Evidence map›Paper›PMID 42229506›Full record

ArticleBiofabrication2026

Large-scale manufacturing of precisely patterned flexible soft tissue implants with high porosity.

Amal Shabazz, Alexandra P Christensen, David Garvey, Mike Pallotta, Sahar Vakili, Stephen Farias, John P Fisher

Abstract read
In one paragraph

Article in Biofabrication, 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

7 authors.

Amal ShabazzFischell Department of Bioengineering, University of Maryland, College Park, MD, United States of America.ORCID 0009-0000-5702-3164
Alexandra P ChristensenFischell Department of Bioengineering, University of Maryland, College Park, MD, United States of America.ORCID 0009-0007-1628-5345
David GarveyThe LaunchPort, Baltimore, MD, United States of America.
Mike PallottaThe LaunchPort, Baltimore, MD, United States of America.
Sahar VakiliFischell Department of Bioengineering, University of Maryland, College Park, MD, United States of America.ORCID 0000-0002-2285-3288
Stephen FariasMateric, Baltimore, MD, United States of America.
John P FisherFischell Department of Bioengineering, University of Maryland, College Park, MD, United States of America.ORCID 0000-0002-4019-348X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As improvements in material compatibility are achieved, stereolithography (SLA) 3D printing allows for the prototyping of soft tissue constructs with high reproducibility and precision. To streamline the Food and Drug Administration approval process, clinical-grade manufacturing must be validated. Here, we present a manufacturing process and post-manufacturing analysis for soft-tissue implants used to reconstruct the nipple-areolar complex (NAC). The NAC is a specialized soft tissue structure that influences aesthetic outcomes in breast reconstruction. Physiologically-sized NAC implants were designed and printed in a good manufacturing practice facility using Formlabs Biomed Elastic 50 A (E 50 A) and Biomed Flexible 80 A (F 80 A) resins. Documentation and procedures were established to standardize and control macroporous soft-tissue implant manufacturing. Post-manufacturing classification based on architectural and mechanical features defined the minimum acceptable criteria for future production. E 50 A macroporous implants resembled the modulus of soft tissue, while F 80 A geometries showed higher reproducibility and preservation of fine architectural features. SLA printing enabled the patterning of implants with porosities of 74.65% and 72.74% for 0.4- and 0.5- mm geometries, respectively. 3D printed implants supported the infusion of gelatin methacryloyl for the delivery of biological cues, with a filling efficiency greater than 97%. This manufacturing platform achieves reproducible fabrication of soft-tissue implants that meet both structural and mechanical requirements. Further, the presented methodology can be adapted for a wide range of complex soft tissues to advance regenerative medicine solutions toward regulatory approval and eventual clinical integration.

Indexed as

Breast ImplantsTissue EngineeringTissue ScaffoldsHumansHydrogelsPorosityPrinting, Three-DimensionalStereolithographyHydrogels3D printingFormlabsgood manufacturing practicestereolithographytissue engineering

Identifiers

PMID42229506
PMCPMC13266584

What OpenQuestion holds

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Registered trials

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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.