Anti‐inflammatory Glycocalyx‐Mimicking Nanoparticles for Colitis Treatment: Construction and In Vivo Evaluation

Author:

Yoo Dohyun12ORCID,Whang Chang‐Hee12ORCID,Hong Jungwoo34,Kim Dohyeon12,Prayogo Monica Celine12,Son Youngju12,Jung Wonsik12,Lee Seojung12,Lee Hee‐Seung34ORCID,Jon Sangyong12ORCID

Affiliation:

1. Department of Biological Sciences, Institute for the BioCentury Korea Advanced Institute of Science and Technology (KAIST) 291 Daehak-ro Daejeon 34141 Republic of Korea

2. Center for Precision Bio-Nanomedicine KAIST 291 Daehak-ro Daejeon 34141 Republic of Korea

3. Department of Chemistry KAIST 291 Daehak-ro Daejeon 34141 Republic of Korea

4. Center for Multiscale Chiral Architectures (CMCA) KAIST 291 Daehak-ro Daejeon 34141 Republic of Korea

Abstract

AbstractCommon medications for treating inflammatory bowel disease (IBD) have limited therapeutic efficacy and severe adverse effects. This underscores the urgent need for novel therapeutic approaches that can effectively target inflamed sites in the gastrointestinal tract upon oral administration, exerting potent therapeutic efficacy while minimizing systemic effects. Here, we report the construction and in vivo therapeutic evaluation of a library of anti‐inflammatory glycocalyx‐mimicking nanoparticles (designated GlyNPs) in a mouse model of IBD. The anti‐inflammatory GlyNP library was created by attaching bilirubin (BR) to a library of glycopolymers composed of random combinations of the five most naturally abundant sugars. Direct in vivo screening of 31 BR‐attached anti‐inflammatory GlyNPs via oral administration into mice with acute colitis led to identification of a candidate GlyNP capable of targeting macrophages in the inflamed colon and effectively alleviating colitis symptoms. These findings suggest that the BR‐attached GlyNP library can be used as a platform to identify anti‐inflammatory nanomedicines for various inflammatory diseases.

Funder

National Research Foundation of Korea

Publisher

Wiley

Subject

General Chemistry,Catalysis

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