Department of Medical Nanotechnology, Faculty of Advanced Sciences and Technology, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran.
Department of Pharmacology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran.
BMC Pharmacol Toxicol. 2021 Oct 3;22(1):54. doi: 10.1186/s40360-021-00525-7.
Berberine (BBR) is a plant alkaloid that possesses anti-inflammatory and anti-oxidant effects with low oral bioavailability. In this study, micelle formulation of BBR was investigated to improve therapeutic efficacy and examined its effect on the secretion of inflammatory cytokines in cerebral ischemia in the animal model.
Nano formulation was prepared by thin-film hydration method, and characterized by particle size, zeta potential, morphology, encapsulation efficacy, and drug release in Simulated Gastric Fluid (SGF) and Simulated Intestine Fluid (SIF). Then, Wistar rats were pretreated with the drug (100 mg/kg) and nano-drug (25, 50, 75, 100 mg/kg) for 14 days. Then, on the fourteenth day, stroke induction was accomplished by Bilateral Common Carotid Artery Occlusion (BCCAO); after that, Tumor Necrosis Factor - Alpha (TNF-α), Interleukin - 1 Beta (IL-1ß), and Malondialdehyde (MDA) levels were measured in the supernatant of the whole brain, then the anti-inflammatory effect of BBR formulations was examined.
Micelles were successfully formed with appropriate characteristics and smaller sizes than 20 nm. The Poly Dispersity Index (PDI), zeta potential, encapsulation efficacy of micelles was 0.227, - 22 mV, 81%, respectively. Also, the stability of nano micelles was higher in SGF as compared to SIF. Our outcomes of TNF-a, IL-1B, and MDA evaluation show a significant ameliorating effect of the Berberine (BBR) and BBR-loaded micelles in pretreated groups.
Our experimental data show that pretreated groups in different doses (nano BBR 100, 75, 50 mg/kg, and BBR 100 mg/kg) successfully showed decreased levels of the inflammatory factors in cerebral ischemia compared with the stroke group and pretreated group with nano BBR in the dose of 25 mg/kg. Nano BBR formulation with a lower dose can be a better candidate than conventional BBR formulation to reduce oxidative and inflammatory factors in cerebral ischemia. Therefore, BBR-loaded micelle formulation could be a promising protective agent on cerebral ischemia.
小檗碱(BBR)是一种植物生物碱,具有抗炎和抗氧化作用,但口服生物利用度低。本研究旨在通过制备胶束来提高 BBR 的治疗效果,并在动物模型中观察其对脑缺血炎症细胞因子分泌的影响。
采用薄膜水化法制备纳米制剂,考察其粒径、Zeta 电位、形态、包封率、在人工胃液(SGF)和人工肠液(SIF)中的释放度。然后,Wistar 大鼠用药物(100mg/kg)和纳米药物(25、50、75、100mg/kg)预处理 14 天。第 14 天,通过双侧颈总动脉闭塞(BCCAO)诱导中风;然后,测量全脑上清液中肿瘤坏死因子-α(TNF-α)、白细胞介素-1β(IL-1β)和丙二醛(MDA)的水平,以考察 BBR 制剂的抗炎作用。
成功制备了具有适当特性和小于 20nm 的胶束。胶束的多分散指数(PDI)、Zeta 电位和包封率分别为 0.227、-22mV 和 81%。此外,纳米胶束在 SGF 中的稳定性高于 SIF。我们对 TNF-α、IL-1β和 MDA 的评价结果表明,BBR 和载 BBR 纳米胶束预处理组在脑缺血中具有显著的改善作用。
本实验数据表明,与卒中组和 25mg/kg 纳米 BBR 预处理组相比,不同剂量(纳米 BBR100、75、50mg/kg 和 BBR100mg/kg)的预处理组可成功降低脑缺血中炎症因子的水平。与传统 BBR 制剂相比,低剂量的纳米 BBR 制剂可能是减少脑缺血中氧化和炎症因子的更好候选药物。因此,载 BBR 胶束制剂可能是一种有前途的脑缺血保护剂。