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DOI 10.1067/mic.2003.41

Медицинская библиотека · American journal of infection control · 2003

Antimicrobial activity of a new intact skin antisepsis formulation.

Russo Antonello, Viotti Pier Luigi, Vitali Matteo, Clementi Massimo

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

UNLABELLED: Different antiseptic formulations have shown limitations when applied to disinfecting intact skin, notably short-term tolerability and/or efficacy. The purpose of this study was optimizing a new antiseptic formulation specifically targeted at intact skin disinfection and evaluating its in vitro microbicidal activity and in vivo efficacy.

METHODS

The biocidal properties of the antiseptic solution containing 0.5% chloramine-T diluted in 50% isopropyl alcohol (Cloral; Eurospital SpA Trieste, Italy) were measured in vitro versus gram-positive-, gram-negative-, and acid-alcohol-resistant germs and fungi with standard suspension tests in the presence of fetal bovine serum. Virus-inhibiting activity was evaluated in vitro against human cytomegalovirus, herpes simplex virus, poliovirus, hepatitis B virus, and hepatitis C virus. Tests used different methods for the different biologic and in vitro replication capacity of these human viruses. Lastly, Cloral tolerability and skin colonization retardation efficacy after disinfection were studied in vivo.

RESULTS

The antiseptic under review showed fast and sustained antimicrobial activity. The efficacy of Cloral against clinically important bacterial and viral pathogens and fungi was highlighted under the experimental conditions described in this article. Finally, microbial regrowth lag and no side effects were documented in vivo after disinfection of 11 volunteers.

CONCLUSIONS

A stable chloramine-T solution in isopropyl alcohol may be suggested for intact skin antisepsis.

Для цитирования: Russo Antonello, Viotti Pier Luigi, Vitali Matteo, Clementi Massimo. Antimicrobial activity of a new intact skin antisepsis formulation.. American journal of infection control. 2003. DOI: 10.1067/mic.2003.41.

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