TY - JOUR
T1 - Berberine-Functionalized Bismuth-Doped Carbon Dots in a Pathogen-Responsive Hydrogel System
T2 - A Multifaceted Approach to Combating Periodontal Diseases
AU - Li, Xuan
AU - Huang, Regina
AU - Li, Pugeng
AU - Tang, Fung Kit
AU - He, Jing
AU - Sun, Hanyu
AU - Wang, Xiaoyu
AU - Wang, Miao
AU - Lan, Xinmiao
AU - Wang, Xinna
AU - Wong, Sarah Sze Wah
AU - Jin, Lijian
AU - Leung, Ken Cham-Fai
AU - Wong, Hai Ming
AU - Wang, Sheng
AU - Guo, Lanping
AU - Ding, Pei-Hui
AU - Yu, Xiaolin
N1 - PMID: 40313185
This work was financially supported by the Health and Medical Research Fund from the Hong Kong Food and Health Bureau (20190682) to X. Li, as well as the National Natural Science Foundation of China (No. 81801012 and 32301133) to X.Y. and X. Lan, respectively.
Publisher Copyright:
© 2025 The Authors. Published by American Chemical Society
PY - 2025/5/2
Y1 - 2025/5/2
N2 - Periodontal disease, a global health burden linked to dysbiotic oral polymicrobial communities and disrupted immune-inflammatory responses, is critically mediated byPorphyromonas gingivalis(Pg)─the keystone pathogen that sabotages host immunity, triggers tissue inflammation and destruction, and disrupts microbiota balance. Effective therapies should combine antimicrobial action, immune modulation, virulence suppression, and microbiome restoration. Bismuth ions and berberine, which exhibit antimicrobial and epithelial barrier-protecting effects, show potential effectiveness in treating periodontal diseases but face practical limitations due to poor water solubility and bioavailability. To address this, we developed bismuth-doped carbon dots functionalized with structure-modified berberine (BiCD-Ber) as a multifunctional nanomedicine. BiCD-Ber eradicated Pg in various forms, restored Pg-perturbed immune responses in gingival fibroblasts, and preserved epithelial barrier integrity. The doped bismuth ions neutralized Pg virulence factors by blocking the catalytic sites of gingipains. To facilitate in vivo delivery, BiCD-Ber was encapsulated in a disulfide-modified hyaluronic acid hydrogel that degrades in response to Pg metabolites. This BiCD-Ber hydrogel system modulated subgingival microbiota, alleviated inflammation in gingiva, and thereby prevented alveolar bone loss. This approach to concurrently eliminating Pg, modulating inflammatory responses , suppressing virulence factors, and restoring microbiota showcases great potential in managing periodontitis effectively.
AB - Periodontal disease, a global health burden linked to dysbiotic oral polymicrobial communities and disrupted immune-inflammatory responses, is critically mediated byPorphyromonas gingivalis(Pg)─the keystone pathogen that sabotages host immunity, triggers tissue inflammation and destruction, and disrupts microbiota balance. Effective therapies should combine antimicrobial action, immune modulation, virulence suppression, and microbiome restoration. Bismuth ions and berberine, which exhibit antimicrobial and epithelial barrier-protecting effects, show potential effectiveness in treating periodontal diseases but face practical limitations due to poor water solubility and bioavailability. To address this, we developed bismuth-doped carbon dots functionalized with structure-modified berberine (BiCD-Ber) as a multifunctional nanomedicine. BiCD-Ber eradicated Pg in various forms, restored Pg-perturbed immune responses in gingival fibroblasts, and preserved epithelial barrier integrity. The doped bismuth ions neutralized Pg virulence factors by blocking the catalytic sites of gingipains. To facilitate in vivo delivery, BiCD-Ber was encapsulated in a disulfide-modified hyaluronic acid hydrogel that degrades in response to Pg metabolites. This BiCD-Ber hydrogel system modulated subgingival microbiota, alleviated inflammation in gingiva, and thereby prevented alveolar bone loss. This approach to concurrently eliminating Pg, modulating inflammatory responses , suppressing virulence factors, and restoring microbiota showcases great potential in managing periodontitis effectively.
KW - alveolar bone loss
KW - immune-responses modulation
KW - pathogen-responsive hydrogel
KW - periopathogen-responsive hydrogeldontitis
KW - subgingival microbiota
KW - periodontitis
UR - https://pubs.acs.org/doi/10.1021/acsnano.5c00561
UR - http://www.scopus.com/inward/record.url?scp=105004031733&partnerID=8YFLogxK
U2 - 10.1021/acsnano.5c00561
DO - 10.1021/acsnano.5c00561
M3 - Journal article
SN - 1936-0851
JO - ACS Nano
JF - ACS Nano
ER -