A Nanocarrier Approach for Oral Peptide Delivery: Evaluation of Cell‐Penetrating‐Peptide‐Modified Liposomal Formulations in Dogs

Abstract: Oral delivery of peptides is severely limited by their instability and poor absorption in the gastrointestinal tract. In contrast to coadministration strategies using medium‐chain fatty acids, which have recently gained regulatory approval with low oral bioavailabilities ≤ 1% (Rybelsus and Mycapssa), efforts to clinically implement delivery systems based on nanocarriers have not been successful to date. The approved drug‐delivery formulations show fairly accurate correlation between clinical results and nonrodent mammal bioavailability, including Beagle dogs for Rybelsus, indicating that Beagle dogs represent a translationally relevant model. Here, a nanocarrier formulation for the oral administration of peptide therapeutics is reported with systemic targets consisting of liposomes decorated with cyclic cell‐penetrating peptides, which significantly increase oral bioavailability in translationally relevant Beagle dogs. This nanocarrier formulation is optimized using the glycopeptide vancomycin, and results in a considerable oral bioavailability of 3.9%. Further, this nanocarrier system increases the oral bioavailability of the large linear peptide therapeutic exenatide 20‐fold, and consistently achieves effective plasma concentrations in Beagle dogs.

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• Location: Deutsche Nationalbibliothek Frankfurt am Main
• Extent: Online-Ressource
• Language: Englisch

References and Relationships

• Bibliographic citation: A Nanocarrier Approach for Oral Peptide Delivery: Evaluation of Cell‐Penetrating‐Peptide‐Modified Liposomal Formulations in Dogs ; day:10 ; month:07 ; year:2023 ; extent:12 ; Advanced therapeutics ; (10.07.2023) (gesamt 12)

Contributors, Places and Time

• Creator: Uhl, Philipp ; Bajraktari‐Sylejmani, Gzona ; Witzigmann, Dominik ; Bay, Cindy ; Zimmermann, Stefan ; Burhenne, Jürgen ; Weiss, Johanna ; Haefeli, Walter E. ; Sauter, Max

Further information

• DOI: 10.1002/adtp.202300021
• URN: urn:nbn:de:101:1-2023071015362198559578
• Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.