Wu Ming, Ding Hui, Tang Xiao, Chen Jiayi, Zhang Meng, Yang Ziqiong, Du Qian, Wang Jun
Institute of Pediatrics, Xuzhou Medical University, Xuzhou, China.
Department of Pediatrics, Xuzhou Medical University Affiliated Hospital, Xuzhou, China.
Front Pharmacol. 2023 Feb 8;14:1111267. doi: 10.3389/fphar.2023.1111267. eCollection 2023.
The aim of this study was to develop a thermosensitive gel (TISG) as an effective rectal delivery platform for delivering extracts (PA) to alleviate ulcerative colitis (UC) and explore the underlying molecular mechanism. Thermosensitive (poloxamer 407) and adhesive polymers (chondroitin sulfate modified carboxymethyl chitosan, CCMTS) were used to construct the gel. CCMTS and aldehyde poloxamer 407 (P407-CHO) were synthesized and chemically cross-linked by Schiff base reaction to formulate thermosensitive gel, which carried extracts (PA/CCMTS-P). The cytotoxicity and cellular uptake of CCMTS-P were investigated in lipopolysaccharide (LPS) -induced macrophages by CCK-8 assay. The anti-inflammatory effects of PA/CCMTS-P were studied in lipopolysaccharide-induced RAW264.7 cells and dextran sulfate sodium (DSS)-induced ulcerative colitis mouse models. In addition, the ability of PA/CCMTS-P to restore the intestinal mucosal barrier after rectal administration was evaluated by immunohistochemical analysis (IHC). PA/CCMTS-P was prepared and characterized as gel with a phase-transition temperature of 32.9°C. The results of the experiments indicated that the hydrogels promoted the cellular uptake of extracts without causing any toxicity as compared to the free gel. PA/CCMTS-P showed superior anti-inflammatory activity both and which restored the damaged intestinal mucosal barrier associated by inhibiting necroptosis in dextran sulfate sodium-induced ulcerative colitis models. The findings from our study show that the rectal administration of PA/CCMTS-P holds a promising potential for the treatment of ulcerative colitis.
本研究的目的是开发一种热敏凝胶(TISG)作为一种有效的直肠给药平台,用于递送提取物(PA)以缓解溃疡性结肠炎(UC),并探索其潜在的分子机制。使用热敏性(泊洛沙姆407)和粘性聚合物(硫酸软骨素修饰的羧甲基壳聚糖,CCMTS)构建凝胶。合成了CCMTS和醛化泊洛沙姆407(P407-CHO),并通过席夫碱反应进行化学交联以制备携带提取物(PA/CCMTS-P)的热敏凝胶。通过CCK-8法研究了CCMTS-P在脂多糖(LPS)诱导的巨噬细胞中的细胞毒性和细胞摄取。在脂多糖诱导的RAW264.7细胞和葡聚糖硫酸钠(DSS)诱导的溃疡性结肠炎小鼠模型中研究了PA/CCMTS-P的抗炎作用。此外,通过免疫组织化学分析(IHC)评估了PA/CCMTS-P直肠给药后恢复肠黏膜屏障的能力。制备的PA/CCMTS-P为凝胶,其相变温度为32.9°C。实验结果表明,与游离凝胶相比,水凝胶促进了提取物的细胞摄取且未引起任何毒性。PA/CCMTS-P在体外和体内均表现出优异的抗炎活性,在葡聚糖硫酸钠诱导的溃疡性结肠炎模型中通过抑制坏死性凋亡恢复了受损的肠黏膜屏障。我们研究的结果表明,PA/CCMTS-P直肠给药在溃疡性结肠炎治疗方面具有广阔的应用前景。