PROSPECTS FOR THE USE OF BLOOD APOLIPOPROTEINS FOR DRUG TRANSPORT THROUGH THE BLOOD-BRAIN BARRIER IN ORDER TO THE EMPOWERMENT OF PHARMACOTHERAP


Cite item

Full Text

Abstract

Blood-brain barrier prevents the transport of drugs into the central nervous system. This limits the possibilities of therapy for many diseases. Thus, the drug transport across the blood-brain barrier remains one of the key problems of modern pharmacology. This study investigated the possibility of using blood apolipoproteins to increase of dalargin transport through the bloodbrain barrier. Antinociceptive activity of dalargin (7,5 mg/kg) adsorbed on nanoparticles with different coating was studied on outbred albino mice by the tail-flick test. Delivery of dalargin to the brain was most effective and safe in case of using nanoparticles with apolipoprotein E coating.

References

  1. Begley D. The blood-brain barrier: principles for targeting peptides and drugs to the central nervous system. J Pharm Pharmacol 1996;48:136-146.
  2. Davson H, Segal M. Physiology of the CSF and Blood-Brain Barrier. CRC Press, Boca Raton 1996:1-192.
  3. Minn A, El-Bacha RDS, Bayol-Denizot C, et al. The Blood-Brain Barrier and Drug Delivery to the CNS. Marcel Dekker, New York. 2000:145-170.
  4. Alyautdin R, Gothier D, Petrov V, et al. Analgesic activity of the hexapeptide dalargin adsorbed on the surface of polysorbate 80 -coated poly(butyl cyanoacrylate) nanoparticles Eur. J Pharm Biopharm 1995;41:44-48.
  5. Kreuter J, Alyautdin RN, Kharkevich DA, et al. Passage of peptides through the blood-brain barrier with colloidal polymer particles (nanoparticles). Brain Res. 1995;674:171-74.
  6. Kreuter J, Petrov VE, Kharkevich DA, et al. Influence of the type of surfactant on the analgesic effects induced by the peptide dalargin after its delivery across the blood-brain barrier using surfactant-coated nanoparticles. J Control Release 1997;49:81-87.
  7. Schroder U, Sabel BA. Nanoparticles, a drug carrier system to pass the blood-brain barrier, permit central analgesic effects of i.v. dalargin injections. Brain Res 1996;710:121-24.
  8. Schroeder U, Sommerfeld P, Ulrich S, et al. Nanoparticle technology for delivery of drugs across the blood-brain barrier. J Pharm Sci. 1998;87:1305-07.
  9. Schroeder U, Sommerfeld P, Sabel BA. Efficacy of oral dalargin-loaded nanoparticle delivery across the blood-brain barrier. Peptides 1998;19:777-80.
  10. Alyautdin RN, Petrov VE, Langer K, et al. Delivery of loperamide across the blood-brain barrier with polysorbate 80-coated polybutylcyanoacrylate nanoparticles. Pharm Res. 1997;14:325-28.
  11. Kreuter J, Alyautdin RN. The Blood-Brain Barrier and Drug Delivery to the CNS. Marcel Dekker, New York, 2000:205-23.
  12. Ramge P, Unger RE, Oltrogge В, et al. Polysorbate-80 coating enhances uptake of polybutylcyanoacrylate (PBCA)-nanoparticles by human and bovine primary brain capillary endothelial cells. Eur J Neurosci 2000;12:1931-40.
  13. Fenart L, Casanova A, Dehouck В, et al. Evaluation of effect of charge and lipid coating on ability of 60-nm nanoparticles to cross an in vitro model of the blood-brain barrier. J Pharmacol Exp Therap 1999;291:1017-22.
  14. Dehouck В, Dehouck MP, Fruchart JC, et al. Upregulation of the low density lipoprotein receptor at the blood-brain barrier: intercommunications between brain capillary endothelial cells and astrocytes. J Cell Biol 1994;126:465-73.
  15. Dehouck В, Fenart L, Dehouck MP, et al. A new function for the LDL receptor: transcytosis of LDL across the blood-brain barrier. J Cell Biol 1997;138:877-89.
  16. Kurakhmaeva KB, Voronina TA, Kapica IG, et al. Antiparkinsonian effect of nerve growth factor adsorbed on polybutylcyanoacrylate nanoparticles coated with polysorbate-80. Bull Exp Biol Med 2008;145(2):259-62.
  17. Kurakhmaeva KB, Djindjikhashvili IA, Petrov VE, et al. Brain targeting of nerve growth factor using poly(butyl cyanoacrylate) nanoparticles. J Drug Target 2009;17(8):564-74.

Supplementary files

Supplementary Files
Action
1. JATS XML

Copyright (c) 2010 Bionika Media

This website uses cookies

You consent to our cookies if you continue to use our website.

About Cookies