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Masses of the peptide fragments were identified using HRMS at an accurate level of mass error below 10 ppm, and their sequences were determined via MS E sequencing using in-source fragmentation, which was also useful for identifying the fatty acid chain modification site

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If these formulations achieve the 50-70% bioavailability seen in some preclinical studies, intranasal delivery could become a practical alternative to injection for a wider range of applications