Targeted drug delivery using genetically engineered diatom biosilica

Publikation: Beitrag in FachzeitschriftForschungsartikelBeigetragenBegutachtung

Beitragende

  • Bahman Delalat - , University of South Australia (Autor:in)
  • Vonda C Sheppard - , Georgia Institute of Technology (Autor:in)
  • Soraya Rasi Ghaemi - , University of South Australia (Autor:in)
  • Shasha Rao - , University of South Australia (Autor:in)
  • Clive A Prestidge - , University of South Australia (Autor:in)
  • Gordon McPhee - , University of South Australia (Autor:in)
  • Mary-Louise Rogers - , Flinders University (Autor:in)
  • Jacqueline F Donoghue - , Hudson Institute of Medical Research (Autor:in)
  • Vinochani Pillay - , Hudson Institute of Medical Research (Autor:in)
  • Terrance G Johns - , Hudson Institute of Medical Research (Autor:in)
  • Nils Kröger - , Fakultät Chemie u. Lebensmittelchemie, Center for Molecular Bioengineering (B CUBE), Georgia Institute of Technology (Autor:in)
  • Nicolas H Voelcker - , University of South Australia (Autor:in)

Abstract

The ability to selectively kill cancerous cell populations while leaving healthy cells unaffected is a key goal in anticancer therapeutics. The use of nanoporous silica-based materials as drug-delivery vehicles has recently proven successful, yet production of these materials requires costly and toxic chemicals. Here we use diatom microalgae-derived nanoporous biosilica to deliver chemotherapeutic drugs to cancer cells. The diatom Thalassiosira pseudonana is genetically engineered to display an IgG-binding domain of protein G on the biosilica surface, enabling attachment of cell-targeting antibodies. Neuroblastoma and B-lymphoma cells are selectively targeted and killed by biosilica displaying specific antibodies sorbed with drug-loaded nanoparticles. Treatment with the same biosilica leads to tumour growth regression in a subcutaneous mouse xenograft model of neuroblastoma. These data indicate that genetically engineered biosilica frustules may be used as versatile 'backpacks' for the targeted delivery of poorly water-soluble anticancer drugs to tumour sites.

Details

OriginalspracheEnglisch
Aufsatznummer8791
FachzeitschriftNature communications
Jahrgang6
PublikationsstatusVeröffentlicht - 10 Nov. 2015
Peer-Review-StatusJa

Externe IDs

Scopus 84946935108

Schlagworte

Schlagwörter

  • Animals, Antibodies, Antineoplastic Agents/administration & dosage, Camptothecin/administration & dosage, Cell Line, Tumor, Cloning, Molecular, Diatoms/genetics, Drug Delivery Systems, Gene Expression Regulation, Genetic Engineering, Immunoglobulin G, Liposomes, Lymphoma, B-Cell/drug therapy, Mice, Micelles, Nanoparticles, Neoplasms, Experimental/drug therapy, Neuroblastoma/drug therapy, Particle Size, Recombinant Fusion Proteins/genetics, Silicon Dioxide/metabolism, Transplantation, Heterologous

Bibliotheksschlagworte