Intranasal delivery of bFGF with nanoliposomes enhances in vivo neuroprotection and neural injury recovery in a rodent stroke model

J Control Release. 2016 Feb 28:224:165-175. doi: 10.1016/j.jconrel.2016.01.017. Epub 2016 Jan 13.

Abstract

Basic fibroblast growth factor (bFGF) may protect stroke patients from cerebral ischemia-reperfusion (I/R) injury. In this study, we report the intranasal use of novel nanoliposomes for the brain delivery of bFGF in a rat model of cerebral I/R. Compared with free bFGF, nanoliposomal therapy was able to significantly improve bFGF accumulation in brain tissues (p<0.05) including the most affected ischemic penumbra regions (e.g. hippocampus, pallium). After intranasal bFGF-nanoliposomal treatment for 3 consecutive days, functional recovery as indicated by improved neurologic deficit score and spontaneous locomotor activity was observed, and the stroke infarct volume was nearly halved (p<0.001) which persisted after 21days. These neuroprotective effects could be blocked by the PI3-K/Akt inhibitor LY294002, indicating the involvement of PI3-K/Akt activation in the therapeutic action. Overall, our results support the intranasal use of nanoliposomal bFGF as an efficient, non-invasive means to bypass the blood-brain barrier for ischemic stroke treatment.

Keywords: Blood–brain barrier; Fibroblast growth factor; Intranasal delivery; Nanoliposome; Stroke.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Intranasal
  • Animals
  • Blood-Brain Barrier
  • Cerebral Infarction / drug therapy
  • Cerebral Infarction / pathology
  • Dentate Gyrus / drug effects
  • Dentate Gyrus / pathology
  • Drug Delivery Systems
  • Female
  • Fibroblast Growth Factor 2 / administration & dosage*
  • Fibroblast Growth Factor 2 / pharmacokinetics
  • Fibroblast Growth Factor 2 / therapeutic use*
  • Liposomes
  • Motor Activity / drug effects
  • Nanoparticles
  • Neuroprotective Agents / administration & dosage*
  • Neuroprotective Agents / pharmacokinetics
  • Neuroprotective Agents / therapeutic use*
  • Rats
  • Rats, Sprague-Dawley
  • Recovery of Function
  • Reperfusion Injury / drug therapy
  • Reperfusion Injury / pathology
  • Stroke / drug therapy*
  • Stroke / pathology

Substances

  • Liposomes
  • Neuroprotective Agents
  • Fibroblast Growth Factor 2