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Since DSIP is not FDA-approved, its long-term safety, purity, and dosing are uncertain
Since the ultimate goal of the project was to produce a clinically relevant molecule that could be delivered peripherally but still exhibit procognitive/antidementia activity, the effectiveness of both the intraperitoneal and oral delivery routes of dihexa administration were determined using the scopolamine model
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JG: Formal Analysis, Writing review and editing, Validation
