Research context and placement

The central process joins electrodes, receiving coils and a soft substrate through different inks. Tissue contact and stimulation provide a secondary connection; placement does not rely on sensing performance alone.

Research background

Wound geometry changes the fit and placement of electrodes and coils. CARE addresses a fabrication workflow that begins with the wound shape. Geometry recognition must be connected to delivered stimulation to assess what customization accomplishes.

Approach and advances

Depth imaging informs electrode and coil design, followed by sequential robotic printing of different inks. The workflow links geometry to fabrication. However, wound data are manually transferred to MATLAB, so the demonstrated process is not fully autonomous.

A not-to-scale concept arranged from left to right: geometry observation by a depth camera, a manually operated design screen, one nozzle printing on a separate flexible carrier, and a separate external coil.
AI-generated concept diagram · not an experimental image

AI-generated, not-to-scale concept of CARE’s geometry-informed, manually assisted design and sequential printing with different inks. The printing scene shows one moment with one active nozzle; other ink stages are omitted. The electrodes and receiving coil on the carrier and the separate external excitation coil are functional symbols, not an actual circuit, experimental evidence or a clinical-treatment result.

A generic phantom, design screen and flexible carrier illustrate fabrication roles only. Other ink-printing stages and detailed electrical routing are omitted. Actual layer count, material colors, circuit connections, nozzle geometry, coil turns or alignment, fields, power-transfer performance, healing, dimensions and proportions are not reconstructed. This is neither microscopy nor a fabrication instruction.

This is not a reproduced paper figure and does not establish permission to reuse the original figure.

Generated in ChatGPT on the web from concepts within the stated public-evidence scope and independently reviewed as a concept. This is not verification of the complete article body or supplementary information. Only display WebP encoding was applied, without cropping, resizing or content editing.

Source paper ↗ · DOI: 10.1002/adhm.202401735 ↗

Evaluation and conditions

Wireless coupling depends on coil geometry, distance and load. Simulated tissue fields and cell proliferation, migration and vascular assays address separate steps. A modeled field is not an in-vivo dose measurement, and cell culture is not animal wound closure.

Key findings

Compared with unstimulated cultures, stimulated fibroblasts and endothelial cells showed greater migration, and endothelial tube assays produced more junctions. Migration and tube assays used a 20% duty cycle with different exposure times; proliferation and other readouts used separate settings. These remain cell-level observations, not demonstrated animal wound closure or patient-specific optimal treatment.

Limits and open questions

Manual data transfer and the external excitation hardware remain workflow constraints. Motion-dependent coupling and reproducible dose also need validation. Biological claims here remain bounded to the inspected fibroblast and endothelial-cell assessments, not clinical treatment efficacy.

Related external research

Corresponding-author verification

Jungmok Seo: corresponding author

This record concerns Jungmok Seo’s correspondence designation. Author order or an asterisk alone is not treated as confirmation; this check is separate from verification of the research content.

  • Correspondence evidence source ↗

    Corresponding Author — Jungmok Seo

    Author information: all three Corresponding Author blocks; local PDF pp. 1–2 email match · public_publisher_author_information_read

  • Correspondence evidence source ↗

    J. Seo; E-mail: [redacted]

    Published PDF page 1: linked author affiliation and E-mail; title and DOI · local_published_pdf_read

Main-text review scope
Read publisher Abstract and pp. 10–12, Figs. 5–6 and Conclusion of the title/DOI-matched local published PDF. Rechecked manual MATLAB transfer, wireless operation and cellular-assay boundaries. Local PDF access is distinct from publisher-web full text.
Supplementary review scope
Supporting information was not comprehensively read. A main-text citation to supplementary results does not count as direct inspection of those results.
Pending verification
Verify supplementary circuit/coil optimization at school; assess any later automation separately from this publication.

COVERAGE & OUTREACH

Coverage and outreach

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Sources and verification scope

Read publisher Abstract and pp. 10–12, Figs. 5–6 and Conclusion of the title/DOI-matched local published PDF. Rechecked manual MATLAB transfer, wireless operation and cellular-assay boundaries. Local PDF access is distinct from publisher-web full text.

The additional commentary is editorially approved within the stated evidence scope. This does not imply complete verification of all main-text and supplementary material.

Additional main-text review scope
Read publisher Abstract and pp. 10–12, Figs. 5–6 and Conclusion of the title/DOI-matched local published PDF. Rechecked manual MATLAB transfer, wireless operation and cellular-assay boundaries. Local PDF access is distinct from publisher-web full text.
Additional supplementary review scope
Supporting information was not comprehensively read. A main-text citation to supplementary results does not count as direct inspection of those results.