ArticleNature communications2026
Injectable hydrogel bioelectrostimulator for wireless deep brain neuromodulation.
Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
2 citing papers in PubMed.
- PEDOT: PSS for Implantable and Wearable Bioelectronics: From Material Engineering and Energy Storage to Clinical Translation.Small (Weinheim an der Bergstrasse, Germany) · 2026Review
- Hydrogel-Based Monitoring in Perioperative Anesthesia: A Conceptual Review and Translational Perspective.International journal of nanomedicine · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
19 authors.
Funding
Abstract
Deep brain stimulation (DBS) is effective for treating neurological and psychiatric disorders. However, its tethered configuration, invasiveness, and limited tissue compatibility motivate wireless, minimally invasive alternatives. Here, we develop an in situ-gelled injectable conductive hydrogel (ICH), enabling wireless neuromodulation via electric-field localization under volume conduction. The ICH forms in vivo through bio-catalyzed polymerization and electrostatic self-assembly, yielding a stable, highly conductive, tissue-soft, and biocompatible network. Under high-frequency capacitive coupling, impedance difference between the ICH and surrounding brain tissue induces interfacial polarization and charge accumulation, locally concentrating the electric field to activate nearby neurons. This mechanism is supported by enhanced calcium signaling, increased c-Fos expression, and electrophysiological evidence of balanced basal ganglia-cortical activity. In a Parkinson's disease rat model, ICH-mediated stimulation improved locomotor behavior, preserved dopaminergic neurons, and restored functional connectivity and structural integrity as revealed by fMRI. This injectable hydrogel bioelectronics provides a platform for minimally invasive, wireless neuromodulation therapies.
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Registered trials
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