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(2024) focused on overcoming the challenges associated with the oral delivery of the vancomycin derivative FU002, which has poor bioavailability

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Cells continuously treated with Peg-rhArgI for 48 h showed no evidence of cytotoxicity or loss of cell viability, but were able to potently inhibit HSV-1 and HSV-2 viral replication, cell-to-cell spread/transmission, production of mature and infectious virus, and virus-mediated cytopathic effects

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