Literature DB >> 25809201

Sucrose Diffusion in Decellularized Heart Valves for Freeze-Drying.

Shangping Wang1, Harriëtte Oldenhof2, Tobias Goecke3, Robert Ramm3, Michael Harder4, Axel Haverich3, Andres Hilfiker3, Willem Frederik Wolkers1.   

Abstract

Decellularized heart valves can be used as starter matrix implants for heart valve replacement therapies in terms of guided tissue regeneration. Decellularized matrices ideally need to be long-term storable to assure off-the-shelf availability. Freeze-drying is an attractive preservation method, allowing storage at room temperature in a dried state. However, the two inherent processing steps, freezing and drying, can cause severe damage to extracellular matrix (ECM) proteins and the overall tissue histoarchitecture and thus impair biomechanical characteristics of resulting matrices. Freeze-drying therefore requires a lyoprotective agent that stabilizes endogenous structural proteins during both substeps and that forms a protective glassy state at room temperature. To estimate incubation times needed to infiltrate decellularized heart valves with the lyoprotectant sucrose, temperature-dependent diffusion studies were done using Fourier transform infrared spectroscopy. Glycerol, a cryoprotective agent, was studied for comparison. Diffusion of both protectants was found to exhibit Arrhenius behavior. The activation energies of sucrose and glycerol diffusion were found to be 15.9 and 37.7 kJ·mol(-1), respectively. It was estimated that 4 h of incubation at 37°C is sufficient to infiltrate heart valves with sucrose before freeze-drying. Application of a 5% sucrose solution was shown to stabilize acellular valve scaffolds during freeze-drying. Such freeze-dried tissues, however, displayed pores, which were attributed to ice crystal damage, whereas vacuum-dried scaffolds in comparison revealed no pores after drying and rehydration. Exposure to a hygroscopic sucrose solution (80%) before freeze-drying was shown to be an effective method to diminish pore formation in freeze-dried ECMs: matrix structures closely resembled those of control samples that were not freeze-dried. Heart valve matrices were shown to be in a glassy state after drying, suggesting that they can be stored at room temperature.

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Year:  2015        PMID: 25809201     DOI: 10.1089/ten.TEC.2014.0681

Source DB:  PubMed          Journal:  Tissue Eng Part C Methods        ISSN: 1937-3384            Impact factor:   3.056


  5 in total

1.  Principles Underlying Cryopreservation and Freeze-Drying of Cells and Tissues.

Authors:  Willem F Wolkers; Harriëtte Oldenhof
Journal:  Methods Mol Biol       Date:  2021

2.  Synergistic Development of Biochips and Cell Preservation Methodologies: A Tale of Converging Technologies.

Authors:  Shangping Wang; Gloria D Elliott
Journal:  Curr Stem Cell Rep       Date:  2017-01-21

3.  Use of sucrose to diminish pore formation in freeze-dried heart valves.

Authors:  Andrés Vásquez-Rivera; Harriëtte Oldenhof; Daniele Dipresa; Tobias Goecke; Artemis Kouvaka; Fabian Will; Axel Haverich; Sotirios Korossis; Andres Hilfiker; Willem F Wolkers
Journal:  Sci Rep       Date:  2018-08-28       Impact factor: 4.379

4.  Fourier transform infrared spectroscopy coupled with machine learning classification for identification of oxidative damage in freeze-dried heart valves.

Authors:  Dejia Liu; Sükrü Caliskan; Bita Rashidfarokhi; Harriëtte Oldenhof; Klaus Jung; Harald Sieme; Andres Hilfiker; Willem F Wolkers
Journal:  Sci Rep       Date:  2021-06-10       Impact factor: 4.379

Review 5.  Accounting for Material Changes in Decellularized Tissue with Underutilized Methodologies.

Authors:  Ryan A Behmer Hansen; Xinming Wang; Gitanjali Kaw; Valinteshley Pierre; Samuel E Senyo
Journal:  Biomed Res Int       Date:  2021-05-31       Impact factor: 3.246

  5 in total

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