Evidence map›Paper›PMID 41524833›Full record

ArticleTissue engineering and regenerative medicine2026

Combining Surface Modification and Bioactive Cues to Enhance Medpor® Implant Integration In Vivo.

Dina Gadalla, Maeve M Kennedy, Jamie E Ganem, Sriya Yeleswarapu, Amanda M Richards, Rachel M Wells, David G Lott

Abstract read
In one paragraph

Article in Tissue engineering and regenerative medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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.

2 · The registry

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3 · Its place in the literature

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4 · The record

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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.

Dina GadallaHead and Neck Regenerative Medicine Laboratory, Phoenix, AZ, 85054, USA.
Maeve M KennedyHead and Neck Regenerative Medicine Laboratory, Phoenix, AZ, 85054, USA.
Jamie E GanemHead and Neck Regenerative Medicine Laboratory, Phoenix, AZ, 85054, USA.
Sriya YeleswarapuHead and Neck Regenerative Medicine Laboratory, Phoenix, AZ, 85054, USA.
Amanda M RichardsHead and Neck Regenerative Medicine Laboratory, Phoenix, AZ, 85054, USA.
Rachel M WellsHead and Neck Regenerative Medicine Laboratory, Phoenix, AZ, 85054, USA.
David G LottHead and Neck Regenerative Medicine Laboratory, Phoenix, AZ, 85054, USA. Lott.david@mayo.edu.ORCID http://orcid.org/0000-0001-6541-9687

Funding

Optimizing a patient-specific regenerative larynx implant for restoration of voiceR01DC019114 · NIDCD · MAYO CLINIC ARIZONA · PI LOTT, DAVID G · 2021 to 2025
$3.1M
NIDCD NIH HHS R01 DC019114
6 · The paper itself

Abstract

backgroundAchieving stable and functional integration of synthetic implants with host tissue remains a key challenge in tissue engineering. Medpor®, a porous high-density polyethylene (HDPE) implant widely used in craniofacial reconstruction, provides excellent mechanical strength but lacks bioactivity, limiting early cell adhesion, vascularization, and extracellular matrix (ECM) deposition.

methodsTo enhance Medpor® biointegration, we employed a multi-faceted modification strategy combining plasma treatment with biologically active components. Treated implants were coated with collagen and fibrin hydrogels and further supplemented with a platelet-derived Purified Exosome Product (PEP). Modified and control implants were evaluated in a subcutaneous mouse model to assess host tissue response, vascularization, and implant integration.

resultsTissue ingrowth was observed in the pores of all Medpor® implants. Plasma treatment significantly increased the surface hydrophilicity of Medpor®, promoting host cell adhesion and tissue infiltration. Implants modified with both hydrogels and PEP exhibited enhanced ECM deposition, greater vascular density, and improved tissue integration compared to untreated Medpor®. The combination of physicochemical surface treatment and biochemical cues led to a synergistic effect, supporting tissue ingrowth and angiogenesis under a controlled host immune response.

conclusionThis study demonstrates that integrating plasma surface modification with bioactive hydrogels and PEP can effectively enhance the biointegration of Medpor® implants in vivo. The combined approach significantly enhances implant vascularization and ECM development, offering a promising translational strategy for improving synthetic implant performance in regenerative and reconstructive biomaterial applications.

Indexed as

Biocompatible MaterialsPolyethylenesProstheses and ImplantsAnimalsCollagenExosomesExtracellular MatrixHydrogelsMiceSurface PropertiesBiocompatible MaterialsCollagenHydrogelsMedporPolyethylenesBioactive hydrogelsExosomesMedpor®Plasma treatmentTissue integration

Identifiers

PMID41524833
PMCPMC13031466

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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.