Pinheiro Andréia C, Ombredane Alicia S, Pinheiro Willie O, Andrade Laise R, Silva Vitória R P, Felice Gisela J, Alves Débora S, Albernaz Aryanne F, Silveira Ariane P, Lima Milena C F, Veiga-Junior Valdir F, Gomes Thamis F S, Damasceno Emanuel A M, Veiga-Souza Fabiane H, Souza Paulo E N, Báo Sônia N, Duarte Eliza C B, Carneiro Marcella L B, Azevedo Ricardo B, Funez Mani I, Joanitti Graziella A
Laboratory of Bioactive Compounds and Nanobiotechnology (LBCNano), Campus Universitário-Centro Metropolitano, University of Brasilia, Ceilândia Sul, Brasília 72220-275, DF, Brazil.
Post-Graduation Program in Nanoscience and Nanobiotechnology, Institute of Biological Sciences, Campus Universitário Darcy Ribeiro, University of Brasilia, Brasília 70910-900, DF, Brazil.
Nanomaterials (Basel). 2022 Nov 30;12(23):4260. doi: 10.3390/nano12234260.
Pequi oil (Caryocar brasiliense) contains bioactive compounds capable of modulating the inflammatory process; however, its hydrophobic characteristic limits its therapeutic use. The encapsulation of pequi oil in nanoemulsions can improve its biodistribution and promote its immunomodulatory effects. Thus, the objective of the present study was to formulate pequi oil-based nanoemulsions (PeNE) to evaluate their biocompatibility, anti-inflammatory, and antinociceptive effects in in vitro (macrophages—J774.16) and in vivo (Rattus novergicus) models. PeNE were biocompatible, showed no cytotoxic and genotoxic effects and no changes in body weight, biochemistry, or histology of treated animals at all concentrations tested (90−360 µg/mL for 24 h, in vitro; 100−400 mg/kg p.o. 15 days, in vivo). It was possible to observe antinociceptive effects in a dose-dependent manner in the animals treated with PeNE, with a reduction of 27 and 40% in the doses of 100 and 400 mg/kg of PeNE, respectively (p < 0.05); however, the treatment with PeNE did not induce edema reduction in animals with carrageenan-induced edema. Thus, the promising results of this study point to the use of free and nanostructured pequi oil as a possible future approach to a preventive/therapeutic complementary treatment alongside existing conventional therapies for analgesia.
巴西坚果油(Caryocar brasiliense)含有能够调节炎症过程的生物活性化合物;然而,其疏水性限制了其治疗用途。将巴西坚果油包裹在纳米乳液中可以改善其生物分布并增强其免疫调节作用。因此,本研究的目的是制备基于巴西坚果油的纳米乳液(PeNE),以评估其在体外(巨噬细胞—J774.16)和体内(褐家鼠)模型中的生物相容性、抗炎和镇痛作用。PeNE具有生物相容性,在所有测试浓度下(体外24小时为90−360 µg/mL;体内口服15天为100−400 mg/kg)均未显示出细胞毒性和遗传毒性作用,也未导致受试动物的体重、生化指标或组织学发生变化。在用PeNE处理的动物中,可以观察到剂量依赖性的镇痛作用,在100和400 mg/kg的PeNE剂量下,疼痛分别减轻了27%和40%(p < 0.05);然而,用PeNE治疗并未使角叉菜胶诱导水肿的动物的水肿减轻。因此,本研究的有前景的结果表明,游离和纳米结构的巴西坚果油有可能作为一种未来的方法,与现有的常规镇痛疗法一起用于预防性/治疗性辅助治疗。