journal article·2025-09-02

Mucoadhesive and Self-Assembled Chitosan Oligosaccharide-Glycyrrhizin Nanoparticle for Oral Nanotherapeutic in Inflammatory Bowel Disease

Gayoung Lim, Ha Rin Kim, Chaerim Yoo, Yu Kyung Oh, Yeon Soo Park, Sijin Park, Seonmi Jang, Lia Priscilla, Dong Yun Lee

ACS Nano· Volume 19· Issue 34
Publisher page

Abstract

Inflammatory bowel disease (IBD) is a chronic inflammatory disorder characterized by severe oxidative stress and intestinal barrier dysfunction. Conventional oral therapies are often limited by low bioavailability and off-target effects. Herein, we report the development of mucoadhesive nanotherapeutics engineered from low molecular weight chitosan oligosaccharide (COS) and glycyrrhizin (GL), a natural anti-inflammatory compound. Hydrophilic COS, selected for its potent antioxidant and mucoadhesive properties, was chemically conjugated with hydrophobic GL to facilitate self-assembly into stable COS-GL nanoparticles (∼129 nm). These nanoparticles exhibit enhanced retention at inflamed intestinal sites and preferential uptake by activated immune and epithelial cells. In vitro evaluations using transwell coculture systems and intestinal organoids revealed that COS-GL nanoparticles effectively suppress pro-inflammatory cytokine secretion, promote M1-to-M2 macrophage remodeling, neutralize reactive oxygen species (ROS), and restore intestinal barrier integrity by upregulating tight junction proteins. In a DSS-induced colitis mouse model, orally administered COS-GL nanoparticles outperform both their individual components and the standard therapeutic 5-aminosalicylic acid (5-ASA), mitigating inflammation and promoting mucosal healing. These findings establish COS-GL nanoparticles as a promising and effective nanotherapeutic platform for the targeted oral treatment of IBD.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Pharmacological Effects of Natural Compounds · Advanced Drug Delivery Systems · Advanced Glycation End Products research

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Bioengineering, College of Engineering

Hanyang University

Division of Oncology, School of Medicine

Stanford University

Biopharmaceutical Chemistry, Applied Chemistry

Kookmin University

Elixir Pharmatech Inc.

Institute for Bioengineering and Biopharmaceutical Research (IBBR), and Institute of Nano Science and Technology (INST)

Funding

National Research Foundation of Korea · Deeptech TIPS program · Korean Fund for Regenerative Medicine

References (55)

Show source-provided references
1. 10.1038/nrgastro.2015.15010.1038/nrgastro.2015.150 ↗
2. 10.1016/s2468-1253(19)30333-410.1016/s2468-1253(19)30333-4 ↗
3. 10.1093/ecco-jcc/jjab02910.1093/ecco-jcc/jjab029 ↗
4. 10.1038/mi.2016.1410.1038/mi.2016.14 ↗
5. 10.3389/fendo.2024.139035110.3389/fendo.2024.1390351 ↗
6. 10.1007/s10620-023-08122-w10.1007/s10620-023-08122-w ↗
7. 10.1016/j.biopha.2024.11730210.1016/j.biopha.2024.117302 ↗
8. 10.1038/s12276-018-0126-x10.1038/s12276-018-0126-x ↗
9. 10.1016/j.jcmgh.2017.03.00710.1016/j.jcmgh.2017.03.007 ↗
10. 10.3389/fmed.2021.76547410.3389/fmed.2021.765474 ↗
11. 10.1016/j.phrs.2020.10507510.1016/j.phrs.2020.105075 ↗
12. 10.1016/j.heliyon.2024.e2535710.1016/j.heliyon.2024.e25357 ↗
13. 10.1016/j.addr.2021.11410110.1016/j.addr.2021.114101 ↗
14. 10.1016/j.biomaterials.2022.12136410.1016/j.biomaterials.2022.121364 ↗
15. 10.1038/nrd436310.1038/nrd4363 ↗
16. 10.1021/acs.jmedchem.7b0113610.1021/acs.jmedchem.7b01136 ↗
17. 10.1016/j.cyto.2024.15653710.1016/j.cyto.2024.156537 ↗
18. 10.1146/annurev-immunol-030409-10132310.1146/annurev-immunol-030409-101323 ↗
19. 10.2147/ITT.S5806410.2147/ITT.S58064 ↗
20. 10.1021/acsnano.3c1108910.1021/acsnano.3c11089 ↗
21. 10.1186/s12974-020-01973-410.1186/s12974-020-01973-4 ↗
22. 10.1038/s41598-021-94928-510.1038/s41598-021-94928-5 ↗
23. 10.1021/acsami.1c0275510.1021/acsami.1c02755 ↗
24. 10.1016/j.phymed.2022.15399910.1016/j.phymed.2022.153999 ↗
25. 10.1211/002235701177573010.1211/0022357011775730 ↗
26. 10.1002/smll.20230233110.1002/smll.202302331 ↗
27. 10.1021/acs.molpharmaceut.0c0124510.1021/acs.molpharmaceut.0c01245 ↗
28. 10.1016/j.pharmthera.2016.10.01310.1016/j.pharmthera.2016.10.013 ↗
29. 10.1021/acsnano.3c0325210.1021/acsnano.3c03252 ↗
30. 10.1038/s41598-021-98931-810.1038/s41598-021-98931-8 ↗
31. 10.3389/fcell.2022.87789210.3389/fcell.2022.877892 ↗
32. 10.1016/j.jconrel.2004.10.01210.1016/j.jconrel.2004.10.012 ↗
33. 10.1021/acsnano.0c0101810.1021/acsnano.0c01018 ↗
34. 10.3390/ijms2019466710.3390/ijms20194667 ↗
35. 10.3390/polym1319325610.3390/polym13193256 ↗
36. 10.1186/s12951-022-01539-x10.1186/s12951-022-01539-x ↗
37. 10.7150/thno.3597210.7150/thno.35972 ↗
38. 10.1038/s41467-021-27463-610.1038/s41467-021-27463-6 ↗
39. 10.1021/acsnano.2c1118810.1021/acsnano.2c11188 ↗
40. 10.1002/smll.20230471310.1002/smll.202304713 ↗
41. 10.1016/j.bbrc.2007.05.04210.1016/j.bbrc.2007.05.042 ↗
42. 10.1038/nrgastro.2015.10910.1038/nrgastro.2015.109 ↗
43. 10.3390/molecules2817629310.3390/molecules28176293 ↗
44. 10.1021/acs.nanolett.3c0011810.1021/acs.nanolett.3c00118 ↗
45. 10.1038/nprot.2007.4110.1038/nprot.2007.41 ↗
46. 10.1046/j.1365-2249.1998.00728.x10.1046/j.1365-2249.1998.00728.x ↗
47. 10.1016/S0168-3659(02)00424-810.1016/S0168-3659(02)00424-8 ↗
48. 10.1007/s12325-015-0206-410.1007/s12325-015-0206-4 ↗
49. 10.1016/j.chembiol.2007.03.00710.1016/j.chembiol.2007.03.007 ↗
50. 10.3389/fendo.2021.61650610.3389/fendo.2021.616506 ↗
51. 10.1128/spectrum.03639-2310.1128/spectrum.03639-23 ↗
52. 10.1016/j.jconrel.2016.06.01610.1016/j.jconrel.2016.06.016 ↗
53. 10.1186/s12951-024-02930-610.1186/s12951-024-02930-6 ↗
54. 10.1007/s11095-014-1613-y10.1007/s11095-014-1613-y ↗
55. 10.1016/j.biomaterials.2011.12.03410.1016/j.biomaterials.2011.12.034 ↗