光毒性
体内
组织蛋白酶B
荧光
分子生物学
自体荧光
材料科学
体外
化学
癌症研究
生物
生物化学
酶
量子力学
物理
生物技术
作者
Xiaoqiang Chen,Da-Young Lee,Sungsook Yu,Gyoungmi Kim,Song Yi Lee,Yejin Cho,Haengdueng Jeong,Ki Taek Nam,Juyoung Yoon
出处
期刊:Biomaterials
[Elsevier]
日期:2017-04-01
卷期号:122: 130-140
被引量:92
标识
DOI:10.1016/j.biomaterials.2017.01.020
摘要
The development of multifunctional reagents for simultaneous specific near-infrared (NIR) imaging and phototherapy of tumors is of great significance. This work describes the design of a cathepsin B-activated fluorescent probe (CyA-P-CyB) and its applications as an NIR imaging probe for tumor cells and as a phototherapy reagent for tumors. In vitro experiments demonstrated that CyA-P-CyB was activated via the cleavage of a peptide linker by cathepsin B in tumor cells to produce fluorescence in the NIR region based on a FRET mechanism. MTT assays showed that the phototoxicity of CyA-P-CyB toward cells depended on the activity of cathepsin B, and the probe exhibited specific phototoxicity toward tumor cells. CyA-P-CyB was also successfully applied to the in vivo imaging and phototherapy of tumors. Histological analysis indicated that CyA-P-CyB had no cytotoxic effects on seven mouse tissues (lung, liver, heart, kidney, pancreas, spleen and brain) after the CyA-P-CyB treatment and laser irradiation.
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