School of Basic Medical Sciences, Xi'an Key Laboratory of Immune Related Diseases, Xi'an Jiaotong University, Xi'an, 710061, Shaanxi, China.
Key Laboratory of Environment and Genes Related to Diseases, Xi'an Jiaotong University, Ministry of Education, Xi'an, 710061, Shaanxi, China.
J Nanobiotechnology. 2022 Mar 2;20(1):99. doi: 10.1186/s12951-022-01299-8.
Ulcerative colitis (UC), a subtype of inflammatory bowel disease (IBD), has evolved into a global burden given its high incidence. There is a clinical need to create better diagnostic and therapeutic approaches to UC.
We fabricated P-selectin binding peptide-decorated poly lactic-co-glycolic acid (PBP-PLGA-NP) doped with two lipophilic dyes, DiL and DiD. Meanwhile, two low-toxic anti-inflammatory natural products (betulinic acid [BA] and resveratrol [Res]) were co-loaded in the PBP-PLGA-NP system. The BA/Res-loaded NPs had an average size of around 164.18 nm with a negative zeta potential (- 25.46 mV). Entrapment efficiencies of BA and Res were 74.54% and 52.33%, respectively, and presented a sustained drug release profile. Further, the resulting PBP-PLGA-NP could be internalized by RAW 264.7 cells and Colon-26 cells efficiently in vitro and preferentially localized to the inflamed colon. When intravenously injected with luminol, MPO-dependent bioluminescence imaging to visualize tissue inflammation was activated by the bioluminescence and fluorescence resonance energy transfer (BRET-FRET) effect. Importantly, injected NPs could remarkably alleviate UC symptoms yet maintain intestinal microbiota homeostasis without inducing organ injuries in the mice models of colitis.
This theranostic nano-platform not only serves as a therapeutic system for UC but also as a non-invasive and highly-sensitive approach for accurately visualizing inflammation.
溃疡性结肠炎(UC)是炎症性肠病(IBD)的一种亚型,由于其发病率高,已成为全球性的负担。因此,需要开发更好的诊断和治疗方法来治疗 UC。
我们制备了 P-选择素结合肽修饰的聚乳酸-羟基乙酸共聚物(PBP-PLGA-NP),并掺杂了两种亲脂性染料 DiL 和 DiD。同时,两种低毒性抗炎天然产物(桦木酸[BA]和白藜芦醇[Res])被共载于 PBP-PLGA-NP 体系中。BA/Res 载药纳米粒的平均粒径约为 164.18nm,带负电荷(-25.46mV)。BA 和 Res 的包封效率分别为 74.54%和 52.33%,并呈现出持续的药物释放模式。此外,所得 PBP-PLGA-NP 可在体外被 RAW 264.7 细胞和 Colon-26 细胞有效内化,并优先定位于炎症结肠。当静脉注射鲁米诺后,通过生物发光和荧光共振能量转移(BRET-FRET)效应激活发光和髓过氧化物酶(MPO)依赖性生物发光成像来可视化组织炎症。重要的是,注射的纳米粒可显著缓解 UC 症状,同时维持肠道微生物组平衡,而不会在结肠炎小鼠模型中引起器官损伤。
这种治疗诊断纳米平台不仅是 UC 的治疗系统,也是一种非侵入性、高灵敏度的方法,可准确地可视化炎症。