Bioconjugate Chemistry · 2020 · 19 citations · 33 references
MedicineEndocrinologyPharmacologyDiabetologyDrug DeliverySignal TransductionDiabetes ManagementDiabetes MellitusGlycemic ControlIncretin-based TherapiesPancreatic HormonesProteolytic ProcessingGlucagon-like PeptidesGlucose-dependent Insulin SecretionGlucose-stimulated Insulin SecretionHormone Secondary StructureIncretin HormonesInsulin Secretion EnhancementProteolytic InactivationProteolytic Stability
Glucagon-like peptide-1 (GLP-1) is of particular interest for treating type 2 diabetes mellitus (T2DM), as it induces insulin secretion in a glucose-dependent fashion and has the potential to facilitate weight control. However, native GLP-1 is a short incretin peptide that is susceptible to fast proteolytic inactivation and rapid clearance from the circulation. Various GLP-1 analogs and bioconjugation of GLP-1 analogs have been developed to counter these issues, but these modifications are frequently accompanied by the sacrifice of potency and the induction of immunogenicity. Here, we demonstrated that with the conjugation of a zwitterionic polymer, poly(carboxybetaine) (pCB), the pharmacokinetic properties of native GLP-1 were greatly enhanced without serious negative effects on its potency and secondary structure. The pCB conjugated GLP-1 further provided glycemic control for up to 6 days in a mouse study. These results illustrate that the conjugation of pCB could realize the potential of using native GLP-1 for prolonged glycemic control in treating T2DM.
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Discovery of the Once-Weekly Glucagon-Like Peptide-1 (GLP-1) Analogue Semaglutide
Jesper Lau, Paw Bloch, Lauge Schäffer et al. · Journal of Medicinal Chemistry · 2015 · 1K citations · Full text
Molecular Understanding and Design of Zwitterionic Materials
Qing Shao, Shaoyi Jiang · Advanced Materials · 2014 · 885 citations