제출 정보
마가은 (건국대학교)
박주호 (건국대학교)
초록
Peptide therapeutics represent an important class of biomacromolecular drugs, yet their clinical application remains limited by poor oral bioavailability. Here, we report a supramolecular biohybrid nanocomplex for oral delivery of the peptide drug semaglutide, where the peptide itself functions as a polymeric therapeutic component. A positively charged bile acid–peptide conjugate forms a reversible non-covalent assembly with semaglutide, enabling transporter-mediated endocytosis via ASBT while preserving peptide integrity under gastrointestinal conditions. This study highlights how biomacromolecular peptides can be engineered through supramolecular interactions, offering a bio-convergent strategy that connects peptide-based polymers with next-generation drug delivery technologies.
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