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BPC-157 stands out for its stability in stomach acid and its broad gastrointestinal record, while TB-500 stands out for its actin-regulation mechanism and wound-closure data

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4.5 Pharmacokinetic, tissue distribution, and excretion studies in rats administered radioactive-labeled BPC157 Thirty intact SD rats, six JVC rats, and six BDC rats (half male and half female subjects) were injected intramuscularly with 100 g/300 Ci/kg of [3H]BPC157

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