Enhanced antitumor efficacy of gemcitabine-loaded temperature-sensitive liposome by hyperthermia in tumor-bearing mice

Drug Dev Ind Pharm. 2014 Apr;40(4):470-6. doi: 10.3109/03639045.2013.768631. Epub 2013 Apr 24.

Abstract

Introduction: Gemcitabine-loaded TSL (Gem-TSL) was used in combination with hyperthermia (HT) to treat the colon adenocarcinoma-bearing BALB/c mice for improved anticancer effect following intravenous administration.

Methods: A new temperature-sensitive liposome (TSL), composed of DPPC:DMPC:DSPC (4:1:1 molar ratio) releasing the encapsulated gemcitabine (Gem) at 41 °C, was developed and evaluated for enhanced antitumor efficacy both in vitro and in vivo.

Results: Drug release from the TSL was sharply increased at 41 °C and in vitro cytotoxicity of Gem-TSL in colon adenocarcinoma cells (CT-26) was 10 times higher than the free drug (IC50 = 0.3 μM versus 3 μM). Apoptosis seemed to be the main mechanism of cell death as the treatment of the cells with Gem-TSL increased the caspse-3/7 activity by 1.5-fold and also caused the fragmentation of chromatin DNA. Gem-TSL suppressed the tumor growth in CT-26-bearing BALB/c mice more stronger than the free gemcitabine after intravenous administration. Moreover, this in vivo antitumor efficacy of Gem-TSL was further increased when HT was added.

Discussion: This study suggests that this new TSL-Gem formulation could serve as a new chemotherapy modality together with HT.

Publication types

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

MeSH terms

  • Adenocarcinoma / drug therapy*
  • Adenocarcinoma / pathology
  • Animals
  • Antibiotics, Antineoplastic / administration & dosage
  • Antibiotics, Antineoplastic / pharmacology
  • Apoptosis / drug effects
  • Caspase 3 / metabolism
  • Caspase 7 / metabolism
  • Chromatin / metabolism
  • Colonic Neoplasms / drug therapy*
  • Colonic Neoplasms / pathology
  • Combined Modality Therapy
  • DNA Fragmentation / drug effects
  • Deoxycytidine / administration & dosage
  • Deoxycytidine / analogs & derivatives*
  • Deoxycytidine / pharmacology
  • Dose-Response Relationship, Drug
  • Gemcitabine
  • Hyperthermia, Induced / methods*
  • Inhibitory Concentration 50
  • Liposomes
  • Mice
  • Mice, Inbred BALB C
  • Temperature

Substances

  • Antibiotics, Antineoplastic
  • Chromatin
  • Liposomes
  • Deoxycytidine
  • Caspase 3
  • Caspase 7
  • Gemcitabine