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allied

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Asian Journal of Biomedical and Pharmaceutical Sciences | ISSN: 2249-622X | Volume 8

&

Joint Event

Chemistry and Organic Chemistry

Biomedicine & Pharmacotherapy

International Conference on

8

th

World Congress on

October 22-23, 2018 | Frankfurt, Germany

Gd

2

O

3

nanoparticles as a MRI contrast agents

Mohammad Wasi Ahmad

Dhofar University, Oman

M

agnetic resonance imaging (MRI) iswidelyused inmodern

clinical medicine as a diagnostic tool, and provides

noninvasive and three-dimensional visualization of biological

phenomena in living organisms with high spatial and temporal

resolution. Therefore, considerable attention has been paid to

magnetic nanoparticles as MRI contrast agents.

We report a facile method to synthesize high quality and bio-

functionalized Gd2O3 nanoparticles (BFNPs) for use as contrast

agents in MRI. The bonding status of BFNPs were confirmed

by FT-IR and TGA analysis. The surface coating amount was

estimated to be from 40% to 60% in weight percent from a TGA

analysis. High voltage electron microscope (HVEM) shows that

the BFNPs were spherical in shape with an average diameter

3M. In addition, the bio-compatibility of the nanoparticles

were measured by cytotoxicity tests by using human prostate

cancer (DU145) and normal mouse hepatocyte (NCTC1469)

cell lines which indicated that BFNPs are not toxic up to 250M.

BFNPs are paramagnetic but have an appreciable magnetic

moment at room temperature. This is because Gd(III) has seven

unpaired 4f-electrons (S = 7/2). Therefore, appreciable r1 and

r2 values are expected from sample solutions, which were in

fact observed in this study. The r1 and r2 values of BFNPs were

estimated to be 13.77 to 64.14 s -1mM -1 respectively. The high

relaxivities provide an opportunity to conduct perfusion MRI

experiments with significantly lower concentrations than those

needed for current commercial agents. A pronounced positive

and negative contrast enhancement was clearly observed in 3

tesla T1 MR images of a rat with a liver tumor after injection of

an aqueous sample solution into a rat tail vein.

e:

mdwasiahmad@gmail.com

Chemistry and Biomedicine 2018, Volume 8

DOI: 10.4066/2249-622X-C4-012