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Hydrogel-Coated Near Infrared Absorbing Nanoshellsas Light-Responsive Drug Delivery Vehicles

机译:水凝胶涂层的近红外吸收纳米壳作为光响应药物输送工具

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摘要

Nanoparticle drug delivery carriers that can modulate drug release based on an exogenous signal, such as light, are of great interest, especially for improving cancer therapy. A light-activated delivery vehicle was fabricated by synthesizing a thin, thermally responsive poly(N-isopropylacrylamide-co-acrylamide) hydrogel coating directly onto the surfaces of individual near-infrared (NIR) absorbing gold-silica nanoshells. This hydrogel was designed to be in a swollen state under physiological conditions and expel large amounts of water, along with any entrapped drug, at elevated temperatures. The required temperature change can be achieved via NIR absorption by the nanoshell, allowing the hydrogel phase change to be triggered by light, which was observed by monitoring changes in particle sizes as water was expelled from the hydrogel network. The phase change was reversible and repeatable. As a model drug, the chemotherapeutic doxorubicin was loaded into this delivery vehicle, and rapid release of doxorubicin occurred upon NIR exposure. Further,colon carcinoma cells exposed to the irradiated platform displayednearly 3 times as much doxorubicin uptake as cells exposed to nonirradiatedparticles or free drug, which in turn resulted in a higher loss ofcell viability. We hypothesize these effects are because the NIR-mediatedheating results in a transient increase in cell membrane permeability,thus aiding in cellular uptake of the drug.
机译:可以基于诸如光的外源信号调节药物释放的纳米颗粒药物递送载体引起了极大的兴趣,尤其是对于改善癌症治疗而言。通过将薄的热响应性聚(N-异丙基丙烯酰胺-共丙烯酰胺)水凝胶涂层直接合成到各个吸收近红外(NIR)的金-二氧化硅纳米壳的表面上,制得了光活化的输送载体。该水凝胶被设计为在生理条件下呈溶胀状态,并在升高的温度下排出大量水以及任何残留的药物。所需的温度变化可以通过纳米壳对NIR的吸收来实现,从而可以通过光触发水凝胶相变,这是通过监测水从水凝胶网络中排出时粒径的变化来观察的。相变是可逆的和可重复的。作为模型药物,将化学疗法阿霉素装载到该递送载体中,并且在暴露NIR后发生了阿霉素的快速释放。进一步,暴露于辐照平台的结肠癌细胞显示阿霉素吸收量几乎是未照射细胞的3倍颗粒或游离药物,进而导致更高的细胞活力。我们假设这些影响是因为NIR介导加热导致细胞膜通透性的瞬时增加,因此有助于药物的细胞吸收。

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