Chitosan coated nanostructured lipid carriers for brain delivery of proteins by intranasal administration

Colloids Surf B Biointerfaces. 2015 Oct 1:134:304-13. doi: 10.1016/j.colsurfb.2015.06.054. Epub 2015 Jul 3.

Abstract

The remarkable increase in the prevalence of neurodegenerative diseases has become a serious public health problem. Considering the lack of effective treatments to address these diseases and the difficulties in accessing the brain due to the blood-brain barrier (BBB), to attain a successful strategy to improve drug delivery to the brain, the administration route becomes a point of interest. The intranasal route provides a non-invasive method to bypass the BBB. Moreover, the development of new technologies for the protection and delivery of peptides is an interesting approach to consider. Thus, in this work, a suitable chitosan coated nanostructured lipid carrier (CS-NLC) formulation with the capacity to reach the brain after being intranasally administered was successfully developed and optimized. The optimal formulation displayed a particle size of 114 nm with a positive surface charge of +28 mV. The in vitro assays demonstrated the biocompatibility of the nanocarrier and its cellular uptake by 16HBE14o- cells. Furthermore, no haemagglutination or haemolysis processes were observed when the particles were incubated with erythrocytes, and no toxicity signals appeared in the nasal mucosa of mice after the administration of CS-NLCs. Finally, the biodistribution study of CS-NLC-DiR demonstrated an efficient brain delivery of the particles after intranasal administration. In conclusion, CS-NLC can be considered to be a safe and effective nanocarrier for nose-to-brain drug delivery; however, to obtain a higher concentration of the drug in the brain following intranasal administration, further modifications are warranted in the CS-NLC formulation.

Keywords: Biodistribution; Blood–brain barrier (BBB); Intranasal administration; Nanostructured lipid carrier (NLC); Neurodegenerative disorders (ND).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Intranasal
  • Animals
  • Brain / metabolism*
  • Cell Line
  • Chitosan / chemistry*
  • Coated Materials, Biocompatible*
  • Drug Carriers*
  • Hemolysis
  • Humans
  • Lipids / administration & dosage*
  • Mice
  • Mice, Inbred C57BL
  • Nanostructures*
  • Proteins / administration & dosage*

Substances

  • Coated Materials, Biocompatible
  • Drug Carriers
  • Lipids
  • Proteins
  • Chitosan