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Nanomedicines for the Treatment of CNS Diseases

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Abstract

Targeting and delivering macromolecular therapeutics to the central nervous system (CNS) has been a major challenge. The blood–brain barrier (BBB) is the main obstacle that must be overcome to allow compounds to reach their targets in the brain. Therefore, much effort has been channelled into improving transport of therapeutics across the BBB and into the CNS including the use of nanoparticles. In this thematic issue, several reviews and original research are presented that address “Nanomedicines for CNS Diseases.” The articles in this issue are concentrated on either CNS-HIV disease or CNS tumors. In regards to CNS-HIV disease, there are two reviews that discuss the role of nanoparticles for improving the delivery of HIV therapeutics to the CNS. In addition, there are two original articles focusing on therapies for CNS-HIV, one of them uses nanoparticles for delivery of siRNA specific to a key protein in autophagy to microglia, and another discusses nanoparticle delivery of a soluble mediator to suppress neuroinflammation. Furthermore, a comprehensive review about gene therapy for CNS neurological diseases is also included. Finally, this issue also includes review articles on enhanced drug targeting to CNS tumors. These articles include a review on the use of nanoparticles for CNS tumors, a review on functionalization (ligands) of nanoparticles for drug targeting to the brain tumor by overcoming BBB, and the final review discusses the use of macrophages as a delivery vehicle to CNS tumors. This thematic issue provides a wealth of knowledge on using nanomedicines for CNS diseases.

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Acknowledgements

New York State Department of Health, Empire Clinical Research Investigator Program (ECRIP) Awards (Reynolds). Authors would also like to acknowledge Dr. Howard Gendelman for his ongoing help and dedication to nanomedicine projects.

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Correspondence to Jessica L. Reynolds.

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Reynolds, J.L., Mahato, R.I. Nanomedicines for the Treatment of CNS Diseases. J Neuroimmune Pharmacol 12, 1–5 (2017). https://doi.org/10.1007/s11481-017-9725-x

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