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Fluorescent Multi-Responsive Cross-Linked P(N-Isopropylacrylamide)-Based Nanocomposites for Cisplatin Delivery Publisher Pubmed



Shakoori Z1 ; Ghanbari H1 ; Omidi Y2 ; Pashaiasl M3, 4 ; Akbarzadeh A5, 6 ; Jomeh Farsangi Z1 ; Rezayat SM1, 7, 8, 9 ; Davaran S5, 10, 11
Authors
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Authors Affiliations
  1. 1. Department of Medical Nanotechnology, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran
  2. 2. Faculty of Pharmacy, Research Center for Pharmaceutical Nanotechnology, Tabriz University of Medical Sciences, Tabriz, Iran
  3. 3. Women’s Reproductive Health Research Centre, Tabriz University of Medical Sciences, Tabriz, Iran
  4. 4. Department of Anatomical Sciences, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran
  5. 5. Drug Applied Research Center, Tabriz University of Medical Sciences, Tabriz, Iran
  6. 6. Universal Scientific Education and Research Network (USERN), Tabriz, Iran
  7. 7. Department of Toxicology and Pharmacology, School of Pharmacy, Pharmaceutical Sciences Branch, Islamic Azad University (IAUPS), Tehran, Iran
  8. 8. Department of Pharmacology, School of Medicine, Tehran University of Medical Sciences, Tehran, Iran
  9. 9. Experimental Medicine Research Center, Tehran University of Medical Sciences, Tehran, Iran
  10. 10. Department of Medical Nanotechnology, Faculty of Advanced Medical Sciences, Tabriz University of Medical Sciences, Tabriz, Iran
  11. 11. Department of Medical Nanotechnology, Faculty of Advanced Medical Sciences, Tabriz University of Medical Sciences, Tabriz, Iran

Source: Drug Development and Industrial Pharmacy Published:2017


Abstract

Magnetic, pH and temperature-sensitive, poly(N-isopropylacrylamide) (PNIPAM)-based nanocomposites with fluorescent properties were synthesized by free radical copolymerization-cross linking of NIPAM, N,N-dimethylaminoethyl methacrylate (DMAEMA) and 4-acrylamidofluorescein (AFA). The model anti-cancer drug, cisplatin (CDDP), was loaded into the resulted nanogel. For the production of CDDP-loaded nanocomposite, Fe3O4 magnetic nanoparticles (MNPs) and CDDP were loaded into the nanogel. Field-emission scanning electron microscopy (FE-SEM) indicated that the size of nanogel and CDDP-loaded nanocomposite were about 90 and 160 nm, respectively. The encapsulation efficiency of CCDP was found up to 65%. The loaded CCDP showed sustained thermal and pH-responsive drug release. A high level of drug release was observed under the conditions of low pH and high temperature. The lower critical solution temperature (LCST) of synthesized nanogel was about 40 °C. CDDP-loaded nanocomposite showed a volume phase transition from 282 to 128 nm at its LCST. Accordingly, in this study, the synthesized nanocomposite can be employed as a stimuli-responsive anti-cancer drug delivery system and the pH and temperature of solution have the potential to monitor the drug release. © 2017 Informa UK Limited, trading as Taylor & Francis Group.