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纳米晶对羟基乙酰苯胺(扑热息痛)和金核壳结构作为一种模型药物输送的有机-无机杂化纳米结构。

Nanocrystalline p-hydroxyacetanilide (paracetamol) and gold core-shell structure as a model drug deliverable organic-inorganic hybrid nanostructure.

机构信息

Department of Chemistry, Indian Institute of Technology Guwahati, Guwahati-781039, Assam, India.

出版信息

Nanoscale. 2013 Oct 7;5(19):9247-54. doi: 10.1039/c3nr03566b. Epub 2013 Aug 14.

Abstract

We report on the generation of core-shell nanoparticles (NPs) having an organic nanocrystal (NC) core coated with an inorganic metallic shell, being dispersed in aqueous medium. First, NCs of p-hydroxyacetanilide (pHA)--known also as paracetamol--were generated in an aqueous medium. Transmission electron microscopy (TEM) and powder X-ray diffraction (XRD) evidenced the formation of pHA NCs and of their crystalline nature. The NCs were then coated with Au to form pHA@Au core-shell NPs, where the thickness of the Au shell was on the order of nanometers. The formation of Au nanoshell--surrounding pHA NC--was confirmed from its surface plasmon resonance (SPR) band in the UV/Vis spectrum and by TEM measurements. Further, on treatment of the core-shell particles with a solution comprising NaCl and HCl (pH < 3), the Au shell could be dissolved, subsequently releasing pHA molecules. The dissolution of Au shell was marked by a gradual diminishing of its SPR band, while the release of pHA molecules in the solution was confirmed from TEM and FTIR studies. The findings suggest that the core-shell NP could be hypothesized to be a model for encapsulating drug molecules, in their crystalline forms, for slow as well as targeted release.

摘要

我们报告了在水相中生成具有核壳结构的纳米粒子(NPs)的方法,这些纳米粒子的内核是有机纳米晶体(NC),外壳是无机金属。首先,在水相中生成了对羟基乙酰苯胺(pHA)——也称为扑热息痛——的 NC。透射电子显微镜(TEM)和粉末 X 射线衍射(XRD)证明了 pHA NC 的形成及其晶体性质。然后,将 NC 用 Au 包覆形成 pHA@Au 核壳 NPs,其中 Au 壳的厚度约为纳米级。从其在紫外/可见光谱中的表面等离子体共振(SPR)带以及 TEM 测量结果证实了 Au 纳米壳(包围 pHA NC)的形成。此外,在用包含 NaCl 和 HCl(pH < 3)的溶液处理核壳颗粒后,Au 壳可以溶解,随后释放出 pHA 分子。Au 壳的溶解伴随着其 SPR 带的逐渐减弱,而 pHA 分子在溶液中的释放则通过 TEM 和 FTIR 研究得到证实。研究结果表明,这种核壳 NP 可以被假设为一种用于封装药物分子的模型,以实现药物的缓慢和靶向释放。

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