In Vitro Calcification of Bioprosthetic Heart Valves: Investigation of Test Fluids.


Journal

Annals of biomedical engineering
ISSN: 1573-9686
Titre abrégé: Ann Biomed Eng
Pays: United States
ID NLM: 0361512

Informations de publication

Date de publication:
Jan 2020
Historique:
received: 06 05 2019
accepted: 16 08 2019
pubmed: 8 9 2019
medline: 17 6 2020
entrez: 8 9 2019
Statut: ppublish

Résumé

Calcification is a major reason for the failure of bioprosthetic heart valves. Therefore, several attempts towards an accelerated in vitro model were undertaken in order to provide a cost- and time-saving method for the analysis of calcification processes. Due to the problem of superficial or spontaneous precipitation, which occurred in the fluids applied, we focused our study on the development of a near-physiological calcification fluid. The desired fluid should not precipitate spontaneously and should neither promote nor inhibit calcification. Eleven different fluid compositions were tested without contact to potentially calcifying materials. Crucial factors regarding the fluid properties were the ionic product, the ionic strength, and the degree of supersaturation concerning dicalciumphosphate-dihydrate, octacalciumphosphate, and hydroxyapatite. The fluids were kept in polyethylene bottles and exposed to a slight vibration within a durability tester at 37 °C. The precipitation propensity was monitored optically and colorimetrically. A structural analysis of the deposits was carried out by x-ray powder diffraction and IR-spectroscopy, which showed the development of the crystal phases that are relevant in vivo. Only two of the fluids did not precipitate. Resulting from the computations of the effective fluid contents, the saturation degree concerning dicalciumphosphate-dihydrate seems to be the key factor for spontaneous precipitation.

Identifiants

pubmed: 31493168
doi: 10.1007/s10439-019-02347-5
pii: 10.1007/s10439-019-02347-5
doi:

Substances chimiques

Phosphates 0
Potassium Chloride 660YQ98I10
Calcium Chloride M4I0D6VV5M

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

282-297

Subventions

Organisme : Interreg Program V-A Maas-Rhine of the European Union
ID : 2016 98602
Organisme : Deutsche Forschungsgemeinschaft (DFG, German Research Foundation)
ID : 403041552

Auteurs

N Kiesendahl (N)

Department of Cardiovascular Engineering, Institute of Applied Medical Engineering, Helmholtz Institute Aachen, RWTH Aachen University, Aachen, Germany.

C Schmitz (C)

Department of Cardiovascular Engineering, Institute of Applied Medical Engineering, Helmholtz Institute Aachen, RWTH Aachen University, Aachen, Germany.

A Von Berg (A)

Institute of Crystallography, RWTH Aachen University, Aachen, Germany.

M Menne (M)

Department of Cardiovascular Engineering, Institute of Applied Medical Engineering, Helmholtz Institute Aachen, RWTH Aachen University, Aachen, Germany.

T Schmitz-Rode (T)

Institute of Applied Medical Engineering, Helmholtz Institute Aachen, RWTH Aachen University, Pauwelsstraße 20, 52074, Aachen, Germany.

J Arens (J)

Department of Cardiovascular Engineering, Institute of Applied Medical Engineering, Helmholtz Institute Aachen, RWTH Aachen University, Aachen, Germany.

U Steinseifer (U)

Department of Cardiovascular Engineering, Institute of Applied Medical Engineering, Helmholtz Institute Aachen, RWTH Aachen University, Aachen, Germany. steinseifer@ame.rwth-aachen.de.
Institute of Applied Medical Engineering, Helmholtz Institute Aachen, RWTH Aachen University, Pauwelsstraße 20, 52074, Aachen, Germany. steinseifer@ame.rwth-aachen.de.
Monash Institute of Medical Engineering and Department of Mechanical and Aerospace Engineering, Monash University, Melbourne, Australia. steinseifer@ame.rwth-aachen.de.

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