Abstract

Alginate as a versatile naturally occurring biomaterial has found widespread use in the biomedical field due to its unique features such as biocompatibility and biodegradability. The ability of its semipermeable hydrogels to provide a favourable microenvironment for clinically relevant cells made alginate encapsulation a leading technology for immunoisolation, 3D culture, cryopreservation as well as cell and drug delivery. The aim of this work is the evaluation of structural properties and swelling behaviour of the core-shell capsules for the encapsulation of multipotent stromal cells (MSCs), their 3D culture and cryopreservation using slow freezing. The cells were encapsulated in core-shell capsules using coaxial electrospraying, cultured for 35 days and cryopreserved. Cell viability, metabolic activity and cell–cell interactions were analysed. Cryopreservation of MSCs-laden core-shell capsules was performed according to parameters pre-selected on cell-free capsules. The results suggest that core-shell capsules produced from the low viscosity high-G alginate are superior to high-M ones in terms of stability during in vitro culture, as well as to solid beads in terms of promoting formation of viable self-assembled cellular structures and maintenance of MSCs functionality on a long-term basis. The application of 0.3 M sucrose demonstrated a beneficial effect on the integrity of capsules and viability of formed 3D cell assemblies, as compared to 10% dimethyl sulfoxide (DMSO) alone. The proposed workflow from the preparation of core-shell capsules with self-assembled cellular structures to the cryopreservation appears to be a promising strategy for their off-the-shelf availability.

Highlights

  • Alginate has been considered as one of the most abundant marine derived naturally occurring biomaterials for the application in cell-based therapies [1], pharmacology [2], tissue regeneration [3], wound healing [4] and others

  • The aim of this work is the evaluation of structural properties and swelling behaviour of the core-shell capsules for the encapsulation of multipotent stromal cells (MSCs), their 3D culture and cryopreservation using slow freezing

  • The results suggest that core-shell capsules produced from the low viscosity high-G alginate are superior to high-M ones in terms of stability during in vitro culture, as well as to solid beads in terms of promoting formation of viable self-assembled cellular structures and maintenance of MSCs functionality on a long-term basis

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Summary

Introduction

Alginate has been considered as one of the most abundant marine derived naturally occurring biomaterials for the application in cell-based therapies [1], pharmacology [2], tissue regeneration [3], wound healing [4] and others. The source of alginate (marine vs bacterial, place of seaweed collection), the extraction, purification and modification methods determine the content and ratio of (1,4)-linked β-D-mannuronate (M) and its C-5 epimer α-L-guluronate (G) (M/G ratio) and their alternating sequences (MG) Due to their distinguished properties, such as ease of gelling with divalent metal cations (ionic cross-linking) forming an “egg-box” structure [5] and 3D environment close to the extracellular matrix of native tissues, high biocompatibility, low immunogenicity in vivo and controlled biodegradability [6,7,8], alginate hydrogels have been widely used in medicine and medicine-related research [3]. Numerous reviews, highlighting the effect of alginate type and source, cross-linking methods and chemical modifications regarding the performance of alginate beads, have been published so far [12,28,29]

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