Cell-based therapies for regenerative medicine have been characterized by the low retention and integration of
injected cells into host structures. Cell immobilization in hydrogels for target cell delivery has been developed to
circumvent this issue. In this work mesenchymal stem cells isolated from Wistar rats bone marrow (rMSCs) were
immobilized in alginate beads fabricated using an innovative approach involving the gellification of the liquid
precursor droplets onto biomimetic superhydrophobic surfaces without the need of any precipitation bath. The
process occurred in mild conditions preventing the loss of cell viability. Furthermore, fibronectin (FN) was also
immobilized inside alginate beads with high efficiency in order to mimic the composition of the extracellular
matrix. This process occurred in a very fast way (around 5 min), at room temperature, without aggressive
mechanical strengths or particle aggregation. The methodology employed allowed the production of alginate
beads exhibiting a homogenous rMSCs and FN distribution. Encapsulated rMSCs remained viable and were
released from the alginate for more than 20 days. In vivo assays were also performed, by implanting these
particles in a calvarial bone defect to evaluate their potential for bone tissue regeneration. Microcomputed
tomography and histological analysis results showed that this hybrid system accelerated bone regeneration
process. The methodology employed had a dual role by preventing cell and FN loss and avoiding any contamination
of the beads or exchange of molecules with the surrounding environment. In principle, the method
used for cell encapsulation could be extended to other systems aimed to be used in tissue regeneration strategies.