Wang Wenyuan, Wu Ya, Wang Yihui, Wang Rui, Deng Cheng, Yi Luyang, Wang Lufang, He Mengrong, Zhou Wuqi, Xie Yuji, Jin Qiaofeng, Chen Yihan, Gao Tang, Zhang Li, Xie Mingxing
Department of Ultrasound Medicine, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China.
Hubei Province Clinical Research Center for Medical Imaging, Wuhan, 430022, China.
Adv Healthc Mater. 2023 Apr;12(9):e2202420. doi: 10.1002/adhm.202202420. Epub 2023 Jan 15.
As macrophage infiltration is significantly related to the progression of inflammatory bowel disease (IBD), monitoring the macrophages is a valuable strategy for IBD diagnosis. However, owing to the harsh physiological environment of the gastrointestinal tract and enzymatic degradation, the development of orally administrable imaging probes for tracking macrophages remains a considerable challenge. Accordingly, herein, an orally administrable aggregation-induced emission biomimetic probe (HBTTPIP/β-glucan particles [GPs]) is developed for tracing macrophages; HBTTPIP/GPs can diagnose and alleviate dextran sulfate sodium (DSS)-induced colonic inflammation and self-report the treatment efficiency. The fluorophore HBTTPIP can effectively aggregate in GPs, restricting intramolecular rotation and activating the fluorescence of HBTTPIP. After being orally administrated, HBTTPIP/GPs are phagocytosed by intestinal macrophages, which then migrate to colonic lesions, enabling non-invasive monitoring of the severity of IBD via in vivo fluorescence imaging. Notably, oral HBTTPIP/GPs ameliorate DSS-induced IBD by inhibiting the expressions of pro-inflammatory factors and improving colonic mucosal barrier function. Furthermore, these HBTTPIP/GPs realize self-feedback of the therapeutic effects of GPs on DSS-induced colitis. The oral biomimetic probe HBTTPIP/GPs reported herein provide a novel theranostic platform for IBD, integrating non-invasive diagnosis of IBD in situ and the corresponding treatment.
由于巨噬细胞浸润与炎症性肠病(IBD)的进展显著相关,监测巨噬细胞是IBD诊断的一种有价值的策略。然而,由于胃肠道恶劣的生理环境和酶降解作用,开发用于追踪巨噬细胞的口服成像探针仍然是一个巨大的挑战。因此,本文开发了一种用于追踪巨噬细胞的口服聚集诱导发光仿生探针(HBTTPIP/β-葡聚糖颗粒[GPs]);HBTTPIP/GPs可以诊断并减轻葡聚糖硫酸钠(DSS)诱导的结肠炎症,并自我报告治疗效果。荧光团HBTTPIP可以在GPs中有效聚集,限制分子内旋转并激活HBTTPIP的荧光。口服后,HBTTPIP/GPs被肠道巨噬细胞吞噬,然后迁移至结肠病变部位,通过体内荧光成像实现对IBD严重程度的无创监测。值得注意的是,口服HBTTPIP/GPs通过抑制促炎因子的表达和改善结肠黏膜屏障功能来减轻DSS诱导的IBD。此外,这些HBTTPIP/GPs实现了GPs对DSS诱导的结肠炎治疗效果的自我反馈。本文报道的口服仿生探针HBTTPIP/GPs为IBD提供了一个新的诊疗平台,将IBD的原位无创诊断和相应治疗整合在一起。