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The pharmacokinetics of pramlintide are comparable to rapid acting insulin

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The impaired interaction decelerated the oxidative half-reaction and decreased the steady-state concentration of available glutathionylated enzyme for the rate-limiting turnover of GSH

When taken orally, this protein gets broken down into its amino acids, just like any protein molecule, so studies show the complete antioxidant doesnt really make it out of digestion intact

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