TY - JOUR
T1 - Redox-responsive nanoparticles with aggregation-induced emission (AIE) characteristic for fluorescence imaging
AU - Cheng, Weiren
AU - Wang, Guan
AU - Pan, Xiaoyong
AU - Zhang, Yong
AU - Tang, Ben Zhong
AU - Liu, Ye
PY - 2014/8
Y1 - 2014/8
N2 - The redox environment between intracellular compartments and extracellular matrix is significantly different, and the cellular redox homeostasis determines many physiological functions. Here, redox-responsive nanoparticles with aggregation-induced emission (AIE) characteristic for fluorescence imaging are developed by encapsulation of fluorophore with redox "turn-on" AIE characteristic, TPE-MI, into the micelles of poly(ethylene glycol) (PEG)- and cholesterol (CE)-conjugated disulfide containing poly(amido amine)s. The redox-responsive fluorescence profiles of the nanoparticles are investigated after reaction with glutathione (GSH). The encapsulation of TPE-MI in micelles leads to a higher efficiency and red shift in emission, and the fluorescence intensity of the nanoparticles increases with the concentration of GSH. Confocal microscopy imaging shows that the nanoparticles can provide obvious contrast between the intracellular compartments and the extracellular matrix in MCF-7 and HepG2 cells. So the nanoparticles with PEG shells and low cytotoxicity are promising to provide fluorescence bioimaging with a high contrast and for differentiation of cellular redox environment. The nanoparticles with PEG shells and low cytotoxcity are fluorescent in intracellular compartments but non-fluorescent in extracellular matrix, therefore, to provide fluorescence imaging with a high contrast. Furthermore, the fluorescent intensity increases with the concentration of thiol, making it promising for differentiation of redox environment using fluorescence imaging.
AB - The redox environment between intracellular compartments and extracellular matrix is significantly different, and the cellular redox homeostasis determines many physiological functions. Here, redox-responsive nanoparticles with aggregation-induced emission (AIE) characteristic for fluorescence imaging are developed by encapsulation of fluorophore with redox "turn-on" AIE characteristic, TPE-MI, into the micelles of poly(ethylene glycol) (PEG)- and cholesterol (CE)-conjugated disulfide containing poly(amido amine)s. The redox-responsive fluorescence profiles of the nanoparticles are investigated after reaction with glutathione (GSH). The encapsulation of TPE-MI in micelles leads to a higher efficiency and red shift in emission, and the fluorescence intensity of the nanoparticles increases with the concentration of GSH. Confocal microscopy imaging shows that the nanoparticles can provide obvious contrast between the intracellular compartments and the extracellular matrix in MCF-7 and HepG2 cells. So the nanoparticles with PEG shells and low cytotoxicity are promising to provide fluorescence bioimaging with a high contrast and for differentiation of cellular redox environment. The nanoparticles with PEG shells and low cytotoxcity are fluorescent in intracellular compartments but non-fluorescent in extracellular matrix, therefore, to provide fluorescence imaging with a high contrast. Furthermore, the fluorescent intensity increases with the concentration of thiol, making it promising for differentiation of redox environment using fluorescence imaging.
KW - aggregation-induced emission
KW - fluorescence
KW - nanoparticles
KW - poly(amido amine)s
KW - redox polymers
UR - https://www.webofscience.com/wos/woscc/full-record/WOS:000342920900001
UR - https://openalex.org/W1483270353
UR - https://www.scopus.com/pages/publications/84906320701
U2 - 10.1002/mabi.201400076
DO - 10.1002/mabi.201400076
M3 - Journal Article
C2 - 24771703
SN - 1616-5187
VL - 14
SP - 1059
EP - 1066
JO - Macromolecular Bioscience
JF - Macromolecular Bioscience
IS - 8
ER -