EFFECT OF CRYOPRESERVATION ON THE INTEGRITY OF COAXIAL ALGINATE CAPSULES

Encapsulation of clinically relevant cells, such as multipotent stromal cells (MSCs), in three-dimensional (3D) core-shell alginate structures is a promising method for the treatment of various diseases as well as drug testing and development. By utilizing the alginate capsules, drugs and active substances can be delivered specifically to the desired place within the patients’ body. The aim of this work was to investigate the effect of cryopreservation on the integrity of cell-free coaxial alginate capsules after thawing using slow freezing to ensure their long-term storage. Alginate capsules were produced by electro-spraying and cryopreserved using different cryoprotective agents (CPAs), incubation time and thawing temperature. The results suggest that the capsules loaded with 10% (v/v) dimethyl sulfoxide (DMSO) and 0.3 M sucrose and using high thawing rates demonstrated a beneficial effect on the integrity of capsules, as compared to 10% (v/v) DMSO alone and applying low thawing rates. This study is a further development towards the application of cryopreservation for long-term storage and the emerging cell-based medicine.

[1]  B. Glasmacher,et al.  Coaxial Alginate Hydrogels: From Self-Assembled 3D Cellular Constructs to Long-Term Storage , 2021, International journal of molecular sciences.

[2]  D. Miklavčič,et al.  Me2SO- and serum-free cryopreservation of human umbilical cord mesenchymal stem cells using electroporation-assisted delivery of sugars. , 2019, Cryobiology.

[3]  B. Glasmacher,et al.  Advances in the application of electrohydrodynamic fabrication for tissue engineering , 2019, Journal of Physics: Conference Series.

[4]  C. Hunt Technical Considerations in the Freezing, Low-Temperature Storage and Thawing of Stem Cells for Cellular Therapies , 2019, Transfusion Medicine and Hemotherapy.

[5]  K. Parivar,et al.  Stemness of spermatogonial stem cells encapsulated in alginate hydrogel during cryopreservation , 2017, Andrologia.

[6]  P. Mohanty,et al.  Impact of alginate concentration on the viability, cryostorage, and angiogenic activity of encapsulated fibroblasts. , 2016, Materials science & engineering. C, Materials for biological applications.

[7]  A. Hoffmann,et al.  Molecular and cellular characteristics of human and non-human primate multipotent stromal cells from the amnion and bone marrow during long term culture , 2015, Stem Cell Research & Therapy.

[8]  B. Glasmacher,et al.  Multipotent stromal cells derived from common marmoset Callithrix jacchus within alginate 3D environment: Effect of cryopreservation procedures. , 2015, Cryobiology.

[9]  B. Glasmacher,et al.  Encapsulating Non-Human Primate Multipotent Stromal Cells in Alginate via High Voltage for Cell-Based Therapies and Cryopreservation , 2014, PloS one.

[10]  B. Glasmacher,et al.  Process engineering of high voltage alginate encapsulation of mesenchymal stem cells. , 2014, Materials science & engineering. C, Materials for biological applications.

[11]  A. Melman,et al.  Photochemical Patterning of Ionically Cross-Linked Hydrogels , 2013 .

[12]  S Sambu,et al.  Predicting the survival rate of mouse embryonic stem cells cryopreserved in alginate beads , 2011, Proceedings of the Institution of Mechanical Engineers. Part H, Journal of engineering in medicine.

[13]  M. T. González-Arnao,et al.  Thermal events in calcium alginate beads during encapsulation dehydration and encapsulation-vitrification protocols. , 2011 .

[14]  Wayne R. Gombotz,et al.  Protein release from alginate matrices. , 1998, Advanced drug delivery reviews.

[15]  J. Hansz,et al.  Successful cryopreservation of suspension cells by encapsulation-dehydration , 1995, Plant Cell, Tissue and Organ Culture.