ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026
A Programmable, 3D Neuron-On-Chip Platform Integrating Near Real-Time Biosensing and Multiaxial Loading for Mechanobiological Injury Profiling.
Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 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.
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Who cites it
4 citing papers in PubMed.
- Translational benchmarking of 3D in vitro models of traumatic brain injury.Trends in biotechnology · 2026Review
- A 3D Human Neuron-on-Chip Platform to Monitor Neuronal Injury Responses.Advanced healthcare materials · 2026Article
- Application and prospects of organoid-on-a-chip in research on the intestinal mucosal barrier.Burns & trauma · 2026Review
- A Programmable, 3D Neuron-On-Chip Platform Integrating Near Real-Time Biosensing and Multiaxial Loading for Mechanobiological Injury Profiling.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026Article
Corrections and comments
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Authors and funding
13 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Mechanical forces imparted to the central nervous system (CNS) generate complex, load-dependent injury patterns, yet the molecular mechanisms linking physical insult to biomarker response remain poorly defined. Here, the Neuron-Injury-on-a-Chip (NIOC) platform is presented as a programmable 3D microfluidic system integrating multiaxial loading with real-time biosensing. The system features a polydimethylsiloxane (PDMS) tube internally coated with polydopamine to support Cath. a-differentiated (CAD) neuron adhesion and viability. Controlled extension, torsion, and combined loads simulate physiologically relevant CNS trauma. Finite element modeling confirms uniform strain transmission, while embedded electrochemical biosensors enable near real-time detection of total tau (T-Tau) and neurofilament light chain (NFL) at picogram levels. qPCR and immunostaining validate gene-level responses (Mapt, Gap-43) and apoptosis (Caspase-3). Load-specific biomarker trajectories and apoptotic thresholds are uncovered, with synergistic injury responses under combined loading. NIOC represents a first-in-class platform for decoding mechanobiological injury, offering new opportunities for biomarker discovery, injury stratification, and neuroprotective screening.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.