Dinuclear iridium(III) complexes activated by light-inducible spatiotemporal control are emerging as promising candidates for cancer therapy. However, broader applications of current light-activated dinuclear iridium(III) complexes are limited by the ineffective tissue penetration and undesirable feedback on guidance activation. Here, an ultrasound (US) triggered near infrared-fluorescent dinuclear iridium(III) nanoparticle, NanoIr, is first reported to precisely and spatiotemporally inhibit tumor growth. It is demonstrated that reactive oxygen species can be generated by NanoIr upon exposure to US irradiation (NanoIr + US), thereby inducing immunogenic cell death. When combined with cisplatin, NanoIr + US elicits synergistic effects in patient-derived tumor xenograft mice models of ovarian cancer. This work first provides a design of dinuclear iridium(III) nanoparticles for immunogenic sonodynamic therapy.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1002/adma.202406815 | DOI Listing |
Phys Chem Chem Phys
September 2024
School of Light Industry Science and Engineering, Beijing Technology and Business University, Beijing 100048, China.
Adv Mater
September 2024
Department of Nuclear Medicine, Peking University People's Hospital, Beijing, 100044, P. R. China.
Inorg Chem
January 2024
Department of Applied Sciences, Northumbria University, Newcastle upon Tyne NE1 8ST, U.K.
Herein, we present two novel cyclometalated Ir(III) complexes of dinuclear and trinuclear design, and , respectively, where is 4,6-di(4-tert-butylphenyl)pyrimidine ligand and is acetylacetonate ligand. In both cases, -diastereomers were isolated during the synthesis. The materials show intense phosphorescence of outstanding rates ( = Φ/τ) with corresponding radiative decay times of only τ = 1/ = 0.
View Article and Find Full Text PDFChem Sci
December 2023
Department of Applied Sciences, Northumbria University Newcastle upon Tyne NE1 8ST UK
The high luminescence efficiency of cyclometallated iridium(iii) complexes, including those widely used in OLEDs, is typically attributed solely to the formally spin-forbidden phosphorescence process being facilitated by spin-orbit coupling with the Ir(iii) centre. In this work, we provide unequivocal evidence that an additional mechanism can also participate, namely a thermally activated delayed fluorescence (TADF) pathway. TADF is well-established in other materials, including in purely organic compounds, but has never been observed in iridium complexes.
View Article and Find Full Text PDFACS Appl Bio Mater
December 2023
Chemical Sciences & Technology Division (CSTD), CSIR-National Institute for Interdisciplinary Science & Technology (CSIR-NIIST), Thiruvananthapuram, Kerala 695019, India.
Photodynamic therapy (PDT) has emerged as an efficient and noninvasive treatment approach utilizing laser-triggered photosensitizers for combating cancer. Within this rapidly advancing field, iridium-based photosensitizers with their dual functionality as both imaging probes and PDT agents exhibit a potential for precise and targeted therapeutic interventions. However, most reported classes of Ir(III)-based photosensitizers comprise mononuclear iridium(III), with very few examples of dinuclear systems.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!