Center for Bioelectrics, Old Dominion University, Norfolk, Virginia, USA.
State Key Lab of Electrical Insulation and Power Equipment, Center for Plasma Biomedicine, Xi'an Jiaotong University, Xi'an, Shaanxi, China.
Gastrointest Endosc. 2019 Jan;89(1):105-114. doi: 10.1016/j.gie.2018.08.009. Epub 2018 Aug 16.
It has been increasingly recognized that the safety of GI endoscopes needs to be improved by addressing the small margin of safety of high-level disinfectants (HLDs) and the failure of HLDs to clear multidrug-resistant organisms and biofilms. There is also an unmet need for effective low-temperature sterilization techniques that have a clear pathway for U.S. Food and Drug Administration clearance. Here, we report the results of our investigation of a novel argon plasma-activated gas (PAG) for disinfection and potentially sterilization of biofilm-contaminated endoscopic channels.
Test polytetrafluoroethylene channel segments were contaminated with 4-, 24- and 48-hour luminal biofilms of methicillin-resistant Staphylococcus aureus, Pseudomonas aeruginosa, or Escherichia coli and were treated by PAG flowing for up to 9 minutes. After PAG treatment, inactivation and dispersal of luminal bacterial biofilms and their regrowth in 48 hours were evaluated. Reactive species induced by PAG were measured with colorimetric probes and electron spin resonance spectrometry. Surface morphology and elemental composition of PAG-treated channel material were analyzed with scanning electron microscopy.
PAG treatment for 9 minutes led to more than 8 log reduction of viable cells and dispersal of 24- and 48-hour luminal biofilms of all 3 bacteria and to suppression of their regrowth, whereas it resulted in little morphologic abnormalities in channel material. Ozone concentration of PAG fell to below .01 ppm within 30 seconds of switching off the plasma. PAG-treated deionized water was acidified with numerous types of reactive species, each with a concentration some 3 orders of magnitude or more below its bacterial inhibition concentration.
PAG is capable of effectively and rapidly disinfecting luminal bacterial biofilms and offers an alternative to the step of HLDs and/or ethylene oxide in the endoscope reprocessing procedure with safety to personnel and environment.
人们越来越认识到,需要通过解决高水平消毒剂(HLD)安全性余量小以及 HLD 无法清除多药耐药菌和生物膜的问题,来提高 GI 内窥镜的安全性。此外,还需要有效的低温灭菌技术,这些技术需要有明确的美国食品和药物管理局(FDA)清除途径。在这里,我们报告了我们对新型氩等离子体激活气体(PAG)用于消毒和潜在生物膜污染内窥镜通道灭菌的研究结果。
用耐甲氧西林金黄色葡萄球菌、铜绿假单胞菌或大肠杆菌的 4 小时、24 小时和 48 小时内腔生物膜污染测试聚四氟乙烯通道段,并通过流动的 PAG 处理长达 9 分钟。PAG 处理后,评估内腔细菌生物膜的失活和分散以及它们在 48 小时内的再生长情况。用比色探针和电子自旋共振光谱法测量 PAG 诱导的反应性物质。用扫描电子显微镜分析 PAG 处理过的通道材料的表面形态和元素组成。
PAG 处理 9 分钟可使 3 种细菌的 24 小时和 48 小时内腔生物膜的活菌数减少 8 个对数以上,并使生物膜分散,同时对通道材料几乎没有形态异常。等离子体关闭后 30 秒内,PAG 的臭氧浓度降至.01 ppm 以下。PAG 处理的去离子水被多种类型的反应性物质酸化,每种物质的浓度比其抑制细菌的浓度低 3 个数量级或更多。
PAG 能够有效地快速消毒内腔细菌生物膜,为内窥镜再处理程序中的 HLD 和/或环氧乙烷步骤提供了替代方案,对人员和环境都具有安全性。