سامانه مدیریت نشریات علمی دانشگاه علوم پزشکی مشهد

Abdollahzade, Aref, Rahimi, Hoda, Yaghoobi, Elnaz, Ramezani, Mohammad, Alibolandi, Mona, Abnous, Khalil, Taghdisi, Seyed Mohammad. (1402). Targeted delivery of doxorubicin and therapeutic FOXM1 aptamer to tumor cells using gold nanoparticles modified with AS1411 and ATP aptamers. , 26(10), 1177-1187. doi: 10.22038/ijbms.2023.71129.15452
Aref Abdollahzade; Hoda Rahimi; Elnaz Yaghoobi; Mohammad Ramezani; Mona Alibolandi; Khalil Abnous; Seyed Mohammad Taghdisi. "Targeted delivery of doxorubicin and therapeutic FOXM1 aptamer to tumor cells using gold nanoparticles modified with AS1411 and ATP aptamers". , 26, 10, 1402, 1177-1187. doi: 10.22038/ijbms.2023.71129.15452
Abdollahzade, Aref, Rahimi, Hoda, Yaghoobi, Elnaz, Ramezani, Mohammad, Alibolandi, Mona, Abnous, Khalil, Taghdisi, Seyed Mohammad. (1402). 'Targeted delivery of doxorubicin and therapeutic FOXM1 aptamer to tumor cells using gold nanoparticles modified with AS1411 and ATP aptamers', , 26(10), pp. 1177-1187. doi: 10.22038/ijbms.2023.71129.15452
Abdollahzade, Aref, Rahimi, Hoda, Yaghoobi, Elnaz, Ramezani, Mohammad, Alibolandi, Mona, Abnous, Khalil, Taghdisi, Seyed Mohammad. Targeted delivery of doxorubicin and therapeutic FOXM1 aptamer to tumor cells using gold nanoparticles modified with AS1411 and ATP aptamers. , 1402; 26(10): 1177-1187. doi: 10.22038/ijbms.2023.71129.15452

Targeted delivery of doxorubicin and therapeutic FOXM1 aptamer to tumor cells using gold nanoparticles modified with AS1411 and ATP aptamers

Iranian Journal of Basic Medical Sciences
مقاله 8، دوره 26، شماره 10، دی 2023، صفحه 1177-1187    اصل مقاله (872.35 K)
نوع مقاله: Original Article
شناسه دیجیتال (DOI): 10.22038/ijbms.2023.71129.15452
نویسندگان
Aref Abdollahzade1؛ Hoda Rahimi1؛ Elnaz Yaghoobi2، 3؛ Mohammad Ramezani2؛ Mona Alibolandi2؛ Khalil Abnous* 2، 4؛ Seyed Mohammad Taghdisi* 5، 6
1School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran
2Pharmaceutical Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran
3Department of Chemistry and Biomolecular Sciences, University of Ottawa, 10 Marie-Curie, Ottawa, ON K1N 6N5, Canada
4Department of Medicinal Chemistry, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran
5Targeted Drug Delivery Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran
6Department of Pharmaceutical Biotechnology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran
چکیده
Objective(s): A targeted delivery platform was prepared to co-deliver both doxorubicin (Dox) as an anticancer drug and FOXM1 aptamer as a therapeutic substance to breast cancer cells (4T1 and MCF-7) to reduce Dox side effects and increase its therapeutic efficacy. The targeted system (AuNPs-AFPA) consisted of FOXM1 aptamer, AS1411 aptamer (targeting oligonucleotide), ATP aptamer, and gold nanoparticles (AuNPs) as a carrier.
Materials and Methods: AuNPs were synthesized by reduction of HAuCl4. Next, after pegylation of ATP aptamer, FOXM1 aptamer-PEGylated ATP aptamer conjugate (FPA) was prepared. Then, the AS1411 aptamer and FPA were exposed to the AuNPs surface through their thiol groups. Subsequently, Dox was loaded into the complex to form a targeted therapeutic complex.
Results: The data of the MTT assay displayed that the targeted complex could remarkably reduce cell viability rate in target cells due to the overexpression of nucleolin on their cell membranes compared to nontarget cells, showing the targeting ability of AuNPs-AFPA-Dox. The in vivo antitumor effect confirmed that AuNPs-AFPA-Dox was capable of remarkably diminishing tumor growth relative to the free Dox in mice bearing 4T1 tumor cells. 
Conclusion: The results confirmed that the targeted system improved the therapeutic effect by loading high amounts of Dox alongside the presence of the therapeutic effect of FOXM1 aptamer. Finally, it can be concluded that AuNPs-AFPA-Dox by enhancing antitumor effectiveness and reducing toxicity toward non-target cells, can be used potentially as an effective strategy for the treatment of breast cancer.v
کلیدواژه‌ها
Aptamers؛ Antineoplastic agents؛ Cell survival؛ Metal nanoparticles؛ Nucleolin؛ Doxorubicin
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