Atomic‐iodine‐substituted polydiacetylene nanospheres with boosted intersystem crossing and nonradiative transition through complete radiative transition blockade for ultraeffective phototherapy
Dan Zhao,
Lingling Zhang,
Mingming Yin,
Zhenyan He,
Fang Fang,
Minle Zhan,
Sidan Tian,
Fanling Meng,
Liang Luo
Affiliations
Dan Zhao
National Engineering Research Center for Nanomedicine, College of Life Science and Technology Huazhong University of Science and Technology Wuhan China
Lingling Zhang
National Engineering Research Center for Nanomedicine, College of Life Science and Technology Huazhong University of Science and Technology Wuhan China
Mingming Yin
National Engineering Research Center for Nanomedicine, College of Life Science and Technology Huazhong University of Science and Technology Wuhan China
Zhenyan He
National Engineering Research Center for Nanomedicine, College of Life Science and Technology Huazhong University of Science and Technology Wuhan China
Fang Fang
National Engineering Research Center for Nanomedicine, College of Life Science and Technology Huazhong University of Science and Technology Wuhan China
Minle Zhan
National Engineering Research Center for Nanomedicine, College of Life Science and Technology Huazhong University of Science and Technology Wuhan China
Sidan Tian
National Engineering Research Center for Nanomedicine, College of Life Science and Technology Huazhong University of Science and Technology Wuhan China
Fanling Meng
National Engineering Research Center for Nanomedicine, College of Life Science and Technology Huazhong University of Science and Technology Wuhan China
Liang Luo
National Engineering Research Center for Nanomedicine, College of Life Science and Technology Huazhong University of Science and Technology Wuhan China
Abstract The energy dissipation pathways of a photosensitizer for phototherapies, including photodynamic therapy (PDT) and photothermal therapy (PTT), compete directly with that of its fluorescence (FL) emission. Enriching heavy atoms on the π‐conjugated systems and aggregation‐caused quenching are two effective methods to turn off the FL emission of photosensitizers, which is expected to boost the intersystem crossing (for PDT) and nonradiative transition (for PTT) of photosensitizers for maximized phototherapeutic efficacy. Following this approach, an all‐iodine‐substituted polydiacetylene aggregate poly(diiododiacetylene) (PIDA) has been developed, which shows a superior near infrared absorption (ε808nm = 26.1 g−1 cm−1 L) with completely blocked FL, as well as high efficiency of reactive oxygen species generation (nearly 45 folds of indocyanine green) and photothermal conversion (33.4%). To make the insoluble fibrillar PIDA aggregates favorable for systemic administration, they are converted into nanospheres through a pre‐polymerization morphology transformation strategy. The in vivo study on a 4T1 tumor‐bearing mouse model demonstrates that PIDA nanospheres can almost eliminate the tumor entirely in 16 days and prolong the survival time of mice to over 60 days, validating their effective phototherapeutic response through the strategy of inhibiting FL for boosted intersystem crossing and nonradiative transition.
