Photonic crystals in biology
Photonic crystals in biology
Photonic crystals in biology
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Poster Session, Tuesday, June 15<br />
Theme A1 - B702<br />
Synthesis and Characterization of CdTeFe 3 O 4 Magnetic Nanoparticles<br />
<br />
1 , Tülay Oymak 1 , 1 *<br />
1 Department of Analytical Chemistry, Faculty of Pharmacy, Gazi University, Ankara 06500, Turkey<br />
Abstract- A simple chemical method for the fabrication of magnetic-fluorescent nanocomposite materials composed of magnetic nanoparticles<br />
and quantum dots at room temperature is described. The nanosutructures were characterized with fluorescence spectrometry, TEM, EDAX and<br />
magnetic measurements.<br />
Recent advance <strong>in</strong> nanotechnology have led to a new class<br />
of labell<strong>in</strong>g based on semiconductor quantum dots (QDs).<br />
Surface passivated QDs exhibit high stablity, large absorption<br />
coefficients, size tunable flurescence. These properties have<br />
made QDs an ideal for label<strong>in</strong>g with broad applications<br />
especially <strong>in</strong> <strong>in</strong> biochemistry [1-2]. The comb<strong>in</strong>ation of<br />
magnetic and fluorescent properties <strong>in</strong> one nanocomposite<br />
provides new nanoscale photonic devices which would be<br />
manipulated us<strong>in</strong>g an external magnetic field [3]. In<br />
immunoassays, QDs are usually used <strong>in</strong> label<strong>in</strong>g of secondary<br />
antibodies. Those QD labeled antibodies can be used after the<br />
IMS of the target molecule <strong>in</strong> order to detect the target. But the<br />
paramagnetic microparticles used <strong>in</strong> IMS cause partial or<br />
complete quench<strong>in</strong>g of QDs and lowers the sensitivity of the<br />
analyze. Therefore, development of magnetic nanoparticles<br />
which do not cause any quench<strong>in</strong>g would be favorable <strong>in</strong><br />
bioassays and <strong>in</strong> some applications like fluorescence<br />
resonance energy transfer (FRET) two different fluorescence<br />
molecules are used as a donor and acceptor. Development of a<br />
nanoparticle which has both magnetic and fluorescence<br />
properties would be an important advance for such systems.<br />
In this work, we describe a simple synthesis method for the<br />
magnetic-florescent, CdTeFe 3 O 4 , nanocomposite material <strong>in</strong><br />
aqueous medium, at room temperature. Characterization of the<br />
core-shell structured Fe 3 O 4 -CdTe nanoparticle proved that the<br />
result<strong>in</strong>g nanoparticles composed of Fe 3 O 4 core and the CdTe<br />
shell. Rapid and room temperature reaction synthesis of CdTe<br />
coated magnetic nanoparticle and subsequent surface<br />
modification may provide b<strong>in</strong>d<strong>in</strong>g properties for sens<strong>in</strong>g<br />
application.<br />
To synthesize CdTe coated iron nanoparaticle, the seed<br />
mediated synthetic method was carried out. First, The Fe3O 4<br />
nanoparticles were prepared by coprecipitation of Fe (II) and<br />
Fe (III). Fe(II) / Fe(III) ratio is kept as 0.5 <strong>in</strong> an alkal<strong>in</strong>e<br />
solution. Briefly, 1.28 M FeCl 3 and 0.64 M FeSO 4 7H 2 O were<br />
dissolved <strong>in</strong> deionized water. The solution was then strirred<br />
vigorously until the iron salts were dissolved. Subsequently, a<br />
solution of 1M NaOH was added dropwise <strong>in</strong>to the mixture<br />
with stirr<strong>in</strong>g for 40 m<strong>in</strong>utes.<br />
After the preparation of the of Fe3O 4 core, CdTeFe 3 O 4<br />
nanocomposite particles were prepared by bubl<strong>in</strong>g the gaseous<br />
tellerium hydride produced by the hydride generation system<br />
through the solution composed of Fe 3 O 4 , 0.03 M CdCl 2 and<br />
0.03 M citrate for 5 m<strong>in</strong>utes. The magnetically active<br />
nanoparticles were collected by a magnet and the supernatant<br />
solution was discarded. The residue was diluted with 5 mL<br />
ethanol and treated with 3-mercaptopropionic acid and shaked<br />
for four hours. The excess of mercaptopropionic acid was<br />
removed by centrifugation. The magnetic separation of these<br />
nanoparticles was easily accomplished and the result<strong>in</strong>g<br />
nanoparticles were characterized with Transmission Electron<br />
Microscopy (TEM), UV-Vis, X Ray Diffraction (XRD) and<br />
magnetic properties of the nanoparticles were also exam<strong>in</strong>ed<br />
by vibrat<strong>in</strong>g sample magnetometer.<br />
Typical morphology of result<strong>in</strong>g nanoparticles is shown <strong>in</strong><br />
Figure 1.<br />
Figure 1. TEM image of CdTeFe 3 O 4 , nanoparticle<br />
The fluorescence spectrum of the nanoparticle is given <strong>in</strong><br />
Figure 2.<br />
R.I.<br />
120<br />
80<br />
40<br />
0<br />
650 675 700 725 750<br />
Wavelength, nm<br />
Figure 2. The fluorescence spectrum of the CdTeFe 3 O 4<br />
nanoparticle exc = 330 nm<br />
*Correspond<strong>in</strong>g author: 1Tnertas@gazi.edu.tr<br />
[1] Sheikh, S. H.; Abela, B. A.; Muchandani, A., Anal Biochem.<br />
2000, 283(1), 33-38<br />
[2] Chan, W.C.; Nie, S., Science, 1998, 281(5385), 2016-2018<br />
[3]Corr, S. A.;Rakovich Y. P.; Gun’ko Y. K., Nanoscale Res. Lett.,<br />
2008, 3, 87-104<br />
6th Nanoscience and Nanotechnology Conference, zmir, 2010 327