Singlet oxygen-based electrosensing by molecular photosensitizers

被引:64
|
作者
Trashin, Stanislav [1 ]
Rahemi, Vanoushe [1 ]
Ramji, Karpagavalli [2 ,3 ]
Neven, Liselotte [1 ]
Gorun, Sergiu M. [2 ,3 ]
De Wael, Karolien [1 ]
机构
[1] Univ Antwerp, Dept Chem, AXES Res Grp, Groenenborgerlaan 171, B-2010 Antwerp, Belgium
[2] Seton Hall Univ, Dept Chem & Biochem, S Orange, NJ 07079 USA
[3] Seton Hall Univ, Ctr Funct Mat, S Orange, NJ 07079 USA
来源
NATURE COMMUNICATIONS | 2017年 / 8卷
基金
美国国家科学基金会;
关键词
C-H BONDS; HORSERADISH-PEROXIDASE; AMPEROMETRIC BIOSENSOR; PHOTODYNAMIC THERAPY; PHENOLIC-COMPOUNDS; PHTHALOCYANINE; DERIVATIVES; POLLUTANTS; OXIDATION; MECHANISM;
D O I
10.1038/ncomms16108
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Enzyme-based electrochemical biosensors are an inspiration for the development of (bio)analytical techniques. However, the instability and reproducibility of the reactivity of enzymes, combined with the need for chemical reagents for sensing remain challenges for the construction of useful devices. Here we present a sensing strategy inspired by the advantages of enzymes and photoelectrochemical sensing, namely the integration of aerobic photocatalysis and electrochemical analysis. The photosensitizer, a bioinspired perfluorinated Zn phthalocyanine, generates singlet-oxygen from air under visible light illumination and oxidizes analytes, yielding electrochemically-detectable products while resisting the oxidizing species it produces. Compared with enzymatic detection methods, the proposed strategy uses air instead of internally added reactive reagents, features intrinsic baseline correction via on/off light switching and shows C-F bonds-type enhanced stability. It also affords selectivity imparted by the catalytic process and nano-level detection, such as 20 nM amoxicillin in mu l sample volumes.
引用
收藏
页数:10
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