Department of Civil and Environmental Engineering, Institute of Critical Technology and Applied Science (ICTAS), and the Center for the Environmental Implications of Nanotechnology (CEINT) , Virginia Tech , 418 Durham Hall , Blacksburg , Virginia 24061-0246 , United States.
Environ Sci Technol. 2018 Mar 6;52(5):2726-2734. doi: 10.1021/acs.est.7b05622. Epub 2018 Feb 13.
Silver nanoparticles (AgNPs) are increasingly being incorporated into a range of consumer products and as such there is significant potential for the environmental release of either the AgNPs themselves or Ag ions. When AgNPs are exposed to environmental systems, the engineered surface coating can potentially be displaced or covered by naturally abundant macromolecules. These capping agents, either engineered or incidental, potentially block reactants from surface sites and can alter nanoparticle transformation rates. We studied how surface functionalization affects the dissolution of uniform arrays of AgNPs fabricated by nanosphere lithography (NSL). Bovine serum albumin (BSA) and two molecular weights of thiolated polyethylene glycol (PEG; 1000 and 5000 Da) were tested as model capping agents. Dissolution experiments were conducted in air-saturated phosphate buffer containing 550 mM NaCl. Tapping-mode atomic force microscopy (AFM) was used to measure changes in AgNP height over time. The measured dissolution rate for unfunctionalized AgNPs was 1.69 ± 0.23 nm/d, while the dissolution rates for BSA, PEG1000, and PEG5000 functionalized samples were 0.39 ± 0.05, 0.20 ± 0.10, and 0.14 ± 0.07 nm/d, respectively. PEG provides a steric barrier restricting mass transfer of reactants to sites on the AgNP surface and thus diminishes the dissolution rate. The effects of BSA, however, are more complicated with BSA initially enhancing dissolution, but providing protection against dissolution over extended time.
银纳米粒子(AgNPs)越来越多地被纳入各种消费产品中,因此,AgNPs 本身或 Ag 离子很有可能被释放到环境中。当 AgNPs 暴露于环境系统中时,其工程表面涂层可能会被天然存在的大分子所取代或覆盖。这些封端剂,无论是工程设计的还是偶然存在的,可能会阻止反应物到达表面位点,并改变纳米粒子的转化速率。我们研究了表面功能化如何影响通过纳米球光刻(NSL)制造的均匀 AgNPs 阵列的溶解。牛血清白蛋白(BSA)和两种分子量的巯基化聚乙二醇(PEG;1000 和 5000 Da)被用作模型封端剂进行测试。溶解实验在含有 550 mM NaCl 的空气饱和磷酸盐缓冲液中进行。原子力显微镜(AFM)的轻敲模式用于测量 AgNP 高度随时间的变化。未功能化的 AgNP 的测量溶解速率为 1.69 ± 0.23 nm/d,而 BSA、PEG1000 和 PEG5000 功能化样品的溶解速率分别为 0.39 ± 0.05、0.20 ± 0.10 和 0.14 ± 0.07 nm/d。PEG 提供了一个阻止反应物向 AgNP 表面位点转移的空间位阻,从而降低了溶解速率。然而,BSA 的影响更为复杂,BSA 最初会增强溶解,但会在延长的时间内提供对溶解的保护。