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. 2014 Jan 22;9(1):e86091. doi: 10.1371/journal.pone.0086091

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© 2014 Assayag et al

This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.

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ASM-024 was administered by (A) nebulization of a solution and (B) orally to OVA-sensitized mice. A dose-related inhibition of inflammation is observed, no further inhibitory effect observed at a dose higher than 10 mg/kg p.o.; Values are mean ± SD. * Significantly different from vehicle control groups; p≤0.001; n = 8–9; ED₅₀ p.o. = 3.55 mg/kg; ED₅₀ inhalation = 0.03 mg/kg.