TY - JOUR
T1 - Pt/PEDOT:PSS modification and SF-doped PEG transient coating of helical neural electrodes for deep-brain implantation and long-term stable recording
AU - Zhou, Chaojie
AU - Xu, Yuchen
AU - Wang, Minghao
AU - Jiang, Hao
AU - Wang, Wenhao
AU - Zhou, Xinhua
AU - Zhao, Xiuqi
AU - Wang, Pengze
AU - Wang, Xinyi
AU - Yang, Wenwei
AU - Zhang, Shaomin
AU - Ji, Bowen
AU - Tan, Zhiping
AU - Wang, Gaofeng
N1 - Publisher Copyright:
© 2026 Elsevier B.V.
PY - 2026/11/1
Y1 - 2026/11/1
N2 - Flexible neural electrodes can reduce mechanical mismatch, but their chronic use remains limited by high interfacial impedance, coating instability, and difficult deep-brain insertion. Here, we report a polyimide-based 3D helical neural electrode integrating Pt/PEDOT:PSS interface modification and a low-dose silk-fibroin (SF)-doped polyethylene glycol (PEG) transient support coating. Sequential Pt/PEDOT:PSS deposition reduced the 1 kHz impedance from 1.93 MΩ to 24 kΩ (98.7%) and increased the charge-storage capacity by 23.5-fold. After 2000 cyclic-voltammetry cycles, the composite-modified electrodes showed a 22.6% impedance increase, compared with 129.4% for PEDOT:PSS-only electrodes. Helical devices retained stable impedance and phase responses after 2000 cycles of 10% tensile strain. Among all tested formulations, PEG/SF (50:1) achieved a 60.8% increase in critical buckling force and maintained a force above 0.8 N after 20 s of immersion in phosphate-buffered saline (PBS), with no detectable in vitro cytotoxicity observed. Pure-PEG-coated probes were implanted in M1 and PEG:SF-coated probes in CA1; because coating formulation and brain target were varied together, these experiments are presented as separate feasibility demonstrations rather than a direct coating comparison. Whisker stimulation elicited region-specific LFP responses. Over 120 days of chronic implantation, the electrodes retained stable impedance, steady signal-to-noise ratio (SNR) of 5.5–6.5 dB, and intact single-unit waveforms. These findings validate the effectiveness of our integrated strategy for electrochemical stabilization, structural compliance improvement, and transient insertion assistance.
AB - Flexible neural electrodes can reduce mechanical mismatch, but their chronic use remains limited by high interfacial impedance, coating instability, and difficult deep-brain insertion. Here, we report a polyimide-based 3D helical neural electrode integrating Pt/PEDOT:PSS interface modification and a low-dose silk-fibroin (SF)-doped polyethylene glycol (PEG) transient support coating. Sequential Pt/PEDOT:PSS deposition reduced the 1 kHz impedance from 1.93 MΩ to 24 kΩ (98.7%) and increased the charge-storage capacity by 23.5-fold. After 2000 cyclic-voltammetry cycles, the composite-modified electrodes showed a 22.6% impedance increase, compared with 129.4% for PEDOT:PSS-only electrodes. Helical devices retained stable impedance and phase responses after 2000 cycles of 10% tensile strain. Among all tested formulations, PEG/SF (50:1) achieved a 60.8% increase in critical buckling force and maintained a force above 0.8 N after 20 s of immersion in phosphate-buffered saline (PBS), with no detectable in vitro cytotoxicity observed. Pure-PEG-coated probes were implanted in M1 and PEG:SF-coated probes in CA1; because coating formulation and brain target were varied together, these experiments are presented as separate feasibility demonstrations rather than a direct coating comparison. Whisker stimulation elicited region-specific LFP responses. Over 120 days of chronic implantation, the electrodes retained stable impedance, steady signal-to-noise ratio (SNR) of 5.5–6.5 dB, and intact single-unit waveforms. These findings validate the effectiveness of our integrated strategy for electrochemical stabilization, structural compliance improvement, and transient insertion assistance.
KW - 3D helical neural electrodes
KW - Deep brain penetration
KW - Long-term neural recording
KW - Pt/PEDOT:PSS composite
KW - Silk fibroin-doped PEG
UR - https://www.scopus.com/pages/publications/105047909168
U2 - 10.1016/j.cej.2026.180921
DO - 10.1016/j.cej.2026.180921
M3 - 文章
AN - SCOPUS:105047909168
SN - 1385-8947
VL - 547
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
M1 - 180921
ER -