Development of clobetasol‐loaded biodegradable nanoparticles as an endodontic intracanal medicament

Author:

Elmsmari Firas123,González Sánchez José Antonio3ORCID,Delgado Luis M.4ORCID,Espina Marta56,Duran‐Sindreu Fernando3,García Maria Luisa567,Sánchez‐López Elena5678

Affiliation:

1. Department of Clinical Sciences, College of Dentistry Ajman University Ajman United Arab Emirates

2. Center of Medical and Bio‐Allied Health Sciences Research Ajman University Ajman United Arab Emirates

3. Department of Endodontics, Faculty of Dentistry Universitat Internacional de Catalunya Barcelona Spain

4. Bioengineering Institute of Technology Universitat Internacional de Catalunya Barcelona Spain

5. Department of Pharmacy, Pharmaceutical Technology and Physical Chemistry, Faculty of Pharmacy and Food Sciences University of Barcelona Barcelona Spain

6. Institute of Nanoscience and Nanotechnology (IN2UB) University of Barcelona Barcelona Spain

7. Networking Research Centre of Neurodegenerative Disease (CIBERNED), Instituto de Salud Juan Carlos III Madrid Spain

8. Unit of Synthesis and Biomedical Applications of Peptides, IQAC‐CSIC Barcelona Spain

Abstract

AbstractAimThe aim of current study is the development and optimization of biodegradable polymeric nanoparticles (NPs) to be used in the field of Endodontics as intracanal medication in cases of avulsed teeth with extended extra‐oral time, utilizing PLGA polymers loaded with the anti‐inflammatory drug clobetasol propionate (CP).MethodologyCP‐loaded nanoparticles (CP‐NPs) were prepared using the solvent displacement method. CP release profile from CP‐NPs was assessed for 48 h against free CP. Using extracted human teeth, the degree of infiltration inside the dentinal tubules was studied for both CP‐NPs and CP. The anti‐inflammatory capacity of CP‐NPs was evaluated in vitro measuring their response and reaction against inflammatory cells, in particular against macrophages. The enzyme‐linked immunosorbent assay (ELISA) was used to examine the cytokine release of IL‐1β and TNF‐α.ResultsOptimized CP‐NPs displayed an average size below 200 nm and a monomodal population. Additionally, spherical morphology and non‐aggregation of CP‐NPs were confirmed by transmission electron microscopy. Interaction studies showed that CP was encapsulated inside the NPs and no covalent bonds were formed. Moreover, CP‐NPs exhibited a prolonged and steady release with only 21% of the encapsulated CP released after 48 h. Using confocal laser scanning microscopy, it was observed that CP‐NPs were able to display enhanced penetration into the dentinal tubules. Neither the release of TNF‐α nor IL‐1β increased in CP‐NPs compared to the LPS control, displaying results similar and even less than the TCP after 48 h. Moreover, IL‐1β release in LPS‐stimulated cells, decreased when macrophages were treated with CP‐NPs.ConclusionsIn the present work, CP‐NPs were prepared, optimized and characterized displaying significant increase in the degree of infiltration inside the dentinal tubules against CP and were able to significantly reduce TNF‐α release. Therefore, CP‐NPs constitute a promising therapy for the treatment of avulsed teeth with extended extra‐oral time.

Publisher

Wiley

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