Published August 1, 2012 | Version v1
Journal article

Cytotoxicity of monodispersed chitosan nanoparticles against the Caco-2 cells

  • 1. Laboratory for Drug Delivery, Pharmacy, Characterisation and Analysis, University of Western Australia (Australia)
  • 2. Centre for Microscopy, Characterisation and Analysis, University of Western Australia (Australia)
  • 3. School of Biomedical, Biomolecular and Chemical Sciences, 35 Stirling Hwy, Crawley 6009 (Australia)

Description

Published toxicology data on chitosan nanoparticles (NP) often lack direct correlation to the in situ size and surface characteristics of the nanoparticles, and the repeated NP assaults as experienced in chronic use. The aim of this paper was to breach these gaps. Chitosan nanoparticles synthesized by spinning disc processing were characterised for size and zeta potential in HBSS and EMEM at pHs 6.0 and 7.4. Cytotoxicity against the Caco-2 cells was evaluated by measuring the changes in intracellular mitochondrial dehydrogenase activity, TEER and sodium fluorescein transport data and cell morphology. Cellular uptake of NP was observed under the confocal microscope. Contrary to established norms, the collective data suggest that the in vitro cytotoxicity of NP against the Caco-2 cells was less influenced by positive surface charges than by the particle size. Particle size was in turn determined by the pH of the medium in which the NP was dispersed, with the mean size ranging from 25 to 333 nm. At exposure concentration of 0.1%, NP of 25 ± 7 nm (zeta potential 5.3 ± 2.8 mV) was internalised by the Caco-2 cells, and the particles were observed to inflict extensive damage to the intracellular organelles. Concurrently, the transport of materials along the paracellular pathway was significantly facilitated. The Caco-2 cells were, however, capable of recovering from such assaults 5 days following NP removal, although a repeat NP exposure was observed to produce similar effects to the 1st exposure, with the cells exhibiting comparable resiliency to the 2nd assault. -- Highlights: ► Chitosan nanoparticles reduced mitochondrial dehydrogenase activity. ► Cellular uptake of chitosan nanoparticles was observed. ► Chitosan nanoparticles inflicted extensive damage to the cell morphology. ► The transport of materials along the paracellular pathway was facilitated.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.taap.2012.04.037

Additional details

Identifiers

DOI
10.1016/j.taap.2012.04.037;
PII
S0041-008X(12)00205-0;

Publishing Information

Journal Title
Toxicology and Applied Pharmacology
Journal Volume
262
Journal Issue
3
Journal Page Range
p. 273-282
ISSN
0041-008X
CODEN
TXAPA9

INIS

Country of Publication
United States
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
45036827
Subject category
S60: APPLIED LIFE SCIENCES;
Descriptors DEI
AMINO ACIDS; FLUORESCEIN; IN VITRO; MITOCHONDRIA; NANOSTRUCTURES; OLIGOSACCHARIDES; PARTICLE SIZE; PH VALUE; SODIUM; TOXICITY
Descriptors DEC
ALKALI METALS; AROMATICS; CARBOHYDRATES; CARBOXYLIC ACIDS; CELL CONSTITUENTS; DYES; ELEMENTS; HYDROXY ACIDS; HYDROXY COMPOUNDS; METALS; ORGANIC ACIDS; ORGANIC COMPOUNDS; PHENOLS; POLYPHENOLS; SACCHARIDES; SIZE

Optional Information

Copyright
Copyright (c) 2012 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.