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EpCAM aptamer-functionalized mesoporous silica nanoparticles for efficient colon cancer cell-targeted drug delivery.

Abstract
Targeted delivery of anticancer agents by functional nanoparticles is an attractive strategy to increase their therapeutic efficacy while reducing toxicity. In this work, doxorubicin (DOX)-loaded mesoporous silica nanoparticles (MSNs) were modified with aptamer (Ap) against the epithelial cell adhesion molecule (EpCAM) for targeted delivery of DOX to colon cancer cells. These nanoparticles (Ap-MSN-DOX) were characterized by particle size, zeta potential, aptamer conjugation efficiency, drug encapsulation efficiency, and drug release properties. The in vitro cell recognition, cellular uptake, EpCAM protein inhibition efficiency, and cytotoxicity of Ap-MSN-DOX were also studied. Results demonstrated that EpCAM conjugation increased binding of Ap-MSN-DOX to EpCAM over-expressing SW620 colon cancer cells but not EpCAM-negative Ramos cells, resulting in enhanced cellular uptake and increased cytotoxicity of the DOX in SW620 cells when compared to non-Ap-modified nanoparticles (MSN-DOX). Additionally, Ap-MSN-DOX exhibited significant inhibition effects on the expression of EpCAM on SW620 cells. These results suggested that Ap-MSN-DOX has the potential for the targeted delivery of therapeutic agents into EpCAM positive colon cancer cells to improve therapeutic index while reducing side effects.
AuthorsXiaodong Xie, Fengqiao Li, Huijuan Zhang, Yusheng Lu, Shu Lian, Hang Lin, Yu Gao, Lee Jia
JournalEuropean journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences (Eur J Pharm Sci) Vol. 83 Pg. 28-35 (Feb 15 2016) ISSN: 1879-0720 [Electronic] Netherlands
PMID26690044 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2015 Elsevier B.V. All rights reserved.
Chemical References
  • Antibiotics, Antineoplastic
  • Aptamers, Nucleotide
  • Epithelial Cell Adhesion Molecule
  • Silicon Dioxide
  • Doxorubicin
Topics
  • Antibiotics, Antineoplastic (administration & dosage, chemistry)
  • Apoptosis (drug effects)
  • Aptamers, Nucleotide (administration & dosage, chemistry)
  • Cell Line, Tumor
  • Cell Survival (drug effects)
  • Colonic Neoplasms (drug therapy, metabolism)
  • Doxorubicin (administration & dosage, chemistry)
  • Drug Delivery Systems
  • Drug Liberation
  • Epithelial Cell Adhesion Molecule (genetics)
  • Humans
  • Nanoparticles (administration & dosage, chemistry)
  • Porosity
  • Silicon Dioxide (administration & dosage, chemistry)

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