Physicochemical Characterization and In Vitro Anti-Inflammatory Assessment of Novel Sodium Alginate Sponges Loading Andiroba Oil ( Carapa guianensis Aubl.) for Skin Dressings

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Authors: Marinaldo V. Souza, Jad Lorena F Simplicio, Fernanda Farias Costa, Aramys S. Reis, Eliana B. Souto, Adenilson O dos Santos, Francisco F. de Sousa
Cited by: 4
References: 64

Abstract

High Resolution Image Download MS PowerPoint Slide This study describes the structural characterization of a novel formulation based on sodium alginate sponges loading the Amazonian andiroba oil ( Carapa guianensis Aubl.) as a strategy for developing topical anti-inflammatory dressings. The characterization by X-ray diffraction revealed the amorphous profile of unloaded and andiroba oil-loaded sponges, indicating structural flexibility suitable for modifying the release profile of bioactives. Scanning electron microscopy revealed a porous, interconnected structure of the unloaded alginate sponges, whereas oil-loaded sponges exhibited smoother, thicker pore walls and localized densification, indicating the oil’s influence on the polymeric matrix architecture. Fourier transform infrared spectra identified the ester, hydroxyl, and carboxylate groups, confirming the chemical signature of the andiroba oil and its interactions with the alginate matrix. Hirshfeld surface analysis of oleic acid, one of the main bioactive components of andiroba oil, revealed a predominance of hydrophobic contacts and hydrogen-bonding interactions, supporting its affinity for biological targets. Surface analysis also indicated high porosity (∼70% void volume), suggesting a potential application for topical delivery. Docking simulations showed favorable binding affinity of oleic acid to the active site of NF-kB (−5.75 kcal/mol) and iNOS (−5.15 kcal/mol), corroborating its anti-inflammatory potential. In silico pharmacokinetic profiling exhibited low skin permeation (Log K p = −2.6 cm/s) of oleic acid, no blood–brain barrier penetration, and no interaction with P-glycoprotein. Andiroba oil-loaded sponges significantly reduced nitric oxide production in lipopolysaccharide-activated RAW 264.7 macrophages without affecting cell viability. The unloaded alginate sponges also showed mild nitric oxide inhibition at high concentration, confirming their inherent biocompatibility. Altogether, these findings support the use of the developed sponges as a promising bioactive dressing for the healing of inflamed wounds and other chronic skin conditions, combining Amazonian phytotherapy with innovative polymeric delivery systems.

Fields of Study & Subjects

Advancements in Transdermal Drug Delivery Wound Healing and Treatments Microencapsulation and Drying Processes

Publication details

Journal / source
ACS Omega
Publisher
American Chemical Society (ACS)
Volume
11
Issue
6
Pages
9937–9949
Publication date
4 February 2026
Language
EN