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A Historical Review of Brain Drug Delivery

Overview
Journal Pharmaceutics
Publisher MDPI
Date 2022 Jun 24
PMID 35745855
Authors
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Abstract

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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References
1.
Cordon-Cardo C, OBrien J, CASALS D, Biedler J, Melamed M, Bertino J . Multidrug-resistance gene (P-glycoprotein) is expressed by endothelial cells at blood-brain barrier sites. Proc Natl Acad Sci U S A. 1989; 86(2):695-8. PMC: 286540. DOI: 10.1073/pnas.86.2.695. View

2.
Logovinsky V, Satlin A, Lai R, Swanson C, Kaplow J, Osswald G . Safety and tolerability of BAN2401--a clinical study in Alzheimer's disease with a protofibril selective Aβ antibody. Alzheimers Res Ther. 2016; 8(1):14. PMC: 4822297. DOI: 10.1186/s13195-016-0181-2. View

3.
Molino Y, David M, Varini K, Jabes F, Gaudin N, Fortoul A . Use of LDL receptor-targeting peptide vectors for and cargo transport across the blood-brain barrier. FASEB J. 2017; 31(5):1807-1827. DOI: 10.1096/fj.201600827R. View

4.
Bies C, Lehr C, Woodley J . Lectin-mediated drug targeting: history and applications. Adv Drug Deliv Rev. 2004; 56(4):425-35. DOI: 10.1016/j.addr.2003.10.030. View

5.
Mullard A . ALS antisense drug falters in phase III. Nat Rev Drug Discov. 2021; 20(12):883-885. DOI: 10.1038/d41573-021-00181-w. View