Nanomedicine Lab, Department of Pharmaceutics, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran 1417614411, Iran.
Department of Pharmaceutics, School of Pharmacy, Hamadan University of Medical Sciences, Pajoohesh Sq., Shahid Fahmideh St., Hamadan, Iran.
Biomed Res Int. 2022 Sep 27;2022:7776092. doi: 10.1155/2022/7776092. eCollection 2022.
The aim of the present study was to investigate the therapeutic potential of budesonide- (BDS-) loaded hyaluronic acid nanoparticles (HANPs) for treatment of inflammatory bowel disease (IBD) using an acute model of colitis in rats. The therapeutic efficacy of BDS-loaded HANPs in comparison with an aqueous suspension of the drug with the same dose (30 g/kg) was investigated 48 h following induction of colitis by intrarectal administration of acetic acid 4% in rats. Microscopic and histopathologic examinations were conducted in inflamed colonic tissue. Tissue concentration of tumor necrosis factor (TNF)- was assessed by ELISA assay kit, while the activity of myeloperoxidase (MPO) was measured spectrophotometrically. Results from in vivo evaluations demonstrated that administrations of BDS-HANPs ameliorated the general endoscopic appearance, quite close to the healthy animals with no signs of inflammation and reduced the cellular infiltration, as well as the TNF- level, and the MPO activity. It was found that delivery by BDS-loaded HANPSs alleviated the induced colitis significantly better than the same dose of the free drug. These data further suggest the potential of HANPs as a targeted drug delivery system to the inflamed colon mucosa.
本研究旨在通过乙酸诱导的大鼠急性结肠炎模型,探讨布地奈德(BDS)负载透明质酸纳米粒(HANPs)治疗炎症性肠病(IBD)的潜在疗效。在诱导结肠炎后 48 小时,通过直肠内给予 4%乙酸,比较了 BDS 负载 HANPs 与相同剂量(30μg/kg)药物水混悬液的治疗效果。对炎症性结肠组织进行了显微镜和组织病理学检查。采用 ELISA 试剂盒检测肿瘤坏死因子(TNF)-的组织浓度,分光光度法测定髓过氧化物酶(MPO)的活性。体内评估结果表明,BDS-HANPs 的给药可改善整体内镜外观,与无炎症迹象且细胞浸润减少的健康动物非常接近,并降低 TNF-水平和 MPO 活性。结果发现,BDS 负载 HANPs 的给药可显著缓解诱导的结肠炎,其效果明显优于相同剂量的游离药物。这些数据进一步表明 HANPs 作为靶向递药系统向炎症性结肠黏膜给药的潜力。