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银离子浸渍隐形眼镜盒中的细菌生物膜。

Bacterial biofilm in silver-impregnated contact lens cases.

机构信息

School of Optometry and Vision Science, University of New South Wales, Sydney, New South Wales, 2052, Australia.

School of Optometry and Vision Science, University of New South Wales, Sydney, New South Wales, 2052, Australia.

出版信息

Cont Lens Anterior Eye. 2020 Aug;43(4):408-412. doi: 10.1016/j.clae.2019.11.004. Epub 2019 Nov 23.

Abstract

PURPOSE

This study investigated the efficacy of pre-conditioning lens cases on bacterial biofilm formation and removal.

METHODS

Silver impregnated (MicroBlock / ProGuard™ & i-Clean) and control storage cases were pre-conditioned for 24 h with their respective multipurpose solutions (MPDSs). Cases were then inoculated with 2 ml of 10 CFU/mL of ocular isolates of either P. aeruginosa or S. aureus and incubated for 48 h. Cases were subsequently disinfected (4-6 hours) as per the manufacturer's recommended disinfecting time (MRDT) followed by the recommended case hygiene procedures - recapping wet (MicroBlock / ProGuard™ cases only) or rinse and air-dry or rinse, tissue-wipe and air dry (mechanical disruption). Surviving bacteria were enumerated using standard techniques.

RESULTS

Pre-conditioning the MicroBlock / ProGuard™ cases with MPDS significantly reduced biofilm formation (-1.1 log CFU, p < 0.01 for P. aeruginosa & -1.3 log, p < 0.001, CFU for S. aureus) compared to the i-Clean lens cases. Maintaining the MicroBlock / ProGuard™ lens cases wet after the MRDT resulted in partial removal of bacterial biofilms (-2.9 log CFU, p < 0.001 for P. aeruginosa and -2.6 log CFU, p < 0.001 for S. aureus). Air-drying of all three types of lens storage cases after MRDT significantly reduced the bacterial biofilm (-5.4 log CFU, p < 0.001 for P. aeruginosa and -3.5 log CFU, p < 0.001 for S. aureus). Mechanical disruption produced the greatest reduction in the levels of bacterial biofilm in all 3 types of lens cases tested (-6.8 log CFU, p < 0.001 for P. aeruginosa and -4.5 log CFU, p < 0.001 for S. aureus). Synergi MPDS was significantly better than AQuify MPDS in removing bacterial biofilm from all 3 lens case types for case hygiene treatments with an air-drying step.

CONCLUSION

Pre-conditioning of silver-impregnated ProGuard™ lens cases inhibited initial bacterial biofilm formation. Synergi MPDS was more effective than AQuify MPDS in removing bacterial biofilm in silver impregnated cases and tissue-wiping significantly improved biofilm removal.

摘要

目的

本研究旨在探究预处理镜片盒对细菌生物膜形成和去除的效果。

方法

采用载银(MicroBlock/ProGuardTM&i-Clean)和对照储存盒,用各自的多功能溶液(MPDS)预处理 24 小时。然后,将 2ml 浓度为 10CFU/ml 的铜绿假单胞菌或金黄色葡萄球菌眼部分离株接种到镜片盒中,并孵育 48 小时。随后,按照制造商推荐的消毒时间(MRDT)进行消毒(4-6 小时),然后按照推荐的镜片盒清洁程序进行操作——湿盖(仅 MicroBlock/ProGuardTM 镜片盒)或冲洗并风干或冲洗、纸巾擦拭并风干(机械破坏)。使用标准技术对存活细菌进行计数。

结果

与 i-Clean 镜片盒相比,用 MPDS 预处理 MicroBlock/ProGuardTM 镜片盒可显著减少生物膜形成(铜绿假单胞菌减少 1.1logCFU,p<0.01;金黄色葡萄球菌减少 1.3logCFU,p<0.001)。MRDT 后保持 MicroBlock/ProGuardTM 镜片盒湿润可部分去除细菌生物膜(铜绿假单胞菌减少 2.9logCFU,p<0.001;金黄色葡萄球菌减少 2.6logCFU,p<0.001)。MRDT 后所有三种类型的镜片储存盒风干均可显著减少细菌生物膜(铜绿假单胞菌减少 5.4logCFU,p<0.001;金黄色葡萄球菌减少 3.5logCFU,p<0.001)。机械破坏可使三种类型的镜片盒中细菌生物膜水平显著降低(铜绿假单胞菌减少 6.8logCFU,p<0.001;金黄色葡萄球菌减少 4.5logCFU,p<0.001)。在所有三种镜片盒类型的镜片盒卫生处理中,Synergi MPDS 比 AQuify MPDS 更能有效地去除细菌生物膜,尤其是在风干步骤后。

结论

载银 ProGuardTM 镜片盒的预处理可抑制初始细菌生物膜形成。Synergi MPDS 比 AQuify MPDS 更能有效地去除载银镜片盒中的细菌生物膜,而纸巾擦拭可显著提高生物膜去除率。

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