...
首页> 外文期刊>Biomaterials >A comparison of the use of an ATP-based bioluminescent assay and image analysis for the assessment of bacterial adhesion to standard HEMA and biomimetic soft contact lenses.
【24h】

A comparison of the use of an ATP-based bioluminescent assay and image analysis for the assessment of bacterial adhesion to standard HEMA and biomimetic soft contact lenses.

机译:使用基于ATP的生物发光测定法和图像分析评估细菌对标准HEMA和仿生软性隐形眼镜的粘附力的比较。

获取原文
获取原文并翻译 | 示例

摘要

The aim of this study was to investigate in vitro adhesion of clinically relevant bacteria to standard HEMA and novel biomimetic soft contact lenses (SCL) using bioluminescent ATP assay and image analysis. Unworn SCL were incubated with Pseudomonas aeruginosa, Staphylococcus epidermidis or Serratia marcescens suspended in sterile phosphate buffered saline (PBS). The level of bacterial adhesion after 1, 2, 4, 6 and 18h, was assessed using both image analysis and a bioluminescent ATP assay. Species differences in the overall level of adhesion to the different types of lens were observed using both measurement techniques. Generally bacterial adhesion was shown to peak at 4-6 h, then decline to a much lower level by 18 h. After 4 h, adhesion of all species of bacteria to the biomimetic SCL (omafilcon A) was found to be significantly lower than to the standard HEMA SCL (polymacon) (p<0.05. Student's t-test, n = 4). Both these techniques demonstrated that novel biomimetic SCL materials exhibit significantly lower bacterial adhesion in vitro compared to standard HEMA SCL materials. SCL manufactured with these novel biomimetic materials may reduce the risk of infection.
机译:这项研究的目的是使用生物发光ATP分析和图像分析研究临床相关细菌对标准HEMA和新型仿生软性隐形眼镜(SCL)的体外粘附。将未用过的SCL与悬浮在无菌磷酸盐缓冲盐水(PBS)中的铜绿假单胞菌,表皮葡萄球菌或粘质沙雷氏菌孵育。使用图像分析和生物发光ATP测定法评估1、2、4、6和18小时后的细菌粘附水平。使用两种测量技术都可以观察到对不同类型镜片的总体粘附力水平上的物种差异。一般情况下,细菌附着力在4-6小时达到峰值,然后在18小时后降至更低的水平。 4小时后,发现所有细菌对仿生SCL(omafilcon A)的粘附力均显着低于标准HEMA SCL(polymacon)(p <0.05。Student's t检验,n = 4)。这两种技术都证明,与标准HEMA SCL材料相比,新型仿生SCL材料在体外的细菌附着力显着降低。用这些新型仿生材料制造的SCL可以降低感染的风险。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号