Sacrificial scaffold-assisted direct ink writing of engineered aortic valve prostheses.


Journal

Biofabrication
ISSN: 1758-5090
Titre abrégé: Biofabrication
Pays: England
ID NLM: 101521964

Informations de publication

Date de publication:
24 08 2023
Historique:
received: 31 12 2022
accepted: 14 08 2023
pmc-release: 24 08 2024
medline: 25 8 2023
pubmed: 15 8 2023
entrez: 14 8 2023
Statut: epublish

Résumé

Heart valve disease has become a serious global health problem, which calls for numerous implantable prosthetic valves to fulfill the broader needs of patients. Although current three-dimensional (3D) bioprinting approaches can be used to manufacture customized valve prostheses, they still have some complications, such as limited biocompatibility, constrained structural complexity, and difficulty to make heterogeneous constructs, to name a few. To overcome these challenges, a sacrificial scaffold-assisted direct ink writing approach has been explored and proposed in this work, in which a sacrificial scaffold is printed to temporarily support sinus wall and overhanging leaflets of an aortic valve prosthesis that can be removed easily and mildly without causing any potential damages to the valve prosthesis. The bioinks, composed of alginate, gelatin, and nanoclay, used to print heterogenous valve prostheses have been designed in terms of rheological/mechanical properties and filament formability. The sacrificial ink made from Pluronic F127 has been developed by evaluating rheological behavior and gel temperature. After investigating the effects of operating conditions, complex 3D structures and homogenous/heterogenous aortic valve prostheses have been successfully printed. Lastly, numerical simulation and cycling experiments have been performed to validate the function of the printed valve prostheses as one-way valves.

Identifiants

pubmed: 37579750
doi: 10.1088/1758-5090/aceffb
pmc: PMC10566457
mid: NIHMS1927034
doi:

Substances chimiques

Hydrogels 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIGMS NIH HHS
ID : P20 GM130459
Pays : United States

Informations de copyright

© 2023 IOP Publishing Ltd.

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Auteurs

Cheng Zhang (C)

State Key Laboratory of High-performance Precision Manufacturing, Dalian University of Technology, Dalian, Liaoning, People's Republic of China.
Department of Mechanical Engineering, University of Nevada, Reno, Reno, NV, United States of America.

Jiangtao Hao (J)

State Key Laboratory of High-performance Precision Manufacturing, Dalian University of Technology, Dalian, Liaoning, People's Republic of China.

Weiliang Shi (W)

State Key Laboratory of High-performance Precision Manufacturing, Dalian University of Technology, Dalian, Liaoning, People's Republic of China.

Ya Su (Y)

School of Chemical Engineering, Dalian University of Technology, Dalian, Liaoning, People's Republic of China.

Kellen Mitchell (K)

Department of Mechanical Engineering, University of Nevada, Reno, Reno, NV, United States of America.

Weijian Hua (W)

Department of Mechanical Engineering, University of Nevada, Reno, Reno, NV, United States of America.

Wenbo Jin (W)

State Key Laboratory of High-performance Precision Manufacturing, Dalian University of Technology, Dalian, Liaoning, People's Republic of China.

Serena Lee (S)

Department of Pharmacology, Center for Molecular and Cellular Signaling in the Cardiovascular System, School of Medicine, University of Nevada, Reno, Reno, NV, United States of America.

Lai Wen (L)

Department of Pharmacology, Center for Molecular and Cellular Signaling in the Cardiovascular System, School of Medicine, University of Nevada, Reno, Reno, NV, United States of America.

Yifei Jin (Y)

Department of Mechanical Engineering, University of Nevada, Reno, Reno, NV, United States of America.

Danyang Zhao (D)

State Key Laboratory of High-performance Precision Manufacturing, Dalian University of Technology, Dalian, Liaoning, People's Republic of China.

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