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Chitosan/Agarose/Graphitic Carbon Nitride Nanocomposite As an Efficient Ph-Sensitive Drug Delivery System for Anticancer Curcumin Releasing Publisher



Rajabzadehkhosroshahi M1 ; Pourmadadi M1 ; Yazdian F2 ; Rashedi H1 ; Navaeinigjeh M3, 4 ; Rasekh B5
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Authors Affiliations
  1. 1. Department of Biotechnology, School of Chemical Engineering, College of Engineering, University of Tehran, Tehran, Iran
  2. 2. Department of Life Science Engineering, Faculty of New Science and Technologies, University of Tehran, Tehran, Iran
  3. 3. Pharmaceutical Sciences Research Center, The Institute of Pharmaceutical Sciences (TIPS), Tehran University of Medical Sciences (TUMS), Tehran, Iran
  4. 4. Department of Pharmaceutical Biomaterials and Medical Biomaterials Research Center, Faculty of Pharmacy, Tehran University of Medical Sciences (TUMS), Tehran, Iran
  5. 5. ALMA MATER STUDIORUM - Universita di Bologna, Via Zamboni, Bologna, 33 - 40126, Italy

Source: Journal of Drug Delivery Science and Technology Published:2022


Abstract

As breast cancer is a common illness that leads to high death rates all over the world, achieving more efficient therapeutic ways such as novel drug delivery can be helpful. In this study, a novel pH-sensitive nanocarrier based on a composite of chitosan (CS)/agarose (AG)/graphitic carbon nitride (g-C3N4) curcumin (Cur) unique properties was developed to deliver curcumin (Cur). Firstly, CS/AG and CS/AG/g-C3N4 hydrogels were prepared as the matrix of the nanocarriers, and Cur was entrapped, then water-in-oil-in-water (W/O/W) emulsification method was applied to form the final nanocarriers. XRD, FTIR, Zeta/DLS, and FESEM characterization analysis confirmed the chemical bonds between CS, AG, and g-C3N4, and also the interactions with the drug and 222 nm mean size was revealed for CS/AG/g-C3N4/Cur nanocomposites with spherical morphology. High Cur loading and entrapment efficiency were obtained. On the other hand, g-C3N4 incorporation with CS/AG enhanced them respectively from 42 to 54% and 83–94%. Release studies, demonstrated an excellent controlled pH-sensitive release profile, furthermore, g-C3N4 nanosheets ameliorated drug release from CS/AG/g-C3N4/Cur nanocarriers. In-vitro cytotoxicity was investigated via MTT assay and flow cytometry analysis. CS/AG/g-C3N4/Cur nanocomposites significantly decreased the viability of the cancer cells to 12% compared to free Cur. The cells treated with CS/AG/g-C3N4/Cur exhibited the most apoptosis rate of 77.8% in breast cancer cell line MCF-7, which reveals the high performance of the nanocomposites in the killing of cancer cells. © 2022 Elsevier B.V.
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