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用于评估抗菌性能的糖酵解和自动菌斑再生长方法

Glycolysis and Automated Plaque Regrowth Method for Evaluation of Antimicrobial Performance.

作者信息

Karlinsey Robert L, Karlinsey Tamara R

机构信息

Custom Dental Formulations, LLC, 1291 Airport Parkway, Suite 400, Greenwood, IN 46143, USA.

出版信息

Dent J (Basel). 2024 May 17;12(5):146. doi: 10.3390/dj12050146.

DOI:10.3390/dj12050146
PMID:38786544
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11119774/
Abstract

PURPOSE

This study explored the potential of a new in vitro method in evaluating antiplaque benefits from five sets of antimicrobial systems including cetylpyridinium chloride (CPC), stannous fluoride (SnF), Listerine essential oil mouthwashes (+/- alcohol), zinc chloride (ZnCl), and sodium fluoride. (NaF).

METHODS

Gingival dental plaque was collected and propagated using sterilized tryptic soy broth and sucrose, and then allocated into separate glycolysis and regrowth recipes for antiplaque evaluations. Glycolysis measurements (in duplicate) were recorded via pH microelectrode on plaque-treatment samples thermomixed (1200 rpm, 37 °C) for 4 h. For plaque regrowth, optical densities (in duplicate) were automatically collected on plaque-treatment samples using a microplate reader (linear shaking, 37 °C) from baseline to 4 h.

RESULTS

Calculations of percent change in pH and optical density were performed and analyzed for each set of antimicrobial treatment groups. Statistical analysis (one-way ANOVA, Student-Newman-Keuls stepwise comparison tests) revealed dose responses and significant differences ( < 0.05) among treatment groups, including between negative and clinically relevant positive controls.

CONCLUSIONS

This lab method produces results consistent with published clinical observations. This glycolysis and plaque growth method is sensitive to antimicrobial mechanisms of action, and may offer a convenient and clinically relevant screening tool in the evaluation of putative antimicrobial agents and formulations.

摘要

目的

本研究探索了一种新的体外方法在评估五组抗菌系统抗牙菌斑益处方面的潜力,这五组抗菌系统包括氯化十六烷基吡啶(CPC)、氟化亚锡(SnF)、李施德林精油漱口水(含/不含酒精)、氯化锌(ZnCl)和氟化钠(NaF)。

方法

收集牙龈牙菌斑,使用无菌胰蛋白胨大豆肉汤和蔗糖进行增殖培养,然后将其分配到单独的糖酵解和再生长配方中进行抗牙菌斑评估。通过pH微电极对在37℃下以1200转/分钟热混合4小时的菌斑处理样品进行糖酵解测量(一式两份)。对于菌斑再生长,使用酶标仪在37℃下对菌斑处理样品从基线到4小时自动收集光密度(一式两份)(线性振荡)。

结果

对每组抗菌治疗组进行pH和光密度变化百分比的计算和分析。统计分析(单因素方差分析、Student-Newman-Keuls逐步比较检验)显示治疗组之间存在剂量反应和显著差异(<0.05),包括阴性对照和临床相关阳性对照之间。

结论

这种实验室方法产生的结果与已发表的临床观察结果一致。这种糖酵解和菌斑生长方法对抗菌作用机制敏感,可能为评估潜在抗菌剂和制剂提供一种方便且与临床相关的筛选工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/859d/11119774/2134af1d0bfb/dentistry-12-00146-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/859d/11119774/21075695c619/dentistry-12-00146-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/859d/11119774/47014e6a773e/dentistry-12-00146-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/859d/11119774/815ffb2f918e/dentistry-12-00146-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/859d/11119774/2134af1d0bfb/dentistry-12-00146-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/859d/11119774/21075695c619/dentistry-12-00146-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/859d/11119774/47014e6a773e/dentistry-12-00146-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/859d/11119774/815ffb2f918e/dentistry-12-00146-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/859d/11119774/2134af1d0bfb/dentistry-12-00146-g004.jpg

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