Enzyme-induced liquid-to-solid phase transition of a mitochondria-targeted AIEgen in cancer theranostics

被引:0
|
作者
Sain, Shreyasri [1 ]
Ramesh, Madhu [1 ]
Bhagavath, Krithi K. [1 ]
Govindaraju, Thimmaiah [1 ]
机构
[1] Jawaharlal Nehru Ctr Adv Sci Res JNCASR, New Chem Unit, Bioorgan Chem Lab, Jakkur PO, Bengaluru 560064, Karnataka, India
关键词
INHIBITOR;
D O I
10.1039/d4mh01692k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Enzyme-instructed self-assembly (EISA) is a promising approach to anti-cancer therapeutics due to its precise targeting and unique cell death mechanism. In this study, we introduce a small molecule, DN6, which undergoes nitroreductase (NTR)-responsive liquid-liquid phase separation (LLPS) followed by a liquid-to-solid phase transition (LST) through a gel-like intermediate state, resulting in the formation of nanoaggregates with spatiotemporal control. The reduced form of DN6 (DN6R), owing to its aggregation-induced emission (AIE) and mitochondria-targeting capabilities, has been employed for organelle-specific imaging of tumor hypoxia. The red-emissive DN6R nanoaggregates in situ generated by NTR induce mitochondrial damage and oxidative stress, culminating in apoptosis in cancer cells and spheroids. The organelle-specific targeting, visualization, and therapeutic outcomes achieved by leveraging LST of NTR-responsive AIEgenic DN6 render it as a promising agent for cancer theranostics.
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页数:7
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