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Development of clobetasol-loaded biodegradable nanoparticles as an endodontic intracanal medicament.
Elmsmari, Firas; González Sánchez, José Antonio; Delgado, Luis M; Espina, Marta; Duran-Sindreu, Fernando; García, Maria Luisa; Sánchez-López, Elena.
Afiliación
  • Elmsmari F; Department of Clinical Sciences, College of Dentistry, Ajman University, Ajman, United Arab Emirates.
  • González Sánchez JA; Center of Medical and Bio-Allied Health Sciences Research, Ajman University, Ajman, United Arab Emirates.
  • Delgado LM; Department of Endodontics, Faculty of Dentistry, Universitat Internacional de Catalunya, Barcelona, Spain.
  • Espina M; Department of Endodontics, Faculty of Dentistry, Universitat Internacional de Catalunya, Barcelona, Spain.
  • Duran-Sindreu F; Bioengineering Institute of Technology, Universitat Internacional de Catalunya, Barcelona, Spain.
  • García ML; Department of Pharmacy, Pharmaceutical Technology and Physical Chemistry, Faculty of Pharmacy and Food Sciences, University of Barcelona, Barcelona, Spain.
  • Sánchez-López E; Institute of Nanoscience and Nanotechnology (IN2UB), University of Barcelona, Barcelona, Spain.
Int Endod J ; 57(8): 1147-1164, 2024 Aug.
Article en En | MEDLINE | ID: mdl-38687284
ABSTRACT

AIM:

The 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).

METHODOLOGY:

CP-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-1ß and TNF-α.

RESULTS:

Optimized 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-1ß increased in CP-NPs compared to the LPS control, displaying results similar and even less than the TCP after 48 h. Moreover, IL-1ß release in LPS-stimulated cells, decreased when macrophages were treated with CP-NPs.

CONCLUSIONS:

In 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.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Clobetasol / Nanopartículas Límite: Humans Idioma: En Revista: Int Endod J Año: 2024 Tipo del documento: Article País de afiliación: Emiratos Árabes Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Clobetasol / Nanopartículas Límite: Humans Idioma: En Revista: Int Endod J Año: 2024 Tipo del documento: Article País de afiliación: Emiratos Árabes Unidos