posted on 2025-09-11, 14:25authored byAnna Raphaella
Autran Colaço, Priscila de Souza Furtado, Daniel Figueiredo Vanzan, Nicole Serqueira da Silva, Flávia Almada do Carmo, Lucio Mendes Cabral, Alice Simon, Jônatas
Caldeira Esteves, Plínio Cunha Sathler
Synthetic, biocompatible, and biodegradable polymers
such as poly-l-lactic acid (PLLA) and polycaprolactone (PCL)
are used in
the form of microparticles (25–200 μm) dispersed in injectable
hydrogels for collagen biostimulation through mechanical stimuli and
subclinical inflammatory responses. However, their clinical application
is limited by adverse effects, including nodule formation and vascular
occlusion. As an alternative, nanoparticles based on poly(lactic-<i>co</i>-glycolic acid) (PLGA), a synthetic, biocompatible, and
biodegradable copolymer, loaded with ascorbic acid (AA), a potent
antioxidant with pro-collagenic activity, may provide enhanced dermal
retention, reduced macrophage recognition, and minimized adverse effects.
This study developed AA-loaded PLGA nanoparticles incorporated into
a hydrogel and evaluated their potential for <i>in vivo</i> dermal biostimulation. Nanoparticles were prepared by nanoprecipitation
and characterized by dynamic light scattering (DLS) to determine average
diameter and polydispersity index (PDI), zeta potential to assess
surface charge, and transmission electron microscopy (TEM) to examine
morphology. AA encapsulation efficiency was assessed spectrophotometrically.
Cytotoxicity was evaluated by the MTT assay using epithelial, macrophage,
and fibroblast cells. The hydrogel was evaluated for stability and
spreadability. The biostimulatory potential of the formulations was
assessed <i>in vivo</i> by measuring hydroxyproline levels,
collagen production, and dermal remodeling. The nanoparticles exhibited
an average diameter below 300 nm, a moderately monodisperse distribution
(PDI <0.2), spherical morphology, and high AA encapsulation efficiency
(>94%). Biocompatibility was confirmed in epithelial and fibroblast
cells (viability >70%), with cytotoxicity observed only in macrophages
at higher concentrations (<70%). <i>In vivo</i>, AA-loaded
PLGA nanoparticles (AANps) induced a 28% increase in collagen production
at 30 days, although this effect declined by 60 days. Collagen fibers
remained denser and more organized, suggesting ongoing tissue remodeling.
Prospectively, after one month, the AANps hydrogel developed in this
study could promote a more pronounced collagen increase compared to
commercial products such as calcium hydroxylapatite (CaHA) microparticles
and PLLA microparticles. These findings suggest that the AA-loaded
PLGA nanoparticle hydrogel is a promising strategy for dermal remodeling.