PLGA公司
生物发光成像
化学
结肠炎
炎症性肠病
Zeta电位
溃疡性结肠炎
炎症
费斯特共振能量转移
共焦显微镜
生物物理学
体外
药理学
荧光
生物化学
荧光素酶
纳米技术
病理
纳米颗粒
细胞生物学
医学
免疫学
材料科学
转染
生物
物理
疾病
量子力学
基因
作者
Xiangji Yan,Chunhua Yang,Mei Yang,Wei Wang,Yuanyuan Zhang,Yujie Zhang,Cui Liu,Qiuran Xu,Kangsheng Tu,Mingzhen Zhang
标识
DOI:10.1186/s12951-022-01299-8
摘要
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.
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