Colloidal gold nanoparticle conjugates of gefitinib

被引:32
|
作者
Anh Thu Ngoc Lam [1 ]
Yoon, Jinha [1 ]
Ganbold, Erdene-Ochir [1 ]
Singh, Dheeraj K. [2 ]
Kim, Doseok [2 ]
Cho, Kwang-Hwi [3 ]
Lee, So Yeong [4 ]
Choo, Jaebum [5 ]
Lee, Kangtaek [6 ]
Joo, Sang-Woo [1 ]
机构
[1] Soongsil Univ, Dept Chem, Seoul 156743, South Korea
[2] Sogang Univ, Dept Phys, Seoul 121742, South Korea
[3] Soongsil Univ, Sch Syst Biomed Sci, Seoul 156743, South Korea
[4] Seoul Natl Univ, Coll Vet Med, Seoul 156743, South Korea
[5] Hanyang Univ, Dept Bionano Technol, Ansan 426791, South Korea
[6] Yonsei Univ, Dept Chem & Biomol Engn, Seoul 120749, South Korea
基金
新加坡国家研究基金会;
关键词
Lung cancer cells; Gold nanoparticle conjugates; Gefitinib; Cell viability; Surface-enhanced Raman scattering; FACTOR RECEPTOR MUTATIONS; SURFACE-ENHANCED RAMAN; CELL LUNG-CANCER; SILVER; SERUM; ADSORPTION;
D O I
10.1016/j.colsurfb.2014.08.021
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Gefitinib (GF) is a US Food and Drug Administration-approved epidermal growth factor receptor (EGFR)tyrosine kinase inhibitor for treating the lung cancers. We fabricated colloidal gold nanoparticle (AuNP) conjugates of the GF anticancer drug by self-assembly to test their potency against A549, NCI-H460, and NCI-H1975 lung cancer cells. GF adsorption on AuNP surfaces was examined by UV vis absorption spectra and surface-enhanced Raman scattering. Density functional theory calculations were performed to estimate the energetic stabilities of the drug-AuNP composites. The N1 nitrogen atom of the quinazoline ring of GF was calculated to be more stable than the N3 in binding Au cluster atoms. The internalizations of GF-coated AuNPs were examined by transmission electron and dark-field microscopy. A cell viability test of AuNP GF conjugates with the EGFR antibody exhibited much higher reductions than free GF for A549, NCI-H460, and NCI-H1975 lung cancer cells after treatment for 48 h. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:61 / 67
页数:7
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