Metabolite-induced in vivo fabrication of substrate-free organic bioelectronics

被引:76
作者
Strakosas, Xenofon [1 ,2 ]
Biesmans, Hanne [1 ]
Abrahamsson, Tobias [1 ]
Hellman, Karin [2 ]
Ejneby, Malin Silvera [1 ]
Donahue, Mary J. [1 ]
Ekstrom, Peter [2 ]
Ek, Fredrik [2 ]
Savvakis, Marios [1 ]
Hjort, Martin [2 ]
Bliman, David [3 ,4 ]
Linares, Mathieu [1 ,5 ]
Lindholm, Caroline [1 ]
Stavrinidou, Eleni [1 ]
Gerasimov, Jennifer Y. [1 ]
Simon, Daniel T. [1 ]
Olsson, Roger [2 ,3 ]
Berggren, Magnus [1 ]
机构
[1] Linkoping Univ, Dept Sci & Technol, Lab Organ Elect, S-60174 Norrkoping, Sweden
[2] Lund Univ, Dept Expt Med Sci, Chem Biol & Therapeut, SE-22184 Lund, Sweden
[3] Univ Gothenburg, Dept Chem & Mol Biol, SE-40530 Gothenburg, Sweden
[4] IRLAB Therapeut AB, Arvid Wallgrens Backe 20, S-41346 Gothenburg, Sweden
[5] Linkoping Univ, Dept Sci & Technol, Sci Visualizat Grp, S-60174 Norrkoping, Sweden
基金
瑞典研究理事会; 欧洲研究理事会;
关键词
POLYMERIZATION; ELECTRODES; GLUCOSE; TRANSPORT; PEDOT;
D O I
10.1126/science.adc9998
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
Interfacing electronics with neural tissue is crucial for understanding complex biological functions, but conventional bioelectronics consist of rigid electrodes fundamentally incompatible with living systems. The difference between static solid-state electronics and dynamic biological matter makes seamless integration of the two challenging. To address this incompatibility, we developed a method to dynamically create soft substrate-free conducting materials within the biological environment. We demonstrate in vivo electrode formation in zebrafish and leech models, using endogenous metabolites to trigger enzymatic polymerization of organic precursors within an injectable gel, thereby forming conducting polymer gels with long-range conductivity. This approach can be used to target specific biological substructures and is suitable for nerve stimulation, paving the way for fully integrated, in vivo-fabricated electronics within the nervous system.
引用
收藏
页码:795 / 802
页数:8
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