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Subsequently, to reduce the dosage intervals and enhance the bio availability, the drug releasing pattern of Glibenclamide was modified by forming mucoadhesive beads using sodium alignate and okra gum for drug entrapment, allowing sustained release for up to 8 h in the body [2, 78]

Bioscience Reports, May 2021, ePublication 3

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Intranasal peptide administration has become an increasingly valuable area of pharmaceutical research because it offers a practical model for evaluating peptide transport and formulation performance