Anti-Porphyromonas gingivalis nanotherapy for maintaining bacterial homeostasis in periodontitis

•Antibody-conjugated liposomal drug carriers with ginsenoside Rh2 (A-L-R) as a targeting nanoagent.•A-L-R targets P. gingivalis with high efficiency and low toxicity.•A-L-R maintains homeostasis with a relatively stable oral microflora.•A-L-R achieves a more precise sterilization effect than other i...

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Veröffentlicht in:International journal of antimicrobial agents 2023-06, Vol.61 (6), p.106801-106801, Article 106801
Hauptverfasser: Chen, Rourong, Ji, Yaoting, Li, Ting, Zhao, Boxuan, Guo, Haiying, Wang, Zijun, Yao, Hantao, Zhang, Zicheng, Liu, Chang, Du, Minquan
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Sprache:eng
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Zusammenfassung:•Antibody-conjugated liposomal drug carriers with ginsenoside Rh2 (A-L-R) as a targeting nanoagent.•A-L-R targets P. gingivalis with high efficiency and low toxicity.•A-L-R maintains homeostasis with a relatively stable oral microflora.•A-L-R achieves a more precise sterilization effect than other interventions in this study. Periodontitis is caused by oral flora imbalance, which leads to immune imbalance. Porphyromonas gingivalis is a keystone pathogen in periodontitis, causing the blooming of inflammophilic microbes, and becoming dormant to resist antibiotics. Targeted interventions are needed to destroy this pathogen and collapse its inflammophilic flora. Therefore, a targeting nanoagent antibody-conjugated liposomal drug carrier with ginsenoside Rh2 (A-L-R) was developed for pleiotropic benefits. A-L-R showed high quality in high-performance liquid chromatography (HPLC), Fourier transform infrared (FTIR), and transmission electron microscope (TEM) detection. Only P. gingivalis was influenced by A-L-R, as shown by live/dead cell staining and a series of antimicrobial effects assays. With fluorescence in situ hybridization (FISH) staining and in propidium monoazide-quantitative polymerase chain reaction (PMA-qPCR), the clearance of P. gingivalis by A-L-R was more than for other groups, and only the proportion of P. gingivalis was reduced by A-L-R in monospecies culture. Moreover, in a periodontitis model, A-L-R targeted P. gingivalis with high efficiency and low toxicity, maintaining homeostasis with a relatively stable oral microflora. This targeting nanomedicine offers new strategies for periodontitis therapy, providing a foundation for the prevention and treatment of periodontitis.
ISSN:0924-8579
1872-7913
DOI:10.1016/j.ijantimicag.2023.106801