Academic Journal

Beyond Transconductance: Cell‐Polymer Coupling Determines Fidelity in Action Potential Recording via Electrolyte‐Gated Polymer Transistors.

Λεπτομέρειες βιβλιογραφικής εγγραφής
Τίτλος: Beyond Transconductance: Cell‐Polymer Coupling Determines Fidelity in Action Potential Recording via Electrolyte‐Gated Polymer Transistors.
Συγγραφείς: Zemignani, Giulia Zoe, Mancinelli, Elena, Tullii, Gabriele, Khudiakov, Aleksandr, Bortolotti, Cristiano, Tanwar, Shubham, Schwartz, Peter J., Sala, Luca, Antognazza, Maria Rosa, Caironi, Mario, Kyndiah, Adrica
Πηγή: Advanced Science; May2026, Vol. 13 Issue 30, p1-11, 11p
Θεματικοί όροι: Action potentials, Cell adhesion, Organic field-effect transistors, Signal integrity (Electronics), Biocompatibility, Electrophysiology
Περίληψη: Organic bioelectronic transistors emerged as powerful tools for probing cellular electrophysiology, offering biocompatibility, mechanical softness, and operational stability in biological environments. Despite these advantages, device benchmarking focused so far exclusively on electrical figures of merit, leaving interfacial processes that contribute to signal recording fidelity largely unexplored. Poly[2‐(3,3′‐bis(2‐(2‐(2‐methoxyethoxy)ethoxy)ethoxy)‐[2,2'‐bithiophen]‐5‐yl)thieno[3,2‐b]thiophene] (p(g2T‐TT)) is a model glycolated organic mixed ionic‐electronic conductor, whose high transconductance and optimal volumetric field‐effect behavior in physiological environment have been widely documented in Organic Electrochemical Transistor (OECT) configurations. Thus, p(g2T‐TT)‐based OECT was assessed as a promising candidate for recording action potentials (APs) from human induced pluripotent stem cell‐derived cardiomyocytes (hiPSC‐CMs). Surprisingly, although AP signal transduction was observed, the recorded AP waveforms failed to reproduce the expected morphology, especially when compared to signals recorded via poly(3‐hexylthiophene‐2,5‐diyl) (P3HT)‐based Electrolyte‐Gated Field‐Effect Transistors (EGOFETs). Immunofluorescence imaging revealed improved adhesion on P3HT with respect to p(g2T‐TT), suggesting weaker cell‐device coupling as the underlying limitation. Our results show that not all polymers combining biocompatibility and high electrical performance can transduce AP signals with high‐fidelity. Instead, interfacial properties govern bioelectronic transduction and provide a foundation for the rational design of polymers and platforms enabling reliable in vitro cellular electrophysiology, with potential translation to in vivo applications. [ABSTRACT FROM AUTHOR]
Copyright of Advanced Science is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
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  Data: <searchLink fieldCode="DE" term="%22Action+potentials%22">Action potentials</searchLink><br /><searchLink fieldCode="DE" term="%22Cell+adhesion%22">Cell adhesion</searchLink><br /><searchLink fieldCode="DE" term="%22Organic+field-effect+transistors%22">Organic field-effect transistors</searchLink><br /><searchLink fieldCode="DE" term="%22Signal+integrity+%28Electronics%29%22">Signal integrity (Electronics)</searchLink><br /><searchLink fieldCode="DE" term="%22Biocompatibility%22">Biocompatibility</searchLink><br /><searchLink fieldCode="DE" term="%22Electrophysiology%22">Electrophysiology</searchLink>
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  Data: Organic bioelectronic transistors emerged as powerful tools for probing cellular electrophysiology, offering biocompatibility, mechanical softness, and operational stability in biological environments. Despite these advantages, device benchmarking focused so far exclusively on electrical figures of merit, leaving interfacial processes that contribute to signal recording fidelity largely unexplored. Poly[2‐(3,3′‐bis(2‐(2‐(2‐methoxyethoxy)ethoxy)ethoxy)‐[2,2'‐bithiophen]‐5‐yl)thieno[3,2‐b]thiophene] (p(g2T‐TT)) is a model glycolated organic mixed ionic‐electronic conductor, whose high transconductance and optimal volumetric field‐effect behavior in physiological environment have been widely documented in Organic Electrochemical Transistor (OECT) configurations. Thus, p(g2T‐TT)‐based OECT was assessed as a promising candidate for recording action potentials (APs) from human induced pluripotent stem cell‐derived cardiomyocytes (hiPSC‐CMs). Surprisingly, although AP signal transduction was observed, the recorded AP waveforms failed to reproduce the expected morphology, especially when compared to signals recorded via poly(3‐hexylthiophene‐2,5‐diyl) (P3HT)‐based Electrolyte‐Gated Field‐Effect Transistors (EGOFETs). Immunofluorescence imaging revealed improved adhesion on P3HT with respect to p(g2T‐TT), suggesting weaker cell‐device coupling as the underlying limitation. Our results show that not all polymers combining biocompatibility and high electrical performance can transduce AP signals with high‐fidelity. Instead, interfacial properties govern bioelectronic transduction and provide a foundation for the rational design of polymers and platforms enabling reliable in vitro cellular electrophysiology, with potential translation to in vivo applications. [ABSTRACT FROM AUTHOR]
– Name: Abstract
  Label:
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  Data: <i>Copyright of Advanced Science is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.)
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