Multifunctional TK-VLPs nanocarrier for tumor-targeted delivery

Int J Pharm. 2016 Apr 11;502(1-2):249-57. doi: 10.1016/j.ijpharm.2016.02.037. Epub 2016 Feb 22.

Abstract

Virus-like particles (VLPs) have been exploited for various biomedical applications, such as the monitoring, prevention, diagnosis and therapy of disease. In this study, a novel multifunctional VLPs nanocarrier (TK-VLPs) was prepared and used for tumor-targeted delivery. The SPR and cell uptake results indicated that the TK peptide is a "bi-functional ligand" with high affinity for Caco-2, HRT-18 and HUVEC cells through the integrin α6β1 and integrin αvβ3 receptors. The results of the direct immunofluorescence, SDS-PAGE and western blot assays demonstrated that the TK-VLPs were successfully prepared using the baculovirus expression system. Confocal laser scanning microscopy and the flow cytometry analysis validated that the TK-VLPs could target to Caco-2, HRT-18 and HUVEC cells. An in vivo study further confirmed that the TK-VLPs could target and efficiently deliver fluorescein to tumor cells and the tumor vasculature in mice bearing subcutaneous tumors. TK-VLPs-DOX displayed a uniform, spherical shape and an average size of approximately 28nm. The results of the cell uptake and cytotoxicity assays indicated that TK-VLPs-DOX could enhance the selectivity for colorectal cancer cells. Together, our studies provide strong evidence that TK-VLPs could target colon tumor cells and tumor angiogenesis with enhanced permeability and retention effects, suggesting that the TK-VLPs are a multifunctional nanocarrier with potential applications in a colon tumor-targeted drug delivery system.

Keywords: Colonic drug delivery; Nanocarrier; Parvovirus capsid protein VP2; TK peptide; Virus-like particles (VLPs).

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antineoplastic Agents / administration & dosage*
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / therapeutic use
  • Baculoviridae / genetics
  • Capsid Proteins / administration & dosage*
  • Capsid Proteins / chemistry
  • Capsid Proteins / genetics
  • Capsid Proteins / therapeutic use
  • Cell Line
  • Cell Line, Tumor
  • Cell Survival / drug effects
  • Doxorubicin / administration & dosage*
  • Doxorubicin / chemistry
  • Doxorubicin / therapeutic use
  • Drug Carriers / administration & dosage*
  • Drug Carriers / chemistry
  • Drug Carriers / therapeutic use
  • Humans
  • Mice, Inbred BALB C
  • Mice, Nude
  • Neoplasms / drug therapy
  • Neoplasms / metabolism
  • Peptides / administration & dosage*
  • Peptides / chemistry
  • Peptides / therapeutic use
  • Recombinant Proteins / administration & dosage
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / genetics
  • Recombinant Proteins / therapeutic use
  • Thymidine Kinase / chemistry*

Substances

  • Antineoplastic Agents
  • Capsid Proteins
  • Drug Carriers
  • Peptides
  • Recombinant Proteins
  • Doxorubicin
  • Thymidine Kinase