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Strategic Approaches to Optimizing Peptide ADME Properties

Journal

AAPS JOURNAL
Volume 17, Issue 1, Pages 134-143

Publisher

SPRINGER
DOI: 10.1208/s12248-014-9687-3

Keywords

ADME; peptides; pharmacokinetics; proteolysis; renal clearance

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Development of peptide drugs is challenging but also quite rewarding. Five blockbuster peptide drugs are currently on the market, and six new peptides received first marketing approval as new molecular entities in 2012. Although peptides only represent 2% of the drug market, the market is growing twice as quickly and might soon occupy a larger niche. Natural peptides typically have poor absorption, distribution, metabolism, and excretion (ADME) properties with rapid clearance, short half-life, low permeability, and sometimes low solubility. Strategies have been developed to improve peptide drugability through enhancing permeability, reducing proteolysis and renal clearance, and prolonging half-life. In vivo, in vitro, and in silico tools are available to evaluate ADME properties of peptides, and structural modification strategies are in place to improve peptide developability.

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