Sugikawa Kouta, Kadota Tatsuya, Matsuo Kotaro, Yasuhara Kazuma, Ikeda Atsushi
Graduate School of Engineering, Hiroshima University, Higashi-Hiroshima 739-8527, Japan.
Graduate School of Materials Science, Nara Institute of Science and Technology, Nara 630-0192, Japan.
Materials (Basel). 2017 Nov 17;10(11):1317. doi: 10.3390/ma10111317.
Anisotropic assembly of nanoparticles (NPs) has attracted extensive attention because of the potential applications in materials science, biology, and medicine. However, assembly control (e.g., the number of assembled NPs) has not been adequately studied. Here, the growth of anisotropic gold NP assemblies on a liposome surface is reported. Citrate-coated gold NPs adsorbed on liposome surfaces were assembled in one dimension at temperatures above the phase transition temperature of the lipid bilayer. Growth of the anisotropic assemblies depended on the heating time. Absorption spectroscopy and transmission electron microscopy revealed that the gradual growth was attributed to liposome fusion, which was strongly affected by the size of the gold NPs. This method enabled us to precisely control the number of NPs in each anisotropic assembly. These results will enable the fabrication of functional materials based on NP assemblies and enable investigations of cell functions and disease causality.
由于在材料科学、生物学和医学领域的潜在应用,纳米颗粒(NPs)的各向异性组装已引起广泛关注。然而,组装控制(例如,组装的NPs数量)尚未得到充分研究。在此,报道了在脂质体表面各向异性金NP组装体的生长情况。吸附在脂质体表面的柠檬酸盐包被金NP在高于脂质双层相变温度的温度下进行一维组装。各向异性组装体的生长取决于加热时间。吸收光谱和透射电子显微镜表明,这种逐渐生长归因于脂质体融合,而脂质体融合受到金NP尺寸的强烈影响。该方法使我们能够精确控制每个各向异性组装体中的NP数量。这些结果将有助于基于NP组装体制造功能材料,并有助于研究细胞功能和疾病因果关系。