Green synthesis and characterisation of Anti-Cancer drug ... · •A novel green method for the...
Transcript of Green synthesis and characterisation of Anti-Cancer drug ... · •A novel green method for the...
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Green synthesis and characterisation of
Anti-Cancer drug carrier, Fe3O4-Ag core-
shell magnetic nanoparticles, supported on
graphene oxide
School of Psychological and Clinical Sciences
Dr Vinuthaa Murthy, Dr Roshanak Khandanlou
& Dr Martin Boland
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Nanomedicine• Great potential for early detection, accurate
diagnosis, and treatment of cancer• 10 to 100nm - 1000 to 10,000 times smaller
than human cells• smaller than large biological molecules such as
enzymes, receptors, and antibodies
• Promise for a “magic gold bullet” against cancer
Green synthesis and characterisation of Anti-Cancer drug carrier nanoparticles
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Synthesis of Nano particles
Some Plant productsNatural Polyphenols - rich in flavonoids, phenolic acids
and tannins.
Inhibitory effect in carcinogenesis and tumor growth
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Parameter optimisation pH
Reaction time
Leaf boiling time.
UV-visible spectra of NPs prepared at different
(a) pH (b) reaction time, and (c) leaf boiling time.
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Characterization of Nanoparticles
XRD pattern of purified NPs synthesized
using leaf extract.
TEM micrograph at different magnifications
SAED pattern
particles size distribution Size:Ranging from 3.56 to 24.5 nm
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Inhibitory Concentration (IC50)
In vitro anticancer activity MTT Cell Proliferation Assay
Cell lines Human breast cancer (MCF-7)liver cancer (HepG2)human dermal fibroblast (HDF-7)
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In vitro anticancer activity MTT Cell Proliferation Assay
MCF-7 : at 500 µgNPs 97.4% Leaf extract 87.9%
HepG2 :at 500 µgNPs 97.4% Leaf extract 99.2%
at 250 µgNPs 91.7% Leaf extract 74.4%
at 250 µgNPs 91.7% Leaf extract 74.4%
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Conclusion
• Proof-of-principle study
• A novel green method for the synthesis of stablecolloidal NPs using leaf extract
• The synthesised NPs have spherical or near sphericalshape with an average size of 8.40 ± 0.084 nm.
• In-vitro anticancer show NPs induced significantcytotoxicity effect against MCF-7 and HepG2 cancercells in a dose dependent manner and with nosignificant cytotoxicity on normal HDF-7 cells.
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Thank you
AcknowledgementsNMIMS Mumbai IndiaProf Dhananjaya Saranath Ms Hetal DamaniCentral Analytical Research Facility (CARF) Institute for Future Environments, Queensland University of Technology (QUT)
Continuing work…