| Literature DB >> 25216919 |
Anh Thu Ngoc Lam1, Jinha Yoon1, Erdene-Ochir Ganbold1, Dheeraj K Singh2, Doseok Kim2, Kwang-Hwi Cho3, So Yeong Lee4, Jaebum Choo5, Kangtaek Lee6, Sang-Woo Joo7.
Abstract
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.Entities:
Keywords: Cell viability; Gefitinib; Gold nanoparticle conjugates; Lung cancer cells; Surface-enhanced Raman scattering
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Year: 2014 PMID: 25216919 DOI: 10.1016/j.colsurfb.2014.08.021
Source DB: PubMed Journal: Colloids Surf B Biointerfaces ISSN: 0927-7765 Impact factor: 5.268