Ultrathin two-dimensional covalent organic framework nanoprobe for interference-resistant two-photon fluorescence bioimaging.

Chem Sci

Molecular Science and Biomedicine Laboratory , State Key Laboratory of Chemo/Biosensing and Chemometrics , College of Chemistry and Chemical Engineering , College of Life Sciences , Collaborative Innovation Center for Chemistry and Molecular Medicine , Hunan University, Changsha , Hunan 410082 , China . Email:

Published: November 2018

AI Article Synopsis

  • The complex environment of living organisms makes it hard for traditional small-molecule fluorescent probes to provide accurate bioimaging.
  • Covalent organic frameworks (COFs) can filter out interfering components, and the study proposes a hybrid COF-based probe that combines the benefits of COFs and small-molecule probes.
  • A new COF nanoprobe developed for targeting hydrogen sulfide shows low toxicity, great photostability, and the ability to provide accurate detection unaffected by intracellular enzymes in a mouse model of cirrhosis.

Article Abstract

The complex environment of living organisms significantly challenges the selectivity of classic small-molecule fluorescent probes for bioimaging. Due to their predesigned topological structure and engineered internal pore surface, covalent organic frameworks (COFs) have the ability to filter out coexisting interference components and help to achieve accurate biosensing. Herein, we propose an effective interference-resistant strategy by creating a COF-based hybrid probe that combines the respective advantages of COFs and small-molecule probes. As a proof of concept, a two-photon fluorescent COF nanoprobe, namely , is developed for targeting hydrogen sulfide (HS) as a model analyte. exhibits limited cytotoxicity, excellent photostability and long-term bioimaging capability. More importantly, compared with the small-molecule probe, achieves accurate detection without the interference from intracellular enzymes. This allows us to monitor the levels of endogenous HS in a mouse model of cirrhosis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6243647PMC
http://dx.doi.org/10.1039/c8sc03393eDOI Listing

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