pH multistage responsive micellar system with charge-switch and PEG layer detachment for co-delivery of paclitaxel and curcumin to synergistically eliminate breast cancer stem cells

Biomaterials. 2017 Dec:147:53-67. doi: 10.1016/j.biomaterials.2017.09.013. Epub 2017 Sep 10.

Abstract

Several studies have demonstrated that cancer stem cells (CSCs) are responsible for replenishing bulk tumor cells, generating new tumors and causing metastasis and relapse. Although combination therapy with multiple chemotherapeutics is considered to be a promising approach for simultaneously eliminating non-CSCs and CSCs, it is difficult to deliver drugs into the inner region of a solid tumor where the CSCs are located due to a lack of capillaries. Here, we synthesized a pH-sensitive polymer, poly(ethylene glycol)-benzoic imine-poly(γ-benzyl-l-aspartate)-b-poly(1-vinylimidazole) block copolymer (PPBV), to develop a pH multistage responsive micellar system for co-delivering paclitaxel and curcumin and synergistically eliminating breast cancer stem cells (bCSCs) and non-bCSCs. This pH multistage responsive micellar system could intelligently switch its surface charge from neutral to positive, de-shield its PEG layer and reduce its size after long-circulation and extravasation from leaky blood vessels at tumor sites, thus facilitating their cellular uptake and deep tumor penetration. These advantages were also beneficial for the combinational therapy efficacy of PTX and CUR to reach the maximum level and achieve superior tumor inhibition activity and effective bCSCs-killing capacity in vivo. Consequently, this pH multistage responsive micellar system is a powerful platform for collaborative therapy with PTX and CUR to simultaneously eliminate bCSCs and non-CSCs.

Keywords: Breast cancer stem cells; Charge-switch; Combination therapy; PEG-Detachment; pH multistage responsive.

MeSH terms

  • Animals
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / pharmacology*
  • Aspartic Acid / analogs & derivatives
  • Aspartic Acid / chemistry
  • Breast Neoplasms
  • Cell Line, Tumor
  • Cell Survival / drug effects
  • Curcumin / chemistry
  • Curcumin / pharmacology*
  • Drug Carriers
  • Drug Liberation
  • Drug Synergism
  • Female
  • Humans
  • Hydrogen-Ion Concentration
  • Imidazoles / chemistry
  • Mice, Inbred BALB C
  • Micelles
  • Nanoparticles / chemistry
  • Neoplastic Stem Cells / drug effects*
  • Neoplastic Stem Cells / pathology
  • Paclitaxel / chemistry
  • Paclitaxel / pharmacology*
  • Particle Size
  • Polyethylene Glycols / chemistry*
  • Polyvinyls / chemistry
  • Surface Properties

Substances

  • Antineoplastic Agents
  • Drug Carriers
  • Imidazoles
  • Micelles
  • Polyvinyls
  • polyvinylimidazole
  • Aspartic Acid
  • Polyethylene Glycols
  • Curcumin
  • Paclitaxel