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- Publisher Website: 10.1021/ja803688x
- Scopus: eid_2-s2.0-50249123111
- PMID: 18661992
- WOS: WOS:000258415900023
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Article: PEGylated nanographene oxide for delivery of water-insoluble cancer drugs
Title | PEGylated nanographene oxide for delivery of water-insoluble cancer drugs |
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Authors | |
Issue Date | 2008 |
Citation | Journal of the American Chemical Society, 2008, v. 130, n. 33, p. 10876-10877 How to Cite? |
Abstract | It is known that many potent, often aromatic drugs are water insoluble, which has hampered their use for disease treatment. In this work, we functionalized nanographene oxide (NGO), a novel graphitic material, with branched polyethylene glycol (PEG) to obtain a biocompatible NGO-PEG conjugate stable in various biological solutions, and used them for attaching hydrophobic aromatic molecules including a camptothecin (CPT) analogue, SN38, noncovalently via π-π stacking. The resulting NGO-PEG-SN38 complex exhibited excellent water solubility while maintaining its high cancer cell killing potency similar to that of the free SN38 molecules in organic solvents. The efficacy of NGO-PEG-SN38 was far higher than that of irinotecan (CPT-11), a FDA-approved water soluble SN38 prodrug used for the treatment of colon cancer. Our results showed that graphene is a novel class of material promising for biological applications including future in vivo cancer treatment with various aromatic, low-solubility drugs. Copyright © 2008 American Chemical Society. |
Persistent Identifier | http://hdl.handle.net/10722/334179 |
ISSN | 2023 Impact Factor: 14.4 2023 SCImago Journal Rankings: 5.489 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Liu, Zhuang | - |
dc.contributor.author | Robinson, Joshua T. | - |
dc.contributor.author | Sun, Xiaoming | - |
dc.contributor.author | Dai, Hongjie | - |
dc.date.accessioned | 2023-10-20T06:46:18Z | - |
dc.date.available | 2023-10-20T06:46:18Z | - |
dc.date.issued | 2008 | - |
dc.identifier.citation | Journal of the American Chemical Society, 2008, v. 130, n. 33, p. 10876-10877 | - |
dc.identifier.issn | 0002-7863 | - |
dc.identifier.uri | http://hdl.handle.net/10722/334179 | - |
dc.description.abstract | It is known that many potent, often aromatic drugs are water insoluble, which has hampered their use for disease treatment. In this work, we functionalized nanographene oxide (NGO), a novel graphitic material, with branched polyethylene glycol (PEG) to obtain a biocompatible NGO-PEG conjugate stable in various biological solutions, and used them for attaching hydrophobic aromatic molecules including a camptothecin (CPT) analogue, SN38, noncovalently via π-π stacking. The resulting NGO-PEG-SN38 complex exhibited excellent water solubility while maintaining its high cancer cell killing potency similar to that of the free SN38 molecules in organic solvents. The efficacy of NGO-PEG-SN38 was far higher than that of irinotecan (CPT-11), a FDA-approved water soluble SN38 prodrug used for the treatment of colon cancer. Our results showed that graphene is a novel class of material promising for biological applications including future in vivo cancer treatment with various aromatic, low-solubility drugs. Copyright © 2008 American Chemical Society. | - |
dc.language | eng | - |
dc.relation.ispartof | Journal of the American Chemical Society | - |
dc.title | PEGylated nanographene oxide for delivery of water-insoluble cancer drugs | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1021/ja803688x | - |
dc.identifier.pmid | 18661992 | - |
dc.identifier.scopus | eid_2-s2.0-50249123111 | - |
dc.identifier.volume | 130 | - |
dc.identifier.issue | 33 | - |
dc.identifier.spage | 10876 | - |
dc.identifier.epage | 10877 | - |
dc.identifier.isi | WOS:000258415900023 | - |