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On-line regeneration of electrochemical biosensor for in vivo repetitive measurements of striatum Cu2+ under global cerebral ischemia/reperfusion events

Author:
Gu, Hui, Hou, Qi, Liu, Yu, Cai, Yujie, Guo, Yanqiu, Xiang, Haoyue, Chen, Shu
Source:
Biosensors & bioelectronics 2019 v.135 pp. 111-119
ISSN:
0956-5663
Subject:
EDTA (chelating agent), biosensors, brain, copper, ischemia, metal ions, microdialysis, moieties, physiology, polyethyleneimine, rats
Abstract:
The detection of Cu2+ ion, one of the metal ions substantial in cerebral physiology, is critical in studying brain activities and understanding brain functions. However, repetitive measurements of Cu2+ in the progress of physiological and pathological events is still challenging, because lack of the platform for repetitive on-line detection-regeneration cycle. Herein we report the design of a regenerated electrochemical biosensor combined with the in vivo microdialysis system. In this biosensor, hyperbranched polyethyleneimine (hPEI) acts as a regenerated recognition unit for Cu2+. Just by a simple rinse of ethylenediaminetetraacetic acid (EDTA) disodium salt, the Cu2+ and Cu+ ions on the biosensor interface were chelated with EDTA disodium salt, thus achieving the regeneration of the biosensor. In addition, 6-(ferrocenyl)hexanethiol (FcHT) serves as the inner reference moiety to elevate the sensing accuracy over regeneration cycles. As a result, this ratiometric electrochemical biosensor not only revealed high sensitivity and selectivity, but also exhibited excellent stability during multiple regeneration processing. This biosensor was capable of determining Cu2+ with a linear range between 0.05 and 12 μM and low detection limit (LOD) of 13 nM. Then, the platform has been successfully applied in repetitive Cu2+ analysis in rat brain under global cerebral ischemia/reperfusion events. The combination of results from 7 rats indicates global cerebral ischemia caused an obvious increase of the Cu2+ level, while reperfusion brought this level back to normal.
Agid:
6346827