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21.
Olsson M Joabsson F Piculell L 《Langmuir : the ACS journal of surfaces and colloids》2005,21(4):1560-1567
The influence of added colloidal particles on the phase separation of mixed aqueous polymer solutions is investigated. Two types of particles (polystyrene latex or silica) and different combinations of segregating polymers (dextran of varying molar mass combined with poly(ethylene oxide) (PEO) of varying molar mass, or Ucon, a copolymer of ethylene oxide and propylene oxide) were used. All systems displayed particle-induced instability effects, but the extent of the effect varied strongly between the various combinations and with the amount of added salt. Very large instability effects were seen in certain mixtures. Two mechanisms, both relying on the adsorption of at least one of the polymers to the particle surface, seem to operate. Close to the cloud-point curve of the particle-free polymer1/polymer2/water mixture, adsorption of PEO or Ucon to the particles gives rise to a capillary-induced phase separation. Close to the dextran/water axis of the phase diagram, the adsorbing polymer gives rise to a surface modification of the particles, which then interacts repulsively with the surrounding dextran solution. 相似文献
22.
Hydrogen peroxide is determined by a chemiluminescence method with a reagent containing 100 μM luminol and 3 μM microperoxidase at pH 10 (carbonate buffer). Microperoxidase is superior to hematin as a catalyst. The method uses an automated flow injection system with a throughput of 2 samples per minute. The log—log calibration plot is linear (slope 1.3) from the detection limit, 3 × 10-9 M up to 10-5 M H2O2. The background emission is low. Impurities in the carrier stream and from some plastics may cause elevated background unless precautions are taken. 相似文献
23.
Siwy Z Trofin L Kohli P Baker LA Trautmann C Martin CR 《Journal of the American Chemical Society》2005,127(14):5000-5001
There is increasing interest in the concept of using nanopores as the sensing elements in biosensors. The nanopore most often used is the alpha-hemolysin protein channel, and the sensor consists of a single channel embedded within a lipid bilayer membrane. An ionic current is passed through the channel, and analyte species are detected as transient blocks in this current associated with translocation of the analyte through the channel-stochastic sensing. While this is an extremely promising sensing paradigm, it would be advantageous to eliminate the very fragile lipid bilayer membrane and perhaps to replace the biological nanopore with an abiotic equivalent. We describe here a new family of protein biosensors that are based on conically shaped gold nanotubes embedded within a mechanical and chemically robust polymeric membrane. While these sensors also function by passing an ion current through the nanotube, the sensing paradigm is different from the previous devices in that a transient change in the current is not observed. Instead, the protein analyte binds to a biochemical molecular-recognition agent at the mouth of the conical nanotube, resulting in complete blockage of the ion current. Three different molecular-recognition agents, and correspondingly three different protein analytes, were investigated: (i) biotin/streptavidin, (ii) protein-G/immunoglobulin, and (iii) an antibody to the protein ricin with ricin as the analyte. 相似文献
24.
Cocquyt J Olsson U Olofsson G Van der Meeren P 《Langmuir : the ACS journal of surfaces and colloids》2004,20(10):3906-3912
Dilute dispersions of the synthetic bilayer forming double-chained cationic lipid dioctadecyldimethylammonium bromide (DODAB) were investigated. In dispersions sonicated above the chain melting temperature Tm (approximately 45 degrees C) it was found by H NMR that about 50% of the surfactant chains remained fluid when the samples were cooled to room temperature, which is 20 degrees C below Tm. In contrast, there was no sign of a fluid fraction in unsonicated samples at room temperature. The addition of the anionic surfactant sodium dodecyl sulfate (SDS) to DODAB dispersions at room temperature resulted in the formation of an essentially stoichiometric DODA-DS complex with frozen chains, as seen by titration calorimetry and H NMR experiments. For sonicated samples, turbidity experiments demonstrated that, after a fast complexation reaction, the system remains colloidally stable unless the SDS-to-DODAB mixing ratio is too close to unity. H NMR experiments also showed that in the unreacted DODAB the fraction of fluid chains remained close to 50%, indicating either that SDS reacts equally fast with fluid and frozen DODAB or that there is a relaxation of the fluid fraction after the complexation. The melting enthalpy and the melting temperature of the alkyl chains rise gradually as the mixing ratio increases. We observed with cryo-TEM that the fraction of large unilamellar vesicles was significantly larger after addition of SDS. This indicates vesicle fusion. Based on both wide- and small-angle X-ray scattering patterns, the structure of the equimolar SDS-DODAB complex at 25 degress C was proposed to be lamellar. 相似文献
25.
Penna Thereza Christina Vessoni Marques Marcelo Machoshvili Irena A. Ishii Marina 《Applied biochemistry and biotechnology》2002,98(1-9):539-551
Large-volume parenteral solutions were submitted to heat treatments after being inoculated with Bacillus stearothermophilus ATCC 7953 (T
r
=121°C) and Bacillus subtilis ATCC 9372 (T
r
=104.5°C) spores. The average decimal reduction time for B. stearothermophilus ranged from a D
121°C value of 1.31 to 3.14 min, in glucophysiologic and Ringer’s solutions respectively. For B. subtilis, D
104.5°C value increased from 0.69 to 1.37 min, in Ringer’s (pH=5.91) and 50% glucose (pH 3.05) solutions respectively. The z value ranged from 7.95°C (20% mannitol solution) to 13.14°C (50% glucose solution), corresponding to an activation energy
(Ea) of 81.48 and 49.30 kcal/mol, respectively. 相似文献
26.
Olsson P 《Physical review letters》1995,75(14):2758-2761
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