Dispersion Characteristics of Zinc Oxide Nanoparticles in Ionic and Non-ionic Isotonic Solution

이온성 및 비이온성 등장액 용매에서 산화아연나노입자의 분산 특성

  • Choi, Jonghye (College of Pharmacy, Dongduk Women's University) ;
  • Kim, Hyejin (College of Pharmacy, Dongduk Women's University) ;
  • Park, Kwangsik (College of Pharmacy, Dongduk Women's University)
  • 최종혜 (동덕여자대학교 약학대학) ;
  • 김혜진 (동덕여자대학교 약학대학) ;
  • 박광식 (동덕여자대학교 약학대학)
  • Received : 2013.05.23
  • Accepted : 2013.07.08
  • Published : 2013.08.31

Abstract

Zinc oxide nanoparticles (ZnONPs) are widely used in a variety of products and cosmetic products including paper, paints, plastics and sunscreen. However, information on the safety of ZnONPs are not enough and many publications suggest possible toxic effects on environmental and human health. Furthermore, physico-chemical characteristics of nanoparticles makes it hard to test toxicity using the test guidelines of chemicals adopted by regulatory bodies. In this study, stability of ZnONPs was investigated using different types of isotonic solution, which is important in the toxicity study of intravenous route. Precipitation, aggregation, size, zeta potential and morphology of ZnONPs were evaluated with different times and concentrations. Precipitation of ZnONPs were observed in ionic isotonic solution including phosphate-buffered saline, Kreb's-Ringer solution, physiological salt solution and cell culture media of DMEM (Dulbecco's Modified Eagle's Medium) with 10% fetal bovine serum. On the other hand, they were stable without precipitation in non-ionic isotonic solution such as 5% glucose and 2% glycerol, respectively, which are biocompatible for intravenous injection. The average size of ZnONPs in 5% glucose and 2% glycerol was stably maintained, which is less than 30 nm and very similar as that in water dispersion of ZnONPs, provided by the manufacturer. The stability was maintained during the experimental period of 5 days and diluted state up to 15,000 ppm. These data suggest that 5% glucose and 2% glycerol solution can be used for the vehicles of ZnONPs in the toxicity study of intravenous injection route.

Keywords

References

  1. Nohynek, G. J. and Dufour, E. K. : Nano-sized cosmetic formulations or solid nanoparticles in sunscreens: a risk to human health? Arch. Toxicol. 86, 1063 (2012). https://doi.org/10.1007/s00204-012-0831-5
  2. Hackenberg, S. and Kleinsasser, N. : Dermal toxicity of ZnO nanoparticles: a worrying feature of sunscreen? Nanomedicine (Lond) 7, 461 (2012). https://doi.org/10.2217/nnm.12.23
  3. Kao, Y. Y., Chen, Y. C., Cheng, T. J., Chiung, Y. M. and Liu, P. S. : Zinc oxide nanoparticles interfere with zinc ion homeostasis to cause cytotoxicity. Toxicol. Sci. 125, 462 (2012). https://doi.org/10.1093/toxsci/kfr319
  4. Sharma, V., Singh, S. K., Anderson, D., Tobin, D. J. and Dhawan, A. : Zinc oxide nanoparticle induced genotoxicity in primary human epidermal keratinocytes. J. Nanosci. Nanotechnol. 11, 3782 (2011). https://doi.org/10.1166/jnn.2011.4250
  5. Roy, R., Tripathi, A., Das, M. and Dwivedi, P. D. : Cytotoxicity and uptake of zinc oxide nanoparticles leading to enhanced inflammatory cytokines levels in murine macrophages: comparison with bulk zinc oxide. J. Biomed. Nanotechnol. 7, 110 (2011). https://doi.org/10.1166/jbn.2011.1226
  6. Sharma, V., Anderson, D. and Dhawan, A. : Zinc oxide nanoparticles induce oxidative stress and genotoxicity in human liver cells (HepG2). J. Biomed Nanotechnol. 7, 98 (2011). https://doi.org/10.1166/jbn.2011.1220
  7. Heng, B. C., Zhao, X., Xiong, S., Ng, K. W., Boey, F. Y. and Loo, J. S. : Toxicity of zinc oxide (ZnO) nanoparticles on human bronchial epithelial cells (BEAS-2B) is accentuated by oxidative stress. Food Chem. Toxicol. 48, 1762 (2010) https://doi.org/10.1016/j.fct.2010.04.023
  8. Wang, L., Wang, L., Ding, W. and Zhang, F. : Acute toxicity of ferric oxide and zinc oxide nanoparticles in rats. J. Nanosci. Nanotechnol. 10, 8617 (2010). https://doi.org/10.1166/jnn.2010.2483
  9. Pasupuleti, S., Alapati, S., Ganapathy, S., Anumolu, G., Pully, N. R. and Prakhya, B. M. : Toxicity of zinc oxide nanoparticles through oral route. Toxicol. Ind. Health 28, 675 (2012). https://doi.org/10.1177/0748233711420473
  10. Surekha, P., Kishore, A. S., Srinivas, A., Selvam, G., Goparaju, A., Reddy, P. N. and Murthy, P. B. : Repeated dose dermal toxicity study of nano zinc oxide with Sprague-Dawley rats. Cutan. Ocul. Toxicol. 31, 26 (2012). https://doi.org/10.3109/15569527.2011.595750
  11. Li, C. H., Shen, C. C., Cheng, Y. W., Huang, S. H., Wu, C. C., Kao, C. C., Liao, J. W., Kang, J. J. : Organ biodistribution, clearance, and genotoxicity of orally administered zinc oxide nanoparticles in mice. Nanotoxicology 6, 746 (2012). https://doi.org/10.3109/17435390.2011.620717
  12. Baek, M., Chung, H. E., Yu, J., Lee, J. A., Kim, T. H., Oh, J. M., Lee, W. J., Paek, S. M., Lee, J. K., Jeong, J., Choy, J. H. and Choi, S. J. : Pharmacokinetics, tissue distribution, and excretion of zinc oxide nanoparticles. Int. J. Nanomedicine. 7, 3081 (2012).
  13. Lee, Y. and Park, K. : The stability of citrate-capped silver nanoparticles in isotonic glycerol solution for intravenous injection. Yakhak Hoeji 56, 74 (2012).
  14. Kim, J. S., Song, K. S., Sung, J. H., Ryu, H. R., Choi, B. G., Cho, H. S., Lee, J. K. and Yu, I. J. : Genotoxicity, acute oral and dermal toxicity, eye and dermal irritation and corrosion and skin sensitisation evaluation of silver nanoparticles. Nanotoxicology PMID: 22417112 (2012)
  15. Kim, Y. S., Kim, J. S., Cho, H. S., Rha, D. S., Kim, J. M., Park, J. D., Choi, B. S., Lim, R., Chang, H. K., Chung, Y. H., Kwon, I. H., Jeong, J., Han, B. S. and Yu, I. J. : Twenty-eight-day oral toxicity, genotoxicity, and gender-related tissue distribution of silver nanoparticles in Sprague-Dawley rats. Inhal. Toxicol. 20, 575 (2008). https://doi.org/10.1080/08958370701874663
  16. Kim, Y. S., Song, M. Y., Park, J. D., Song, K. S., Ryu, H. R., Chung, Y. H., Chang, H. K., Lee, J. H., Oh, K. H., Kelman, B. J., Hwang, I. K. and Yu, I. J. : Subchronic oral toxicity of silver nanoparticles. Part Fibre Toxicol. 7, 20. (2010). https://doi.org/10.1186/1743-8977-7-20
  17. Park, E. J., Bae, E., Yi, J., Kim, Y., Choi, K., Lee, S. H., Yoon, J., Lee, B. C. and Park, K. : Repeated-dose toxicity and inflammatory responses in mice by oral administration of silver nanoparticles. Environ. Toxicol. Pharmacol. 30, 162. (2010). https://doi.org/10.1016/j.etap.2010.05.004
  18. Park, K., Park, E. J., Chun, I., Choi, K., Lee, S. H., Yoon, J. and Lee, B. C. : Bioavailability and toxicokinetics of citrate-coated silver nanoparticles in rats. Arch. Pharm. Res. 34, 153 (2011). https://doi.org/10.1007/s12272-011-0118-z
  19. Lee, Y., Kim, P., Yoon, J., Lee, B., Choi, K., Kil, K. and Park, K : Serum kinetics, distribution and excretion of silver in rabbits following 28 days after a single intravenous injection of silver nanoparticles. Nanotoxicology PMID22770226 (2012).
  20. Hong, J. S., Kim, S., Lee, S. H., Jo, E., Lee, B., Yoon, J., Eom, I., Kim, H. M., Kim, P., Choi, K., Lee, M. Y., Seo, Y. R., Kim, Y., Lee, Y., Choi, J. and Park, K. : Combined repeated dose toxicity study of silver nanoparticles with the reproduction/ developmental toxicity screening test. Nanotoxicology PMID: 23432083 (2013).