Skip to main content
Log in

Bioeffects of different functionalized silica nanoparticles on HaCaT cell line

  • Articles
  • Published:
Chinese Science Bulletin

    We’re sorry, something doesn't seem to be working properly.

    Please try refreshing the page. If that doesn't work, please contact support so we can address the problem.

Abstract

The bioeffects of silica nanoparticles (SiNP), phosphorylate-terminated nanoparticles (PO4NP) and amino-terminated nanoparticles (NH2NP) on HaCaT cell line have been studied in this paper. The effects of the three kinds of functionalized silica nanoparticles on adherence, proliferation and cycle of HaCaT cells have been investigated. And the cellular uptake of the three kinds of functionalized silica nanoparticles by HaCaT cells has also been examined. Results indicated that the bioeffects of the three kinds of functionalized nanoparticles on HaCaT cells were concentration-dependent. And the three kinds of functionalized nanoparticles all exhibited well biocompatibility if the concentration was below 0.2 μg/μL. While the cytotoxicities of the three kinds of functionalized nanoparticles on HaCaT cells would increase with the increasing of nanoparticles concentration, and the following order was observed: NH2NP > SiNP > PO4NP. In addition, the quantity and rapidity of cellular uptake of nanoparticles by HaCaT cells were diverse due to the different functional groups. Under the same conditions, NH2NP was most and fast internalized by HaCaT cells, followed by SiNP, and PO4NP was the least and slowest. These results provided theoretical foundation for the safe application and further modification of silica nanoparticles, which could broaden the application of silica nanoparticles in biomedicine.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Akerman M E, Chan W C W, Laakkonen P, et al. Nanocrystal targeting in vivo. PNAS, 2002, 99: 12617–12621

    Article  Google Scholar 

  2. Santra S, Zhang P, Wang K M, et al. Conjugation of biomolecules with luminophore-doped silica nanoparticles for photostable biomarkers. Anal Chem, 2001, 73: 4988–4993

    Article  Google Scholar 

  3. He X X, Wang K M, Tan W H, et al. Bioconjugated nanoparticles for DNA protection from cleavage. J Am Chem Soc, 2003, 125: 7168–7169

    Article  Google Scholar 

  4. Service R F. Nanomaterials show signs of toxicity. Science, 2003, 300(11): 243

    Article  Google Scholar 

  5. Zhang W X. Environmental technologies at the nanoscale. Environ Sci Technol, 2003, 37(5): 103–108

    Google Scholar 

  6. Kelly K L. Nanotechnology grows up. Science, 2004, 304: 1732–1734

    Article  Google Scholar 

  7. Jia G, Wang H F, Yan L, et al. Cytotoxicity of carbon nanomaterials: single-wall nanotube, multi-wall nanotube, and fullerene. Environ Sci Technol, 2005, 39:1378–1383

    Article  Google Scholar 

  8. Ajay K G, Mona G. Cytotoxicity suppression and cellular uptake enhancement of surface modified magnetic nanoparticles. Biomaterials, 2005, 26: 1565–1573

    Article  Google Scholar 

  9. Afaq F, Abidi P, Matin R, et al. Cytotoxicity, pro-oxidant effects and antioxidant depletion in rat lung alveolar macrophages exposed to ultrafine titanium dioxide. J Appl Toxicol, 1998, 18: 307–312

    Article  Google Scholar 

  10. Scholer N, Hahn H, Muller R H, et al. Effect of lipid matrix and size of solid lipid nanoparticles (SLN) on the viability and cytokine production of macrophages. Int J Pharm, 2002, 231: 167–176

    Article  Google Scholar 

  11. Ziady A G, Gedeon C R, Muhammad O, et al. Minimal toxicity of stabilized compacted DNA nanoparticles in the murine lung. Mol Ther, 2003, 8(6): 948–956

    Article  Google Scholar 

  12. Akiyoshi H, Kouki F, Taisuke O, et al. Physicochemical properties and cellular toxicity of nanocrystal quantum dots depend on their surface modification. Nano Lett, 2004, 4(11): 2163–2169

    Article  Google Scholar 

  13. Oberdörster G, Ferin J, Gelein R, et al. Role of the alveolar macrophage in lung injury: studies with ultrafine particles. Environ Health Perspec, 1992, 97: 193–199

    Google Scholar 

  14. Deng Y, Xu H B, Huang K X, et al. Size effects of realgar particles on apoptosis in a Human Umbilical Vein Endothelial Cell line: ECV-304. Pharmacol Res, 2001, 44(6): 513–518

    Article  Google Scholar 

  15. Sayes C M, John D F, Guo W, et al. The differential cytotoxicity of water-soluble fullerenes. Nano Lett, 2004, 4(10): 1881–1887

    Article  Google Scholar 

  16. Catherine M G, Catherine D M, Tuna Y, et al. Toxicity of gold nanoparticles functionalized with cationic and anionic side chains. Bioconjug Chem, 2004, 15: 897–900

    Article  Google Scholar 

  17. He X X, Wang K M, Tan W H, et al. Concentration of trace amounts oligonucleotide using super-paramagnetic DNA nano-enricher. Chem J Chinese U, 2003, 24(1): 40–42

    Google Scholar 

  18. Bruce I J, Sen T. Surface modification of magnetic nanoparticles with alkoxysilanes and their application in magnetic bioseparations. Langmuir, 2005, 21: 7029–7035

    Article  Google Scholar 

  19. He X X, Wang K M, Tan W H, et al. A novel fluorescent label based on biological fluorescent nanoparticles and its application in cell recognition. Chin Sci Bull, 2001, 46(16): 1353–1356

    Google Scholar 

  20. Wang L, Yang C Y, Tan W H. Dual-luminophore-doped silica nanoparticles for multiplexed signaling. Nano Lett, 2005, 5(1): 37–43

    Article  Google Scholar 

  21. Zhao X J, Tapec-Dytioco R, Tan W H. Ultrasensitive DNA detection using highly fluorescent bioconjugated nanoparticles. J Am Chem Soc, 2003, 125: 11474–11475

    Article  Google Scholar 

  22. He X X, Wang K M, Tan W H, et al. A novel gene carrier based on SiO2 amino nanoparticles. Chin Sci Bull, 2002, 47(18): 1365–1369

    Google Scholar 

  23. Yang H H, Zhang S Q, Chen X L, et al. Magnetite containing spherical silica nanoparticles for biocatalysis and bioseparations. Anal Chem, 2004, 76(5): 1316–1321

    Article  Google Scholar 

  24. Li D, He X X, Wang K M, et al. Cytotoxicity detection of silica nanoparticles. Human University Bull, 2002, 29(6): 1–6

    Google Scholar 

  25. Zhu S G, Gan K, Li Z, et al. Polylisine—the biocompatibility study of silica nanoparticles. Cancer, 2003, 22(10): 1114–1117

    Google Scholar 

  26. Inbaraj J J, Chignell C F. Cytotoxic action of juglone and plumbagin: a mechanistic study using HaCaT keratinocytes. Chem Res Toxicol, 2004, 17: 55–62

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Wang Kemin.

About this article

Cite this article

He, X., Liu, F., Wang, K. et al. Bioeffects of different functionalized silica nanoparticles on HaCaT cell line. CHINESE SCI BULL 51, 1939–1946 (2006). https://doi.org/10.1007/s11434-006-2077-1

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11434-006-2077-1

Keywords

Navigation