莱菔硫烷
透明质酸
活力测定
药理学
化学
止痛药
一氧化氮
泊洛沙姆
医学
细胞
生物化学
共聚物
解剖
有机化学
聚合物
作者
Juliana Zampoli Boava Papini,B. Esteves,Vagner Gomes de Souza Oliveira,Henrique Ballassani Abdalla,Cíntia Maria Saia Cereda,Daniele Ribeiro de Araújo,Giovana Radomille Tófoli
出处
期刊:Gels
[Multidisciplinary Digital Publishing Institute]
日期:2024-07-13
卷期号:10 (7): 460-460
被引量:5
摘要
Sulforaphane (SFN) has shown potential as an antioxidant and anti-inflammatory agent. To improve its druggability, we developed new analgesic formulations with sulforaphane-loaded hyaluronic acid (HA)-poloxamer (PL) hydrogel. This study evaluated the pre-clinical safety and effectiveness of these formulations. Effectiveness was tested on Wistar rats divided into groups (n = 15) receiving (IM, 10 mg/kg) SFN formulations or control groups (without SFN). This study used a hind paw incision postoperative pain model to evaluate mechanical hypersensitivity with von Frey filaments. TNF-α, IL-1β, substance P, and CGRP levels verified anti-inflammatory activity in the hind paw tissue. Histopathology of tissues surrounding the injection site was assessed after 2 and 7 days post-treatment. To corroborate drug safety, cell viability of 3T3 and RAW 264.7 cultures was assessed. Additionally, RAW 264.7 cultures primed with carrageenan evaluated nitric oxide (NO) levels. All animals exhibited post-incisional hypersensitivity, and F2 (PL 407/338 (18/2%) + HA 1% + SFN 0.1%) showed a longer analgesic effect (p < 0.05). F2 reduced TNF-α, IL-1β, and CGRP levels (p < 0.05). Histopathological evaluation showed mild to moderate inflammatory reactions after the formulations' injections. F2 produced no significant difference in cell viability (p > 0.05) but reduced NO production (p < 0.05). Thus, our results highlight the biocompatibility and effectiveness of F2.
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