Functionalized graphene oxide/Fe3O4 nanocomposite: A biocompatible and robust nanocarrier for targeted delivery and release of anticancer agents

[Display omitted] •Graphene oxide nanosheets were decorated with superparamagnetic iron oxid nanoparticles (SPMGO).•The conjugation of methotrexate on functionalized SPMGO was confirmed by different techniques.•This MTX nanocarrier demonstrated high drug loading and optimum ability for a controlled...

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Veröffentlicht in:Journal of biotechnology 2021-04, Vol.331, p.26-36
Hauptverfasser: Taheri-Kafrani, Asghar, Shirzadfar, Hamidreza, Abbasi Kajani, Abolghasem, Kudhair, Bassam K., Jasim Mohammed, Layth, Mohammadi, Shima, Lotfi, Fatemeh
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Sprache:eng
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Zusammenfassung:[Display omitted] •Graphene oxide nanosheets were decorated with superparamagnetic iron oxid nanoparticles (SPMGO).•The conjugation of methotrexate on functionalized SPMGO was confirmed by different techniques.•This MTX nanocarrier demonstrated high drug loading and optimum ability for a controlled drug release.•The in vitro assay results showed that the drug carrier system was a hemocompatible. The development of efficient drug nanocarriers has remained an important challenge in advanced drug delivery in human body. Combination of graphene-based nanomaterials and cyanuric chloride (CC), as a linker, may improve the success of drug delivery. Herein, a simple approach was used for the synthesis of superparamagnetic graphene oxide (SPMGO) nanocomposite through a chemical precipitation method. The nanocomposite was readily functionalized with cyanuric chloride as a linker for loading the drug. The FTIR spectroscopy confirmed the efficient synthesis of nanocarriers. So did the transmission electron microscopy, atomic force microscopy, and thermo-gravimetric analysis, X-ray diffraction and X-ray photoelectron spectroscopy. Subsequently, the synthesized nanocarriers were studied in terms of their potential for biomedical applications. Immobilization of methotrexate (MTX), as a drug for treatment of cancer was taken into action on the SPMGO and SPMGO/CC. The in vitro assays indicated that the drug nanocarrier systems, SPMGO/MTX and SPMGO/CC/MTX, are hemo-compatible and increase the efficiency of MTX against Caov-4, HeLa and MCF-7 cell lines. The MTX nanocarriers represented a considerably high drug loading and controlled drug release. The overall results indicated the great potential of SPMGO/CC/MTX nanocarrier for targeted drug delivery, particularly in MTX chemotherapy.
ISSN:0168-1656
1873-4863
DOI:10.1016/j.jbiotec.2021.03.005