Impact of Three Different Processing Techniques on the Strength and Structure of Juvenile Ovine Pulmonary Homografts.

cryopreservation decellularization glutaraldehyde-fixation homografts ischaemic harvesting

Journal

Polymers
ISSN: 2073-4360
Titre abrégé: Polymers (Basel)
Pays: Switzerland
ID NLM: 101545357

Informations de publication

Date de publication:
27 Jul 2022
Historique:
received: 19 05 2022
revised: 15 06 2022
accepted: 20 06 2022
entrez: 27 7 2022
pubmed: 28 7 2022
medline: 28 7 2022
Statut: epublish

Résumé

Homografts are routinely stored by cryopreservation; however, donor cells and remnants contribute to immunogenicity. Although decellularization strategies can address immunogenicity, additional fixation might be required to maintain strength. This study investigated the effect of cryopreservation, decellularization, and decellularization with additional glutaraldhyde fixation on the strength and structure of ovine pulmonary homografts harvested 48 h post-mortem. Cells and cellular remnants were present for the cryopreserved group, while the decellularized groups were acellular. The decellularized group had large interfibrillar spaces in the extracellular matrix with uniform collagen distribution, while the additional fixation led to the collagen network becoming dense and compacted. The collagen of the cryopreserved group was collapsed and appeared disrupted and fractured. There were no significant differences in strength and elasticity between the groups. Compared to cryopreservation, decellularization without fixation can be considered an alternative processing technique to maintain a well-organized collagen matrix and tissue strength of homografts.

Identifiants

pubmed: 35894000
pii: polym14153036
doi: 10.3390/polym14153036
pmc: PMC9332750
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Johannes J van den Heever (JJ)

Department of Cardiothoracic Surgery, Faculty of Health Sciences, University of the Free State (UFS), P.O. Box 339 (Internal Box G32), Bloemfontein 9300, South Africa.

Christiaan J Jordaan (CJ)

Department of Cardiothoracic Surgery, Faculty of Health Sciences, University of the Free State (UFS), P.O. Box 339 (Internal Box G32), Bloemfontein 9300, South Africa.

Angélique Lewies (A)

Department of Cardiothoracic Surgery, Faculty of Health Sciences, University of the Free State (UFS), P.O. Box 339 (Internal Box G32), Bloemfontein 9300, South Africa.

Jacqueline Goedhals (J)

Department of Anatomical Pathology, Faculty of Health Sciences, University of the Free State (UFS), P.O. Box 339 (Internal Box G32), Bloemfontein 9300, South Africa.

Dreyer Bester (D)

Department of Cardiothoracic Surgery, Faculty of Health Sciences, University of the Free State (UFS), P.O. Box 339 (Internal Box G32), Bloemfontein 9300, South Africa.

Lezelle Botes (L)

Department of Health Sciences, Central University of Technology, Free State (CUT), Private Bag X20539, P.O. Box 339 (Internal Box G32), Bloemfontein 9300, South Africa.

Pascal M Dohmen (PM)

Department of Cardiothoracic Surgery, Faculty of Health Sciences, University of the Free State (UFS), P.O. Box 339 (Internal Box G32), Bloemfontein 9300, South Africa.
Klinikdirektor (k), Klinik und Poliklinik für Herzchirurgie, Universitätsmedizin Rostock, Schillingallee 35, 18057 Rostock, Germany.

Francis E Smit (FE)

Department of Cardiothoracic Surgery, Faculty of Health Sciences, University of the Free State (UFS), P.O. Box 339 (Internal Box G32), Bloemfontein 9300, South Africa.

Classifications MeSH