Graduate School of Chemical Sciences and Engineering, Hokkaido University, Sapporo, Hokkaido, 060-8628, Japan.
Division of Applied Chemistry, Faculty of Engineering, Hokkaido University, Sapporo, Hokkaido, 060-8628, Japan.
Nat Commun. 2020 Nov 30;11(1):6089. doi: 10.1038/s41467-020-19947-8.
Nano-sized metal particles are attracting much interest in industrial and biomedical applications due to the recent progress and development of nanotechnology, and the surface-modifications by appropriate polymers are key techniques to stably express their characteristics. Herein, we applied cyclic poly(ethylene glycol) (c-PEG), having no chemical inhomogeneity, to provide a polymer topology-dependent stabilization for the surface-modification of gold nanoparticles (AuNPs) through physisorption. By simply mixing c-PEG, but not linear counterparts, enables AuNPs to maintain dispersibility through freezing, lyophilization, or heating. Surprisingly, c-PEG endowed AuNPs with even better dispersion stability than thiolated PEG (HS-PEG-OMe). The stronger affinity of c-PEG was confirmed by DLS, ζ-potential, and FT-IR. Furthermore, the c-PEG system exhibited prolonged blood circulation and enhanced tumor accumulation in mice. Our data suggests that c-PEG induces physisorption on AuNPs, supplying sufficient stability toward bio-medical applications, and would be an alternative approach to the gold-sulfur chemisorption.
由于纳米技术的最新进展和发展,纳米级金属颗粒在工业和生物医学应用中引起了广泛关注,通过适当的聚合物进行表面修饰是稳定表达其特性的关键技术。在这里,我们应用环状聚(乙二醇)(c-PEG),由于没有化学不均匀性,通过物理吸附为金纳米粒子(AuNPs)的表面修饰提供了一种与聚合物拓扑结构相关的稳定化作用。通过简单地混合 c-PEG,但不混合线性类似物,使 AuNPs 能够通过冷冻、冻干或加热保持分散性。令人惊讶的是,c-PEG 赋予 AuNPs 比巯基化聚乙二醇(HS-PEG-OMe)更好的分散稳定性。通过 DLS、ζ-电位和 FT-IR 证实了 c-PEG 的更强亲和力。此外,c-PEG 体系在小鼠中表现出更长的血液循环和增强的肿瘤积累。我们的数据表明,c-PEG 在 AuNPs 上诱导物理吸附,为生物医学应用提供了足够的稳定性,并且可能是金-硫化学吸附的替代方法。
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