Sun Wei, Li Zhibo, Zhang Xiaohao, Luo Qiang, Wei Lijuan, Xiao Chunsheng
Department of Gastroenterology and Digestive Endoscopy Center, The Second Hospital of Jilin University, 4026 Yatai Street, Changchun, 130041, PR China.
Department of Cardiology, The Second Hospital of Jilin University, 4026 Yatai Street, Changchun, 130041, PR China.
Biomaterials. 2026 Jan;324:123462. doi: 10.1016/j.biomaterials.2025.123462. Epub 2025 Jun 2.
Inflammatory bowel disease (IBD) is a chronic, challenging condition characterized by epithelial barrier disruption, immune dysregulation, and alterations in gut microbiota, leading to symptoms such as abdominal pain, diarrhea, and weight loss, affecting millions of patients worldwide. The etiology and pathogenesis of IBD are multifactorial, involving a combination of genetic factors, environmental influences, microbial dysbiosis, and other elements. Current treatments for IBD include aminosalicylates, antibiotics, corticosteroids, and immunosuppressants, all aimed at reducing inflammation and achieving clinical remission. However, the frequent and prolonged use of these medications results in significant adverse effects, including joint pain, diabetes, and osteoporosis. Therefore, targeting drug delivery to affected areas, extending the duration of drug action, and minimizing systemic exposure are crucial for effective IBD management. Emerging strategies that target excess reactive oxygen species, modulate local inflammation, and restore gut microbiota homeostasis show promise for improving IBD treatment. Biomaterials have demonstrated considerable potential in precisely delivering therapeutic agents selectively to inflamed tissues, thereby minimizing off-target effects and improving efficacy. This review highlights recent advancements in biomaterials for IBD treatment and explores future directions and challenges in their clinical application.
炎症性肠病(IBD)是一种慢性、具有挑战性的疾病,其特征为上皮屏障破坏、免疫失调和肠道微生物群改变,导致腹痛、腹泻和体重减轻等症状,影响全球数百万患者。IBD的病因和发病机制是多因素的,涉及遗传因素、环境影响、微生物失调和其他因素的综合作用。目前IBD的治疗方法包括氨基水杨酸类药物、抗生素、皮质类固醇和免疫抑制剂,所有这些都旨在减轻炎症并实现临床缓解。然而,这些药物的频繁和长期使用会导致严重的不良反应,包括关节疼痛、糖尿病和骨质疏松症。因此,将药物递送至受影响区域、延长药物作用持续时间并尽量减少全身暴露对于IBD的有效管理至关重要。针对过量活性氧、调节局部炎症和恢复肠道微生物群稳态的新兴策略有望改善IBD治疗。生物材料已显示出在将治疗剂精确地选择性递送至炎症组织方面具有相当大的潜力,从而最大限度地减少脱靶效应并提高疗效。本综述重点介绍了用于IBD治疗的生物材料的最新进展,并探讨了其临床应用的未来方向和挑战。