Novel theranostic zinc phthalocyanine-phospholipid complex self-assembled nanoparticles for imaging-guided targeted photodynamic treatment with controllable ROS production and shape-assisted enhanced cellular uptake

Colloids Surf B Biointerfaces. 2018 Feb 1:162:76-89. doi: 10.1016/j.colsurfb.2017.10.061. Epub 2017 Oct 24.

Abstract

The novel drug delivery system based on self-assembly of zinc phthalocyanine-soybean phosphatidylcholine (ZnPc-SPC) complex was developed by a co-solvent method followed by a nanoprecipitaion technique. DSPE-PEG-methotrexate (DSPE-PEG-MTX) was introduced on the surface of ZnPc-SPC self-assembled nanoparticles (ZS) to endow them with folate receptor-targeting property. NMR, XRD, FTIR, and UV-vis-NIR analysis demonstrated the weak molecular interaction between ZnPc and SPC. The ZS functionalized with DSPE-PEG-MTX (ZSPM) was successfully constructed with an average particle size of ∼170nm, a narrow size distribution, and could remain physiologically stable for at least 7days. In vitro cellular uptake and cytotoxicity studies demonstrated that ZSPM exhibited stronger cellular uptake efficacy and photodynamic cytotoxicity against HeLa and MCF-7 cells than ZS functionalized with DSPE-mPEG (ZSP) and free ZnPc. More importantly, ZSPM showed the enhanced accumulation effect at the tumor region compared with ZSP by the active-plus-passive targeting via enhanced permeability and retention (EPR) effect and folate receptor-mediated endocytosis. Furthermore, in vivo antitumor effect and histological analysis demonstrated the superior tumor growth inhibition effect of ZSPM. In addition, the needle-shape ZSP (ZSPN) exhibited better in vitro cellular uptake and in vivo tumor accumulation compared with ZSP due to the shape-assisted effect. Moreover, the interesting off-on switch effect of reactive oxygen species (ROS) production of ZnPc-SPC complex-based nanoparticles was discovered to achieve photodynamic treatment in a controllable way. These findings suggested that the ZnPc-SPC complex-based self-assembled nanoparticles could serve as a promising and effective formulation to achieve tumor-targeting fluorescence imaging and enhanced photodynamic treatment.

Keywords: Phospholipid complex; Photodynamic treatment; Self-assembly; Shape-assisted effect; Tumor-targeting; Zinc phthalocyanine.

MeSH terms

  • Animals
  • Drug Delivery Systems / methods*
  • Endocytosis
  • Female
  • Folate Receptors, GPI-Anchored / genetics
  • Folate Receptors, GPI-Anchored / metabolism
  • HeLa Cells
  • Humans
  • Indoles / pharmacokinetics
  • Indoles / pharmacology*
  • Injections, Subcutaneous
  • Isoindoles
  • MCF-7 Cells
  • Mammary Neoplasms, Animal / genetics
  • Mammary Neoplasms, Animal / metabolism
  • Mammary Neoplasms, Animal / pathology
  • Mammary Neoplasms, Animal / therapy*
  • Methotrexate / pharmacokinetics
  • Methotrexate / pharmacology*
  • Mice
  • Mice, Nude
  • Nanoparticles / administration & dosage
  • Nanoparticles / chemistry*
  • Optical Imaging / methods
  • Organometallic Compounds / pharmacokinetics
  • Organometallic Compounds / pharmacology*
  • Particle Size
  • Phosphatidylcholines / chemistry
  • Phosphatidylethanolamines / chemistry
  • Photochemotherapy / methods
  • Photosensitizing Agents / pharmacokinetics
  • Photosensitizing Agents / pharmacology*
  • Polyethylene Glycols / chemistry
  • Reactive Oxygen Species / agonists*
  • Reactive Oxygen Species / metabolism
  • Theranostic Nanomedicine / methods
  • Zinc Compounds

Substances

  • Folate Receptors, GPI-Anchored
  • Indoles
  • Isoindoles
  • Organometallic Compounds
  • Phosphatidylcholines
  • Phosphatidylethanolamines
  • Photosensitizing Agents
  • Reactive Oxygen Species
  • Zinc Compounds
  • polyethylene glycol-distearoylphosphatidylethanolamine
  • Zn(II)-phthalocyanine
  • Polyethylene Glycols
  • Methotrexate