The biocompatibility of fluorescent nanodiamonds and their mechanism of cellular uptake.

Abstract

The labeling of cells with fluorescent nanoparticles is promising for various biomedical applications. The objective of this study is to evaluate the biocompatibility and the mechanism of the cellular uptake of fluorescent nanodiamonds (FNDs) in cancer cells (HeLa) and pre-adipocytes (3T3-L1). With flow cytometry and the use of a battery of metabolic and cytoskeletal inhibitors, we found that the mechanism of the FND uptake in both cells is by energy-dependent clathrin-mediated endocytosis. In addition, the surface charge of FND influences its cellular uptake, as the uptake of poly-L-lysine-coated FNDs is better than that of oxidative-acid-purified FNDs at the same concentration in regular medium with or without serum. We also confirm that the proliferative potential of FND-treated and untreated cells does not exhibit any significant differences when measured at bulk cultures, and more stringently at clonal cell density. Further biocompatibility studies indicate that the in vitro differentiation of 3T3-L1 pre-adipocytes and 489-2 osteoprogenitors is not affected by the FND treatment. Our results show that FNDs are biocompatible and ideal candidates for potential applications in human stem cell research.

• Authors: Vairakkannu Vaijayanthimala, Yan-Kai Tzeng, Huan-Cheng Chang, Chung-Leung Li
• Journal: Nanotechnology (Nanotechnology) Vol. 20 Issue 42 Pg. 425103 (Oct 21 2009) ISSN: 1361-6528 [Electronic] England
• PMID: 19779240 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Biocompatible Materials
• Culture Media, Conditioned
• Fluorescent Dyes
• Diamond
• Lysine

Topics

• Adipocytes (metabolism)
• Animals
• Biocompatible Materials (chemistry, pharmacokinetics)
• Cattle
• Cell Differentiation
• Cell Line
• Cell Proliferation
• Culture Media, Conditioned
• Diamond (chemistry, pharmacokinetics, pharmacology)
• Endocytosis (drug effects)
• Flow Cytometry
• Fluorescent Dyes (chemistry, pharmacokinetics, pharmacology)
• HeLa Cells
• Humans
• Lysine (chemistry)
• Materials Testing (methods)
• Mice
• Nanostructures (chemistry)
• Serum (metabolism)