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Research from the original patent holders of BPC-157 suggests the arginate form can boost oral bioavailability from less than 3% to greater than 90%
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BPC-157 appears to remain stable and active when taken orally
That being said, the high doses of the nootropic measured at 0.5 mg/kg/day for intraperitoneal delivery and 2.0 mg/kg/day for oral delivery, and resulted in a performance that was indistinguishable from the control group and significantly better than the animals treated with scopolamine alone [2]
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