Performance evaluation of bactericidal effect and endotoxin inactivation by low‐temperature ozone/hydrogen peroxide mixed gas exposure

Author:

Nomura Yusuke1,Yamamura Junji2,Fukui Chie1,Fujimaki Hideo3,Sakamoto Kazuyuki2,Matsuo Ken‐ichi2,Kuromatsu Hisashi2,Kikuchi Yutaka4,Haishima Yuji1

Affiliation:

1. Division of Medical Devices National Institute of Health Sciences Kawasaki‐shi Kanagawa Japan

2. Environment and Cleran Group, Strategy Development Department Industrial Systems and General‐Purpose Machinery Business Area, IHI Corporation Tokyo Japan

3. Research Department Public Welfare Institute of Scientific Research Foundation Tokyo Japan

4. Division of Microbiology National Institute of Health Sciences Kawasaki‐shi Kanagawa Japan

Publisher

Wiley

Subject

Biomedical Engineering,Biomaterials

Reference31 articles.

1. A compendium of processes materials test methods and acceptance criteria for cleaning reusable medical devices. Technical information report. AMMI TIR30: 2011/(R)2016.

2. DGKH DGSV AKI.Validation and routine monitoring of automated cleaning and thermal disinfection processes for medical devices (5thed. 2017) Zentral Sterilisation suppl2017.

3. Guideline for evaluation and assessment of medical instrument cleanliness. Japanese Society of Medical Instrumentation 2012.

4. Gram‐negative bacterial endotoxin and the pathogenesis of fever;Snell ES;Prog Drug Res,1975

5. Role of hypothalamic interleukin‐6 and tumor necrosis factor‐alpha in LPS fever in rat;Klir JJ;Am J Physiol,1993

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