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Its selective lipolytic action, minimal systemic effects, and ability to mobilize fatty acids make it invaluable in preclinical studies of obesity, metabolic function, and adipocyte biology

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The second is dose and route translation : even where an effect is real in a mouse, the human-equivalent dose is not a simple body-weight scaling, and as the route section above stressed there is no human bioavailability figure to anchor an oral-versus-injected comparison

In that scenario, three 10 mg vials over twelve weeks costs more per milligram but wastes nothing