Cargando…
Physicochemical properties and formulation development of a novel compound inhibiting Staphylococcus aureus biofilm formation
The emergence of antibiotic resistance over the past several decades has given urgency to new antibacterial strategies that apply less selective pressure. A new class of anti-virulence compounds were developed that are active against methicillin-resistant Staphylococcus aureus (MRSA), by inhibiting...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7870075/ https://www.ncbi.nlm.nih.gov/pubmed/33556134 http://dx.doi.org/10.1371/journal.pone.0246408 |
_version_ | 1783648739719643136 |
---|---|
author | Wang, Nan Qi, Feng Yu, Haqing Yestrepsky, Bryan D. Larsen, Scott D. Shi, Honglan Ji, Juan Anderson, David W. Li, Hao Sun, Hongmin |
author_facet | Wang, Nan Qi, Feng Yu, Haqing Yestrepsky, Bryan D. Larsen, Scott D. Shi, Honglan Ji, Juan Anderson, David W. Li, Hao Sun, Hongmin |
author_sort | Wang, Nan |
collection | PubMed |
description | The emergence of antibiotic resistance over the past several decades has given urgency to new antibacterial strategies that apply less selective pressure. A new class of anti-virulence compounds were developed that are active against methicillin-resistant Staphylococcus aureus (MRSA), by inhibiting bacterial virulence without hindering their growth to reduce the selective pressure for resistance development. One of the compounds CCG-211790 has demonstrated potent anti-biofilm activity against MRSA. This new class of anti-virulence compounds inhibited the gene expression of virulence factors involved in biofilm formation and disrupted the biofilm structures. In this study, the physicochemical properties of CCG-211790, including morphology, solubility in pure water or in water containing sodium dodecyl sulfate, solubility in organic solvents, and stability with respect to pH were investigated for the first time. Furthermore, a topical formulation was developed to enhance the therapeutic potential of the compound. The formulation demonstrated acceptable properties for drug release, viscosity, pH, cosmetic elegance and stability of over nine months. |
format | Online Article Text |
id | pubmed-7870075 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-78700752021-02-11 Physicochemical properties and formulation development of a novel compound inhibiting Staphylococcus aureus biofilm formation Wang, Nan Qi, Feng Yu, Haqing Yestrepsky, Bryan D. Larsen, Scott D. Shi, Honglan Ji, Juan Anderson, David W. Li, Hao Sun, Hongmin PLoS One Research Article The emergence of antibiotic resistance over the past several decades has given urgency to new antibacterial strategies that apply less selective pressure. A new class of anti-virulence compounds were developed that are active against methicillin-resistant Staphylococcus aureus (MRSA), by inhibiting bacterial virulence without hindering their growth to reduce the selective pressure for resistance development. One of the compounds CCG-211790 has demonstrated potent anti-biofilm activity against MRSA. This new class of anti-virulence compounds inhibited the gene expression of virulence factors involved in biofilm formation and disrupted the biofilm structures. In this study, the physicochemical properties of CCG-211790, including morphology, solubility in pure water or in water containing sodium dodecyl sulfate, solubility in organic solvents, and stability with respect to pH were investigated for the first time. Furthermore, a topical formulation was developed to enhance the therapeutic potential of the compound. The formulation demonstrated acceptable properties for drug release, viscosity, pH, cosmetic elegance and stability of over nine months. Public Library of Science 2021-02-08 /pmc/articles/PMC7870075/ /pubmed/33556134 http://dx.doi.org/10.1371/journal.pone.0246408 Text en © 2021 Wang et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Wang, Nan Qi, Feng Yu, Haqing Yestrepsky, Bryan D. Larsen, Scott D. Shi, Honglan Ji, Juan Anderson, David W. Li, Hao Sun, Hongmin Physicochemical properties and formulation development of a novel compound inhibiting Staphylococcus aureus biofilm formation |
title | Physicochemical properties and formulation development of a novel compound inhibiting Staphylococcus aureus biofilm formation |
title_full | Physicochemical properties and formulation development of a novel compound inhibiting Staphylococcus aureus biofilm formation |
title_fullStr | Physicochemical properties and formulation development of a novel compound inhibiting Staphylococcus aureus biofilm formation |
title_full_unstemmed | Physicochemical properties and formulation development of a novel compound inhibiting Staphylococcus aureus biofilm formation |
title_short | Physicochemical properties and formulation development of a novel compound inhibiting Staphylococcus aureus biofilm formation |
title_sort | physicochemical properties and formulation development of a novel compound inhibiting staphylococcus aureus biofilm formation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7870075/ https://www.ncbi.nlm.nih.gov/pubmed/33556134 http://dx.doi.org/10.1371/journal.pone.0246408 |
work_keys_str_mv | AT wangnan physicochemicalpropertiesandformulationdevelopmentofanovelcompoundinhibitingstaphylococcusaureusbiofilmformation AT qifeng physicochemicalpropertiesandformulationdevelopmentofanovelcompoundinhibitingstaphylococcusaureusbiofilmformation AT yuhaqing physicochemicalpropertiesandformulationdevelopmentofanovelcompoundinhibitingstaphylococcusaureusbiofilmformation AT yestrepskybryand physicochemicalpropertiesandformulationdevelopmentofanovelcompoundinhibitingstaphylococcusaureusbiofilmformation AT larsenscottd physicochemicalpropertiesandformulationdevelopmentofanovelcompoundinhibitingstaphylococcusaureusbiofilmformation AT shihonglan physicochemicalpropertiesandformulationdevelopmentofanovelcompoundinhibitingstaphylococcusaureusbiofilmformation AT jijuan physicochemicalpropertiesandformulationdevelopmentofanovelcompoundinhibitingstaphylococcusaureusbiofilmformation AT andersondavidw physicochemicalpropertiesandformulationdevelopmentofanovelcompoundinhibitingstaphylococcusaureusbiofilmformation AT lihao physicochemicalpropertiesandformulationdevelopmentofanovelcompoundinhibitingstaphylococcusaureusbiofilmformation AT sunhongmin physicochemicalpropertiesandformulationdevelopmentofanovelcompoundinhibitingstaphylococcusaureusbiofilmformation |