Poly(vinyl alcohol) potentiating an inert d-amino acid-based drug for boron neutron capture therapy

Since the discovery of d -amino acids, they have been considered inactive and have not been used as potent drugs. Here, we report that simple mixing with poly(vinyl alcohol) (PVA) unleashed latent potentials of d -amino acids in boron neutron capture therapy (BNCT). PVA formed boronate esters with seemingly useless boronated d -amino acids and induced tumor-associated amino acid transporter-superselective internalization and prolonged intracellular retention, accomplishing complete cure of tumors. The superselective internalization was achieved by switching the internalization pathway from ineffective pass through the transporter to the transporter-mediated endocytosis. The acidic environment in the endo−/lysosome dissociated the boronate esters and elicited the stealthiness of the drugs, preventing their externalization and prolonging intracellular retention time. In a subcutaneous tumor model, this system accomplished surprisingly high tumor-selective accumulation that could not be achieved by conventional approaches and induced drastic BNCT effects. PVA may be a unique material to unlock potentials of seemingly inert molecules. • Simple addition of poly(vinyl alcohol) revealed latent effects of seemingly inert molecules. • Our system interacts specifically with LAT1 and shows astonishingly high tumor accumulation. • We unlocked the potential of a d -amino acid-based drug for cancer therapy.