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Collagen type I and hyaluronic acid based hybrid scaffolds for heart valve tissue engineering

Abstract:
Tissue engineers have achieved limited success so far in designing an ideal scaffold for aortic valve; scaffolds lack in mechanical compatibility, appropriate degradation rate, and microstructural similarity. This paper, therefore, has demonstrated a carbodiimide‐based sequential crosslinking technique to prepare aortic valve extracellular matrix mimicking (ECM) hybrid scaffolds from collagen type I and hyaluronic acid (HA), the building blocks of heart valve ECM, with tailorable crosslinking densities. Swelling studies revealed that crosslinking densities of parent networks increased with increasing the concentration of the crosslinking agents whereas crosslinking densities of hybrid scaffolds averaged from those of parent collagen and HA networks. Hybrid scaffolds also offered a wide range of pore size (66‐126 μm) which fulfilled the criteria for valvular tissue regeneration. Scanning electron microscopy and images of Alcian blue‐Periodic acid Schiff stained samples suggested that our crosslinking technique yielded an ECM mimicking microstructure with interlaced bands of collagen and HA in the hybrid scaffolds. The mutually reinforcing networks of collagen and HA also resulted in increased bending moduli up to 1660 kPa which spanned the range of natural aortic valves. Cardio sphere‐derived cells (CDCs) from rat hearts showed that crosslinking density affected the available cell attachment sites on the surface of the scaffold. Increased bending moduli of CDCs seeded scaffolds up to two folds (2‐6 kPa) as compared to the non‐seeded scaffolds (1 kPa) suggested that an increase in crosslinking density of the scaffolds could not only increase the in vitro bending modulus but also prevented its disintegration in the cell culture medium.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1002/bip.23278

Authors


More by this author
Role:
Author
ORCID:
0000-0003-0537-2551
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Institution:
University of Oxford
Division:
MSD
Department:
Physiology Anatomy & Genetics
Oxford college:
Pembroke College
Role:
Author
ORCID:
0000-0003-0102-5261


Publisher:
Wiley
Journal:
Biopolymers More from this journal
Volume:
110
Issue:
8
Article number:
e23278
Publication date:
2019-04-08
Acceptance date:
2019-03-21
DOI:
EISSN:
1097-0282
ISSN:
0006-3525
Pmid:
30958569


Language:
English
Keywords:
Pubs id:
pubs:991966
UUID:
uuid:d7cd2785-a1e9-4e04-92d5-2fb81e7d0fdd
Local pid:
pubs:991966
Source identifiers:
991966
Deposit date:
2019-07-25

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