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Article: Circulation and long-term fate of functionalized, biocompatible single-walled carbon nanotubes in mice probed by Raman spectroscopy

TitleCirculation and long-term fate of functionalized, biocompatible single-walled carbon nanotubes in mice probed by Raman spectroscopy
Authors
KeywordsBiodistribution
Blood circulation
Excretion
Nanoparticles
Toxicity
Issue Date2008
Citation
Proceedings of the National Academy of Sciences of the United States of America, 2008, v. 105, n. 5, p. 1410-1415 How to Cite?
AbstractCarbon nanotubes are promising new materials for molecular delivery in biological systems. The long-term fate of nanotubes intravenously injected into animals in vivo is currently unknown, an issue critical to potential clinical applications of these materials. Here, using the intrinsic Raman spectroscopic signatures of single-walled carbon nanotubes (SWNTs), we measured the blood circulation of intravenously injected SWNTs and detect SWNTs in various organs and tissues of mice ex vivo over a period of three months. Functionalization of SWNTs by branched polyethyleneglycol (PEG) chains was developed, enabling thus far the longest SWNT blood circulation up to 1 day, relatively low uptake in the reticuloendothelial system (RES), and near-complete clearance from the main organs in ∼2 months. Raman spectroscopy detected SWNT in the intestine, feces, kidney, and bladder of mice, suggesting excretion and clearance of SWNTs from mice via the biliary and renal pathways. No toxic side effect of SWNTs to mice was observed in necropsy, histology, and blood chemistry measurements. These findings pave the way to future biomedical applications of carbon nanotubes. © 2008 by The National Academy of Sciences of the USA.
Persistent Identifierhttp://hdl.handle.net/10722/334161
ISSN
2023 Impact Factor: 9.4
2023 SCImago Journal Rankings: 3.737
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLiu, Zhuang-
dc.contributor.authorDavis, Corrine-
dc.contributor.authorCai, Weibo-
dc.contributor.authorHe, Lina-
dc.contributor.authorChen, Xiaoyuan-
dc.contributor.authorDai, Hongjie-
dc.date.accessioned2023-10-20T06:46:10Z-
dc.date.available2023-10-20T06:46:10Z-
dc.date.issued2008-
dc.identifier.citationProceedings of the National Academy of Sciences of the United States of America, 2008, v. 105, n. 5, p. 1410-1415-
dc.identifier.issn0027-8424-
dc.identifier.urihttp://hdl.handle.net/10722/334161-
dc.description.abstractCarbon nanotubes are promising new materials for molecular delivery in biological systems. The long-term fate of nanotubes intravenously injected into animals in vivo is currently unknown, an issue critical to potential clinical applications of these materials. Here, using the intrinsic Raman spectroscopic signatures of single-walled carbon nanotubes (SWNTs), we measured the blood circulation of intravenously injected SWNTs and detect SWNTs in various organs and tissues of mice ex vivo over a period of three months. Functionalization of SWNTs by branched polyethyleneglycol (PEG) chains was developed, enabling thus far the longest SWNT blood circulation up to 1 day, relatively low uptake in the reticuloendothelial system (RES), and near-complete clearance from the main organs in ∼2 months. Raman spectroscopy detected SWNT in the intestine, feces, kidney, and bladder of mice, suggesting excretion and clearance of SWNTs from mice via the biliary and renal pathways. No toxic side effect of SWNTs to mice was observed in necropsy, histology, and blood chemistry measurements. These findings pave the way to future biomedical applications of carbon nanotubes. © 2008 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.subjectBiodistribution-
dc.subjectBlood circulation-
dc.subjectExcretion-
dc.subjectNanoparticles-
dc.subjectToxicity-
dc.titleCirculation and long-term fate of functionalized, biocompatible single-walled carbon nanotubes in mice probed by Raman spectroscopy-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1073/pnas.0707654105-
dc.identifier.pmid18230737-
dc.identifier.scopuseid_2-s2.0-40349112868-
dc.identifier.volume105-
dc.identifier.issue5-
dc.identifier.spage1410-
dc.identifier.epage1415-
dc.identifier.eissn1091-6490-
dc.identifier.isiWOS:000253077900007-

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