Brain targeted delivery of anticancer drugs: prospective approach using solid lipid nanoparticles

IET Nanobiotechnol. 2019 Jun;13(4):353-362. doi: 10.1049/iet-nbt.2018.5322.

Abstract

A brain tumour is amongst most devastating and challenging condition to overcome with suitable treatment as the drug has to cross the blood-brain barrier (BBB) with several physiological barriers like opsonisation by the reticuloendothelial system. Presently various techniques such as surgical, chemotherapeutic agents, and radiotherapy techniques have performed to extend the lifespan of patients diagnosed with glioblastoma, which did not maximise the overall survival of patients with a tumour. Nanotechnology is relied upon to diminish the requirement for intrusive methods for conveyance of therapeutics to the central nervous system. Colloidal nanocarriers sizing range 1-1000 nm have been utilised to cross BBB delivers the drug at cell levels with enhanced bioavailability and reduced toxicity. However, solid lipid nanoparticles (SLNs) are considered a highly flexible carrier for more successful remedially in brain tumour. The treatment of a brain tumour via SLNs is gaining greater potency due to its inimitable size and lipidic nature. This review focuses and represents the current strategies of SLNs in the brain tumour treatment with appropriate techniques adopted are highlighted. Based on this review, the authors concluded that SLNs embrace exclusive promising lipidic nanocarrier that could be utilised to target a brain tumour effectively.

Publication types

  • Review

MeSH terms

  • Animals
  • Antineoplastic Agents* / metabolism
  • Antineoplastic Agents* / pharmacokinetics
  • Antineoplastic Agents* / therapeutic use
  • Brain / metabolism*
  • Brain Neoplasms / drug therapy
  • Brain Neoplasms / metabolism
  • Drug Delivery Systems*
  • Humans
  • Lipids* / chemistry
  • Lipids* / pharmacokinetics
  • Liposomes
  • Mice
  • Micelles
  • Nanomedicine
  • Nanoparticles* / chemistry

Substances

  • Antineoplastic Agents
  • Lipids
  • Liposomes
  • Micelles