Published August 15, 2011 | Version v1
Journal article

The uptake and intracellular fate of a series of different surface coated quantum dots in vitro

  • 1. Department of Clinical Research, Division of Pneumology, Inselspital University Hospital, University of Bern, Postfach 44, Bern 3008 (Switzerland)
  • 2. Lung Biology Laboratory, Department of Medicine, Columbia University 630 West, 168 Street, 10032 NY (United States)
  • 3. Nanosafety Research Group, School of Life Sciences, Heriot-Watt University, Edinburgh EH14 4AS (United Kingdom)

Description

Highlights: → Assessing an important issue relevant to the toxicity of nanoparticles. → Use of novel confocal laser scanning and electron microscopy techniques. → Novel findings for intracellular fate of quantum dots in vitro. -- Abstract: Quantum dots (QDs) are potentially beneficial semi-conductor nanocrystals for use in diagnostics and therapeutics. The chemical composition of QDs however, has raised concerns as to their potential toxicity. Although a thorough examination using specific biochemical endpoints is necessary to assess QD toxicity, an understanding of the interaction of QDs, specifically their uptake and intracellular fate, with biological systems is also essential in determining their potential hazardous effects. The aim of this study was to investigate the uptake and intracellular fate of a series of different surface coated QDs (organic, carboxylated (COOH) and amino (NH2) polyethylene glycol (PEG)) in J774.A1 'murine macrophage-like' cells. Model 20 nm and 200 nm COOH polystyrene beads (PBs) were also studied. Results showed that COOH and NH2 (PEG) QDs, as well as 20 nm and 200 nm PBs were located within lysosomes and the mitochondria of macrophages after 2 h. Additionally, elemental transmission electron microscopy confirmed both COOH and NH2 (PEG) QDs to be located within membrane-bound compartments at this time point. The data from this study combined with current knowledge, indicates that the intracellular localisation of QDs could be directly related to their toxicity.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.tox.2011.05.006

Additional details

Identifiers

DOI
10.1016/j.tox.2011.05.006;
PII
S0300-483X(11)00186-7;

Publishing Information

Journal Title
Toxicology
Journal Volume
286
Journal Issue
1-3
Journal Page Range
p. 58-68
ISSN
0300-483X
CODEN
TXCYAC

Optional Information

Copyright
Copyright (c) 2011 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.