Vitamin E-rich Nanoemulsion Enhances the Antitumor Efficacy of Low-Dose Paclitaxel by Driving Th1 Immune Response

Pharm Res. 2017 Jun;34(6):1244-1254. doi: 10.1007/s11095-017-2141-3. Epub 2017 Mar 21.

Abstract

Purpose: To overcome the drawbacks of high dose regimen and improve the outcomes of chemotherapy at a low dose, an immunotherapeutic nanoemulsion based combination of chemotherapeutic agent (paclitaxel) with immunomodulatory agent (vitamin E) was developed and evaluated for their antitumor effect against breast cancer.

Methods: A total of five nanoemulsions loaded with various content of vitamin E were prepared and characterized. The immunoregulatory effects of vitamin E along with the overall antitumor efficacy of vitamin E-rich nanoemulsion with a low dose of paclitaxel were investigated through in vitro and in vivo experiments.

Results: Vitamin E-rich nanoemulsion exhibited relatively narrow size distribution, high entrapment efficiency and controlled in vitro release profile. In RAW264.7 cells, vitamin E-rich nanoemulsion significantly enhanced the secretion of Th1 cytokines and down-regulated the secretion of Th2 cytokine. In a co-culture system, vitamin E-rich nanoemulsion induced a high apoptosis rate in MDA-MB-231 cells as compared with vitamin E-low nanoemulsion. Furthermore, vitamin E-rich nanoemulsion exhibited superior in vivo antitumor efficacy in comparison with Taxol and vitamin E-low nanoemulsion at a paclitaxel dose of 4 mg/kg.

Conclusions: Vitamin E-rich nanoemulsion has great potential for the treatment of breast cancers with a low dose of paclitaxel via driving Th1 immune response.

Keywords: Th1 immune response; immunochemotherapy; low-dose paclitaxel; nanoemulsion; vitamin E.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / pharmacology*
  • Apoptosis
  • Breast Neoplasms / drug therapy
  • Breast Neoplasms / immunology
  • Cell Line, Tumor
  • Coculture Techniques
  • Cytokines / immunology*
  • Cytokines / metabolism
  • Drug Carriers
  • Drug Interactions
  • Emulsions
  • Female
  • Humans
  • Mice, Inbred C57BL
  • Nanoparticles / chemistry*
  • Paclitaxel / chemistry
  • Paclitaxel / pharmacology*
  • Signal Transduction
  • Vitamin E / chemistry
  • Vitamin E / pharmacology*

Substances

  • Antineoplastic Agents
  • Cytokines
  • Drug Carriers
  • Emulsions
  • Vitamin E
  • Paclitaxel