Synergistic cytotoxicity of irinotecan and cisplatin in dual-drug targeted polymeric nanoparticles. Academic Article uri icon

Overview

abstract

  • AIM: Two unexplored aspects for irinotecan and cisplatin (I&C) combination chemotherapy are: actively targeting both drugs to a specific diseased cell type, and delivering both drugs on the same vehicle to ensure their synchronized entry into the cell at a well-defined ratio. In this work, the authors report the use of targeted polymeric nanoparticles (NPs) to coencapsulate and deliver I&C to cancer cells expressing the prostate-specific membrane antigen. MATERIALS & METHODS: Targeted NPs were prepared in a single step by mixing four different precursors inside microfluidic devices. RESULTS: I&C were encapsulated in 55-nm NPs and showed an eightfold increase in internalization by prostate-specific membrane antigen-expressing LNCaP cells compared with nontargeted NPs. NPs coencapsulating both drugs exhibited strong synergism in LNCaP cells with a combination index of 0.2. CONCLUSION: The strategy of coencapsulating both I&C in a single NP targeted to a specific cell type could potentially be used to treat different types of cancer.

publication date

  • October 17, 2012

Research

keywords

  • Antineoplastic Agents
  • Camptothecin
  • Cisplatin
  • Drug Delivery Systems
  • Nanoparticles
  • Prostate
  • Prostatic Neoplasms

Identity

PubMed Central ID

  • PMC3694785

Scopus Document Identifier

  • 84877680982

Digital Object Identifier (DOI)

  • 10.2217/nnm.12.134

PubMed ID

  • 23075285

Additional Document Info

volume

  • 8

issue

  • 5