Targeting specific cells in the brain with nanomedicines for CNS therapies

Research output: Contribution to journalArticlepeer-review

38 Scopus citations

Abstract

Treatment of Central Nervous System (CNS) disorders still remains a major clinical challenge. The Blood–Brain Barrier (BBB), known as the major hindrance, greatly limits therapeutics penetration into the brain. Moreover, even though some therapeutics can cross BBB based on their intrinsic properties or via the use of proper nanoscale delivery vehicles, their therapeutic efficacy is still often limited without the specific uptake of drugs by the cancer or disease-associated cells. As more studies have started to elucidate the pathological roles of major cells in the CNS (for example, microglia, neurons, and astrocytes) for different disorders, nanomedicines that can enable targeting of specific cells in these diseases may provide great potential to boost efficacy. In this review, we aim to briefly cover the pathological roles of endothelial cells, microglia, tumor-associated microglia/macrophage, neurons, astrocytes, and glioma in CNS disorders and to highlight the recent advances in nanomedicines that can target specific disease-associated cells. Furthermore, we summarized some strategies employed in nanomedicine to achieve specific cell targeting or to enhance the drug neuroprotective effects in the CNS. The specific targeting at the cellular level by nanotherapy can be a more precise and effective means not only to enhance the drug availability but also to reduce side effects.

Original languageEnglish (US)
Pages (from-to)212-226
Number of pages15
JournalJournal of Controlled Release
Volume240
DOIs
StatePublished - Oct 28 2016

Keywords

  • BBB
  • CNS disorders
  • Microglia
  • Nanomedicine
  • Neuron
  • Targeted therapy

ASJC Scopus subject areas

  • Pharmaceutical Science

Fingerprint

Dive into the research topics of 'Targeting specific cells in the brain with nanomedicines for CNS therapies'. Together they form a unique fingerprint.

Cite this