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To overcome these limitations, this review discusses a range of structural modifications, including N-terminal and C-terminal substitutions, fatty acid conjugation, and large molecule fusion technologies, which have collectively contributed to enhanced half-life, increased stability, improved receptor affinity, and retained or augmented bioactivity of GLP-1 analogs

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These medications work by binding to GLP-1 receptors in the body, which increases insulin production in response to food intake and suppresses glucagon, a hormone that raises blood sugar