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Cyclodextrins, blood-brain barrier, and treatment of neurological diseases.

Authors :
Vecsernyés M
Fenyvesi F
Bácskay I
Deli MA
Szente L
Fenyvesi É
Source :
Archives of medical research [Arch Med Res] 2014 Nov; Vol. 45 (8), pp. 711-29. Date of Electronic Publication: 2014 Dec 04.
Publication Year :
2014

Abstract

Biological barriers are the main defense systems of the homeostasis of the organism and protected organs. The blood-brain barrier (BBB), formed by the endothelial cells of brain capillaries, not only provides nutrients and protection to the central nervous system but also restricts the entry of drugs, emphasizing its importance in the treatment of neurological diseases. Cyclodextrins are increasingly used in human pharmacotherapy. Due to their favorable profile to form hydrophilic inclusion complexes with poorly soluble active pharmaceutical ingredients, they are present as excipients in many marketed drugs. Application of cyclodextrins is widespread in formulations for oral, parenteral, nasal, pulmonary, and skin delivery of drugs. Experimental and clinical data suggest that cyclodextrins can be used not only as excipients for centrally acting marketed drugs like antiepileptics, but also as active pharmaceutical ingredients to treat neurological diseases. Hydroxypropyl-β-cyclodextrin received orphan drug designation for the treatment of Niemann-Pick type C disease. In addition to this rare lysosomal storage disease with neurological symptoms, experimental research revealed the potential therapeutic use of cyclodextrins and cyclodextrin nanoparticles in neurodegenerative diseases, stroke, neuroinfections and brain tumors. In this context, the biological effects of cyclodextrins, their interaction with plasma membranes and extraction of different lipids are highly relevant at the level of the BBB.<br /> (Copyright © 2015 IMSS. Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1873-5487
Volume :
45
Issue :
8
Database :
MEDLINE
Journal :
Archives of medical research
Publication Type :
Academic Journal
Accession number :
25482528
Full Text :
https://doi.org/10.1016/j.arcmed.2014.11.020