Ex vivo porcine vaginal mucosal model of infection for determining effectiveness and toxicity of antiseptics

被引:14
作者
Anderson, M. J. [1 ]
Scholz, M. T. [2 ]
Parks, P. J. [3 ]
Peterson, M. L. [1 ]
机构
[1] Univ Minnesota, Dept Expt & Clin Pharmacol, Coll Pharm, Minneapolis, MN 55455 USA
[2] 3M Co, Infect Prevent, St Paul, MN 55144 USA
[3] 3M Co, Crit & Chron Care Solut, St Paul, MN 55144 USA
关键词
antiseptic; decolonization; MRSA; mucosal model; toxicity; RESISTANT STAPHYLOCOCCUS-AUREUS; MUPIROCIN RESISTANCE; HAND DISINFECTION; NASAL CARRIAGE; BUCCAL MUCOSA; SKIN; CULTURE; TISSUE; HIV-1; EPIDEMIOLOGY;
D O I
10.1111/jam.12277
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Aims: To develop a semi-high-throughput ex vivo mucosal model for determining efficacy and toxicity of antiseptics. Methods and Results: Explants (5mm) from freshly excised, porcine vaginal mucosa were infected with methicillin-sensitive Staphylococcus aureus (1x10(6)CFU) at the epithelial surface for 2h. Haematoxylin and eosin staining revealed healthy uninfected tissue and only minor disruptions in tissue infected with methicillin susceptible Staph. aureus (MSSA), which remained in outer epithelial cell layers. After 2h infection, 10l of chlorhexidine digluconate (CHG, 3%), povidone-iodine (PI, 7<bold>5</bold>%), octenidine dihydrochloride (OCT, 0<bold>1</bold>%) or polyhexamethylene biguanide (PHMB, 0<bold>1</bold>%) was applied. Antiseptics significantly reduced MSSA (1-4 log(10)CFU/explants) after 0<bold>25</bold>h to 4h. CHG, PHMB and OCT exhibited persistence at 24h. In broth culture, CHG 0<bold>012</bold>% and PI 0<bold>625</bold>% achieved >6 log(10) reductions at 2h. PI-based formulations were more efficacious than unformulated PI. PI-based formulations exhibited no significant cytotoxicity on explants using an MTT assay. Conclusions: All antiseptics tested in the mucosal MSSA infection model reduced MSSA. CHG and PI were more potent in broth culture. Significance and Impact of the Study: We developed a semi-high-throughput mucosal model that can identify compounds or formulations with promising antimicrobial and limited cytotoxic properties.
引用
收藏
页码:679 / 688
页数:10
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