Codelivery of salinomycin and doxorubicin using nanoliposomes for targeting both liver cancer cells and cancer stem cells

Nanomedicine (Lond). 2016 Oct;11(19):2565-2579. doi: 10.2217/nnm-2016-0137. Epub 2016 Sep 20.

Abstract

Aim: To develop salinomycin-loaded nanoliposomes (SLN), doxorubicin-loaded nanoliposomes (DLN) and nanoliposomes codelivering salinomycin and doxorubicin (SDLN) to target both liver cancer cells and cancer stem cells.

Materials & methods: The characterization and antitumor activity of SLN, DLN and SDLN were evaluated.

Results & conclusion: The doxorubicin/salinomycin sodium mole ratio of 1:1 had the best synergistic combination index value, and was chosen as the drug ratio in SDLN. SDLN could maintain the drug ratio between 1:1 and 3:1 in 12 h in vivo. SDLN and SLN + DLN showed the best tumor inhibitory rate, and could significantly decrease the percentage of liver cancer stem cells in vivo. SDLN and SLN + DLN may serve as an effective approach to treat liver cancer.

Keywords: cancer stem cells; combined therapy; doxorubicin; liver cancer; nanoliposomes; salinomycin.

MeSH terms

  • Animals
  • Antineoplastic Combined Chemotherapy Protocols / administration & dosage*
  • Antineoplastic Combined Chemotherapy Protocols / chemistry
  • Apoptosis
  • Carcinoma, Hepatocellular / drug therapy*
  • Carcinoma, Hepatocellular / pathology
  • Cell Survival
  • Doxorubicin / administration & dosage
  • Drug Liberation
  • Hep G2 Cells
  • Humans
  • Liposomes / chemistry*
  • Liver Neoplasms / drug therapy
  • Liver Neoplasms / pathology
  • Male
  • Mice, Nude
  • Nanocapsules / chemistry*
  • Neoplastic Stem Cells / drug effects*
  • Particle Size
  • Pyrans / administration & dosage
  • Surface Properties

Substances

  • Liposomes
  • Nanocapsules
  • Pyrans
  • salinomycin
  • Doxorubicin