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Au Nanoclusters Sensitized Black TiO 2− x Nanotubes for Enhanced Photodynamic Therapy Driven by Near‐Infrared Light
Author(s) -
Yang Dan,
Gulzar Arif,
Yang Guixin,
Gai Shili,
He Fei,
Dai Yunlu,
Zhong Chongna,
Yang Piaoping
Publication year - 2017
Publication title -
small
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.785
H-Index - 236
eISSN - 1613-6829
pISSN - 1613-6810
DOI - 10.1002/smll.201703007
Subject(s) - nanoclusters , anatase , materials science , photodynamic therapy , photocatalysis , nanotechnology , visible spectrum , photochemistry , optoelectronics , chemistry , catalysis , biochemistry , organic chemistry
The low reactive oxygen species production capability and the shallow tissue penetration of excited light (UV) are still two barriers in photodynamic therapy (PDT). Here, Au cluster anchored black anatase TiO 2− x nanotubes (abbreviated as Au 25 /B‐TiO 2− x NTs) are synthesized by gaseous reduction of anatase TiO 2 NTs and subsequent deposition of noble metal. The Au 25 /B‐TiO 2− x NTs with thickness of about 2 nm exhibit excellent PDT performance. The reduction process increased the density of Ti 3+ on the surface of TiO 2 , which effectively depresses the recombination of electron and hole. Furthermore, after modification of Au 25 nanoclusters, the PDT efficiency is further enhanced owing to the changed electrical distribution in the composite, which forms a shallow potential well on the metal–TiO 2 interface to further hamper the recombination of electron and hole. Especially, the reduction of anatase TiO 2 can expend the light response range (UV) of TiO 2 to the visible and even near infrared (NIR) light region with high tissue penetration depth. When excited by NIR light, the nanoplatform shows markedly improved therapeutic efficacy attributed to the photocatalytic synergistic effect, and promotes separation or restrained recombination of electron and hole, which is verified by experimental results in vitro and in vivo.