Effects of a Mouthrinse Containing Silver Nanoparticles on Polymicrobial Oral Biofilms.

IF 1.4 4区 医学 Q3 DENTISTRY, ORAL SURGERY & MEDICINE
Kiyoshi Tomiyama, Kiyoko Watanabe, Junko Iizuka, Nobushiro Hamada, Yoshiharu Mukai
{"title":"Effects of a Mouthrinse Containing Silver Nanoparticles on Polymicrobial Oral Biofilms.","authors":"Kiyoshi Tomiyama, Kiyoko Watanabe, Junko Iizuka, Nobushiro Hamada, Yoshiharu Mukai","doi":"10.3290/j.ohpd.b5816545","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>To investigate the antimicrobial effects of a mouthrinse containing silver nanoparticles (AgNP) on polymicrobial biofilms in vitro.</p><p><strong>Materials and methods: </strong>Polymicrobial biofilms were grown on glass cover slips following the method of Exterkate. Saliva collected from a healthy human was added to McBain medium (including 0.2% sucrose) to achieve a 50-fold dilution. Glass coverslips were attached to the lid of a 24-well culture plate and suspended in the medium of each well. After 24 h of cultivating, coverslips with biofilms were immersed in each of four treatment solutions or sterile deionized water for 5 min. The control and four treatment groups were as follows: 1) control: sterile deionized water; 2) nanosilver (NS): mouthrinse containing AgNP; 3) 0.05C: 0.05% chlorhexidine gluconate; 4) 0.2C: 0.2% chlorhexidine gluconate; 5) Xyl: 25% xylitol. The biofilms were further regrown for 48 h. After removing the biofilms ultrasonically, they were cultured on blood agar, viable cells were counted, and the amount of lactic acid in the biofilms was analysed using a colorimetric assay.</p><p><strong>Results: </strong>Mouthrinse containing AgNP suppressed viable cells in the biofilm to the same degree or more than with chlorhexidine gluconate. Amounts of lactic acid after 72 h cultivation of biofilms treated with 0.2C and NS showed consistently low values.</p><p><strong>Conclusion: </strong>The mouthrinse containing AgNP suppressed viable cells in polymicrobial biofilms to the same level as 0.2% chlorhexidine or higher.</p>","PeriodicalId":19696,"journal":{"name":"Oral health & preventive dentistry","volume":"22 ","pages":"567-572"},"PeriodicalIF":1.4000,"publicationDate":"2024-11-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11619913/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Oral health & preventive dentistry","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3290/j.ohpd.b5816545","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"DENTISTRY, ORAL SURGERY & MEDICINE","Score":null,"Total":0}
引用次数: 0

Abstract

Purpose: To investigate the antimicrobial effects of a mouthrinse containing silver nanoparticles (AgNP) on polymicrobial biofilms in vitro.

Materials and methods: Polymicrobial biofilms were grown on glass cover slips following the method of Exterkate. Saliva collected from a healthy human was added to McBain medium (including 0.2% sucrose) to achieve a 50-fold dilution. Glass coverslips were attached to the lid of a 24-well culture plate and suspended in the medium of each well. After 24 h of cultivating, coverslips with biofilms were immersed in each of four treatment solutions or sterile deionized water for 5 min. The control and four treatment groups were as follows: 1) control: sterile deionized water; 2) nanosilver (NS): mouthrinse containing AgNP; 3) 0.05C: 0.05% chlorhexidine gluconate; 4) 0.2C: 0.2% chlorhexidine gluconate; 5) Xyl: 25% xylitol. The biofilms were further regrown for 48 h. After removing the biofilms ultrasonically, they were cultured on blood agar, viable cells were counted, and the amount of lactic acid in the biofilms was analysed using a colorimetric assay.

Results: Mouthrinse containing AgNP suppressed viable cells in the biofilm to the same degree or more than with chlorhexidine gluconate. Amounts of lactic acid after 72 h cultivation of biofilms treated with 0.2C and NS showed consistently low values.

Conclusion: The mouthrinse containing AgNP suppressed viable cells in polymicrobial biofilms to the same level as 0.2% chlorhexidine or higher.

含银纳米颗粒的漱口水对多微生物口腔生物膜的影响
目的:研究含银纳米粒子(AgNP)的漱口水对体外多微生物生物膜的抗菌效果:按照 Exterkate 的方法,在玻璃盖玻片上培养多微生物生物膜。在麦克贝恩培养基(含 0.2% 蔗糖)中加入从健康人身上采集的唾液,稀释到 50 倍。将玻璃盖玻片固定在 24 孔培养板的盖子上,悬浮在每孔的培养基中。培养 24 小时后,将带有生物膜的盖玻片分别浸入四种处理溶液或无菌去离子水中 5 分钟。对照组和四个处理组如下:1)对照组:无菌去离子水;2)纳米银(NS):含 AgNP 的漱口水;3)0.05C:0.05% 葡萄糖酸洗必泰;4)0.2C:0.2% 葡萄糖酸洗必泰;5)Xyl:25% 木糖醇。用超声波去除生物膜后,将其放在血琼脂上培养,计数存活细胞,并用比色法分析生物膜中的乳酸含量:结果:含 AgNP 的漱口水对生物膜中存活细胞的抑制程度与葡萄糖酸氯己定相同,甚至更强。经 0.2C 和 NS 处理的生物膜在培养 72 小时后的乳酸量始终很低:含有 AgNP 的漱口水对多微生物生物膜中存活细胞的抑制作用与 0.2% 的洗必泰相同,甚至更高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Oral health & preventive dentistry
Oral health & preventive dentistry DENTISTRY, ORAL SURGERY & MEDICINE-
CiteScore
3.00
自引率
0.00%
发文量
51
审稿时长
>12 weeks
期刊介绍: Clinicians, general practitioners, teachers, researchers, and public health administrators will find this journal an indispensable source of essential, timely information about scientific progress in the fields of oral health and the prevention of caries, periodontal diseases, oral mucosal diseases, and dental trauma. Central topics, including oral hygiene, oral epidemiology, oral health promotion, and public health issues, are covered in peer-reviewed articles such as clinical and basic science research reports; reviews; invited focus articles, commentaries, and guest editorials; and symposium, workshop, and conference proceedings.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信