The Platin-X series: activation, targeting, and delivery

Dalton Trans. 2016 Aug 16;45(33):12992-3004. doi: 10.1039/c6dt01738j.

Abstract

Anticancer platinum (Pt) complexes have long been considered to be one of the biggest success stories in the history of medicinal inorganic chemistry. Yet there remains the hunt for the "magic bullet" which can satisfy the requirements of an effective chemotherapeutic drug formulation. Pt(iv) complexes are kinetically more inert than the Pt(ii) congeners and offer the opportunity to append additional functional groups/ligands for prodrug activation, tumor targeting, or drug delivery. The ultimate aim of functionalization is to enhance the tumor selective action and attenuate systemic toxicity of the drugs. Moreover, an increase in cellular accumulation to surmount the resistance of the tumor against the drugs is also of paramount importance in drug development and discovery. In this review, we will address the attempts made in our lab to develop Pt(iv) prodrugs that can be activated and delivered using targeted nanotechnology-based delivery platforms.

Publication types

  • Review

MeSH terms

  • Animals
  • Antineoplastic Agents* / administration & dosage
  • Antineoplastic Agents* / chemistry
  • Antineoplastic Agents* / pharmacology
  • Drug Delivery Systems
  • Humans
  • Organoplatinum Compounds* / administration & dosage
  • Organoplatinum Compounds* / chemistry
  • Organoplatinum Compounds* / pharmacology
  • Platinum Compounds* / administration & dosage
  • Platinum Compounds* / chemistry
  • Platinum Compounds* / pharmacology
  • Prodrugs* / administration & dosage
  • Prodrugs* / chemistry
  • Prodrugs* / pharmacology

Substances

  • Antineoplastic Agents
  • Organoplatinum Compounds
  • Platinum Compounds
  • Prodrugs