4.3 Article

Correlation of particle properties with cytotoxicity and cellular uptake of hydroxyapatite nanoparticles in human gastric cancer cells

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ELSEVIER
DOI: 10.1016/j.msec.2016.05.034

Keywords

Hydroxyapatite nanoparticles; Particle properties; Cancer cell; Cytotoxicity; Uptake; Intracellular calcium concentration

Funding

  1. National Basic Research Program of China (973 Program) [2012CB933600]
  2. National Natural Science Foundation of China [31271010]
  3. Program for New Century Excellent Talents in University [NCET-11-0639]

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Three types of hydroxyapatite nanoparticles (HAPNs) were synthesized employing a sonochemistry-assisted microwave method by changing microwave power (from 200 to 300 W) or using calcination treatment: 1200 (200 W, lyophilization), 1300 (300 W, lyophilization) and C200 (200 W, lyophilization & calcination). Their physiochemical properties were characterized and correlated with cytotoxicity to human gastric cancer cells (MGC80-3). The major differences among these HAPN preparations were their size and specific surface area, with the 1200 showing a smaller size and higher specific surface area. Although all HAPNs inhibited cell proliferation and induced apoptosis of cancer cells,1200 exhibited the greatest toxicity. All types of HAPNs were internalized through energy-dependent pathways, but the 1200 nanoparticles were more efficiently uptaken by MGC80-3 cells. Inhibitor studies with dynasore and methyl-beta-cyclodextrin suggested that caveolae-mediated endocytosis and, to a much lesser extent, clathrin-mediated endocytosis, were involved in cellular uptake of the various preparations, whereas the inhibition of endocytosis was more obvious for L200. Using fluorescein isothiocyanate-labeled HAPNs and laser-scanning confocal microscopy, we found that all forms of nanoparticles were present in the cytoplasm, and some L200 HAPNs were even found within nuclei. Treatment with all HAPN preparations led to the increase in the intracellular calcium level with the highest level detected for L200. (C) 2016 Elsevier B.V. All rights reserved.

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