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Nucleus‐Targeted Organoiridium–Albumin Conjugate for Photodynamic Cancer Therapy
Author(s) -
Zhang Pingyu,
Huang Huaiyi,
Banerjee Samya,
Clarkson Guy J.,
Ge Chen,
Imberti Cinzia,
Sadler Peter J.
Publication year - 2019
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/anie.201813002
Subject(s) - photodynamic therapy , photosensitizer , human serum albumin , cytotoxicity , chemistry , conjugate , biophysics , albumin , cancer cell , serum albumin , spheroid , phosphorescence , phototoxicity , cancer research , cancer , in vitro , fluorescence , biochemistry , photochemistry , medicine , biology , organic chemistry , mathematical analysis , mathematics , physics , quantum mechanics
An organoiridium–albumin bioconjugate ( Ir1‐HSA ) was synthesized by reaction of a pendant maleimide ligand with human serum albumin. The phosphorescence of Ir1‐HSA was enhanced significantly compared to parent complex Ir1 . The long phosphorescence lifetime and high 1 O 2 quantum yield of Ir1‐HSA are highly favorable properties for photodynamic therapy. Ir1‐HSA mainly accumulated in the nucleus of living cancer cells and showed remarkable photocytotoxicity against a range of cancer cell lines and tumor spheroids (light IC 50 ; 0.8–5 μ m , photo‐cytotoxicity index PI=40–60), while remaining non‐toxic to normal cells and normal cell spheroids, even after photo‐irradiation. This nucleus‐targeting organoiridium‐albumin is a strong candidate photosensitizer for anticancer photodynamic therapy.
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