Evidence map›Paper›PMID 42368015›Full record

ArticlebioRxiv : the preprint server for biology2026

Simultaneous regeneration of skin and bone in full-thickness cranial composite defects.

Mirae Kim, Yi Zhu, Shivakalyani Adepu, Caralyn P Collins, Maria Mendez-Santos, Cheng Sun, Tong-Chuan He, Russell R Reid, Guillermo A Ameer

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Mirae KimDepartment of Biomedical Engineering, Northwestern University, Evanston, IL, 60208, USA.
Yi ZhuMolecular Oncology Laboratory, Department of Orthopedic Surgery and Rehabilitation Medicine, The University of Chicago Medical Center; Chicago, IL, 60637, USA.
Shivakalyani AdepuDepartment of Biomedical Engineering, Northwestern University, Evanston, IL, 60208, USA.
Caralyn P CollinsCenter for Advanced Regenerative Engineering, Northwestern University, Evanston, IL, 60208, USA.
Maria Mendez-SantosDepartment of Biomedical Engineering, Northwestern University, Evanston, IL, 60208, USA.
Cheng SunCenter for Advanced Regenerative Engineering, Northwestern University, Evanston, IL, 60208, USA.ORCID 0000-0002-2744-0896
Tong-Chuan HeCenter for Advanced Regenerative Engineering, Northwestern University, Evanston, IL, 60208, USA.
Russell R ReidDepartment of Surgery, Section of Plastic and Reconstructive Surgery, The University of Chicago Medicine and Biological Sciences, Chicago, IL, 60637, USA.
Guillermo A AmeerQuerrey Simpson Institute for Regenerative Engineering at Northwestern University, Chicago, IL, 60611, USA.

Funding

Tumor Environment and Metastasis (TEAM) Research ProgramP30CA060553 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Devalingam Mahalingam · 1993 to 2026
$153.9M
The Institute for Translational MedicineUL1TR002389 · NCATS · UNIVERSITY OF CHICAGO · PI Joshua J Jacobs, DAVID O MELTZER · 2017 to 2026
$71.6M
Multi-Tissue Craniofacial Engineering using 3D-BMP9-Notch-Synergized Graphene Citrate Composite ScaffoldsR01DE030480 · NIDCR · UNIVERSITY OF CHICAGO · PI REID, RUSSELL R. · 2021 to 2025
$2.3M
NCATS NIH HHS UL1 TR002389NCI NIH HHS P30 CA060553NIDCR NIH HHS R01 DE030480
6 · The paper itself

Abstract

Traumatic cranial defects often involve concurrent loss of soft and hard tissues and can progress to chronic defects due to delayed healing associated with infection or other co-morbidities. Despite autologous reconstruction remaining the clinical standard, it requires staged procedures using heterogeneous tissues, increasing operative time, costs, and surgical risks. Moreover, current tissue engineering approaches focus on single tissues or acute tissue defect models, limiting their clinical applications. Herein, we describe an acellular, material-driven 3D-printed composite scaffold designed to regenerate both bone and skin within composite cranial defects. The scaffold integrates controlled copper ion release from both organic and inorganic components with 3D-printed citrate polymer and citrate polymer-ceramic composites. Integrated thermoresponsive citrate-based hydrogels further enable spatially defined dermoconductive and osteoconductive properties, supporting a one-step surgical approach. At 12 weeks post-implantation, our scaffold enhanced keratinocyte organization, collagen deposition, and defect coverage with mature bone, achieving histological outcomes comparable to autografts. Furthermore, the system suppressed bacterial burden. Thus, this acellular platform represents a clinically promising synchronized strategy to address the complex demands of traumatic craniofacial composite defects.

Indexed as

3D printingacellular regenerative platformcitrate-based materialscraniofacial composite defectsoft and bone regeneration

Identifiers

PMID42368015
PMCPMC13308115

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.