TY - JOUR
T1 - Readily Available Oral Prebiotic Protein Reactive Oxygen Species Nanoscavengers for Synergistic Therapy of Inflammation and Fibrosis in Inflammatory Bowel Disease
AU - Yu, Yang
AU - Yang, Dairong
AU - Lin, Bingru
AU - Zhu, Lin
AU - Li, Chong
AU - Li, Xin
N1 - This work was supported by the National Natural Science Foundation of China (82270692 and 81603047), Medical Science and Technology Project of Zhejiang Province (2022488040), Chongqing Science Fund for Distinguished Young Scholars (CSTB2023NSCQ-JQX0021), and Chongqing University Innovation Research Group (CXQT20006).
Publisher Copyright:
© 2024 American Chemical Society
PY - 2024/5/28
Y1 - 2024/5/28
N2 - A significant gap exists in the demand for safe and effective drugs for inflammatory bowel disease (IBD), and its associated intestinal fibrosis. As oxidative stress plays a central role in the pathogenesis of IBD, astaxanthin (AST), a good antioxidant with high safety, holds promise for treating IBD. However, the application of AST is restricted by its poor solubility and easy oxidation. Herein, different protein-based nanoparticles (NPs) are fabricated for AST loading to identify an oral nanovehicle with potential clinical applicability. Through systematic validation via molecular dynamics simulation and in vitro characterization of properties, whey protein isolate (WPI)-driven NPs using a simple preparation method without the need for cross-linking agents or emulsifiers were identified as the optimal carrier for oral AST delivery. Upon oral administration, the WPI-driven NPs, benefiting from the intrinsic pH sensitivity and mucoadhesive properties, effectively shielded AST from degradation by gastric juices and targeted release of AST at intestinal lesion sites. Additionally, the AST NPs displayed potent therapeutic efficacy in both dextran sulfate sodium (DSS)-induced acute colitis and chronic colitis-associated intestinal fibrosis by ameliorating inflammation, oxidative damage, and intestinal microecology. In conclusion, the AST WPI NPs hold a potential therapeutic value in treating inflammation and fibrosis in IBD.
AB - A significant gap exists in the demand for safe and effective drugs for inflammatory bowel disease (IBD), and its associated intestinal fibrosis. As oxidative stress plays a central role in the pathogenesis of IBD, astaxanthin (AST), a good antioxidant with high safety, holds promise for treating IBD. However, the application of AST is restricted by its poor solubility and easy oxidation. Herein, different protein-based nanoparticles (NPs) are fabricated for AST loading to identify an oral nanovehicle with potential clinical applicability. Through systematic validation via molecular dynamics simulation and in vitro characterization of properties, whey protein isolate (WPI)-driven NPs using a simple preparation method without the need for cross-linking agents or emulsifiers were identified as the optimal carrier for oral AST delivery. Upon oral administration, the WPI-driven NPs, benefiting from the intrinsic pH sensitivity and mucoadhesive properties, effectively shielded AST from degradation by gastric juices and targeted release of AST at intestinal lesion sites. Additionally, the AST NPs displayed potent therapeutic efficacy in both dextran sulfate sodium (DSS)-induced acute colitis and chronic colitis-associated intestinal fibrosis by ameliorating inflammation, oxidative damage, and intestinal microecology. In conclusion, the AST WPI NPs hold a potential therapeutic value in treating inflammation and fibrosis in IBD.
KW - Astaxanthin
KW - Intestinal inflammation and fibrosis
KW - Intestinal microecology
KW - Prebiotic protein nanoparticles
KW - Synergistic therapeutics
UR - http://www.scopus.com/inward/record.url?scp=85193241772&partnerID=8YFLogxK
UR - https://pubs.acs.org/doi/10.1021/acsnano.3c13114
U2 - 10.1021/acsnano.3c13114
DO - 10.1021/acsnano.3c13114
M3 - Journal article
C2 - 38740518
AN - SCOPUS:85193241772
SN - 1936-0851
VL - 18
SP - 13583
EP - 13598
JO - ACS Nano
JF - ACS Nano
IS - 21
ER -