of single-walled carbon nanotubes (SWNTs) in this special spectral window, an intrinsic property of SWNTs, can be used for optical stimulation of nanotubes inside living cells to afford multifunctional nanotube biological transporters. For oligonucleotides transported inside living cells by nanotubes, the oligos can translocate into cell nucleus upon endosomal rupture triggered by NIR laser pulses. Continuous NIR radiation can cause cell death because of excessive local heating of SWNT in vitro. Selective cancer cell destruction can be achieved by functionalization of SWNT with a folate moiety, selective internalization of SWNTs inside cells labeled with folate receptor tumor markers, and NIR-triggered cell death, without harming receptor-free normal cells. Thus, the transporting capabilities of carbon nanotubes combined with suitable functionalization chemistry and their intrinsic optical properties can lead to new classes of novel nanomaterials for drug delivery and cancer therapy. © 2005 by The National Academy of Sciences of the USA.-
dc.languageeng-
dc.relation.ispartofProceedings of the National Academy of Sciences of the United States of America-
dc.subjectCancer cells-
dc.subjectDrug delivery nanobiotechnology-
dc.subjectOptical excitation-
dc.subjectRadiation therapy-
dc.titleCarbon nanotubes as multifunctional biological transporters and near-infrared agents for selective cancer cell destruction-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1073/pnas.0502680102-
dc.identifier.pmid16087878-
dc.identifier.scopuseid_2-s2.0-23844531202-
dc.identifier.volume102-
dc.identifier.issue33-
dc.identifier.spage11600-
dc.identifier.epage11605-
dc.identifier.isiWOS:000231317000008-

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