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Silica nanoparticles containing nano-silver and chlorhexidine to suppress Porphyromonas gingivalis biofilm and modulate multispecies biofilms toward healthy tendency.
Fang, Lixin; Zhang, Yishuang; Cheng, Long; Zheng, Hao; Wang, Yiyi; Qin, Lu; Cai, Yingchun; Cheng, Lei; Zhou, Wen; Liu, Fei; Wang, Suping.
Affiliation
  • Fang L; Stomatology Center, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
  • Zhang Y; The Academy of Medical Sciences, Zhengzhou University, Zhengzhou, China.
  • Cheng L; Stomatology Center, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
  • Zheng H; The Academy of Medical Sciences, Zhengzhou University, Zhengzhou, China.
  • Wang Y; Stomatology Center, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
  • Qin L; The Academy of Medical Sciences, Zhengzhou University, Zhengzhou, China.
  • Cai Y; Stomatology Center, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
  • Cheng L; The Academy of Medical Sciences, Zhengzhou University, Zhengzhou, China.
  • Zhou W; Stomatology Center, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
  • Liu F; The Academy of Medical Sciences, Zhengzhou University, Zhengzhou, China.
  • Wang S; Stomatology Center, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
J Oral Microbiol ; 16(1): 2361403, 2024.
Article in En | MEDLINE | ID: mdl-38847000
ABSTRACT

Objectives:

This research first investigated the effect of mesoporous silica nanoparticles (nMS) carrying chlorhexidine and silver (nMS-nAg-Chx) on periodontitis-related biofilms. This study aimed to investigate (1) the antibacterial activity on Porphyromonas gingivalis (P. gingivalis) biofilm; (2) the suppressing effect on virulence of P. gingivalis biofilm; (3) the regulating effect on periodontitis-related multispecies biofilm.

Methods:

Silver nanoparticles (nAg) and chlorhexidine (Chx) were co-loaded into nMS to form nMS-nAg-Chx. Inhibitory zone test and minimum inhibitory concentration (MIC) against P. gingivalis were tested. Growth curves, crystal violet (CV) staining, live/dead staining and scanning electron microscopy (SEM) observation were performed. Biofilm virulence was assessed. The 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) assay and Quantitative Real Time-PCR (qPCR) were performed to validate the activity and composition changes of multispecies biofilm (P. gingivalis, Streptococcus gordonii and Streptococcus sanguinis).

Results:

nMS-nAg-Chx inhibited P. gingivalis biofilm dose-dependently (p<0.05), with MIC of 18.75 µg/mL. There were fewer live bacteria, less biomass and less virulence in nMS-nAg-Chx groups (p<0.05). nMS-nAg-Chx inhibited and modified periodontitis-related biofilms. The proportion of pathogenic bacteria decreased from 16.08 to 1.07% and that of helpful bacteria increased from 82.65 to 94.31% in 25 µg/mL nMS-nAg-Chx group for 72 h.

Conclusions:

nMS-nAg-Chx inhibited P. gingivalis growth, decreased biofilm virulence and modulated periodontitis-related multispecies biofilms toward healthy tendency. pH-sensitive nMS-nAg-Chx inhibit the pathogens and regulate oral microecology, showing great potential in periodontitis adjunctive therapy.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Oral Microbiol Year: 2024 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Oral Microbiol Year: 2024 Document type: Article Affiliation country: China