Author/Authors :
Lam، نويسنده , , Anh Thu Ngoc and Yoon، نويسنده , , Jinha and Ganbold، نويسنده , , Erdene-Ochir and Singh، نويسنده , , Dheeraj K. and Kim، نويسنده , , Doseok and Cho، نويسنده , , Kwang-Hwi and Lee، نويسنده , , So Yeong and Choo، نويسنده , , Jaebum and Lee، نويسنده , , Kangtaek and Joo، نويسنده , , Sang-Woo، نويسنده ,
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 h.
Keywords :
Lung cancer cells , gefitinib , Gold nanoparticle conjugates , surface-enhanced Raman scattering , Cell viability