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银纳米粒子合成:用于激光触发聚电解质胶囊的新途径。

Silver nanoparticle synthesis: novel route for laser triggering of polyelectrolyte capsules.

机构信息

Department of Materials Engineering, Indian Institute of Science, Bangalore 560012, India.

出版信息

ACS Appl Mater Interfaces. 2011 Sep;3(9):3419-24. doi: 10.1021/am200651t. Epub 2011 Sep 2.

Abstract

We have demonstrated the synthesis of light-sensitive polyelectrolyte capsules (PECs) by utilizing a novel polyol reduction method and investigated its applicability as photosensitive drug delivery vehicle. The nanostructured capsules were prepared via layer by layer (LbL) assembly of poly(allylamine hydrochloride) (PAH) and dextran sulfate (DS) on silica particles followed by in-situ synthesis of silver nanoparticles (NPs). Capsules without silver NPs were permeable to low molecular weight (M(w), 479 g/mol) rhodamine but impermeable to higher molecular weight fluorescence labeled dextran (FITC-dextran). However, capsules synthesized with silver NPs showed porous morphology and were permeable to higher molecular weight (M(w) 70 kDa) FITC-dextran also. These capsules were loaded with FITC-dextran using thermal encapsulation method by exploiting temperature induced shrinking of the capsules. During heat treatment the porous morphology of the capsules transformed into smooth pore free structure which prevents the movement of dextran into bulk during the loading process. When these loaded capsules are exposed to laser pulses, the capsule wall ruptured, resulting in the release of the loaded drug/dye. The rupture of the capsules was dependent on particle size, laser pulse energy and exposure time. The release was linear with time when pulse energy of 400 μJ was used and burst release was observed when pulse energy increased to 600 μJ.

摘要

我们已经通过一种新的多元醇还原方法展示了对光敏感的聚电解质胶囊(PECs)的合成,并研究了其作为光敏药物传递载体的适用性。通过在二氧化硅颗粒上逐层(LbL)组装聚(盐酸烯丙胺)(PAH)和葡聚糖硫酸盐(DS),然后进行银纳米粒子(NPs)的原位合成,制备了纳米结构胶囊。没有银 NPs 的胶囊对低分子量(M(w),479 g/mol)罗丹明是可渗透的,但对高分子量荧光标记葡聚糖(FITC-葡聚糖)是不可渗透的。然而,合成有银 NPs 的胶囊显示出多孔形态,并且对高分子量(M(w)70 kDa)FITC-葡聚糖也是可渗透的。这些胶囊通过利用胶囊的热收缩,使用热包封方法装载 FITC-葡聚糖。在热处理过程中,胶囊的多孔形态转变为光滑无孔的结构,从而防止在装载过程中葡聚糖进入主体。当这些装载的胶囊暴露于激光脉冲时,胶囊壁破裂,导致装载的药物/染料释放。胶囊的破裂取决于粒径、激光脉冲能量和暴露时间。当使用 400 μJ 的脉冲能量时,释放是线性的,当脉冲能量增加到 600 μJ 时,会观察到爆发释放。

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