Reprint

Non-invasive Device-Mediated Brain Drug Delivery across the Blood-Brain Barrier

Edited by
April 2024
244 pages
  • ISBN978-3-7258-0680-5 (Hardback)
  • ISBN978-3-7258-0679-9 (PDF)

This is a Reprint of the Special Issue Non-invasive Device-Mediated Brain Drug Delivery across the Blood-Brain Barrier that was published in

Biology & Life Sciences
Chemistry & Materials Science
Medicine & Pharmacology
Summary

It is well known that the blood–brain barrier (BBB), substantially composed of tight junctions between the capillary endothelial cells and efflux transporters such as MDR1 at the apical membrane of the capillary endothelial cells, prevents drugs from entering the brain. Accordingly, drug delivery into the brain across the BBB is a challenging task, particularly in central nervous system diseases such as Alzheimer’s disease and Parkinson’s disease, as well as brain cancers such as glioma. It is true that drugs in systemic circulation go through intentional membrane disruption or intentional tight junction disruption into the brain across the BBB, but bystander harmful compounds can enter the brain together. Moreover, although craniotomy is often conducted for surgical removal or direct drug administration, this process burdens and torments patients. Thus, non-invasive, device-mediated brain drug delivery across the BBB should be developed to improve not only patient health, but also quality of life. At present, brain drug delivery systems that utilize biological transport machineries such as carrier-mediated transport, receptor-mediated transcytosis, lipid-raft-mediated transcytosis, or macropinocytosis at the BBB have been extensively investigated. This Special Issue aims to share recent progress and trends in this field.

Format
  • Hardback
License and Copyright
© 2022 by the authors; CC BY-NC-ND license
Keywords
glioblastoma; focused ultrasound; blood-brain barrier; PET; SPECT; drug delivery; rotigotine; lecithin-chitosan hybrid nanoparticles; intranasal delivery; nose-to-brain uptake; brain distribution study; in vitro model; blood–brain barrier (BBB); nanoparticles; drug delivery; targeted receptor-mediated transcytosis; ligand conjugation; nicotinic acetylcholine receptor; nanobody; VHH; transferrin receptor; blood-brain barrier; receptor-mediated transcytosis; nanoparticle; liposome; extracellular vesicle; chemotherapy; targeted therapy; drug delivery; blood–brain barrier; brain tumor; glioma; cell-penetrating peptides (CPPs); endosomal entrapment; homing peptides; blood–brain barrier (BBB); tumour-specific markers; siRNA-CPP delivery; blood–brain barrier; nanoparticles; porous silicon nanoparticles; BBB-on-a-chip; ligand density; organ-on-a-chip; nanomedicine; microfluidic model; neurodegenerative disorders; blood–brain barrier; non-invasive delivery; device-related delivery; Alzheimer’s disease; Parkinson’s disease; ALS; Down syndrome; CNS disorders; nasal delivery; biologics; nose-to-brain; the blood–brain barrier; mesenchymal stem cell-based drug delivery; transmembrane drug delivery; n/a

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