Delivery of Multifunctional Nanoparticles to the Brain

Abstract

Protein nanoparticles derived from non-enveloped viruses have several advantageous properties for the installation of new function. We used virus-like particles (VLPs) based on bacteriophage Q-beta, which means that the capsid structure has no natural and specific mammalian cell receptors. We therefore started with a structure that can interact with mammalian tissues only through nonspecific properties such as surface charge or hydrophobicity. While it can be difficult to eliminate such interactions, it is usually possible to do so, and specificity in binding and internalization can be separately introduced by the attachment of interacting groups on the particle surface.

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Document Details

Document Type
Technical Report
Publication Date
Mar 04, 2022
Accession Number
AD1195285

Entities

People

  • M. Finn

Organizations

  • Georgia Tech Research Corporation

Tags

DTIC Thesaurus Topics

  • Antibodies
  • Attachment
  • Bacteriophages
  • Biochemistry
  • Blood
  • Blood-Brain Barrier
  • Brain
  • Cells
  • Chemical Compounds
  • Chemical Synthesis
  • Chemistry
  • Cultured Cells
  • Immunogenicity
  • Leviviridae
  • Medical Personnel
  • Molecules
  • Nanoparticles
  • Packaging
  • Particles
  • Polymer Chemistry
  • Production
  • Proteins
  • Targets
  • Viral Structures
  • Viruses

Readers

  • Molecular and Cellular Biochemistry
  • Nanocomposite Materials Science
  • Virology (or Medical Virology).

Technology Areas

  • Biotechnology