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A multi-storey DNA nanostructure containing doxorubicin and AS1411 aptamer for targeting breast cancer cells.
Yaghoobi, Elnaz; Zavvar, TaranehSadat; Ramezani, Mohammad; Alibolandi, Mona; Rahimzadeh Oskuei, Sara; Zahiri, Mahsa; Alinezhad Nameghi, Morteza; Abnous, Khalil; Taghdisi, Seyed Mohammad.
Affiliation
  • Yaghoobi E; Pharmaceutical Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran.
  • Zavvar T; Department of Chemistry and Biomolecular Sciences, University of Ottawa, Ottawa, ON, Canada.
  • Ramezani M; Pharmaceutical Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran.
  • Alibolandi M; Department of Medicinal Chemistry, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran.
  • Rahimzadeh Oskuei S; Pharmaceutical Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran.
  • Zahiri M; Pharmaceutical Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran.
  • Alinezhad Nameghi M; Department of Medicinal Chemistry, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran.
  • Abnous K; Biotechnology Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
  • Taghdisi SM; Department of Pharmaceutical Nanotechnology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran.
J Drug Target ; 30(10): 1106-1112, 2022 12.
Article in En | MEDLINE | ID: mdl-35736221
ABSTRACT
Herein, we presented a novel DOX-loaded multi-storey DNA nanostructure, including AS1411 aptamer as a targeting agent for treatment of target cells (MCF-7 and 4T1). Gel retardation test and fluorometric analysis were used to examine the construction of DNA nanostructure and loading of DOX in the complex. At pH 5.5 and 7.4, the release patterns of DOX from the prepared formulation were studied. Cell viability test was conducted to analyse the cell cytotoxicity ability of the DOX loaded multi-storey DNA nanostructure compared to free DOX in 4T1, MCF-7 (target) and CHO cells (non-target). Flow cytometry analysis was used to examine the DOX-loaded DNA nanostructure internalisation. Finally, the developed DOX-loaded multi-storey DNA nanostructure was tested in vivo to see if it could prevent tumour growth. The drug was released from the nanocomplex in a pH-related process (higher release in acidic pH compared to neutral pH). According to MTT assay, DOX-loaded DNA nanostructure damaged nucleolin positive cells while not significantly affecting nucleolin negative cells. The formulation was efficaciously internalised into target cells (4T1 and MCF-7), but not into non-target ones. Moreover, DOX-loaded DNA nanostructure can restrict tumour growth, increase survival rate, and accumulate significantly more in the tumour site than free DOX.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Breast Neoplasms / Nanostructures / Aptamers, Nucleotide Limits: Animals / Female / Humans Language: En Journal: J Drug Target Journal subject: FARMACOLOGIA Year: 2022 Document type: Article Affiliation country: Irán

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Breast Neoplasms / Nanostructures / Aptamers, Nucleotide Limits: Animals / Female / Humans Language: En Journal: J Drug Target Journal subject: FARMACOLOGIA Year: 2022 Document type: Article Affiliation country: Irán