The phrase "acid ear" is not a standard or widely recognized expression in written English.
It may be used in specific contexts, such as in music or art discussions, to describe a particular sensitivity or reaction to certain sounds or styles.
Example: "Her acid ear for music allows her to pick out the most intricate details in a song that others might miss."
Alternatives: "keen ear" or "sensitive ear".
As expected, 2.5% ketoprofen gel nearly completely suppressed the arachidonic acid induced ear swelling (Fig. 3).
Arachidonic acid (AA) ear edema was performed according to Young et al. [ 15].
Bucladesine, administered topically as water-free cream formulation, was capable of reducing the arachidonic acid induced ear swelling.
In the arachidonic acid induced ear oedema model in mice, single or multiple administration of an emulsion containing 1.5% was capable of significantly reducing the inflammatory oedema.
The anti-inflammatory activity of methanol extract was evaluated by using three screening protocols, namely, carrageenan-induced paw edema, arachidonic acid-induced ear edema, and formaldehyde-induced arthritis.
Suitable acute (carrageenan-induced paw edema, arachidonic acid-induced ear edema, xylene-induced ear edema) and chronic (cotton pellet granuloma) models were employed to investigate in vivo the anti-inflammatory activity.
He tried to pour acid into his ears to block out the 'noise' of the world, leaving one ear permanently deaf".
Here, three distinctive meadow types are developing before our eyes – with lesser stitchwort, meadow buttercups and sorrel on the silty, acid soil; mouse-ear-hawkweed, birds-foot trefoil and ox-eyes on the lime-rich, brashy forest marble and loam soils; and clustered rush and common spotted orchids (500 spikes in one spot) on poorly-draining clays.
flush your dog's ears with a product containing salicylic acid (which helps wet ear canals dry).
Topical application of OG but not 5- tetradecyloxy -2-furoic acid significantly reduced hamster ear sebaceous gland size, indicating that this pro-drug approach was critical to obtain the desired activity in vivo.
