The penetration of therapeutics across the blood-brain barrier: Classic case studies and clinical implications.

Cell Rep Med

Geriatric Research Education and Clinical Center, Veterans Affairs Puget Sound Health Care System, Seattle, WA 98108, USA; Division of Gerontology and Geriatric Medicine, Department of Medicine, University of Washington School of Medicine, Seattle, WA 98104, USA.

Published: November 2024

AI Article Synopsis

  • The blood-brain barrier (BBB) protects the brain from harmful substances but also complicates drug development for central nervous system (CNS) conditions.
  • The review discusses how various transport mechanisms work, such as lipid solubility and different transport systems, which affect drug delivery to the brain.
  • It also explores how diseases can disrupt the BBB, allowing for potential treatment methods, and highlights the historical significance of the BBB in drug delivery strategies.

Article Abstract

The blood-brain barrier (BBB) plays central roles in the maintenance and health of the brain. Its mechanisms to safeguard the brain against xenobiotics and endogenous toxins also make the BBB the primary obstacle to the development of drugs for the central nervous system (CNS). Here, we review classic examples of the intersection of clinical medicine, drug delivery, and the BBB. We highlight the role of lipid solubility (heroin), saturable brain-to-blood (efflux: opiates) and blood-to-brain (influx: nutrients, vitamins, and minerals) transport systems, and adsorptive transcytosis (viruses and incretin receptor agonists). We examine how the disruption of the BBB that occurs in certain diseases (tumors) can also be modulated (osmotic agents and microbubbles) and used to deliver treatments, and the role of extracellular pathways in gaining access to the CNS (albumin and antibodies). In summary, this review provides a historical perspective of the key role of the BBB in delivery of drugs to the brain in health and disease.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11604479PMC
http://dx.doi.org/10.1016/j.xcrm.2024.101760DOI Listing

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