Prevention of murine influenza A virus pneumonitis by surfactant nano-emulsions

被引:38
作者
Donovan, BW
Reuter, JD
Cao, ZY
Myc, A
Johnson, KJ
Baker, JR [1 ]
机构
[1] Univ Michigan, Ctr Biol Nanotechnol, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Internal Med, Div Allergy, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Unit Lab Anim Med, Ann Arbor, MI 48109 USA
[4] Univ Michigan, Dept Pathol, Ann Arbor, MI 48109 USA
关键词
non-ionic surfactant; nano-emulsion; mice; enveloped virus; influenza A virus;
D O I
10.1177/095632020001100104
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Non-ionic surfactant nano-emulsions have extensive anti-microbial activity and are biocompatible with skin and mucous membranes at effective concentrations. Two nano-emulsion formulations (8N8 and 20N10) made from soybean oil, tributyl phosphate and Triton X-100, were tested for their ability to prevent murine influenza virus pneumonia in vivo. In the initial study, CD-1 mice were administered various dilutions of the nano-emulsions intranasally, and safe dosages and concentrations were determined. Non-toxic concentrations of the nano-emulsions were then mixed with influenza virus and applied to the nares of mice. Animals receiving mixtures of two different emulsions (8N8 or 20N10) and a LD,, of virus survived the challenge without evidence of viral infection. To determine if the nano-emulsions could prevent influenza virus infection in vivo when used as a prophylactic treatment, the nano-emulsions (8N8 at 1.0% and 20N10 at 1.0% or 0.2%) were applied to mouse nares 90 min before exposure to 5 x 10(5) p.f.u./ml virus by nebulized aerosol. Animals pretreated with the nano-emulsions had significantly decreased clinical signs of infection. Only 26.0% (8N8 at 1.0%), 31.25% (20N10 at 1.0%) and 37.0% (20N10 at 0.2%) of animals pretreated with nano-emulsion died from pneumonitis, whereas >80.0% of mock pretreated animals succumbed to infection (P < 0.005). These findings suggest that nonionic surfactant nano-emulsions have therapeutic potential for the prevention of influenza virus infection in vivo.
引用
收藏
页码:41 / 49
页数:9
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