Evidence map›Paper›PMID 39976571›Full record

ArticleSoft matter2025

Poroelasticity and permeability of fibrous polymer networks under compression.

Paul Mollenkopf, Jakub A Kochanowski, Yifei Ren, Kyle H Vining, Paul A Janmey, Prashant K Purohit

Abstract read
In one paragraph

Article in Soft matter, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Modeling tumor transport and growth with poroelastic biopolymer networks.bioRxiv : the preprint server for biology · 2025
    Article
  6. Fluid effects on the fracture toughness of gels.Journal of the mechanics and physics of solids · 2025
    Article
  7. Article
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

6 authors.

Paul MollenkopfDepartment of Physiology, University of Pennsylvania, Philadelphia, PA, 19104, USA. janmey@pennmedicine.upenn.edu.ORCID http://orcid.org/0000-0003-4653-1643
Jakub A KochanowskiDepartment of Physiology, University of Pennsylvania, Philadelphia, PA, 19104, USA. janmey@pennmedicine.upenn.edu.ORCID http://orcid.org/0009-0006-0008-1463
Yifei RenDepartment of Mechanical Engineering and Applied Mechanics, University of Pennsylvania, Philadelphia, PA 19104, USA.ORCID http://orcid.org/0009-0000-4712-0657
Kyle H ViningDepartment of Preventive and Restorative Sciences, Department of Materials Science and Engineering, University of Pennsylvania, Philadelphia, PA 19104, USA.ORCID http://orcid.org/0000-0002-4009-879X
Paul A JanmeyDepartment of Physiology, University of Pennsylvania, Philadelphia, PA, 19104, USA. janmey@pennmedicine.upenn.edu.ORCID http://orcid.org/0000-0002-3495-3286
Prashant K PurohitDepartment of Mechanical Engineering and Applied Mechanics, University of Pennsylvania, Philadelphia, PA 19104, USA.ORCID http://orcid.org/0000-0002-1939-907X

Funding

Regulation of cell, tissue, and nucleus function by mechanical properties of biopolymer networksR35GM136259 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI Paul A Janmey · 2020 to 2026
$3.2M
Mechanisms of mechano-chemical rupture of blood clots and thrombiR01HL148227 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI PUROHIT, PRASHANT KISHORE · 2020 to 2023
$2.5M
NHLBI NIH HHS R01 HL148227NIGMS NIH HHS R35 GM136259
6 · The paper itself

Abstract

Soft biopolymer networks play pivotal roles in governing cellular mechanics, tissue structure, and physiological processes such as blood coagulation. Understanding their permeability and mechanical responses under compression is crucial for elucidating mass transport phenomena and their impact on extra- and intra-cellular behavior as well as processes affecting functionality of blood clots, cartilage and other fibrous tissues. The nonlinear responses of these networks to mechanical stresses prevent application of established linear poro-elasticity models. Despite extensive studies of fibrous network viscoelastic properties under shear deformations, their dynamic responses to compressive deformations remain poorly understood, particularly in physiological contexts of growth and collective migration of solid bodies. Conventional experimental techniques face challenges in accurately evaluating the permeability of these networks, hindering comprehensive understanding of their poromechanical behavior. In this study, we employ a novel poroelastic hybrid approach combining rheometer-based compression rheology with camera-facilitated sample shape detection to directly measure fluid flux and network permeability under controlled compressive strains. Accompanying experimental investigations, a continuum model implemented in finite elements, and an analytical model are developed to interpret the findings. The experimental data align well with the analytical model, revealing the emergence and disappearance of distinct densification regimes within the gel under mechanical stress. This study advances our understanding of the intricate interplay between mechanical forces, fluid flow, and structural properties in soft biopolymer networks, with a specific focus on fibrin- and collagen-based gels which represent the most abundant protein networks in the extracellular environment.

Indexed as

CollagenElasticityFibrinCompressive StrengthPermeabilityPorosityRheologyStress, MechanicalCollagenFibrin

Identifiers

PMID39976571
PMCPMC11841696

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.