Design and Characterization of Biomimetic Hybrid Construct Based on Hyaluronic Acid and Alginate Bioink for Regeneration of Articular Cartilage
Metadatos
Mostrar el registro completo del ítemAutor
Galocha-León, Cristina; Sntich Acedo, Cristina; Clares Naveros, Beatriz; Voltes Martínez, Ana; Marchal Corrales, Juan Antonio; Gálvez Martín, PatriciaEditorial
MDPI
Materia
hyaluronic acid mesenchymal stromal cell bioprinting
Fecha
2024-11-07Referencia bibliográfica
Galocha León, C. et. al. Pharmaceutics 2024, 16, 1422. [https://doi.org/10.3390/pharmaceutics16111422]
Patrocinador
Ministerio de Economía, Industria y Competitividad (FEDER funds, project RTC-2016-5451-1); Ministry of Economy and Competitiveness, Instituto de Salud Carlos III (FEDER funds, projects DTS19/00143 and DTS17/00087); Consejería de Economía, Conocimiento, Empresas y Universidad de la Junta de Andalucía (P18-FR-2470, PYC20 RE 015 UGR, A-CTS-180-UGR20 and B-CTS-230-UGR18); Fundación Mutua Madrileña (project FMM-AP17196-2019); AdvanceCat with the support of ACCIÓ (Catalonia Trade & Investment; Generalitat de Catalunya) under the Catalonian European Regional Development Fund operational program, 2014–2020Resumen
Background/Objectives: Three-dimensional bioprinting technology has enabled great
advances in the treatment of articular cartilage (AC) defects by the biofabrication of biomimetic
constructs that restore and/or regenerate damaged tissue. In this sense, the selection of suitable cells
and biomaterials to bioprint constructs that mimic the architecture, composition, and functionality of
the natural extracellular matrix (ECM) of the native tissue is crucial. In the present study, a novel
cartilage-like biomimetic hybrid construct (CBC) was developed by 3D bioprinting to facilitate and
promote AC regeneration. Methods: The CBC was biofabricated by the co-bioprinting of a bioink
based on hyaluronic acid (HA) and alginate (AL) loaded with human mesenchymal stromal cells
(hMSCs), with polylactic acid supporting the biomaterial, in order to mimic the microenvironment
and structural properties of native AC, respectively. The CBC was biologically in vitro characterized.
In addition, its physiochemical characteristics were evaluated in order to determine if the presence of
hMSCs modified its properties. Results: Results from biological analysis demonstrated that CBC
supported the high viability and proliferation of hMSCs, facilitating chondrogenesis after 5 weeks
in vitro. The evaluation of physicochemical properties in the CBCs confirmed that the CBC developed
could be suitable for use in cartilage tissue engineering. Conclusions: The results demonstrated
that the use of bioprinted CBCs based on hMSC-AL/HA-bioink for AC repair could enhance the
regeneration and/or formation of hyaline cartilaginous tissue.