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Eur J Pharmacol ; 919: 174809, 2022 Mar 15.
Artículo en Inglés | MEDLINE | ID: mdl-35151648

RESUMEN

Cutaneous wounds deteriorate the health of patients and liable for high economic loss. Previous studies showed promising wound healing potentials of bilirubin, however, this macromolecule constrained with poor water solubility and skin penetration. In this study, Pluronic F-127, a non-ionic copolymer surfactant, was used for the encapsulation of the wound healing agent the bilirubin. With this strategy, spherical shaped bilirubin nanoparticles of ∼100-150 nm with zeta potential ranging from -13.43 ± 0.56 to -17.53 ± 0.43 mV were obtained. Topical applications of bilirubin nanoparticle (0.3%) on cutaneous wounds of rats showed promising wound healing in comparison with other topical treatments. This topical nano-formulation also modulates the cytokine and growth factor responses in the treated group. On day 7 of healing, bilirubin nanoparticles treatment significantly reduced TNF-α and increased IL-10 levels with increased VEGF and TGF-ß1 expressions. Simultaneously, prominent pro-healing activities could be observed histopathologically. These include increased blood vessels, reduced inflammatory cells, more myofibroblasts, increased deposition of collagen fibres, and early re-epithelialization. The changes were prominent in bilirubin nanoparticles (0.3%) treated group indicating better granulation tissue, quality of healing and wound maturity. In conclusion, the proposed new encapsulated bilirubin nanoparticles strategy significantly improved wound healing by modulation of cytokines and growth factors response in comparison with native bulk bilirubin. These observations support its potential as a novel biomaterial for wound healing in the future.


Asunto(s)
Bilirrubina/farmacología , Nanopartículas , Poloxámero , Cicatrización de Heridas/efectos de los fármacos , Administración Cutánea , Animales , Bilirrubina/administración & dosificación , Bilirrubina/uso terapéutico , Materiales Biocompatibles , Citocinas/metabolismo , Modelos Animales de Enfermedad , Humanos , Masculino , Ratas , Ratas Wistar , Factor A de Crecimiento Endotelial Vascular/metabolismo
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