In vitro biological effects of sodium titanate materials

R. R. Davis, P. E. Lockwood, D. T. Hobbs, Regina L W Messer, R. J. Price, J. B. Lewis, J. C. Wataha

Research output: Contribution to journalArticle

30 Citations (Scopus)

Abstract

Monosodium titanate (MST) particles effectively bind specific metals and are therefore promising compounds for delivery or sequestration of metals in biological contexts. Yet, the biological properties of MST are largely unexplored. Our previous study showed that the cytotoxicity of these compounds was mild, but the nature of the dose response curves suggested that residual titanates in culture may have interfered with the assay. In the current study, we assessed the importance of these artifacts, and extended our previous results using fibroblasts for biological evaluation. We also assessed the biological response to a new type of titanate (referred to as amorphous peroxo-titanate or APT) that shows more promising metal binding properties than MST. Methods: The degree of titanate-induced interference in the MTT (mitochondrial activity assay) was estimated by means of cell-free assays with and without a final centrifugation step to remove residual titanate particulate. Cytotoxic responses to titanates were assessed by measuring succinate dehydrogenase activity (by MTT) in THP1 monocytes or L929 fibroblasts after 24-72 h exposures. Monocytic activation by APT was assessed by TNFα secretion (ELISA) from monocytes: with or without lipopolysaccharide (LPS) activation. Results: We confirmed that residual titanate particulates may alter the SDH activity assay, but that this effect is eliminated by adding a final centrifugation step to the standard MTT procedure. Addition of MST or APT at concentrations up to 100 mg/L altered succinate dehydrogenase activity by < 25% in both monocytes and fibroblasts. Fibroblasts displayed time-dependent adaptation to the MST. APT did not trigger TNFα secretion or modulate LPS-induced TNFα secretion from monocytes. Conclusions: Although further in vitro and in vivo assessment is needed, MST and APT exhibit biological properties that are promising for their use as agents to sequester or deliver metals in biological systems.

Original languageEnglish (US)
Pages (from-to)505-511
Number of pages7
JournalJournal of Biomedical Materials Research - Part B Applied Biomaterials
Volume83
Issue number2
DOIs
StatePublished - Nov 1 2007

Fingerprint

Fibroblasts
Assays
Sodium
Monocytes
Metals
Centrifugation
Succinate Dehydrogenase
Chemical activation
Lipopolysaccharides
Sequestering Agents
Biological systems
Cytotoxicity
Artifacts
Enzyme-Linked Immunosorbent Assay
APT
sodium titanate
In Vitro Techniques
Oxidoreductases

Keywords

  • Cell-culture
  • Cytotoxicity
  • Drug-delivery
  • Fibroblast
  • MTT
  • Monocyte

ASJC Scopus subject areas

  • Biomaterials
  • Biomedical Engineering

Cite this

In vitro biological effects of sodium titanate materials. / Davis, R. R.; Lockwood, P. E.; Hobbs, D. T.; Messer, Regina L W; Price, R. J.; Lewis, J. B.; Wataha, J. C.

In: Journal of Biomedical Materials Research - Part B Applied Biomaterials, Vol. 83, No. 2, 01.11.2007, p. 505-511.

Research output: Contribution to journalArticle

Davis, R. R. ; Lockwood, P. E. ; Hobbs, D. T. ; Messer, Regina L W ; Price, R. J. ; Lewis, J. B. ; Wataha, J. C. / In vitro biological effects of sodium titanate materials. In: Journal of Biomedical Materials Research - Part B Applied Biomaterials. 2007 ; Vol. 83, No. 2. pp. 505-511.
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