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A Historical Review of Brain Drug Delivery

Journal

PHARMACEUTICS
Volume 14, Issue 6, Pages -

Publisher

MDPI
DOI: 10.3390/pharmaceutics14061283

Keywords

blood-brain barrier; endothelium; receptor-mediated transport; carrier-mediated transport; genetic engineering; IgG fusion proteins; nanoparticles; liposomes

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This article reviews the history of brain drug delivery and discusses different technologies and methods. Due to the restricted transport across the blood-brain barrier, FDA-approved drugs for the central nervous system are generally limited to lipid-soluble small molecules.
The history of brain drug delivery is reviewed beginning with the first demonstration, in 1914, that a drug for syphilis, salvarsan, did not enter the brain, due to the presence of a blood-brain barrier (BBB). Owing to restricted transport across the BBB, FDA-approved drugs for the CNS have been generally limited to lipid-soluble small molecules. Drugs that do not cross the BBB can be re-engineered for transport on endogenous BBB carrier-mediated transport and receptor-mediated transport systems, which were identified during the 1970s-1980s. By the 1990s, a multitude of brain drug delivery technologies emerged, including trans-cranial delivery, CSF delivery, BBB disruption, lipid carriers, prodrugs, stem cells, exosomes, nanoparticles, gene therapy, and biologics. The advantages and limitations of each of these brain drug delivery technologies are critically reviewed.

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