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- Publisher Website: 10.1021/acsami.5b06250
- Scopus: eid_2-s2.0-84940848334
- PMID: 26278410
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Article: Solvent-Free Click-Mechanochemistry for the Preparation of Cancer Cell Targeting Graphene Oxide
Title | Solvent-Free Click-Mechanochemistry for the Preparation of Cancer Cell Targeting Graphene Oxide |
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Authors | |
Keywords | antibody breast cancer drug delivery nanomedicine toxicity |
Issue Date | 2015 |
Citation | ACS Applied Materials and Interfaces, 2015, v. 7, n. 34, p. 18920-18923 How to Cite? |
Abstract | Polyethylene glycol-functionalized nanographene oxide (PEGylated n-GO) was synthesized from alkyne-modified n-GO, using solvent-free click-mechanochemistry, i.e., copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC). The modified n-GO was subsequently conjugated to a mucin 1 receptor immunoglobulin G antibody (anti-MUC1 IgG) via thiol-ene coupling reaction. n-GO derivatives were characterized with Fourier-transformed infrared (FT-IR) spectroscopy, thermogravimetric analysis (TGA), Bradford assay, sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE), and atomic force microscopy (AFM). Cell targeting was confirmed in vitro in MDA-MB-231 cells, either expressing or lacking MUC1 receptors, using flow cytometry, confocal laser scanning microscopy (CLSM) and multiphoton (MP) fluorescence microscopy. Biocompatibility was assessed using the modified lactate dehydrongenase (mLDH) assay. |
Persistent Identifier | http://hdl.handle.net/10722/349084 |
ISSN | 2023 Impact Factor: 8.3 2023 SCImago Journal Rankings: 2.058 |
DC Field | Value | Language |
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dc.contributor.author | Rubio, Noelia | - |
dc.contributor.author | Mei, Kuo Ching | - |
dc.contributor.author | Klippstein, Rebecca | - |
dc.contributor.author | Costa, Pedro M. | - |
dc.contributor.author | Hodgins, Naomi | - |
dc.contributor.author | Wang, Julie Tzu Wen | - |
dc.contributor.author | Festy, Frederic | - |
dc.contributor.author | Abbate, Vincenzo | - |
dc.contributor.author | Hider, Robert C. | - |
dc.contributor.author | Chan, Ka Lung Andrew | - |
dc.contributor.author | Al-Jamal, Khuloud T. | - |
dc.date.accessioned | 2024-10-17T06:56:09Z | - |
dc.date.available | 2024-10-17T06:56:09Z | - |
dc.date.issued | 2015 | - |
dc.identifier.citation | ACS Applied Materials and Interfaces, 2015, v. 7, n. 34, p. 18920-18923 | - |
dc.identifier.issn | 1944-8244 | - |
dc.identifier.uri | http://hdl.handle.net/10722/349084 | - |
dc.description.abstract | Polyethylene glycol-functionalized nanographene oxide (PEGylated n-GO) was synthesized from alkyne-modified n-GO, using solvent-free click-mechanochemistry, i.e., copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC). The modified n-GO was subsequently conjugated to a mucin 1 receptor immunoglobulin G antibody (anti-MUC1 IgG) via thiol-ene coupling reaction. n-GO derivatives were characterized with Fourier-transformed infrared (FT-IR) spectroscopy, thermogravimetric analysis (TGA), Bradford assay, sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE), and atomic force microscopy (AFM). Cell targeting was confirmed in vitro in MDA-MB-231 cells, either expressing or lacking MUC1 receptors, using flow cytometry, confocal laser scanning microscopy (CLSM) and multiphoton (MP) fluorescence microscopy. Biocompatibility was assessed using the modified lactate dehydrongenase (mLDH) assay. | - |
dc.language | eng | - |
dc.relation.ispartof | ACS Applied Materials and Interfaces | - |
dc.subject | antibody | - |
dc.subject | breast cancer | - |
dc.subject | drug delivery | - |
dc.subject | nanomedicine | - |
dc.subject | toxicity | - |
dc.title | Solvent-Free Click-Mechanochemistry for the Preparation of Cancer Cell Targeting Graphene Oxide | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1021/acsami.5b06250 | - |
dc.identifier.pmid | 26278410 | - |
dc.identifier.scopus | eid_2-s2.0-84940848334 | - |
dc.identifier.volume | 7 | - |
dc.identifier.issue | 34 | - |
dc.identifier.spage | 18920 | - |
dc.identifier.epage | 18923 | - |
dc.identifier.eissn | 1944-8252 | - |