Pabari Ritesh M, Tambuwala Murtaza M, Lajczak-McGinley Natalia, Aljabali Alaa, Kirby Brian P, Keely Stephen, Ramtoola Zebunissa
RCSI, University of Medicine and Health Sciences, Dublin, Ireland.
School of Pharmacy and Pharmaceutical Sciences, Ulster University, Coleraine, County, Londonderry BT52 1SA, Northern Ireland, United Kingdom.
Int J Pharm. 2021 Jul 15;604:120717. doi: 10.1016/j.ijpharm.2021.120717. Epub 2021 May 18.
Our recent study showed that novel infliximab (INF) loaded polyesterurethane (INF-PU) and INF-PU-PEG particulate formulations reduced inflammation in an in-vitro epithelial inflammation model. In this study we investigated therapeutic potential of novel INF-PU and INF-PU-PEG particulate formulations to reduce inflammation in a dextran sodium sulfate (DSS) induced murine model of colitis. Severity of colitis was assessed by measurement of disease activity index (DAI) score, inflammatory markers (neutrophil infiltration, TNFα) and histological score. Treatment groups orally administered with INF-PU and INF-PU-PEG particulate formulations showed improvement in the clinical signs of colitis, similar to that observed with intraperitoneally administered INF, in both, moderate and severe DSS induced colitis model. This was related to a significant reduction in inflammatory cytokines, resulting in a significant reduction in histological score (ANOVA; p < 0.05), indicative of mucosal healing, a key goal of IBD therapy. This could be attributed to its targeted delivery to the inflamed colon and higher permeation of these particulate formulations across the inflamed colonic mucosa, as observed by the confocal images, resulting in local inhibition of TNFα at its site of production. These promising preliminary results warrant further investigation of orally administered INF and its novel particulate formulations in a wider preclinical study.
我们最近的研究表明,新型负载英夫利昔单抗(INF)的聚酯聚氨酯(INF-PU)和INF-PU-PEG颗粒制剂在体外上皮炎症模型中可减轻炎症。在本研究中,我们调查了新型INF-PU和INF-PU-PEG颗粒制剂在葡聚糖硫酸钠(DSS)诱导的小鼠结肠炎模型中减轻炎症的治疗潜力。通过测量疾病活动指数(DAI)评分、炎症标志物(中性粒细胞浸润、TNFα)和组织学评分来评估结肠炎的严重程度。在中度和重度DSS诱导的结肠炎模型中,口服INF-PU和INF-PU-PEG颗粒制剂的治疗组在结肠炎临床症状方面均有改善,类似于腹腔注射INF所观察到的情况。这与炎症细胞因子的显著减少有关,导致组织学评分显著降低(方差分析;p<0.05),表明黏膜愈合,这是炎症性肠病治疗的一个关键目标。这可能归因于其靶向递送至炎症结肠以及这些颗粒制剂通过炎症结肠黏膜的更高渗透性,如共聚焦图像所示,从而在TNFα产生部位进行局部抑制。这些有前景的初步结果值得在更广泛的临床前研究中进一步研究口服INF及其新型颗粒制剂。