4.7 Article

Polydopamine-enabled surface functionalization of gold nanorods for cancer cell-targeted imaging and photothermal therapy

期刊

NANOMEDICINE
卷 8, 期 1, 页码 17-28

出版社

FUTURE MEDICINE LTD
DOI: 10.2217/NNM.12.82

关键词

antibody; biomimetic adhesion; EGF receptor; mussel foot proteins; nanoparticle; optical imaging; photothermal therapy; plasmon; surface modification

资金

  1. Ruth Kirschstein National Research Service Award from National Institute of Dental and Craniofacial Research [NIH F31 DE019750]
  2. NIH [RO1 EB005772, R37 DE014193, R01 CA128641, R01 EB003682]
  3. National Science Foundation Graduate Research Fellowship [DGE-0824162]
  4. NSF [CBET-0937987]

向作者/读者索取更多资源

Aim: A novel biomimetic strategy was employed for presenting antibodies on gold nanorods (NRs) to target growth factor receptors on cancer cells for use in photothermal therapy. Materials & methods: Polydopamine (PD) was polymerized onto gold NRs, and EGF receptor antibodies (anti-EGFR) were immobilized onto the layer. Cell-binding affinity and light-activated cell death of cancer cells incubated with anti-EGFR-PD-NRs were quantified by optical imaging. Results: PD was deposited onto gold NRs, and antibodies were bound to PD-coated NRs. Anti-EGFR-PD-NRs were stable in media, and were specifically bound to EGFR-overexpressing cells. Illumination of cells targeted with anti-EGFR-PD-NRs enhanced cell death compared with nonirradiated controls and cells treated with antibody-free NRs. Conclusion: PD facilitates the surface functionalization of gold NRs with biomolecules, allowing cell targeting and photothermal killing of cancer cells. PD can potentially coat a large variety of nanoparticles with targeting ligands as a strategy for biofunctionalization of diagnostic and therapeutic nanoparticles.

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