Abstract

본 연구는 P. aeruginosa와 E. hirae을 대상으로 ortho-phenylphenol 20%를 함유한 훈증소독제, Fumagari <TEX>$OPP^{(R)}$</TEX>의 살균효과를 평가하기 위해 수행되었다. 예비 시험에서, P. aeruginosa와 E. hirae의 현탁액 균수는 각각 <TEX>$2.8{\times}10^8$</TEX>와 <TEX>$3.6{\times}10^8CFU/mL$</TEX>이었으며, 모든 훈증소독제에 노출시킨 담체의 균수는 모두 평판배지법과 여과법으로 배양한 시험균주 현탁액의 균수의 50%보다 많았다. 또한, 대조 담체로부터 회복된 P. aeruginosa와 E. hirae 균수는 각각 <TEX>$2.9{\times}10^6$</TEX>와 <TEX>$2.7{\times}10^6CFU/mL$</TEX>이었다. 훈증소독제의 살균효과 시험에서는, 훈증소독제를 처리한 담체의 P. aeruginosa와 E. hirae의 감소 균수는 각각 6.46와 5.19 logCFU/mL로 나타났다. 이상의 결과로부터, 훈증소독제, Fumagari <TEX>$OPP^{(R)}$</TEX>는 P. aeruginosa와 E. hirae에 대해 효과적인 살균력을 갖는 것으로 확인되었으며, 병원성 세균에 오염된 식품재료 및 주방용품의 소독에 적용할 수 있을 것으로 사료된다. This test was performed to evaluate the bactericidal efficacy of a fumigation disinfectant containing 20% ortho-phenylphenol against Pseudomonas aeruginosa (P. aeruginosa) and Enterococcus hirae (E. hirae). In preliminary tests, P. aeruginosa and E. hirae working culture suspension number (N value) were <TEX>$2.8{\times}10^8$</TEX> and <TEX>$4.0{\times}10^8CFU/mL$</TEX>, respectively. And all the colony numbers on the carriers exposed to the fumigant (n1, n2, n3) were higher than 0.5N1 (the number of bacterial test suspentions by pour plate method), 0.5N2 (the number of bacterial test suspentions by filter membrane method) and 0.5N1, respectively. In addition, the mean number of P. aeruginosa and E. hirae recovered on the control-carriers (T value) was <TEX>$2.8{\times}10^8$</TEX> and <TEX>$3.4{\times}10^6CFU/mL$</TEX>, respectively. In the bactericidal effect of the fumigant, the reduction number of <TEX>$2.8{\times}10^8$</TEX> (d value) was 6.46 and 5.19 logCFU/mL, respectively. According to the French standard for the fumigant, the d value for the effective bactericidal fumigant should be over than 5 logCFU/mL. With the results from this study, the fumigation disinfectant containing 20% ortho-phenylphenol has an effective bactericidal activity, then the fumigant can be applied to disinfect food materials and kitchen appliances contaminated with the pathogenic bacteria.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.