Structure, mechanical properties, and modeling of cyclically compressed pulmonary emboli.

Cyclic compression Hysteresis Phase transition Pulmonary emboli

Journal

Journal of the mechanical behavior of biomedical materials
ISSN: 1878-0180
Titre abrégé: J Mech Behav Biomed Mater
Pays: Netherlands
ID NLM: 101322406

Informations de publication

Date de publication:
05 2020
Historique:
received: 10 07 2019
revised: 11 02 2020
accepted: 13 02 2020
entrez: 14 4 2020
pubmed: 14 4 2020
medline: 15 5 2021
Statut: ppublish

Résumé

Pulmonary embolism occurs when blood flow to a part of the lungs is blocked by a venous thrombus that has traveled from the lower limbs. Little is known about the mechanical behavior of emboli under compressive forces from the surrounding musculature and blood pressure. We measured the stress-strain responses of human pulmonary emboli under cyclic compression, and showed that emboli exhibit a hysteretic stress-strain curve. The fibrin fibers and red blood cells (RBCs) are damaged during the compression process, causing irreversible changes in the structure of the emboli. We showed using electron and confocal microscopy that bundling of fibrin fibers occurs due to compression, and damage is accumulated as more cycles are applied. The stress-strain curves depend on embolus structure, such that variations in composition give quantitatively different responses. Emboli with a high fibrin component demonstrate higher normal stress compared to emboli that have a high RBC component. We compared the compression response of emboli to that of whole blood clots containing various volume fractions of RBCs, and found that RBCs rupture at a certain critical stress. We describe the hysteretic response characteristic of foams, using a model of phase transitions in which the compressed foam is segregated into coexisting rarefied and densified phases whose fractions change during compression. Our model takes account of the rupture of RBCs in the compressed emboli and stresses due to fluid flow through their small pores. Our results can help in classifying emboli as rich in fibrin or rich in red blood cells, and can help in understanding what responses to expect when stresses are applied to thrombi in vivo.

Identifiants

pubmed: 32279846
pii: S1751-6161(19)30961-0
doi: 10.1016/j.jmbbm.2020.103699
pmc: PMC7241098
mid: NIHMS1574171
pii:
doi:

Substances chimiques

Fibrin 9001-31-4

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

103699

Subventions

Organisme : NHLBI NIH HHS
ID : R01 HL135254
Pays : United States

Informations de copyright

Copyright © 2020 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest No conflicts of interest.

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Auteurs

Irina N Chernysh (IN)

Department of Cell Biology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, 19104, USA.

Russell Spiewak (R)

Department of Mechanical Engineering and Applied Mechanics, University of Pennsylvania, Philadelphia, PA, 19104, USA.

Carolyn L Cambor (CL)

Department of Pathology and Laboratory of Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, 19104, USA.

Prashant K Purohit (PK)

Department of Mechanical Engineering and Applied Mechanics, University of Pennsylvania, Philadelphia, PA, 19104, USA.

John W Weisel (JW)

Department of Cell Biology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, 19104, USA. Electronic address: weisel@pennmedicine.upenn.edu.

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