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可激活铁蛋白纳米复合物用于光动力学治疗期间胱天蛋白酶-3 激活的实时监测。

Activatable Ferritin Nanocomplex for Real-Time Monitoring of Caspase-3 Activation during Photodynamic Therapy.

机构信息

State Key Laboratory of Molecular Vaccinology and Molecular Diagnostics & Center for Molecular Imaging and Translational Medicine, School of Public Health, Xiamen University , Xiamen 361005, China.

China-Japan Union Hospital, Jilin University , Changchun 130033, China.

出版信息

ACS Appl Mater Interfaces. 2015 Oct 21;7(41):23248-56. doi: 10.1021/acsami.5b07316. Epub 2015 Oct 12.

Abstract

One mechanism of photodynamic therapy (PDT) for the ablation of tumors is to induce apoptosis. Visualization of apoptosis during PDT in real-time is of great benefit for predicting and evaluating therapeutic outcomes. Herein, we engineered a highly stable and sensitive caspase-3 ferritin activatable probe (FABP/ZnPc) for simultaneous delivery of a photosensitizer (ZnPc) and real-time visualization of apoptosis during PDT. Upon near-infrared (NIR) light irradiation, ZnPc becomes active and initiates apoptosis, upon which the outer layer of the FABP/ZnPc is degraded by the apoptotic marker, caspase-3, to boost strong fluorescent signals, ultimately allowing real-time imaging of apoptosis. Our results demonstrate the utility of FABP/ZnPc as a tool for PDT and simultaneous imaging of caspase-3 activation in vitro and in vivo. Overall, the ability of FABP/ZnPc to image apoptosis during PDT will not only facilitate optimizing and personalizing the PDT strategy but is also important for understanding the mechanisms of PDT.

摘要

一种用于肿瘤消融的光动力疗法 (PDT) 的机制是诱导细胞凋亡。在 PDT 过程中实时可视化细胞凋亡对于预测和评估治疗效果非常有益。在此,我们设计了一种高度稳定和敏感的 caspase-3 铁蛋白激活探针 (FABP/ZnPc),用于同时递送光敏剂 (ZnPc) 并在 PDT 过程中实时可视化细胞凋亡。近红外 (NIR) 光照射后,ZnPc 变得活跃并引发细胞凋亡,此时凋亡标志物 caspase-3 会降解 FABP/ZnPc 的外层,从而增强强烈的荧光信号,最终允许实时成像细胞凋亡。我们的结果证明了 FABP/ZnPc 作为 PDT 工具以及体外和体内同时成像 caspase-3 激活的工具的效用。总体而言,FABP/ZnPc 在 PDT 过程中成像细胞凋亡的能力不仅将有助于优化和个性化 PDT 策略,而且对于理解 PDT 机制也很重要。

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