TY - JOUR
T1 - A PEGylated fluorescent turn-on sensor for detecting fluoride ions in totally aqueous media and its imaging in live cells
AU - Zheng, Fangyuan
AU - Zeng, Fang
AU - Yu, Changmin
AU - Hou, Xianfeng
AU - Wu, Shuizhu
PY - 2013/1/14
Y1 - 2013/1/14
N2 - Owing to the considerable significance of fluoride anions for health and environmental issues, it is of great importance to develop methods that can rapidly, sensitively and selectively detect the fluoride anion in aqueous media and biological samples. Herein, we demonstrate a robust fluorescent turn-on sensor for detecting the fluoride ion in a totally aqueous solution. In this study, a biocompatible hydrophilic polymer poly(ethylene glycol) (PEG) is incorporated into the sensing system to ensure water solubility and to enhance biocompatibility. tert-Butyldiphenylsilyl (TBDPS) groups were then covalently introduced onto the fluorescein moiety, which effectively quenched the fluorescence of the sensor. Upon addition of fluoride ion, the selective fluoride-mediated cleavage of the Si-O bond leads to the recovery of the fluorescein moiety, resulting in a dramatic increase in fluorescence intensity under visible light excitation. The sensor is responsive and highly selective for the fluoride anion over other common anions; it also exhibits a very low detection limit of 19ppb. In addition, this sensor is operative in some real samples such as running water, urine, and serum and can ac
AB - Owing to the considerable significance of fluoride anions for health and environmental issues, it is of great importance to develop methods that can rapidly, sensitively and selectively detect the fluoride anion in aqueous media and biological samples. Herein, we demonstrate a robust fluorescent turn-on sensor for detecting the fluoride ion in a totally aqueous solution. In this study, a biocompatible hydrophilic polymer poly(ethylene glycol) (PEG) is incorporated into the sensing system to ensure water solubility and to enhance biocompatibility. tert-Butyldiphenylsilyl (TBDPS) groups were then covalently introduced onto the fluorescein moiety, which effectively quenched the fluorescence of the sensor. Upon addition of fluoride ion, the selective fluoride-mediated cleavage of the Si-O bond leads to the recovery of the fluorescein moiety, resulting in a dramatic increase in fluorescence intensity under visible light excitation. The sensor is responsive and highly selective for the fluoride anion over other common anions; it also exhibits a very low detection limit of 19ppb. In addition, this sensor is operative in some real samples such as running water, urine, and serum and can ac
KW - fluorescence
KW - fluorescent probes
KW - fluoride
KW - sensors
UR - http://www.scopus.com/inward/record.url?scp=84872198473&partnerID=8YFLogxK
U2 - 10.1002/chem.201202732
DO - 10.1002/chem.201202732
M3 - 文章
C2 - 23197478
AN - SCOPUS:84872198473
SN - 0947-6539
VL - 19
SP - 936
EP - 942
JO - Chemistry - A European Journal
JF - Chemistry - A European Journal
IS - 3
ER -