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Preparation and characterization of chitosan—Polyethylene glycol‐polyvinylpyrrolidone‐coated superparamagnetic iron oxide nanoparticles as carrier system: Drug loading and in vitro drug release study
Author(s) -
Prabha G.,
Raj V.
Publication year - 2016
Publication title -
journal of biomedical materials research part b: applied biomaterials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.665
H-Index - 108
eISSN - 1552-4981
pISSN - 1552-4973
DOI - 10.1002/jbm.b.33637
Subject(s) - polyvinylpyrrolidone , polyethylene glycol , nuclear chemistry , chitosan , nanoparticle , zeta potential , fourier transform infrared spectroscopy , peg ratio , chemistry , drug delivery , chemical engineering , materials science , nanotechnology , organic chemistry , finance , engineering , economics
In the present research work, the anticancer drug “curcumin” is loaded with Chitosan (CS)—polyethylene glycol (PEG)‐polyvinylpyrrolidone (PVP) (CS‐PEG‐PVP) polymer nanocomposites coated with superparamagnetic iron oxide (Fe 3 O 4 ) nanoparticles. The system can be used for targeted and controlled drug delivery of anticancer drugs with reduced side effects and greater efficiency. The prepared nanoparticles were characterized by Fourier transmission infrared spectroscopy (FTIR), vibrating sample magnetometry (VSM), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). Curcumin drug‐loaded Fe 3 O 4 ‐CS, Fe 3 O 4 ‐CS‐ PEG and Fe 3 O 4 ‐CS‐PEG‐PVP nanoparticles exhibited the mean particle size in the range of 183 − 390 nm with a zeta potential value of 26 mV−41 mV as measured using Malvern Zetasizer. The encapsulation efficiency, loading capacity and in‐vitro drug release behaviour of curcumin drug‐loaded Fe 3 O 4 ‐CS, Fe 3 O 4 ‐CS‐PEG, and Fe 3 O 4 ‐CS‐PEG‐PVP nanoparticles were studied using UV spectrophotometer. Besides, the cytotoxicity of the prepared nanoparticles using MTT assay was also studied. The curcumin drug release was examined at different pH medium (4.5 and 7.4) and temperature (37°C and 45°C), and it was proved that the drug release depends upon the pH medium and temperature in addition to the nature of matrix. © 2016 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 104B: 808–816, 2016.