Evidence map›Paper›PMID 41780217›Full record

ArticleJournal of the mechanical behavior of biomedical materials2026

Tissue compliance characterization for human umbilical arteries after decellularization.

Kun Gou, Jin-Jia Hu, Seungik Baek

Abstract read
In one paragraph

Article in Journal of the mechanical behavior of biomedical materials, 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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0citing papers 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

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

3 authors.

Kun GouDepartment of Computational, Engineering, and Mathematical Sciences, Texas A&M University-San Antonio, San Antonio, TX, USA. Electronic address: kgou@tamusa.edu.
Jin-Jia HuDepartment of Mechanical Engineering, National Yang Ming Chiao Tung University, Hsinchu 300, Taiwan. Electronic address: jjhu@nycu.edu.tw.
Seungik BaekDepartment of Mechanical Engineering, Michigan State University, East Lansing, MI, USA. Electronic address: sbaek@egr.msu.edu.

Funding

Growth and Remodeling Model of Abdominal Aortic Aneurysm: Toward Clinical ApplicaR01HL115185 · NHLBI · MICHIGAN STATE UNIVERSITY · PI BAEK, SEUNGIK · 2012 to 2015
$753k
NHLBI NIH HHS R01 HL115185
6 · The paper itself

Abstract

Human umbilical arteries (HUAs) are promising candidates for small-diameter vascular grafts due to their ability to closely replicate the mechanical behavior and structural integrity of native arteries. To minimize immunogenic responses and promote integration with host tissue following implantation, decellularization is required to remove cellular components from HUAs. A thorough understanding of the mechanical properties of decellularized HUAs (Dec-HUAs) is critical for predicting their mechanical compatibility and adaptability within the host circulation. This study aims to characterize the mechanical alterations induced by decellularization using a hyperelastic constitutive model that incorporates both isotropic and anisotropic damage parameters. Five HUA samples are subjected to mechanical characterization following removal of the abluminal layer and subsequent decellularization. The mechanical response is modeled within a modified hyperelastic damage framework, and model parameters are estimated using an improved fitting approach. Statistical analyses are then performed to evaluate the mean, standard deviation, and significance of changes in mechanical properties. The mechanical analysis of stress-strain behavior under large transmural pressure differences shows that Dec-HUAs exhibit reduced compliance compared with native HUAs. The results reveal a notable increase in compliance (C) following abluminal layer removal, whereas decellularization causes a mild decrease in compliance. Both stored strain energy (W) and compliance (C) serve as indices of vessel compliance, but statistical comparisons indicate that W more effectively captures alterations in compliance during the graft preparation process than C. Overall, these findings highlight the key mechanical changes introduced by decellularization and establish a robust parameter-estimation framework for assessing vessel mechanics. This framework can support future studies on mechanical adaptation of Dec-HUAs and ultimately aid in the development of mechanically compatible and durable vascular grafts.

Indexed as

Mechanical PhenomenaUmbilical ArteriesBiomechanical PhenomenaComplianceHumansMaterials TestingStress, MechanicalDecellularizationParameter fittingTissue damageUmbilical arteryVascular graft

Identifiers

PMID41780217
PMCPMC13277210

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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.