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Synthesis and evaluation of radiolabeled, folic acid-PEG conjugated, amino silane coated magnetic nanoparticles in tumor bearing Balb/C mice

Treść / Zawartość
Identyfikatory
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
To design a potent agent for positron emission tomography/magnetic resonance imaging (PET/MRI) imaging and targeted magnetic hyperthermia-radioisotope cancer therapy radiolabeled surface modified superparamagnetic iron oxide nanoparticles (SPIONs) were used as nanocarriers. Folic acid was conjugated for increasing selective cellular binding and internalization through receptor-mediated endocytosis. SPIONs were synthesized by the thermal decomposition of tris (acetylacetonato) iron (III) to achieve narrow and uniform nanoparticles. To increase the biocompatibility of SPIONs, they were coated with (3-aminopropyl) triethoxysilane (APTES), and then conjugated with synthesized folic acid-polyethylene glycol (FA-PEG) through amine group of (3-aminopropyl) triethoxysilane. Finally, the particles were labeled with 64Cu (t1/2 = 12.7 h) using 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid mono (N-hydroxy succinimide ester) DOTA-NHS chelator. After the characterization of SPIONs, their cellular internalization was evaluated in folate receptor (FR) overexpressing KB (established from a HeLa cell contamination) and mouse fibroblast cell (MFB) lines. Eventually, active and passive targeting effects of complex were assessed in KB tumor-bearing Balb/C mice through biodistribution studies. Synthesized bare SPIONs had low toxicity effect on healthy cells, but surface modification increased their biocompatibility. Moreover, KB cells viability was reduced when using folate conjugated SPIONs due to FR-mediated endocytosis, while having little effect on healthy cells (MFB). Moreover, this radiotracer had tolerable in vivo characteristics and tumor uptake. In the receptor blocked case, tumor uptake was decreased, indicating FR-specifi c uptake in tumor tissue while enhanced permeability and retention effect was major mechanism for tumor uptake.
Czasopismo
Rocznik
Strony
497--502
Opis fizyczny
Bibliogr. 27 poz., rys.
Twórcy
autor
  • Department of Engineering, Garmsar Branch, Islamic Azad University, Garmsar, Iran, Tel.: +9891 0942 2335, Fax: 026 3446 4053
autor
  • Department of Energy Engineering and Physics, Amirkabir University of Technology, Tehran, Iran
autor
  • Young Researchers and Elite Club, South Tehran Branch, Islamic Azad University, Tehran, Iran
  • Biomedical Engineering Department, Science and Research Branch, Islamic Azad University, Tehran, Iran
  • Nuclear Medicine Research Group, Alborz Research Center, Karaj, Iran
  • Nuclear Engineering Department, East Tehran Branch, Islamic Azad University, Tehran, Iran
Bibliografia
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  • 6. Feng, B., Hong, R. Y., Wang, L. S., Guoc, L., Li, H. Z., Dingd, J., Zhenge, Y., & Wei, D. G. (2008). Synthesis of Fe3O4/APTES/PEG diacid functionalized magnetic nanoparticles for MR imaging B. Colloid.Surf. A-Physicochem. Eng. Asp., 328, 52–59. DOI:10.1016/j.colsurfa.2008.06.024.
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  • 15. Sun, G., Hagooly, A., Xu, J., Nystrom, A. M., Li, Z., Rossin, R., Moore, D. A., Wooley, K. L., & Welch, M. J. (2008). Facile, efficient approach to accomplish tunable chemistries and variable biodistributions for shell crosslinked nanoparticles. Biomacromolecules, 9, 1997–2006. DOI: 10.1021/bm800246x.
  • 16. Sun, X., Rossin, R., Turner, J. L., Becker, M. L., Joralemon, M. J., Welch, M. J., & Wooley, K. L. (2005).An assessment of the effects of shell cross-linked nanoparticle size, core composition, and surface PEGylation on in vivo biodistribution. Biomacromolecules, 6, 2541–2554. DOI: 10.1021/bm050260e.
  • 17. Sun, X., & Anderson, C. (2004). Production and applications of copper-64 radiopharmaceuticals. Method. Enzymol., 386, 237–261. DOI: 10.1016/S0076-6879(04)86011-7.
  • 18. McCarthy, D., Shefer, R., Klinkowstein, R., Bass, L.,Margeneau, W., Cutler, C., Anderson, C., & Welch, M. (1997). Efficient production of high specific activity 64Cu using a biomedical cyclotron. Nucl. Med. Biol., 24, 35–43. DOI: 10.1016/S0969-8051(96)00157-6.
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  • 21. Heidari Majd, M., Asgari, D., Barara, J., Valizadeh, H., Kafi l, V., Abadpour, A., Moumivand, E., Shahbazi Mojarrad, J., Rashidi, M. R., Coukos, G., & Omidi, Y. (2013). Tamoxifen loaded folic acid armed PEGylated magnetic nanoparticles for targeted imaging and therapy of cancer. J. Colloid. Surf. B-Biointerfaces,106, 117–125. DOI: 10.1016/j.colsurfb.2013.01.051.
  • 22. Yang, X., Hong, H., Grailer, J. J., Rowland, I. J., Javadi, A., Hurley, S. A., Xiao, Y., Yang, Y., Zhang, Y., Nickles, R. J., Cai, W., Steeber, D. A., & Gonge, S. (2011).RGD-functionalized, DOX-conjugated, and 64Cu--labeled superparamagnetic iron oxide nanoparticles for targeted anticancer drug delivery and SPECT/MR imaging. J. Biomater., 32(17), 4151–4160. DOI:10.1016/j.biomaterials.2011.02.006.
  • 23. Xu, Z., Shen, C., Hou, Y., Gao, H., & Sun, S. (2009).Oleylamine as both reducing agent and stabilizer in a facile synthesis of magnetite nanoparticles. J. Chem. Mater., 21, 1778–1780. DOI: 10.1021/cm802978z.
  • 24. Xie, J., Xu, C., Xu, Z., Hou, Y., Young, K. L., Wang, S. X., Pourmand, N., & Sun, S. (2006). Linking hydrophilic macromolecules to monodisperse magnetite (Fe3O4) nanoparticles via trichloro-s-triazine.J. Chem. Mater., 18(3), 5401–5403. DOI: 10.1021/cm061793c.
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  • 26. Rossin, R., Pan, D., Qi, K., Turner, J. L., Sun, X., Wooley, K. L., & Welch, M. J. (2005). 64Cu-labeled folate-conjugated shell cross-linked nanoparticles for tumor imaging and radiotherapy: synthesis, radiolabeling, and biologic evaluation J. Nucl. Med.,46, 1210–1218.
  • 27. Zolata, H., Afarideh, H., & Abbasi-Davani, F. (2014).Radio-immunoconjugated, Dox-loaded, surface--modified superparamagnetic iron oxide nanoparticles (SPIONs) as a bioprobe for breast cancer tumor theranostics. J. Radioanal. Nucl. Chem., 301, 451–460.DOI: 10.1007/s10967-014-3101-6.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-b42b5726-b5d4-4004-b18e-d3ee1f5c008e
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