TY - JOUR
T1 - High UV-VIS-NIR light-induced antibacterial activity by heterostructured TiO2-FeS2 nanocomposites
AU - Mutalik, Chinmaya
AU - Hsiao, Yu Cheng
AU - Chang, Yi Hsuan
AU - Krisnawati, Dyah Ika
AU - Alimansur, Moh
AU - Jazidie, Achmad
AU - Nuh, Mohammad
AU - Chang, Chia Che
AU - Wang, Di Yan
AU - Kuo, Tsung Rong
N1 - Publisher Copyright:
© 2020 Mutalik et al. Tphp and incorporate the.
PY - 2020
Y1 - 2020
N2 - Purpose: Antibiotic resistance issues associated with microbial pathogenesis are considered to be one of the most serious current threats to health. Fortunately, TiO2, a photoactive semiconductor, was proven to have antibacterial activity and is being widely utilized. However, its use is limited to the short range of absorption wavelength. Methods: In this work, heterostructured TiO2-FeS2 nanocomposites (NCs) were success-fully prepared by a facile solution approach to enhance light-induced antibacterial activity over a broader absorption range. Results: In TiO2-FeS2 NCs, FeS2 NPs, as light harvesters, can effectively increase light absorption from the visible (Vis) to near-infrared (NIR). Results of light-induced antibacterial activities indicated that TiO2-FeS2 NCs had better antibacterial activity than that of only TiO2 nanoparticles (NPs) or only FeS2 NPs. Reactive oxygen species (ROS) measurements also showed that TiO2-FeS2 NCs produced the highest relative ROS levels. Unlike TiO2 NPs, TiO2-FeS2 NCs, under light irradiation with a 515-nm filter, could absorb light wavelengths longer than 515 nm to generate ROS. In the mechanistic study, we found that TiO2 NPs in TiO2-FeS2 NCs could absorb ultraviolet (UV) light to generate photoinduced electrons and holes for ROS generation, including ⋅O2 − and ⋅OH; FeS2 NPs efficiently harvested Vis to NIR light to generate photoinduced electrons, which then were transferred to TiO2 NPs to facilitate ROS generation. Conclusion: TiO2-FeS2 NCs with superior light-induced antibacterial activity could be a promising antibacterial agent against bacterial infections.
AB - Purpose: Antibiotic resistance issues associated with microbial pathogenesis are considered to be one of the most serious current threats to health. Fortunately, TiO2, a photoactive semiconductor, was proven to have antibacterial activity and is being widely utilized. However, its use is limited to the short range of absorption wavelength. Methods: In this work, heterostructured TiO2-FeS2 nanocomposites (NCs) were success-fully prepared by a facile solution approach to enhance light-induced antibacterial activity over a broader absorption range. Results: In TiO2-FeS2 NCs, FeS2 NPs, as light harvesters, can effectively increase light absorption from the visible (Vis) to near-infrared (NIR). Results of light-induced antibacterial activities indicated that TiO2-FeS2 NCs had better antibacterial activity than that of only TiO2 nanoparticles (NPs) or only FeS2 NPs. Reactive oxygen species (ROS) measurements also showed that TiO2-FeS2 NCs produced the highest relative ROS levels. Unlike TiO2 NPs, TiO2-FeS2 NCs, under light irradiation with a 515-nm filter, could absorb light wavelengths longer than 515 nm to generate ROS. In the mechanistic study, we found that TiO2 NPs in TiO2-FeS2 NCs could absorb ultraviolet (UV) light to generate photoinduced electrons and holes for ROS generation, including ⋅O2 − and ⋅OH; FeS2 NPs efficiently harvested Vis to NIR light to generate photoinduced electrons, which then were transferred to TiO2 NPs to facilitate ROS generation. Conclusion: TiO2-FeS2 NCs with superior light-induced antibacterial activity could be a promising antibacterial agent against bacterial infections.
KW - Antibacterial agent
KW - Antibacterial mechanism
KW - Light harvester
KW - Light-induced antibacterial activity
KW - Reactive oxygen species
UR - http://www.scopus.com/inward/record.url?scp=85096044728&partnerID=8YFLogxK
U2 - 10.2147/IJN.S282689
DO - 10.2147/IJN.S282689
M3 - Article
C2 - 33209024
AN - SCOPUS:85096044728
SN - 1176-9114
VL - 15
SP - 8911
EP - 8920
JO - International Journal of Nanomedicine
JF - International Journal of Nanomedicine
ER -