Precise ligand engineering of Ir(III)‐based photosensitizer with aggregation‐induced emission for image‐guided photodynamic therapy

Author:

Tong Jialin1,Liu Ao1,Huang Shanshan1,Zhou Dan1,Gao Ying2,Wang Yan3,Shan Guo‐Gang1ORCID

Affiliation:

1. Institute of Functional Material Chemistry and National & Local United Engineering Lab for Power Battery, Faculty of Chemistry Northeast Normal University Changchun China

2. Jilin Provincial Key Laboratory of Straw‐Based Functional Materials, Institute for Interdisciplinary Biomass Functional Materials Studies Jilin Engineering Normal University Changchun China

3. Engineering Research Center of Advanced Ferroelectric Functional Materials, College of Chemistry and Chemical Engineering, Baoji University of Arts and Sciences Key Laboratory of Phytochemistry of Shaanxi Province Baoji China

Abstract

AbstractPhotodynamic therapy (PDT), which relies on the production of reactive oxygen species (ROS) induced by a photosensitizer to kill cancer cells, has become a non‐invasive approach to combat cancer. However, the conventional aggregation‐caused quenching effect, as well as the low ROS generation ability of photosensitizers, restrict their biological applications. In this work, a new Ir(III) complex with a dendritic ligand has been strategically designed and synthesized by ingenious modification of the ancillary ligand of a reported Ir(III) complex (Ir‐1). The extended π‐conjugation and multiple aromatic donor moieties endow the resulting complex Ir‐2 with obvious aggregation‐induced emission (AIE) activity and bathochromic emission. In in vitro experiments, importantly, Ir‐2 nanoparticles exhibit the excellent photoinduced ROS generation capabilities of O2•− and 1O2, as well as excellent biocompatibility and the lipid droplets (LDs) targeting feature. This study would provide useful guidance to design efficient Ir(III)‐based photosensitizers used in biological applications in the future.

Publisher

Wiley

Subject

Chemistry (miscellaneous),Biophysics

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