Laboratório de Nanoestruturas Plasmônicas, Instituto de Ciências Exatas, Universidade Federal de Juiz de Fora, Juiz de Fora, MG, Brazil.
Núcleo de Pesquisa e Inovação em Ciências da Saúde, Faculdade de Farmácia, Universidade Federal de Juiz de Fora, Juiz de Fora, MG, Brazil.
Colloids Surf B Biointerfaces. 2018 Oct 1;170:712-717. doi: 10.1016/j.colsurfb.2018.07.001. Epub 2018 Jul 4.
Gold nanoparticles (AuNP) were synthesized and modified with anti-folate receptor antibody (AB), folic acid (FA), crystal violet (CV), poly (ethyleneglycol) methyl ether thiol and the antineoplastic drug tamoxifen (TAM). Such a preparation was incubated in vitro with MCF-7 human breast cancer cells, showing a decrease in the TAM dosage for the reduction of cell viability. The adsorption of TAM on gold surface was investigated by surface-enhanced Raman scattering (SERS) spectroscopy and the assignment based on Density Functional Theory calculations showed that the ether moiety was involved in the interactions with the metal. Such a chemical affinity was correlated with the carrying of TAM in the biological media. CV was included in the preparation as a molecular probe for SERS spectroscopy, whose signal was monitored to analyse the efficiency of the modified AuNP in the target of neoplastic cells. The results showed AB, FA and TAM components had complementary roles in the cell recognition and, therefore, in the efficiency of the drug carrier nanosystem.
金纳米粒子 (AuNP) 经合成并修饰为叶酸受体抗体 (AB)、叶酸 (FA)、结晶紫 (CV)、聚乙二醇甲醚硫醇和抗肿瘤药物他莫昔芬 (TAM)。这种制剂在体外与 MCF-7 人乳腺癌细胞孵育,显示出 TAM 剂量减少,细胞活力降低。通过表面增强拉曼散射 (SERS) 光谱研究了 TAM 在金表面的吸附,基于密度泛函理论计算的分配表明醚部分参与了与金属的相互作用。这种化学亲和力与在生物介质中携带 TAM 有关。CV 被包含在制剂中作为 SERS 光谱的分子探针,监测其信号以分析修饰的 AuNP 在肿瘤细胞靶标中的效率。结果表明,AB、FA 和 TAM 成分在细胞识别中具有互补作用,因此在药物载体纳米系统的效率中具有互补作用。