Nanoenabled Immunomodulatory Scaffolds for Cartilage Tissue Engineering

Author:

Pereira Vasconcelos Daniela1ORCID,Leite Pereira Catarina1ORCID,Couto Marina1ORCID,Neto Estrela1ORCID,Ribeiro Beatriz1ORCID,Albuquerque Filipe12ORCID,Freitas Alexandra12ORCID,Alves Cecília J.1ORCID,Klinkenberg Geir3,McDonagh Birgitte Hjelmeland3ORCID,Schmid Ruth Baumberger3ORCID,Seitz Andreas M.4ORCID,de Roy Luisa4,Ignatius Anita4ORCID,Haaparanta Anne‐Marie5ORCID,Muhonen Virpi5,Sarmento Bruno16ORCID,Lamghari Meriem1ORCID

Affiliation:

1. i3S ‐ Instituto de Inovação e Investigação em Saúde INEB ‐ Instituto Nacional de Engenharia Biomédica Universidade do Porto Rua Alfredo Allen, 208 Porto 4200‐135 Portugal

2. School of Medicine and Biomedical Sciences (ICBAS‐UP) Faculdade de Engenharia (FEUP) Universidade do Porto Porto 4050‐313 Portugal

3. SINTEF Industry Department of Biotechnology and Nanomedicine Trondheim 7034 Norway

4. Institute of Orthopedic Research and Biomechanics Center for Trauma Research Ulm University Medical Center Ulm 89081 Ulm Germany

5. Askel Healthcare Ltd Siltasaarenkatu 8‐10 Helsinki 00530 Finland

6. Instituto de Investigação e Formação Avançada em Ciências e Tecnologias da Saúde Gandra 4585‐116 Portugal

Abstract

AbstractArticular cartilage regeneration is a challenge in tissue engineering. Although diverse materials have been developed for this purpose, cartilage regeneration remains suboptimal. The integration of nanomaterials into 3D network materials holds great potential in the improvement of key mechanical properties, particularly important for osteochondral replacement scaffolds and even to function as carriers for disease‐modifying drugs or other regulatory signals. In this study, a simple yet effective cell‐free nanoenabled Col‐PLA scaffold specially designed to enhance cartilage regeneration and modulate inflammatory response is proposed, by incorporating poly(lactic‐co‐glycolic acid) (PLGA) ibuprofen nanoparticles (NPs) into a collagen/polylactide (Col‐PLA) matrix. The developed nanoenabled scaffold successfully decreases IL‐1β release and leads to primary human chondrocytes survival, ultimately restoring extracellular matrix (ECM) production under inflammatory conditions. The nanoenabled Col‐PLA scaffolds secretome effectively decreases macrophage invasion in vitro, as well as neutrophil infiltration and inflammatory mediators’, namely the complement component C5/C5a, C‐reactive protein, IL‐1β, MMP9, CCL20, and CXCL1/KC production in vivo in a rodent air‐pouch model. Overall, the established nanoenabled scaffold has the potential to support chondrogenesis as well as modulate inflammatory response, overcoming the limitations of traditional tissue engineering strategies.

Publisher

Wiley

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