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Description
Background Despite the effectiveness of glucagon-like peptide-1 agonist (GLP-1A) in the treatment of diabetes, its large molecular weight and high hydrophilicity result in poor cellular permeability, thus limiting its oral bioavailability
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However, staying attuned to systemic health trends is equally critical, especially with the rise of GLP-1 receptor agonists (like semaglutide and liraglutide) in managing diabetes and obesity.
