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Description
The development of therapies for central nervous system disorders is still a major pharmacological challenge. Efflux transporters (ABC transporters) expressed at the blood brain barrier (BBB) and at the blood-cerebrospinal fluid barrier (BCSFB), are main obstacles for the delivery of therapeutic compounds into the CNS, compromising the effective treatment of brain cancer, brain metastasis from peripheral cancers and many other neurologic diseases (1). Reducing the expression and activity of these transporters while treating a brain disorder or choosing the time of the day when their activity