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Sericin Grafted Multifunctional Curcumin Loaded Fluorinated Graphene Oxide Nanomedicines With Charge Switching Properties for Effective Cancer Cell Targeting Publisher Pubmed



Jahanshahi M1 ; Kowsari E1 ; Haddadiasl V2 ; Khoobi M3 ; Lee JH4 ; Kadumudi FB5 ; Talebian S6, 7 ; Kamaly N4, 8 ; Mehrali M5
Authors
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Authors Affiliations
  1. 1. Amirkabir University of Technology, Department of Chemistry, Tehran, 1591634311, Iran
  2. 2. Amirkabir University of Technology, Department of Polymer Engineering and Color Technology, Tehran, 1591634311, Iran
  3. 3. The Institute of Pharmaceutical Sciences (TIPS), Tehran University of Medical Sciences, Tehran, 1417614411, Iran
  4. 4. Technical University of Denmark, Department of Micro and Nanotechnology, DTU Nanotech, Bioinspired Nanomaterials Lab, Kgs. Lyngby, 2800, Denmark
  5. 5. Technical University of Denmark, Department of Health Technology, Center for Intestinal Absorption and Transport of Biopharmaceuticals, Kgs. Lyngby, 2800, Denmark
  6. 6. University of Wollongon, Illawarra Health and Medical Research Institute, 2522, NSW, Australia
  7. 7. University of Wollongong, Intelligent Polymer Research Institute, ARC Centre of Excellence for Electromaterials Science, AIIM Facility, 2522, NSW, Australia
  8. 8. Imperial College London, Department of Chemistry, Molecular Science Research Hub, W12 0BZ London, United Kingdom

Source: International Journal of Pharmaceutics Published:2019


Abstract

Fluorinated graphene has recently gained much attention for cancer drug delivery, owing to its peculiar properties including high electronegativity difference, magnetic resonance imaging contrast agent, and the photothermal effect. However, the hydrophobic nature of fluorinated graphene greatly hinders its application as a biological material. Herein, a novel green method is reported for synthesis of a pH-sensitive charge-reversal and water-soluble fluorinated graphene oxide, modified with polyethyleneimine anchored to sericin-polypeptide (FPS). This nanocarrier was further loaded with curcumin (Cur), and characterized as a nanocarrier for anti-cancer drug delivery. The synthesized nanocarriers contain two different pH-sensitive amide linkages, which are negatively charged in blood pH (≈7.4) and can prolong circulation times. The amide linkages undergo hydrolysis once they reach the mildly acidic condition (pH≈6.5, corresponding to tumor extracellular matrix), and subsequently once reached the lower acidic condition (pH≈5.5, corresponded to endo/lysosomes microenvironment), the FPS charge can be switched to positive (≈+28 mV), which aids the nuclear release. This nanocarrier was designed to selectively enhance cell internalization and nuclear-targeted delivery of curcumin in HeLa, SkBr3 and PC-3 cancer cells. Moreover, FPS-Cur demonstrated high curcumin loading capacity, prolonged curcumin release and promotion of apoptosis in HeLa, SkBr3 and PC-3 cells. Therefore, with its pH-responsive charge-reversal properties, FPS-Cur would be a promising candidate for chemotherapy of cervical, breast and prostate cancers. © 2019 Elsevier B.V.