TY - JOUR
T1 - Aggregation-Induced Emission Luminogens with the Capability of Wide Color Tuning, Mitochondrial and Bacterial Imaging, and Photodynamic Anticancer and Antibacterial Therapy
AU - Zhao, Na
AU - Li, Pengfei
AU - Zhuang, Jiabao
AU - Liu, Yanyan
AU - Xiao, Yuxin
AU - Qin, Ruilin
AU - Li, Nan
N1 - Publisher Copyright:
© 2019 American Chemical Society.
PY - 2019/3/27
Y1 - 2019/3/27
N2 - Recently, luminogens with the aggregation-induced emission characteristic (AIEgens) have received much attention in the field of bioimaging and therapeutic applications. However, the development of AIEgens that are derived from the simple core skeleton with emission color tuning for imaging and therapy is still a formidable challenge. To address this constraint, we present a series of cationic AIEgens based on cyanopyridinium salts (CP1-CP5). The AIEgens can be facilely prepared by varying the aromatic electron donor while fixing the cyanopyridinium group as the electron acceptor within a single benzene ring. The obtained AIEgens possess wide color tunability, large Stokes shifts, and bright emission in the condensed state. Due to their good biocompatibility and cationic nature, these AIEgens can be utilized for multiple-color imaging of intracellular mitochondria as well as Gram-negative and Gram-positive bacteria. Importantly, these AIEgens exhibit remarkable structure-dependent singlet-oxygen generation ability under white light illumination (25 mW cm -2 ), and CP4 was optimized to serve as an excellent photosensitizer for photodynamic anticancer and antibacterial therapy.
AB - Recently, luminogens with the aggregation-induced emission characteristic (AIEgens) have received much attention in the field of bioimaging and therapeutic applications. However, the development of AIEgens that are derived from the simple core skeleton with emission color tuning for imaging and therapy is still a formidable challenge. To address this constraint, we present a series of cationic AIEgens based on cyanopyridinium salts (CP1-CP5). The AIEgens can be facilely prepared by varying the aromatic electron donor while fixing the cyanopyridinium group as the electron acceptor within a single benzene ring. The obtained AIEgens possess wide color tunability, large Stokes shifts, and bright emission in the condensed state. Due to their good biocompatibility and cationic nature, these AIEgens can be utilized for multiple-color imaging of intracellular mitochondria as well as Gram-negative and Gram-positive bacteria. Importantly, these AIEgens exhibit remarkable structure-dependent singlet-oxygen generation ability under white light illumination (25 mW cm -2 ), and CP4 was optimized to serve as an excellent photosensitizer for photodynamic anticancer and antibacterial therapy.
KW - aggregation-induced emission
KW - bacterial imaging
KW - mitochondrial imaging
KW - photosensitizer
KW - wide color tuning
UR - http://www.scopus.com/inward/record.url?scp=85063508306&partnerID=8YFLogxK
U2 - 10.1021/acsami.9b01655
DO - 10.1021/acsami.9b01655
M3 - Article
C2 - 30843393
AN - SCOPUS:85063508306
SN - 1944-8244
VL - 11
SP - 11227
EP - 11237
JO - ACS Applied Materials and Interfaces
JF - ACS Applied Materials and Interfaces
IS - 12
ER -