Ristig Simon, Kozlova Diana, Meyer-Zaika Wolfgang, Epple Matthias
Inorganic Chemistry and Centre for Nanointegration Duisburg-Essen (CeNIDE), University of Duisburg-Essen, Universitaetsstr. 5-7, 45117 Essen, Germany.
J Mater Chem B. 2014 Dec 7;2(45):7887-7895. doi: 10.1039/c4tb01010h. Epub 2014 Oct 10.
A one-pot synthesis of fluorescent bimetallic silver-gold nanoparticles in aqueous medium is presented. Carboxylic acid-functionalized nanoparticles were prepared with different metal compositions from 90 : 10 to 10 : 90 (n : n) for silver : gold with a diameter of 1.8 ± 0.4 nm. Pure silver and gold nanoparticles were prepared for comparison. Spectroscopic analyses showed that the ligand, i.e. 11-mercaptoundecanoic acid, binds to the particle surface by the thiol group, leaving the carboxylic acid accessible for further functionalization, e.g. by suitable coupling reactions. Nanoparticles with a silver content up to 60 : 40 showed autofluorescence with a large Stokes shift of about 250-300 nm (maximum wavelength of the emission between 608 nm and 645 nm). The intracellular localization of bimetallic silver-gold nanoparticles was studied in HeLa cells by confocal laser scanning microscopy (CLSM). The alloyed silver-gold nanoparticles showed no significant cytotoxicity at a metal concentration of 5 μg mL for 24 h, but were cytotoxic to some degree at 50 μg mL at higher silver content.
本文介绍了在水介质中一锅法合成荧光双金属银金纳米颗粒的方法。制备了羧酸官能化的纳米颗粒,其银与金的金属组成比例从90 : 10到10 : 90(n : n)不等,直径为1.8 ± 0.4 nm。制备了纯银和金纳米颗粒用于比较。光谱分析表明,配体,即11-巯基十一烷酸,通过硫醇基团与颗粒表面结合,使羧酸可用于进一步功能化,例如通过合适的偶联反应。银含量高达60 : 40的纳米颗粒表现出自发荧光,斯托克斯位移约为250 - 300 nm(发射的最大波长在608 nm至645 nm之间)。通过共聚焦激光扫描显微镜(CLSM)研究了双金属银金纳米颗粒在HeLa细胞中的细胞内定位。在金属浓度为5 μg mL下处理24 h时,合金化的银金纳米颗粒没有显示出明显的细胞毒性,但在银含量较高时,在50 μg mL时会有一定程度的细胞毒性。