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Validation of Bioanalytical Method The validation was executed as per Guidance for industry: Bioanalytical Method Validation from the United States Food and Drug Administration ( Selectivity The selectivity of the method was evaluated by analyzing blank plasma samples prior to spiking

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Products are supplied as lyophilised powder for stability during storage and transport

The only peptides that survive oral administration are those specifically modified with protective groups or encapsulated in enteric coatings