Design of smart HPMA copolymer-based nanomedicines

J Control Release. 2016 Oct 28:240:9-23. doi: 10.1016/j.jconrel.2015.10.003. Epub 2015 Oct 3.

Abstract

The state-of-the art in water-soluble macromolecular therapeutics has been reviewed. First the design principles for polymer-drug conjugates are discussed followed by two recent developments in the field: a) The design, synthesis and properties of backbone degradable N-(2-hydroxypropyl)methacrylamide (HPMA) copolymer-drug conjugates. The enhanced intravascular half-life of such conjugates creates a concentration gradient (blood vs. tumor) for an extended time interval resulting in increased solid tumor accumulation by enhanced permeability and retention (EPR) effect with concomitant increase in efficacy. b) Drug-free macromolecular therapeutics is a new paradigm in macromolecular therapeutics. Apoptosis in malignant cell is induced by crosslinking of cell surface non-internalizing receptors. Crosslinking of receptors is mediated by the biorecognition of two nanoconjugates containing high-fidelity complementary motifs (peptides or oligonucleotides). Results for the treatment of B cell lymphomas in animal models and patient cells demonstrate the high translational potential of this approach.

Keywords: Coiled-coil peptides; Degradable polymeric carriers; Drug-free macromolecular therapeutics; HPMA; Oligonucleotides; Self-assembly.

Publication types

  • Review
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Apoptosis / physiology
  • Drug Design*
  • Humans
  • Methacrylates / administration & dosage
  • Methacrylates / chemistry*
  • Methacrylates / metabolism
  • Nanomedicine / methods*
  • Nanomedicine / trends
  • Neoplasms / drug therapy
  • Neoplasms / metabolism
  • Polymers / administration & dosage
  • Polymers / chemistry*
  • Polymers / metabolism

Substances

  • Methacrylates
  • Polymers
  • hydroxypropyl methacrylate