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      Gold-Coated Iron Composite Nanospheres Targeted the Detection of Escherichia coli

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          Abstract

          We report the preparation and characterization of spherical core-shell structured Fe 3O 4–Au magnetic nanoparticles, modified with two component self-assembled monolayers (SAMs) consisting of 3–mercaptophenylboronic acid (3–MBA) and 1–decanethiol (1–DT). The rapid and room temperature synthesis of magnetic nanoparticles was achieved using the hydroxylamine reduction of HAuCl 4 on the surface of ethylenediaminetetraacetic acid (EDTA)-immobilized iron (magnetite Fe 3O 4) nanoparticles in the presence of an aqueous solution of hexadecyltrimetylammonium bromide (CTAB) as a dispersant. The reduction of gold on the surface of Fe 3O 4 nanoparticles exhibits a uniform, highly stable, and narrow particle size distribution of Fe 3O 4–Au nanoparticles with an average diameter of 9 ± 2 nm. The saturation magnetization value for the resulting nanoparticles was found to be 15 emu/g at 298 K. Subsequent surface modification with SAMs against glucoside moieties on the surface of bacteria provided effective magnetic separation. Comparison of the bacteria capturing efficiency, by means of different molecular recognition agents 3–MBA, 1–DT and the mixed monolayer of 3–MBA and 1–DT was presented. The best capturing efficiency of E. coli was achieved with the mixed monolayer of 3–MBA and 1–DT-modified nanoparticles. Molecular specificity and selectivity were also demonstrated by comparing the surface-enhanced Raman scattering (SERS) spectrum of E. coli-nanoparticle conjugates with bacterial growth media.

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          A DNA-based method for rationally assembling nanoparticles into macroscopic materials.

          Colloidal particles of metals and semiconductors have potentially useful optical, optoelectronic and material properties that derive from their small (nanoscopic) size. These properties might lead to applications including chemical sensors, spectroscopic enhancers, quantum dot and nanostructure fabrication, and microimaging methods. A great deal of control can now be exercised over the chemical composition, size and polydispersity of colloidal particles, and many methods have been developed for assembling them into useful aggregates and materials. Here we describe a method for assembling colloidal gold nanoparticles rationally and reversibly into macroscopic aggregates. The method involves attaching to the surfaces of two batches of 13-nm gold particles non-complementary DNA oligonucleotides capped with thiol groups, which bind to gold. When we add to the solution an oligonucleotide duplex with 'sticky ends' that are complementary to the two grafted sequences, the nanoparticles self-assemble into aggregates. This assembly process can be reversed by thermal denaturation. This strategy should now make it possible to tailor the optical, electronic and structural properties of the colloidal aggregates by using the specificity of DNA interactions to direct the interactions between particles of different size and composition.
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            Seeding of Colloidal Au Nanoparticle Solutions. 2. Improved Control of Particle Size and Shape

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              Characterization of aqueous dispersions of Fe(3)O(4) nanoparticles and their biomedical applications.

              A newly developed non-polymer coated Fe(3)O(4) nanoparticles showing well-dispersion were synthesized using Fe(II) and Fe(III) salt chemical coprecipitation with tetramethylammonium hydroxide (N(CH(3))(4)OH) in an aqueous solution. Transmission electron microscopy (TEM), X-ray diffraction (XRD), Fourier transform infrared spectrometer (FT-IR), X-ray photoelectron spectrometer (XPS) and superconducting quantum interference measurement device (SQUID) measurements were employed to investigate the iron oxide properties. The resulting iron oxide particles were manipulated to be as small as 9 nm diameter in size. Based on FT-IR and X-ray photoelectron spectrometer results, it is suggested that the surfaces of the magnetite (Fe(3)O(4)) particles are covered with hydroxide (-OH) groups incorporated with (CH(3))(4)N(+) through electrostatic interaction. The in vitro cytotoxicity test revealed that the magnetite particles exhibited excellent biocompatibility, suggesting that they may be further explored for biomedical applications. NMR measurements revealed significantly reduced water proton relaxation times T1 and T2. The MR images of the nanoparticles in water, serum, and whole blood were investigated using a 1.5 T clinical MR imager. Significant reduction of the background medium signal was achieved in the T2-weighted and the T2*-weighted sequence especially in the serum and whole blood. Combining the advantage of MRI signal contrast, the non-polymer-coated surface chemistry for distinct bioconjugation and the homogenous nanometer size for better controlled biodistribution, these preliminary experiments demonstrated the potential of the as-synthesized magnetite material in functional molecular imaging for biomedical research and clinical diagnosis.
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                Author and article information

                Journal
                Int J Mol Sci
                Int J Mol Sci
                ijms
                International Journal of Molecular Sciences
                Molecular Diversity Preservation International (MDPI)
                1422-0067
                March 2013
                18 March 2013
                : 14
                : 3
                : 6223-6240
                Affiliations
                [1 ]Department of Analytical Chemistry, Faculty of Pharmacy, Gazi University, Etiler, Ankara 06330, Turkey; E-Mail: ednah87@ 123456hotmail.com
                [2 ]Science Teaching Programme, Faculty of Education, Gazi University, Besevler, Ankara 06330, Turkey; E-Mail: demetcetin@ 123456gazi.edu.tr
                [3 ]Department of Biology, Faculty of Science, Gazi University, Besevler, Ankara 06330, Turkey; E-Mail: zekiyes@ 123456gazi.edu.tr
                [4 ]Department of Food Engineering, Hacettepe University, Beytepe, Ankara 06530, Turkey; Food Research Center, Hacettepe University, 06800 Beytepe, Ankara, Turkey; E-Mails: ihb@ 123456hacettepe.edu.tr (I.H.B.); tumaytemiz89@ 123456gmail.com (H.T.T.)
                [5 ]Institut des Molécules et Matériaux du Mans IMMM, LUNAM Université, Université du Maine, UMR CNRS 6283 F–72085 Le Mans 9, France; E-Mail: daniel@ 123456univ-lemans.fr
                [6 ]Department of Engineering Physics, Faculty of Engineering, Ankara University, Besevler, Ankara 06100, Turkey; E-Mails: idincer@ 123456eng.ankara.edu.tr (İ.D.); elerman@ 123456ankara.edu.tr (Y.E.)
                Author notes
                [†]

                These authors contributed equally to this work.

                [* ]Author to whom correspondence should be addressed; E-Mail: utamer@ 123456gazi.edu.tr ; Tel.: +90-312-202-3110.
                Article
                ijms-14-06223
                10.3390/ijms14036223
                3634437
                23507756
                a506e20b-bdf9-4902-8e66-79aae79b448f
                © 2013 by the authors; licensee MDPI, Basel, Switzerland.

                This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license ( http://creativecommons.org/licenses/by/3.0/).

                History
                : 28 November 2012
                : 28 February 2013
                : 28 February 2013
                Categories
                Article

                Molecular biology
                magnetic gold nanoparticle,sers,immunomagnetic separation,e. coli,surface functionalisation of particles

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