TY - JOUR
T1 - A new near-infrared phosphorescent iridium(iii) complex conjugated to a xanthene dye for mitochondria-Targeted photodynamic therapy
AU - Wu, Yongquan
AU - Wu, Jie
AU - Wong, Wai Yeung
N1 - Funding Information:
This work was financially supported by the National Natural Science Foundation of China (51873176 and 21967001), Hong Kong Research Grants Council (PolyU153058/19P), Guangdong-Hong Kong-Macao Joint Laboratory of Optoelectronic and Magnetic Functional Materials (2019B121205002), the Hong Kong Polytechnic University (1-ZE1C), Ms Clarea Au for the Endowed Professorship in Energy (847S), and the Double-Thousand Talents Plan of Jiangxi Province (2019). We also gratefully acknowledge Prof. Huifang Li of Qingdao University of Science and Technology for the support of DFT calculations.
Publisher Copyright:
© The Royal Society of Chemistry.
PY - 2021/7/21
Y1 - 2021/7/21
N2 - Iridium(iii) complexes are potent candidates for photodynamic therapy (PDT), but some key drawbacks still hamper clinical translation, such as poor operability in the phototherapeutic window, high dark toxicity, and low reactive oxygen species (ROS) production efficiency. In this work, a near-infrared phosphorescent Ir(iii) complex conjugated to a xanthene dye, NIR-Ir-XE, is reported with highly favourable properties for mitochondria-Targeted imaging and cancer phototherapy. The generation of the triplet excited state of a xanthene moiety endows the NIR-Ir-XE to form singlet oxygen (1O2) for use as a photodynamic therapy agent after irradiation with visible light. Compared with the xanthene-free Ir(iii) counterpart (NIR-Ir-bpy), the xanthene-modified cyclometalated Ir(iii) photosensitizer NIR-Ir-XE exhibits higher 1O2 generation efficiency, negligible dark toxicity and a better therapeutic effect. Importantly, a clear correlation between cell death and intracellular generation of 1O2 derived from NIR-Ir-XE after light irradiation was demonstrated. The corresponding in vivo photo-Antitumor performance was further demonstrated to be effective in tumor-bearing mice. The observed properties of NIR-Ir-XE qualify it as a promising PDT agent.
AB - Iridium(iii) complexes are potent candidates for photodynamic therapy (PDT), but some key drawbacks still hamper clinical translation, such as poor operability in the phototherapeutic window, high dark toxicity, and low reactive oxygen species (ROS) production efficiency. In this work, a near-infrared phosphorescent Ir(iii) complex conjugated to a xanthene dye, NIR-Ir-XE, is reported with highly favourable properties for mitochondria-Targeted imaging and cancer phototherapy. The generation of the triplet excited state of a xanthene moiety endows the NIR-Ir-XE to form singlet oxygen (1O2) for use as a photodynamic therapy agent after irradiation with visible light. Compared with the xanthene-free Ir(iii) counterpart (NIR-Ir-bpy), the xanthene-modified cyclometalated Ir(iii) photosensitizer NIR-Ir-XE exhibits higher 1O2 generation efficiency, negligible dark toxicity and a better therapeutic effect. Importantly, a clear correlation between cell death and intracellular generation of 1O2 derived from NIR-Ir-XE after light irradiation was demonstrated. The corresponding in vivo photo-Antitumor performance was further demonstrated to be effective in tumor-bearing mice. The observed properties of NIR-Ir-XE qualify it as a promising PDT agent.
UR - http://www.scopus.com/inward/record.url?scp=85110295398&partnerID=8YFLogxK
U2 - 10.1039/d1bm00128k
DO - 10.1039/d1bm00128k
M3 - Journal article
C2 - 33998610
AN - SCOPUS:85110295398
SN - 2047-4830
VL - 9
SP - 4843
EP - 4853
JO - Biomaterials Science
JF - Biomaterials Science
IS - 14
ER -