ArticleResearch (Washington, D.C.)2025
Immersion Phase Separation 3-Dimensional Printing for Strain-Stiffening Hydrogel Scaffolds.
Article in Research (Washington, D.C.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
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
1 citing paper in PubMed.
- Adhesive-Electrocoupling Hydrogels for Tissue Regeneration: Design, Mechanisms, and Perspectives.Research (Washington, D.C.) · 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
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Strain-stiffening hydrogels, which mimic the nonlinear mechanical behavior of biological tissues such as skin, arteries, and cartilage, hold transformative potential for biomedical applications. This study introduces immersion phase separation (IPS) 3-dimensional (3D) printing, an innovative technique that enables the one-step fabrication of strain-stiffening hydrogel scaffolds with intricate, hierarchical architectures. This technique addresses the long-standing challenge of balancing structural complexity and intrinsic mechanoresponsive behavior in traditional hydrogel fabrication methods. By leveraging dynamic hydrophobic interactions and solvent exchange kinetics, IPS 3D printing achieves multiscale control over pore architectures (5 to 200 μm) and anisotropic microchannels while preserving J-shaped stress-strain curves (fracture stress: ~0.7 MPa; elongation: >1,000%). The physically cross-linked network enables closed-loop recyclability (>95% material recovery) without performance degradation, while functional fillers (e.g., carbon nanotubes, copper, and hydroxyapatite) enhance properties such as electrical conductivity (2-orders-of-magnitude improvement) and real-time motion sensing capabilities. This platform facilitates the creation of patient-specific implants with tailored mechanical properties and paves the way for adaptive biohybrid devices that mimic the dynamic behavior of native tissues, holding promise for regenerative medicine, soft robotics, and advanced biomedical applications. IPS 3D printing uniquely resolves the trade-off between structural sophistication and functional biomimicry, establishing a paradigm for replicating dynamic biological tissues.
Identifiers
What OpenQuestion holds
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.