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

被引:5
|
作者
Black, Kvar C. L. [1 ,2 ]
Yi, Ji [1 ]
Rivera, Jose G. [1 ]
Zelasko-Leon, Daria C. [1 ]
Messersmith, Phillip B. [1 ]
机构
[1] Northwestern Univ, Evanston, IL 60208 USA
[2] Washington Univ, Sch Med, Dept Radiol, St Louis, MO 63110 USA
基金
美国国家科学基金会;
关键词
antibody; biomimetic adhesion; EGF receptor; mussel foot proteins; nanoparticle; optical imaging; photothermal therapy; plasmon; surface modification; GROWTH-FACTOR RECEPTOR; BREAST-CANCER; ADHESIVE PROTEIN; PEPTIDE LIGANDS; ORAL-CANCER; NANOPARTICLES; MUSSEL; DOPAMINE; OXIDE; SPECTROSCOPY;
D O I
10.2217/NNM.12.82
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
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.
引用
收藏
页码:17 / 28
页数:12
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