A Biomimetic Nanoplatform with Improved Inflammatory Targeting Behavior for ROS Scavenging‐Based Treatment of Ulcerative Colitis

Author:

Wang Xiaofen1,Jiao Menglu2,Tian Fangzhen3,Lu Xuan4,Xiong Huihuang1,Liu Fan5,Wan Yiqun1,Zhang Xiaodong23,Wan Hao6ORCID

Affiliation:

1. School of Chemistry and Chemical Engineering Nanchang University Nanchang 330031 China

2. Department of Physics and Tianjin Key Laboratory of Low Dimensional Materials Physics and Preparing Technology School of Sciences Tianjin University Tianjin 300350 China

3. Tianjin Key Laboratory of Brain Science and Neural Engineering Academy of Medical Engineering and Translational Medicine Tianjin University Tianjin 300072 China

4. College of Food Science and Technology Nanchang University Nanchang 330031 China

5. Center of Analysis and Testing Nanchang University Nanchang 330047 China

6. State Key Laboratory of Food Science and Resources Nanchang University Nanchang 330047 China

Abstract

AbstractUlcerative colitis (UC), a refractory disease, has become a global problem. Herein, a biomimetic nanoplatform (AU‐LIP‐CM) comprising Au cluster enzymes (AU)‐loaded liposomes (AU‐LIP) camouflaged with the fusion membrane (CM) consisting of neutrophil (NC) and red blood cell (RBC) membrane is designed for the treatment of UC. Briefly, revealed by second near‐infrared (NIR‐II) imaging through collection of fluorescence emitting >1200 nm from AU, the improved inflammatory targeting behavior contributed by CM cloaking, which inherits abilities of inflammatory targeting and immune escape from NC and RBC, respectively, promotes specific accumulation of AU within inflammatory intestines with up to ≈11.5 times higher than that of bare AU. Afterward, AU possessing superoxide dismutase‐ and catalase‐like activities realizes high‐efficiency scavenging of reactive oxygen species (ROS), leading to repair of intestinal barriers, regulation of the immune system, and modulation of gut microbiota, which surpass first‐line UC drug. In addition, study of underlying therapeutic mechanism demonstrated that the treatment with AU‐LIP‐CM can alter the gene signature associated with response to ROS for UC mice to a profile similar to that of healthy mice, deciphering related signal pathways. The strategy developed here provides insights of learning from properties of natural bio‐substances to empower biomimetic nanoplatform to confront diseases.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Publisher

Wiley

Subject

Pharmaceutical Science,Biomedical Engineering,Biomaterials

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