Hydrolysis-Sensitive Dithiolethione Prodrug Micelles

Macromol Biosci. 2015 Nov;15(11):1512-22. doi: 10.1002/mabi.201500156. Epub 2015 Jun 23.

Abstract

Prodrug micelles carrying 5-(4-hydroxyphenyl)-3H-1,2-dithiole-3-thione (ADT-OH), a compound possessing chemopreventive properties, are prepared from amphiphilic block copolymers linking ADT-OH via an ester bond using glycine (PAM-PGlyADT) and isoleucine linkers (PAM-PIleADT). The release of ADT-OH from the PAM-PIleADT micelles is much slower than the PAM-PGlyADT micelles. The PAM-PGlyADT micelles show comparable toxicity with ADT-OH in different cancer cell lines, whereas the PAM-PIleADT micelles are not toxic up to 400 µM. This ADT-ester prodrug micelle approach enables to modulate the release rate of ADT-OH and thus might find application in cancer therapy and prevention.

Keywords: block copolymer; cytotoxicity; dithiolehthiones; micelle; prodrug.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anethole Trithione / chemistry*
  • Anethole Trithione / therapeutic use
  • Antineoplastic Agents / chemistry*
  • Antineoplastic Agents / therapeutic use
  • Humans
  • Hydrolysis
  • Micelles*
  • Neoplasms / drug therapy
  • Prodrugs / chemistry*
  • Prodrugs / therapeutic use

Substances

  • Antineoplastic Agents
  • Micelles
  • Prodrugs
  • Anethole Trithione