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Targeted multimodal theranostics via biorecognition controlled aggregation of metallic nanoparticle composites

机译:通过生物识别控制的金属纳米粒子复合材料的聚集进行靶向多峰治疗学

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摘要

We have developed a theranostic nanocomposite of metallic nanoparticles that uses two distinct fluorescence mechanisms: Förster Resonance Energy Transfer (FRET) and Metal-Enhanced Fluorescence (MEF) controlled by ligand–receptor interaction. Supramolecular assembly of the fluorophore-labeled glycoligands to cyclodextrin-capped gold nanoparticles produces a nanocomposite with a quenched fluorescence due to FRET from the fluorophore to the proximal particle. Subsequently, interaction with a selective protein receptor leads to an aggregation of the composite, reactivating the fluorescence by MEF from the distal metallic particles to fluorophores encapsulated in the aggregates. The aggregation also causes a red-shift in absorbance of the composite, thereby enhancing the production of reactive oxygen species (ROS) on red-light irradiation. Our nanocomposite has proven suitable for targeted cancer cell imaging as well as multimode therapy using both the photodynamic and drug delivery properties of the composite.
机译:我们已经开发了一种金属纳米粒子的治疗论纳米复合物,它使用两种不同的荧光机制:由配体-受体相互作用控制的福斯特共振能量转移(FRET)和金属增强荧光(MEF)。荧光团标记的糖苷配体与环糊精封端的金纳米粒子的超分子组装产生了纳米复合材料,该复合材料由于从荧光团到近端粒子的FRET而具有猝灭的荧光。随后,与选择性蛋白质受体的相互作用导致复合物的聚集,通过MEF将荧光从远端金属颗粒重新活化为封装在聚集物中的荧光团。聚集还导致复合材料的吸收率发生红移,从而增强了红光照射下活性氧(ROS)的产生。我们的纳米复合材料已被证明适用于靶向癌细胞成像以及利用复合材料的光动力和药物传递特性进行的多模式治疗。

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