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Real-Time Monitoring Surface Chemistry-Dependent In Vivo Behaviors of Protein Nanocages via Encapsulating an NIR-II Ag2S Quantum Dot

机译:通过封装NIR-II Ag2S量子点实时监测蛋白纳米笼子表面化学依赖性的体内行为

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Protein nanocages (PNCs) have been recognized as a promising platform for nanomedicine innovation. Real-time in vivo tracking of PNCs can provide critically important information for the development of PNC-based diagnostics and therapeutics. Here we demonstrate a general strategy for monitoring the behaviors of PNCs in vivo by encapsulating a Ag2S quantum dot (QD) with fluorescence in the second near-infrared window (NIR-II, 1000-1700 nm) inside the PNC, using simian virus 40 (SV40) PNC (PNCSV40) as a model. Benefiting from the high spatiotemporal resolution and deep tissue penetration of NIR-II fluorescence imaging, the dynamic distribution of the PNCSV40 in living mice was tracked in real time with high fidelity, and adopting the PEGylation strategy, surface chemistry-dependent in vivo behaviors of PNCSV40 were clearly revealed. This study represents the first evidence of real-time tracking of the intrinsic behaviors of PNCs in vivo without interference in PNC-host interactions by encapsulating nanoprobes inside. The as-described imaging strategy will facilitate the study of interactions between exogenously introduced PNCs and host body and prompt the development of future protein-based drugs, sensors, and high-efficacy targeted delivery systems.
机译:蛋白质纳米笼(PNC)已被公认为是纳米医学创新的有前途的平台。 PNC的实时体内跟踪可以为开发基于PNC的诊断和治疗方法提供至关重要的信息。在这里,我们通过使用猿猴病毒40在PNC内部的第二个近红外窗口(NIR-II,1000-1700 nm)中封装了带有荧光的Ag2S量子点(QD),展示了一种监控PNC体内行为的通用策略(SV40)PNC(PNCSV40)作为模型。得益于NIR-II荧光成像的高时空分辨率和深层组织穿透性,能够以高保真度实时跟踪PNCSV40在活小鼠中的动态分布,并采用PEG化策略,PNCSV40的表面化学依赖性体内行为被清楚地揭示出来。这项研究代表了实时跟踪PNC体内行为的第一个证据,而不会通过将纳米探针包裹在体内而干扰PNC与宿主之间的相互作用。所描述的成像策略将有助于研究外源引入的PNC与宿主之间的相互作用,并促进未来基于蛋白质的药物,传感器和高效靶向递送系统的发展。

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