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Several pharmacokinetic characteristics significantly contribute to the low bioavailability of catechins: - low chemical stability within the conditions of the gastrointestinal tract
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Quantity::5 MG
the molecule may not be absorbed effectively in the digestive tract the dose may be too small to influence cellular physiology the compound may break down before reaching target tissues the body may rapidly eliminate it through the liver or kidneys Even when a compound is absorbed into the bloodstream, that does not necessarily mean it will influence cellular biology
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