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The intestinal flora of mice treated with AOB was significantly different from that of mice fed high-fat diet
Three key modifications optimize its pharmacokinetics: Aib substitution at position 2 resists DPP-4 cleavage C18 fatty diacid via a hydrophilic linker at Lys26 enables strong, non-covalent albumin binding Arg substitution at position 34 prevents fatty acid binding at the wrong site These modifications produce a half-life of approximately 165 hours (7 days), enabling true once-weekly pharmacokinetics without microsphere encapsulation, plus a daily oral formulation (Rybelsus) using the SNAC absorption enhancer
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The liver is responsible for detoxifying harmful substances and metabolizing drugs
Published January 27, 2021.
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