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Neither conclusion can be applied to humans at typical compounded doses (250 to 500 mcg subcutaneously) because: Rodent doses (10 mcg/kg intraperitoneally) do not translate linearly to human subcutaneous pharmacokinetics
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It is studied for its involvement in cellular signaling pathways, structural protein support, regenerative processes, and oxidative stress models
Injectable administration is hypothesized to provide systemic distribution, but human pharmacokinetic data for this route does not exist
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