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      Surfactant Concentration Regime in Miniemulsion Polymerization for the Formation of MMA Nanodroplets by High-Pressure Homogenization

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          Abstract

          This article focuses on the adequate surfactant concentration regime in which MMA droplets are stabilized sufficiently against coalescence during high-pressure homogenization but still no diffusion processes from droplets to micelles take place in the polymerization. Monomer miniemulsions with different surfactant concentrations were prepared with different energy inputs. Emulsions result that depend either on the surfactant concentration or on the energy input of the homogenization process. For both cases, the occupancy of the interface is compared as a function of the droplet size. It is shown that the surfactant concentration needed for the stabilization of a specified interface area decreases with increasing droplet size. For the dependence of droplet size on the energy input, it is shown that more surfactant can be applied before emulsion polymerization starts, but the applicable surfactant concentration is lower than the cmc and also depends on droplet size.

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          Hydrolytic stability of organic monolayers supported on TiO2 and ZrO2.

          The hydrolytic stability of C18 monolayers supported on TiO2 and ZrO2 was studied. Three types of monolayers were prepared from the following octadecyl modifiers: (1) octadecyldimethylchlorosilane (C18H37Si(CH3)2Cl); (2) octadecylsilane (C18H37SiH3); and (3) octadecylphosphonic acid (C18H37P(O)(OH)2). The hydrolysis of the surfaces prepared was studied under static conditions at 25 and 65 degrees C at pH 1-10. On the basis of the loss of grafted material, the stability of the monolayers fall in the following range: C18H37P(O)(OH)2 > or = C18H37SiH3 > C18H37Si(CH3)2Cl. At 25 degrees C, monolayers from C18H37P(O)(OH)2 showed only approximately 2-5% loss in grafting density after one week at pH 1-10. The high stability of these monolayers was explained because of the strong interactions of the phosphonic acids with the substrates. Monolayers from C18H37Si(CH3)2Cl showed poor hydrolytic stability at any pH, which was explained because of the low stability of Ti-O-Si and Zr-O-Si bonds. Unlike monofunctional silanes, trifunctional silane (C18H37SiH3) yielded surfaces that showed good hydrolytic stability. This suggests that the stability of the monolayers from trifunctional silanes is primarily due to "horizontal" bonding (Si-O-Si or Si-OH...HO-Si) rather than due to bondingwith the matrix (M-O-Si). At 65 degrees C, all C18 surfaces become more susceptible to hydrolysis; however, the trend observed for 25 degrees C remained unchanged. Low-temperature nitrogen adsorption was used to study the adsorption properties of the monolayers as a function of their grafting density. The energy of adsorption interactions showed a significant increase as the grafting density of the monolayers decreased. The order of the alkyl groups in the monolayers, as assessed from CH2 stretching, decreased as the grafting density of the monolayers decreased.
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            A hybrid DNA aptamer-dendrimer nanomaterial for targeted cell labeling.

            Antibodies are natural nanomaterials and have been widely used for targeted cell labeling. However, the applications of antibodies are often limited by their large size and instability. The purpose of this study is to develop a new type of multifunctional nanomaterial that is comprised of a nucleic acid aptamer and a dendrimer, both of which are stable. This nanomaterial is approximately 8 nm in size. Moreover, it could not only carry multiple signal molecules, but also bind to target cancer cells with high affinity and specificity. This sub-10 nm multifunctional nanomaterial is expected to be useful in basic biomedical research and clinical medicine.
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              Cellular uptake behavior of unfunctionalized and functionalized PBCA particles prepared in a miniemulsion.

              Fluorescent dye labeled unfunctionalized and functionalized poly(n-butylcyanoacrylate) nanoparticles were prepared using a miniemulsion technique. Amino acid and methoxyPEG functionalization could be introduced by using aqueous solutions as an initiator for the anionic polymerization in the heterophase. All the particles prepared had sizes smaller than 250 nm and negative zeta-potentials. The molar mass distribution of the polymer was dependent on the acid used as the continuous phase and the initiator solution applied. Cells of three lines (HeLa, Jurkat and mesenchymal stem cells) were incubated with the particles. The molar mass of the polymer determined the onset and extent of apoptosis, and the total uptake was determined by the size and functionalization of the particles. Different uptake kinetics were obtained with HeLa and Jurkat cells after incubation with the same particle batch. The intracellular particle distribution, visualized by confocal laser scanning microscopy, did not show significant differences for either of the cell lines or particle batches.
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                Author and article information

                Journal
                Langmuir
                la
                langd5
                Langmuir
                American Chemical Society
                0743-7463
                1520-5827
                11 February 2011
                15 March 2011
                : 27
                : 6
                : 2279-2285
                Affiliations
                []Karlsruhe Institute of Technology (KIT), Institute for Process Engineering in Life Science, Section I: Food Process Engineering, Karlsruhe, Germany
                []Max-Planck-Institute for Polymer Research, Mainz, Germany
                Author notes
                [* ]E-mail: lena.hecht@ 123456kit.edu . Tel: +49 721 608 43614. Fax: +49 721 45967.
                Article
                10.1021/la104480s
                3052788
                21314152
                ea4ee0b1-0c88-41af-b508-428fdd5e3251
                Copyright © 2011 American Chemical Society

                This is an open-access article distributed under the ACS AuthorChoice Terms & Conditions. Any use of this article, must conform to the terms of that license which are available at http://pubs.acs.org.

                History
                : 10 November 2010
                : 06 January 2011
                : 11 February 2011
                : 15 March 2011
                Categories
                Article
                Custom metadata
                la104480s
                la-2010-04480s

                Physical chemistry
                Physical chemistry

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