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Electrospun Doxorubicin-Loaded Peo/Pcl Core/Sheath Nanofibers for Chemopreventive Action Against Breast Cancer Cells Publisher



Darbasizadeh B1, 2 ; Mortazavi SA1 ; Kobarfard F3 ; Jaafari MR4 ; Hashemi A5 ; Farhadnejad H1 ; Feyzibarnaji B6
Authors
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Authors Affiliations
  1. 1. Department of Pharmaceutics and Pharmaceutical Nanotechnology, School of Pharmacy, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  2. 2. Student Research Committee, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  3. 3. Department of Medicinal Chemistry, School of Pharmacy, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  4. 4. Department of Pharmaceutical Nanotechnology, School of Pharmacy, Mashhad University of Medical Sciences, Mashhad, Iran
  5. 5. Department of Pharmaceutical Biotechnology, School of Pharmacy, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  6. 6. Department of Pharmaceutical Nanotechnology, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran

Source: Journal of Drug Delivery Science and Technology Published:2021


Abstract

In the present study, polyethylene oxide (PEO)/polycaprolactone (PCL) core/sheath nanofibers were prepared via co-axial electrospinning method. Doxorubicin hydrochloride (DOX) was loaded into the core section of the electrospun nanofibers and their sustained drug release and the cytotoxicity against the MCF-7 breast cancer cell lines were evaluated. The PEO/PCL core/sheath nanofibers were characterized by Fourier-transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), X-ray diffraction (XRD), scanning electron microscope (SEM) and transmission electron microscopy (TEM). Moreover, their tensile strength and degradation behavior were investigated. In-vitro release of DOX from the nanofibers in phosphate buffer solution (PBS) at pH = 7.4 and its release kinetics were also evaluated. Finally, the cytotoxicity of the pristine and DOX loaded nanofibers was investigated. The degradation rate of the fiber mats was slow, indicating that the drug release was controlled by diffusion process. Nearly 20–30% of the drug was released at first day and till 28 days up to 60% of the drug was released. Their cell viability toward the MCF-7 breast cancer cells was examined via MTT assay at 1, 3, and 8 day. They showed no toxicity effect. Also, our results revealed high activity of the DOX-loaded core/sheath nanofibers against the MCF-7 breast cancer cells. © 2021 Elsevier B.V.
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