Active wrinkles to drive self-cleaning: A strategy for anti-thrombotic surfaces for vascular grafts.


Journal

Biomaterials
ISSN: 1878-5905
Titre abrégé: Biomaterials
Pays: Netherlands
ID NLM: 8100316

Informations de publication

Date de publication:
02 2019
Historique:
received: 04 09 2018
revised: 24 10 2018
accepted: 03 11 2018
pubmed: 21 11 2018
medline: 19 3 2020
entrez: 21 11 2018
Statut: ppublish

Résumé

The inner surfaces of arteries and veins are naturally anti-thrombogenic, whereas synthetic materials placed in blood contact commonly experience thrombotic deposition that can lead to device failure or clinical complications. Presented here is a bioinspired strategy for self-cleaning anti-thrombotic surfaces using actuating surface topography. As a first test, wrinkled polydimethylsiloxane planar surfaces are constructed that can repeatedly transition between smooth and wrinkled states. When placed in contact with blood, these surfaces display markedly less platelet deposition than control samples. Second, for the specific application of prosthetic vascular grafts, the potential of using pulse pressure, i.e. the continual variation of blood pressure between systole and diastole, to drive topographic actuation was investigated. Soft cylindrical tubes with a luminal surface that transitioned between smooth and wrinkled states were constructed. Upon exposure to blood under continual pressure pulsation, these cylindrical tubes also showed reduced platelet deposition versus control samples under the same fluctuating pressure conditions. In both planar and cylindrical cases, significant reductions in thrombotic deposition were observed, even when the wrinkles had wavelengths of several tens of μm, far larger than individual platelets. We speculate that the observed thrombo-resistance behavior is attributable to a biofilm delamination process in which the bending energy within the biofilm overcomes interfacial adhesion. This novel strategy to reduce thrombotic deposition may be applicable to several types of medical devices placed into the circulatory system, particularly vascular grafts.

Identifiants

pubmed: 30458358
pii: S0142-9612(18)30782-8
doi: 10.1016/j.biomaterials.2018.11.005
pmc: PMC7248685
mid: NIHMS1578285
pii:
doi:

Substances chimiques

Biocompatible Materials 0
Dimethylpolysiloxanes 0
baysilon 63148-62-9

Types de publication

Journal Article 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

226-234

Subventions

Organisme : NHLBI NIH HHS
ID : R56 HL142743
Pays : United States

Informations de copyright

Copyright © 2018 Elsevier Ltd. All rights reserved.

Auteurs

Luka Pocivavsek (L)

Department of Surgery, The University of Chicago, Chicago, IL, 60637, USA. Electronic address: Luka.Pocivavsek@uchospitals.edu.

Sang-Ho Ye (SH)

Department of Surgery, University of Pittsburgh Medical Center, Pittsburgh, PA, 15213, USA; McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, PA 15219, USA.

Joseph Pugar (J)

Department of Chemical Engineering, University of Pittsburgh, Pittsburgh, PA, 15213, USA.

Edith Tzeng (E)

Department of Surgery, University of Pittsburgh Medical Center, Pittsburgh, PA, 15213, USA.

Enrique Cerda (E)

Department of Physics, Universidad de Santiago de Chile, Santiago, Chile.

Sachin Velankar (S)

Department of Chemical Engineering, University of Pittsburgh, Pittsburgh, PA, 15213, USA; Department of Mechanical Engineering, University of Pittsburgh, Pittsburgh, PA, 15213, USA. Electronic address: velankar@pitt.edu.

William R Wagner (WR)

Department of Surgery, University of Pittsburgh Medical Center, Pittsburgh, PA, 15213, USA; Department of Chemical Engineering, University of Pittsburgh, Pittsburgh, PA, 15213, USA; McGowan Institute for Regenerative Medicine, University of Pittsburgh, Pittsburgh, PA 15219, USA.

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Classifications MeSH