Cargando…
Inhibited biofilm formation and improved antibacterial activity of a novel nanoemulsion against cariogenic Streptococcus mutans in vitro and in vivo
The aim of this study was to prepare a novel nanoemulsion loaded with poorly water-soluble chlorhexidine acetate (CNE) to improve its solubility, and specifically enhance the antimicrobial activity against Streptococcus mutans in vitro and in vivo. In this study, a novel CNE nanoemulsion with an ave...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4296965/ https://www.ncbi.nlm.nih.gov/pubmed/25624759 http://dx.doi.org/10.2147/IJN.S72920 |
_version_ | 1782353075684507648 |
---|---|
author | Li, Yun Fei Sun, Hong Wu Gao, Rong Liu, Kai Yun Zhang, Hua Qi Fu, Qi Huan Qing, Sheng Li Guo, Gang Zou, Quan Ming |
author_facet | Li, Yun Fei Sun, Hong Wu Gao, Rong Liu, Kai Yun Zhang, Hua Qi Fu, Qi Huan Qing, Sheng Li Guo, Gang Zou, Quan Ming |
author_sort | Li, Yun Fei |
collection | PubMed |
description | The aim of this study was to prepare a novel nanoemulsion loaded with poorly water-soluble chlorhexidine acetate (CNE) to improve its solubility, and specifically enhance the antimicrobial activity against Streptococcus mutans in vitro and in vivo. In this study, a novel CNE nanoemulsion with an average size of 63.13 nm and zeta potential of −67.13 mV comprising 0.5% CNE, 19.2% Tween 80, 4.8% propylene glycol, and 6% isopropyl myristate was prepared by the phase inversion method. Important characteristics such as the content, size, zeta potential, and pH value of CNE did not change markedly, stored at room temperature for 1 year. Also, compared with chlorhexidine acetate water solution (CHX), the release profile results show that the CNE has visibly delayed releasing effect in both phosphate-buffered saline and artificial saliva solutions (P<0.005). The minimum inhibitory concentration and minimum bactericidal concentration of CHX for S. mutans (both 0.8 μg/mL) are both two times those of CNE (0.4 μg/mL). Besides, CNE of 0.8 μg/mL exhibited fast-acting bactericidal efficacy against S. mutans, causing 95.07% death within 5 minutes, compared to CHX (73.33%) (P<0.01). We observed that 5 mg/mL and 2 mg/mL CNE were both superior to CHX, significantly reducing oral S. mutans numbers and reducing the severity of carious lesions in Sprague Dawley rats (P<0.05), in an in vivo test. CNE treatment at a concentration of 0.2 μg/mL inhibited biofilm formation more effectively than CHX, as indicated by the crystal violet staining method, scanning electron microscopy, and atomic force microscopy. The cell membrane of S. mutans was also severely disrupted by 0.2 μg/mL CNE, as indicated by transmission electron microscopy. These results demonstrated that CNE greatly improved the solubility and antimicrobial activity of this agent against S. mutans both in vitro and in vivo. This novel nanoemulsion is a promising medicine for preventing and curing dental caries. |
format | Online Article Text |
id | pubmed-4296965 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-42969652015-01-26 Inhibited biofilm formation and improved antibacterial activity of a novel nanoemulsion against cariogenic Streptococcus mutans in vitro and in vivo Li, Yun Fei Sun, Hong Wu Gao, Rong Liu, Kai Yun Zhang, Hua Qi Fu, Qi Huan Qing, Sheng Li Guo, Gang Zou, Quan Ming Int J Nanomedicine Original Research The aim of this study was to prepare a novel nanoemulsion loaded with poorly water-soluble chlorhexidine acetate (CNE) to improve its solubility, and specifically enhance the antimicrobial activity against Streptococcus mutans in vitro and in vivo. In this study, a novel CNE nanoemulsion with an average size of 63.13 nm and zeta potential of −67.13 mV comprising 0.5% CNE, 19.2% Tween 80, 4.8% propylene glycol, and 6% isopropyl myristate was prepared by the phase inversion method. Important characteristics such as the content, size, zeta potential, and pH value of CNE did not change markedly, stored at room temperature for 1 year. Also, compared with chlorhexidine acetate water solution (CHX), the release profile results show that the CNE has visibly delayed releasing effect in both phosphate-buffered saline and artificial saliva solutions (P<0.005). The minimum inhibitory concentration and minimum bactericidal concentration of CHX for S. mutans (both 0.8 μg/mL) are both two times those of CNE (0.4 μg/mL). Besides, CNE of 0.8 μg/mL exhibited fast-acting bactericidal efficacy against S. mutans, causing 95.07% death within 5 minutes, compared to CHX (73.33%) (P<0.01). We observed that 5 mg/mL and 2 mg/mL CNE were both superior to CHX, significantly reducing oral S. mutans numbers and reducing the severity of carious lesions in Sprague Dawley rats (P<0.05), in an in vivo test. CNE treatment at a concentration of 0.2 μg/mL inhibited biofilm formation more effectively than CHX, as indicated by the crystal violet staining method, scanning electron microscopy, and atomic force microscopy. The cell membrane of S. mutans was also severely disrupted by 0.2 μg/mL CNE, as indicated by transmission electron microscopy. These results demonstrated that CNE greatly improved the solubility and antimicrobial activity of this agent against S. mutans both in vitro and in vivo. This novel nanoemulsion is a promising medicine for preventing and curing dental caries. Dove Medical Press 2015-01-09 /pmc/articles/PMC4296965/ /pubmed/25624759 http://dx.doi.org/10.2147/IJN.S72920 Text en © 2015 Li et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Li, Yun Fei Sun, Hong Wu Gao, Rong Liu, Kai Yun Zhang, Hua Qi Fu, Qi Huan Qing, Sheng Li Guo, Gang Zou, Quan Ming Inhibited biofilm formation and improved antibacterial activity of a novel nanoemulsion against cariogenic Streptococcus mutans in vitro and in vivo |
title | Inhibited biofilm formation and improved antibacterial activity of a novel nanoemulsion against cariogenic Streptococcus mutans in vitro and in vivo |
title_full | Inhibited biofilm formation and improved antibacterial activity of a novel nanoemulsion against cariogenic Streptococcus mutans in vitro and in vivo |
title_fullStr | Inhibited biofilm formation and improved antibacterial activity of a novel nanoemulsion against cariogenic Streptococcus mutans in vitro and in vivo |
title_full_unstemmed | Inhibited biofilm formation and improved antibacterial activity of a novel nanoemulsion against cariogenic Streptococcus mutans in vitro and in vivo |
title_short | Inhibited biofilm formation and improved antibacterial activity of a novel nanoemulsion against cariogenic Streptococcus mutans in vitro and in vivo |
title_sort | inhibited biofilm formation and improved antibacterial activity of a novel nanoemulsion against cariogenic streptococcus mutans in vitro and in vivo |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4296965/ https://www.ncbi.nlm.nih.gov/pubmed/25624759 http://dx.doi.org/10.2147/IJN.S72920 |
work_keys_str_mv | AT liyunfei inhibitedbiofilmformationandimprovedantibacterialactivityofanovelnanoemulsionagainstcariogenicstreptococcusmutansinvitroandinvivo AT sunhongwu inhibitedbiofilmformationandimprovedantibacterialactivityofanovelnanoemulsionagainstcariogenicstreptococcusmutansinvitroandinvivo AT gaorong inhibitedbiofilmformationandimprovedantibacterialactivityofanovelnanoemulsionagainstcariogenicstreptococcusmutansinvitroandinvivo AT liukaiyun inhibitedbiofilmformationandimprovedantibacterialactivityofanovelnanoemulsionagainstcariogenicstreptococcusmutansinvitroandinvivo AT zhanghuaqi inhibitedbiofilmformationandimprovedantibacterialactivityofanovelnanoemulsionagainstcariogenicstreptococcusmutansinvitroandinvivo AT fuqihuan inhibitedbiofilmformationandimprovedantibacterialactivityofanovelnanoemulsionagainstcariogenicstreptococcusmutansinvitroandinvivo AT qingshengli inhibitedbiofilmformationandimprovedantibacterialactivityofanovelnanoemulsionagainstcariogenicstreptococcusmutansinvitroandinvivo AT guogang inhibitedbiofilmformationandimprovedantibacterialactivityofanovelnanoemulsionagainstcariogenicstreptococcusmutansinvitroandinvivo AT zouquanming inhibitedbiofilmformationandimprovedantibacterialactivityofanovelnanoemulsionagainstcariogenicstreptococcusmutansinvitroandinvivo |