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Synergistic effects of Titanium dioxide nanoparticles and Paclitaxel combination on the DNA structure and their antiproliferative role on MDA-MB-231cells | ||
Journal of Nanoanalysis | ||
دوره 7، شماره 2، شهریور 2020، صفحه 152-165 اصل مقاله (1.22 M) | ||
نوع مقاله: Original Research Paper | ||
شناسه دیجیتال (DOI): 10.22034/jna.2020.677396 | ||
نویسندگان | ||
Azadeh Hekmat* 1؛ Masoumeh Afrough1؛ Saeed Hesami Tackallou2؛ Faizan Ahmad3 | ||
1Department of Biology, Science and Research Branch, Islamic Azad University, Tehran, Iran | ||
2Department of Biology, Central Tehran Branch, Islamic Azad University, Tehran, Iran | ||
3Centre for Interdisciplinary Research in Basic Sciences, Jamia Millia Islamia, New Delhi, India | ||
چکیده | ||
Objective(s): The objective of this investigation was to evaluate the synergistic effect of paclitaxel (PTX) combined with titanium dioxide nanoparticles (TiO2NPs) on DNA structure and to examine the proliferation of MDA-MB-231cells. Methods: This investigation performed with Ultraviolet spectroscopy, zeta potential investigation, circular dichroism (CD) spectroscopy, ELISA reader and fluorescence spectroscopy. Results: The Ultraviolet results indicated that the structure of DNA in the presence of PTX and TiO2NPs (at a lower concentration) changed significantly rather than TiO2NPs or PTX alone. The fluorescence results exposed that PTX+TiO2NPs could form a complex via non-intercalative mechanism and the PTX+TiO2NPs affinity to DNA increased considerably. The thermodynamics parameters displayed that PTX+TiO2NPs interact with DNA strongly and in this interaction, the hydrophobic force plays an important role. The CD data confirmed that DNA structure was modified by PTX+TiO2NPs via a simple and reasonable mechanism: change in DNA conformation from B to C-form. The negative charge of DNA reduced strongly after addition of PTX+TiO2NPs. The anticancer property of PTX+TiO2NPs by MTT assay demonstrates that this combination can tremendously diminish the proliferation of MDA-MB-231cells compared to PTX or TiO2NPs alone. Conclusions: Based on this investigation TiO2NPs could enhance the affinity and binding of PTX (at a lower concentration) on DNA structure and PTX+NDs can promote mortality of MDA-MB-231 cells. This study can offer an innovative strategy for designing the ideal anti-tumor agents. | ||
کلیدواژهها | ||
Titanium dioxide nanoparticles (TiO2NPs) Paclitaxel (PTX) Spectroscopy C؛ form DNA MDA؛ MB؛ 231cells | ||
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