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Large (10 × 10 cm) sheets of surface-enhanced Raman spectroscopy (SERS) active polymer have been prepared by stabilising metal nanoparticle aggregates within dry hydroxyethylcellulose (HEC) films. In these films the aggregates are protected by the polymer matrix during storage but in use they are released when aqueous analyte droplets cause the films to swell to their gel form. The fact that these “Poly-SERS” films can be prepared in bulk but then cut to size and stored in air before use means that they provide a cost effective and convenient method for routine SERS analysis. Here we have tested both Ag and Au Poly-SERS films for use in point-of-care monitoring of therapeutic drugs, using phenytoin as the test compound. Phenytoin in water could readily be detected using Ag Poly-SERS films but dissolving the compound in phosphate buffered saline (PBS) to mimic body fluid samples caused loss of the drug signal due to competition for metal surface sites from Cl− ions in the buffer solution. However, with Au Poly-SERS films there was no detectable interference from Cl− and these materials allowed phenytoin to be detected at 1.8 mg L−1, even in PBS. The target range of detection of phenytoin in therapeutic drug monitoring is 10–20 mg L−1. With the Au Poly-SERS films, the absolute signal generated by a given concentration of phenytoin was lower for the films than for the parent colloid but the SERS signals were still high enough to be used for therapeutic monitoring, so the cost in sensitivity for moving from simple aqueous colloids to films is not so large that it outweighs the advantages which the films bring for practical applications, in particular their ease of use and long shelf life. 相似文献
2.
A simple and robust static adsorptive (dynamic) coating process using 2% hydroxyethylcellulose was developed for surface modification of poly(methyl methacrylate) (PMMA) microfluidic chips for DNA separations, suitable for usage over extended periods, involving hundreds of runs. The coating medium was also used as a sieving matrix for the DNA separations following the coating process. Four consecutive static treatments, by simply filling the PMMA chip channels with sieving matrix once every day, were required for obtaining a stable coating and optimum performance. The performance of the coated chips at different phases of the coating process was studied by consecutive gel electrophoretic separations with LIF detection using a PhiX-174/HaeIII DNA digest sample. The coated chip, with daily renewal of the sieving matrix, showed high stability in performance during a 25-day period of systematic study, involving more than 100 individual runs. The performance of the coated chip also remained almost the same after 3 months of continuous usage, during which over 200 separations were performed. The average precision of migration time for the 603-bp fragment was 1.31% RSD (n = 6) during the 25-day study, with a separation efficiency of 6.5 x 10(4) plates (effective separation length 5.4 cm). 相似文献
3.
B. Vijaya Kumar Naidu K.S.V. Krishna Rao Tejraj M. Aminabhavi 《Journal of membrane science》2005,260(1-2):131-141
Sodium alginate and hydroxyethylcellulose blend membranes were prepared by solution casting, crosslinked with glutaraldehyde and urea–formaldehyde–sulfuric acid mixture. Crosslinking was confirmed by Fourier transform infrared spectroscopy, while the blend compatibility was studied by differential scanning calorimetry and scanning electron microscopy. Membranes were tested for pervaporation separation of feed mixtures ranging from 10 to 50 mass% water in water + 1,4-dioxane and water + tetrahydrofuran mixtures at 30 °C. For 10 mass% of the feed mixture, pervaporation experiments were also carried out at higher temperatures (40 and 50 °C). By increasing the temperature, a slight increase in flux with a considerable decrease in selectivity was observed for all the membranes and for both the mixtures. The blend membranes exhibited different pervaporation performance for both the binary mixtures investigated. For water + 1,4-dioxane mixture, the pervaporation performance did not improve much after blending, whereas for water + tetrahydrofuran mixture, the pervaporation performance has improved considerably over that of plain sodium alginate membrane. 相似文献
4.
L.-M. Zhang 《Colloid and polymer science》1999,277(9):886-890
Homogeneous blends of two solutions of carboxymethylcellulose and hydroxyethylcellulose (HEC) were studied with respect to
viscosity properties at different blending ratios, shear rates and temperatures. The blends exhibited viscosity synergism
at all blending ratios, as well as improved shear and temperature stability. Maximum synergism was observed for the blend
containing 67% of HEC. The UV and IR spectra showed that the hydrogen-bonding interaction between the blended components is
the main reason for the synergism.
Received: 9 February 1999 Accepted in revised form: 15 April 1999 相似文献
5.
Analysis of small interfering RNA by capillary electrophoresis in hydroxyethylcellulose solutions
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Chenchen Liu Yoshinori Yamaguchi Xifang Zhu Zhenqing Li Yi Ni Xiaoming Dou 《Electrophoresis》2015,36(14):1651-1657
The analysis of small interfering RNA (siRNA) is important for gene function studies and drug developments. We employed CE to study the separation of siRNA ladder marker, which were ten double‐stranded RNA (dsRNA) fragments ranged from 20 to 1000 bp, in solutions of hydroxyethylcellulose (HEC) polymer with different concentrations and molecular weights (Mws). Migration mechanism of dsRNA during CE was studied by the mobility and resolution length (RL) plots. We found that the RL depended on not only the concentration of HEC, but also the Mw of HEC. For instance, RL of small dsRNA fragment was more influenced by concentration of high Mw HEC than large dsRNA fragment and RL of large dsRNA fragment was more influenced by concentration of low Mw HEC than small dsRNA fragment. In addition, we found electrophoretic evidence that the structure of dsRNA was more compact than dsDNA with the same length. In practice, we succeeded to separate the glyceraldehyde 3‐phosphate dehydrogenase siRNA in the mixture of the siRNA ladder marker within 4 min. 相似文献
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Almantas Danilevicius Justina Dobiliene Christoph Wutz Jolanta Liesiene 《Cellulose (London, England)》2007,14(4):321-329
A new amphiphilic cellulose derivative phenoxyhydroxypropylhydroxyethylcellulose of substitution degree up to 0.67 was synthesized
by reaction of water-soluble hydroxyethylcellulose with 2,3-epoxypropylphenylether in the presence of sodium hydroxide as
a catalyst. The chemical composition of the derivative was confirmed by means of UV, IR- and 13C-NMR-spectroscopy. The derivatives with substitution degree up to 0.12 are soluble in water and water–alcohol mixtures. With
increasing substitution degree, the polymers lose their water solubility, but still dissolve in water–alcohol mixtures. All
products are soluble in aprotic solvents. The effect of the reaction conditions, such as temperature and molar ratios of reaction
components, on both the reaction rate and degree of substitution was investigated. 相似文献
7.
Summary
l-Phenylalanine was immobilized on nylon membranes with two pore diameters (0.45 μm and 1 μm), by activation with 1,4-butanediol
diglycidyl ether, and the effect of pore size on the affinity adsorption of γ-globulin studied by batch and kinetic methods.
Experiment shows that adsorption on both affinity membranes obeys the Freundlich model. The accessible pore volume for adsorption
of proteins on the membrane with 0.45 μm diameter pores is less than for that with 1 μm diameter pores. The adsorption capacity
of affinity membranes with 1 μm diameter pores is 2.5-fold that of membranes with 0.45 μm diameter pores. Feed-rate has a
larger effect on affinity adsorption on the membrane with 0.45 μm diameter pores than on that with 1 μm diameter pores. Small
pores on the affinity membrane do not cause broadening of the elution peak. It is concluded that affinity interaction and
separation occur mainly in the large pores, and small pore size does not favor improvement of adsorption capacity. γ-Globulin
85.1% pure can be obtained in one step from human plasma by use of the affinity membrane with 0.45 μm diameter pores. 相似文献
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