Orally available exendin
By forming a complex with incretin or its analogues and a hydrophobic ionic agent and encapsulating it in SEDDS, the problems of insufficient stability and bioavailability of oral formulations in the prior art are solved, and the effects of prolonged glycemic control and HbA1c reduction are achieved.
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- ALBUNEXT LLC
- Filing Date
- 2024-12-16
- Publication Date
- 2026-06-30
AI Technical Summary
Existing oral insulin and GLP-1 analog formulations have shortcomings in terms of stability and bioavailability, especially in cases where long-term blood glucose reduction is required, making it difficult to achieve effective blood glucose control.
Incretin or its analogues are combined with hydrophobic ionic agents to form hydrophobic ionic complexes, which are then encapsulated in a self-emulsifying drug delivery system (SEDDS). The lipid phase of the SEDDS is used for formulation to create a stable oral formulation.
It achieves prolonged glycemic control after oral administration, reduces blood glucose levels and HbA1c, and has stable drug release and improved bioavailability.
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Figure CN122318976A_ABST
Abstract
Citation Information
Patent Citations
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