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Asymmetric Si-rhodamine scaffolds: rational design of pH-durable protease-activated NIR probes <i>in vivo</i>

Min Li, Chuanfeng Wang, Ting Wang, Mengting Fan, Ning Wang, Danying Ma, Ting Hu, Xiaoyan Cui

2020Chemical Communications20 citationsDOI

Abstract

A group of asymmetric Si-rhodamine scaffolds was designed for protease-activated NIR probes. Dual pH-inertia for both spirocyclized fluorescent probes and fluorescent products of zwitterions form over a wide range of pH (4.0-11.0). Leucine aminopeptidase (LAP) and γ-glutamyl transpeptidase (GGT) were monitored by fluorescent imaging in vivo.

Topics & Concepts

In vivoRational designChemistryRhodamineRhodamine BCombinatorial chemistryNanotechnologyMaterials scienceBiophysicsFluorescenceOrganic chemistryCatalysisPhotocatalysisBiotechnologyPhysicsQuantum mechanicsBiologyAdvanced biosensing and bioanalysis techniquesClick Chemistry and ApplicationsRNA Interference and Gene Delivery
Asymmetric Si-rhodamine scaffolds: rational design of pH-durable protease-activated NIR probes <i>in vivo</i> | Litcius