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二氧化硅包裹金纳米颗粒的浓缩胶体:胶体稳定性、细胞毒性及X射线吸收

Concentrated colloids of silica-encapsulated gold nanoparticles: colloidal stability, cytotoxicity, and X-ray absorption.

作者信息

Park Yeon-Su, Kasuya Atsuo, Dmytruk Andriy, Yasuto Noda, Takeda Motohiro, Ohuchi Noriaki, Sato Yoshinori, Tohji Kazuyuki, Uo Motohiro, Watari Fumio

机构信息

Center for Interdisciplinary Research, Tohoku University, Aoba-ku, Sendai 980-8578, Japan.

出版信息

J Nanosci Nanotechnol. 2007 Aug;7(8):2690-5. doi: 10.1166/jnn.2007.601.

Abstract

As an effort to develop a new, effective, nontoxic X-ray contrast agent, the concentrated colloids of silica-encapsulated gold nanoparticles (Au@SiO2 NPs) were fabricated and their colloidal stability, cytotoxicity, and X-ray absorption were investigated. The concentrated colloidal NPs were manufactured by forming a 4 nm-thick silica shell on the surface of each Au NP with 15 nm diameter, followed by enrichment to [Au] = 100 mM. They were very stable in water: the NPs were well separated each other without forming agglomerates and their optical property was very similar to that before enrichment. The colloidal stability of the NPs in biological environment was strongly dependent on their previous morphology in water. The NPs with minor shell damage were stable in phosphate buffered saline (PBS) solution: both in water and in PBS solution, they showed very similar morphology and optical property. However, the NPs with profound shell damage formed big agglomerates in PBS solution, resulting in the red-shift and broadening of the Au surface plasmon resonance peak. Cell viability and proliferation assessments revealed the biocompatibility of the Au@SiO2 NPs: no apparent cytotoxicity was observed even at 100 ppm NPs. The concentrated colloidal NPs showed very strong X-ray absorption. Their relative X-ray transmittance to water was comparable to that of a commercial agent. Considering these, the concentrated colloids of the Au@SiO2 NPs are suitable for an X-ray contrast agent.

摘要

为了开发一种新型、有效、无毒的X射线造影剂,制备了二氧化硅包覆金纳米颗粒(Au@SiO2 NPs)的浓缩胶体,并研究了其胶体稳定性、细胞毒性和X射线吸收情况。通过在直径为15 nm的每个金纳米颗粒表面形成4 nm厚的二氧化硅壳层,随后富集至[Au]=100 mM来制备浓缩胶体纳米颗粒。它们在水中非常稳定:纳米颗粒彼此分离良好,未形成团聚体,其光学性质与富集前非常相似。纳米颗粒在生物环境中的胶体稳定性强烈依赖于它们在水中的先前形态。壳层损伤较小的纳米颗粒在磷酸盐缓冲盐水(PBS)溶液中稳定:在水和PBS溶液中,它们都表现出非常相似的形态和光学性质。然而,壳层损伤严重的纳米颗粒在PBS溶液中形成大的团聚体,导致金表面等离子体共振峰发生红移和展宽。细胞活力和增殖评估揭示了Au@SiO2纳米颗粒的生物相容性:即使在100 ppm纳米颗粒的情况下也未观察到明显的细胞毒性。浓缩胶体纳米颗粒表现出非常强的X射线吸收。它们相对于水的X射线透过率与商业造影剂相当。考虑到这些,Au@SiO2纳米颗粒的浓缩胶体适合用作X射线造影剂。

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