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71.
Observations of the activity of two hydrolyzing enzymes—protease and α-amylase—entrapped inside the reversed micelles formed
by surfactants in hexane, benzene, and cyclohexane are reported. The surfactants chosen for this study are: Tween 80, a nonionic
surfactant, Cetyl pyridinium chloride, a cationic surfactant, and two anionic surfactants, sodium lauryl sulfate and Aerosol
OT.
Tween 80 enhances the activity of both protease and α-amylase. Sodium lauryl sulfate and Aerosol OT, which are ionic surfactants,
enhance the activity of protease, but inhibit the activity of α-amylase. Cetyl pyridinium chloride, however, enhances the
activity of α-amylase, but inhibits the activity of protease. Enhanced activity is generally severalfold greater in comparison
to the activity observed in the usual aqueous system in the absence of reversed micelles. It has also been observed that the
enhanced activity of the enzymes entrapped inside the reversed micelles remains preserved for a much longer period of time
in comparison to the activity in the usual aqueous systems. These observations, which support the view that with proper choice
of surfactant and the organic solvent, reversed micelles act like a microreactor that provides a favorable aqueous microenvironment
for enzyme activity, have biotechnological overtones. 相似文献
72.
H. Etori H. Hirata Y. Yamada H. Okabayashi M. Furusaka 《Colloid and polymer science》1997,275(3):263-273
Potassium salts of N-decanoylglycine and N-decanoyl-L-alanine oligopeptides (monomer, dimer and trimer) were synthesized.
For these oligomer salts in aqueous solutions, the microstructures of micelles have been investigated by small-angle neutron-scattering
(SANS). In the calculation of SANS intensity data, the thickness of the hydrophilic layer was altered by changing the conformation
of the oligomer moiety (helical and β-sheet structures). For micelles of the trimer salts, the helical structure models provide
the best fit to the observed SANS intensity data. For micelles of the monomer-and dimer-salts, the β-sheet model provides
the best fit to the observed data. For the monomer-and dimer-micelles, the aggregation number (n) is not dependent on the species of amino acid residue, imply-ing that the decanoyl group plays a critical role in micelle
formation. However, for the trimer micelles, the n value is dependent on the species of amino acid residue.
Received: 11 July 1996 Accepted: 11 September 1996 相似文献
73.
Refractive index measurements on water/AOT/n-heptane microemulsions as a function of the volume fraction of the dispersed phase (water plus AOT) and of the water/AOT molar ratio R have been performed at 25°C. The refractive index was found to vary monotonically with without any change in rate during the crossover of the percolation threshold. Such a behavior suggested that, well above the percolation threshold, the water-AOT-n-heptane microemulsions are still formed by water-containing AOT reversed micelles dispersed in the oil phase. The analysis of the experimental data allowed an evaluation the fraction of the water molecules bonded to the AOT head group as a function of R. 相似文献
74.
Gohy JF Lohmeijer BG Schubert US 《Chemistry (Weinheim an der Bergstrasse, Germany)》2003,9(15):3472-3479
The formation of asymmetric bis-complexes, based on terpyridine ligands and ruthenium ions, is described as a powerful tool for the self-assembly of polymer blocks end-functionalized with terpyridine units. This is illustrated in this contribution for the synthesis of amphiphilic metallo-supramolecular block copolymers, which are further used to produce aqueous micelles. Finally, the reversibility of the supramolecular bond opens new avenues for the preparation and manipulation of these nano-objects. 相似文献
75.
I. Shimizu H. Okabayashi N. Hattori K. Taga A. Yoshino C. J. O’Connor 《Colloid and polymer science》1997,275(3):293-297
Changes in the 13C and 1H NMR chemical shifts of the silane coupling agent (3-aminopropyltri-ethoxysilane, APTS) in toluene, which were detected as
the concentration of APTS increased, have been interpreted in terms of the formation of micelles and the presence of a critical
micelle concentration (CMC) equal to ca. 0.47 mol 1-1. For the protons of the n-propyl segment, 1H NMR splitting patterns have been analyzed and conformations of the propyl segment have been discussed. Plots of relative
absorbance of the two NH2 stretch IR bands at 3324 and 3384 cm-1 against concentration provided an inflection point (corresponding to the CMC) at a value equal to 0.46 mol 1-1. Thus, consideration of the interaction of APTS with a surface must take into account the presence of both APTS aggregates
as well as APTS monomers.
Received: 16 August 1996 Accepted: 26 September 1996 相似文献
76.
The enthalpies of mixing of some n-nitriles (from acetonitrile to valeronitrile) aqueous solutions with dodecyltzimethylammonium bromide, sodium dodecylsulfate and dodecyltzimethylammonium oxide micellar solutions were determined. The measurements were performed by systematically changing the surfactant concentration at a given solute concentration. The experimental enthalpies were rationalized in terms of the standard enthalpy of transfer of solute from the aqueous to the micellar phase and of the distribution constant between the two phase. Information on the effect of the nature of the surfactant on the standard thermodynamic quantities of transfer(G
t
o
, H
t
o
, TS
t
o
) is reported. The present data are compared to those previously reported for primary alcohols and the solubilizing properties shown by the different types of micelles are discussed. 相似文献
77.
78.
79.
Xiao‐Lan Wei Rong Han Xiao Hu Li‐Hui Quan Chun‐Yu Liu Qi Chang Yong‐Hong Liao 《Biomedical chromatography : BMC》2013,27(5):636-640
Six esterase inhibitors, namely EDTA·2Na+, NaF, phenylmethanesulfonyl fluoride, dichlorvos, bis‐nitrophenyl phosphate (BNPP) and thenoyltrifluoroacetone, and the mixture of NaF and BNPP, were evaluated for the stabilization of labile benzoate containing zeylenone in rat plasma. The mixture appeared to exhibit the most effectively stabilizing effect with the degraded content of zeylenone decreasing from >60% (in the absence of inhibitors) to <6%. Following the stabilization by the addition of NaF (5 mm ) and BNPP (5 mm ), the analytes in rat plasma were acidified by formic acid and extracted into ethyl acetate at 0°C. After chromatographic separation, the detection of zeylenone was performed on a 3200 Q‐Trap with positive ion electrospray mode, monitoring the ion transition m/z 383.2 → 105.0. The method was validated over the range from 2.68 to 1340 ng/mL with inter‐ and intra‐run precision for the quality control samples being less than 6.8%. The assay accuracy was within 100 ± 7.0%. The validated method was successfully applied to a pharmacokinetic study in rats after the intratracheal administration of zeylenone in free drug or polymeric micellar solutions. The results showed that the pulmonary absorption of zeylenone loaded in micelles was significantly retarded compared with that of free drug solutions. Copyright © 2012 John Wiley & Sons, Ltd. 相似文献
80.