Polymeric nanomicelles for sustained delivery of anti-cancer drugs

Mutat Res. 2014 Oct:768:47-59. doi: 10.1016/j.mrfmmm.2014.04.009. Epub 2014 Apr 24.

Abstract

In the first section of this paper, the existing and emerging nanotechnology-based cancer therapies--nanoparticles, drug conjugates, nanomicelles--are reviewed. In a second part, we present our original and unpublished findings on the sustained release of anti-cancer drugs such as paclitaxel, doxorubicin and camptothecin using block copolymer micelles [PEG-b-poly(dioxanone-co-methyl dioxanone)]. Copolymers with variable lengths of hydrophobic and hydrophilic blocks have been synthesized and successfully loaded with paclitaxel, doxorubicin and camptothecin anti-cancer drugs, with micelles size in the range 130-300 nm. Drug encapsulation efficiencies varied between 15% and 70% depending on drug and copolymer composition. The drug binding constants, which give a good insight into drug encapsulation and release, were evaluated from UV spectroscopy as we reported previously for anti-TB drugs. Through variation of the methyl dioxanone content of the copolymer, our systems can be tailored for sustained release of the different drugs.

Keywords: Anti-cancer; Camptothecin; Doxorubicin; Paclitaxel; Polymeric micelles; Sustained delivery.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / pharmacology*
  • Delayed-Action Preparations / chemistry
  • Delayed-Action Preparations / pharmacology
  • Humans
  • Micelles*
  • Nanostructures / chemistry*
  • Neoplasms / drug therapy*
  • Neoplasms / metabolism
  • Neoplasms / pathology
  • Polydioxanone / chemistry
  • Polydioxanone / pharmacology
  • Polyethylene Glycols / chemistry
  • Polyethylene Glycols / pharmacology

Substances

  • Antineoplastic Agents
  • Delayed-Action Preparations
  • Micelles
  • Polydioxanone
  • Polyethylene Glycols