Reversible Self-Assembly of Glutathione-Coated Gold Nanoparticle Clusters via pH-Tunable Interactions

星团(航天器) 化学 纳米颗粒 亚稳态 离解(化学) 金团 水溶液 位阻效应 氢键 谷胱甘肽 自组装 PEG比率 结晶学 成核 化学物理 分子 纳米技术 立体化学 有机化学 材料科学 计算化学 密度泛函理论 经济 财务 程序设计语言 计算机科学
作者
Ehsan Moaseri,Jonathan A. Bollinger,Behzad Changalvaie,Lindsay T. Johnson,Joseph Schroer,Keith P. Johnston,Thomas M. Truskett
出处
期刊:Langmuir [American Chemical Society]
卷期号:33 (43): 12244-12253 被引量:53
标识
DOI:10.1021/acs.langmuir.7b02446
摘要

Nanoparticle (NP) clusters with diameters ranging from 20 to 100 nm are reversibly assembled from 5 nm gold (Au) primary particles coated with glutathione (GSH) in aqueous solution as a function of pH in the range of 5.4 to 3.8. As the pH is lowered, the GSH surface ligands become partially zwitterionic and form interparticle hydrogen bonds that drive the self-limited assembly of metastable clusters in <1 min. Whereas clusters up to 20 nm in size are stable against cluster–cluster aggregation for up to 1 day, clusters up to 80 nm in size can be stabilized over this period via the addition of citrate to the solution in equal molarity with GSH molecules. The cluster diameter may be cycled reversibly by tuning pH to manipulate the colloidal interactions; however, modest background cluster–cluster aggregation occurs during cycling. Cluster sizes can be stabilized for at least 1 month via the addition of PEG-thiol as a grafted steric stabilizer, where PEG-grafted clusters dissociate back to starting primary NPs at pH 7 in fewer than 3 days. Whereas the presence of excess citrate has little effect on the initial size of the metastable clusters, it is necessary for both the cycling and dissociation to mediate the GSH–GSH hydrogen bonds. In summary, these metastable clusters exhibit significant characteristics of equilibrium self-limited assembly between primary particles and clusters on time scales where cluster–cluster aggregation is not present.
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