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31.
S. Ezrahi Ido Nir Abraham Aserin Nick Kozlovich Yuri Feldman Nissim Garti 《Journal of Dispersion Science and Technology》2013,34(1-3):351-378
The hydration behavior of the system polyoxyethylene (10) oleylalcohol [C18:1 (EO)10 or Brij 97]/water/dodecane/butanol (model system B) was investigated along a dilution line for which the respective weight ratio of dodecane:butanol:Brij 97 is 3:3:4. Two experimental methods were applied: time domain dielectric spectroscopy (TDDS) and sub-zero temperature differential scanning calorimetry (SZT-DSC). Two types of bound water (with melting peaks at -25 and -11°C) were detected by SZT-DSC (using the endothermic mode), whereas TDDS revealed only one such type. Nevertheless, roughly the same total amount of bound water was estimated from these two techniques. The average number of bound water molecules per ethylene oxide (EO) group, NW/EO is 2.3 (TDDS data) or 2.5 (SZT-DSC data) in good agreement with the observation that 1–2 water layers are formed in the hydration of ethoxylated surfactants. We have also shown that butanol is involved in the formation of the bound water that melts at -25°C. We suggest that butanol molecules occupy binding sites within the second hydration shell, thereby reducing the expected total bound water content. 相似文献
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When certain catalysts that display a low apparent metathesis activity on terminal olefins are employed on mixtures of terminal and internal olefins, they lead to a selective formation of cross metathesis products. Critical experimentation using deuterated 1-pentene reveals that terminal olefins prefer to scramble “head-to-tail”. A study of the macrocyclics distribution produced at various conversions during 1,5-cycloocta-diene polymerization suggests that these are being formed exclusively via an intramolecular transalkylidenation. The significance of the two sets of results is discussed in terms of two basic mechanistic schemes. 相似文献
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Journal of Thermal Analysis and Calorimetry - 相似文献
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Pemberton C Hoffman R Aserin A Garti N 《Journal of magnetic resonance (San Diego, Calif. : 1997)》2011,208(2):262-269
Silica is used as an important component for NMR “chromatography”. In this study the effect of the binding strength to silica of a variety of compounds on their diffusion rate is measured for the first time. Over two orders of magnitude of diffusion difference enhancement was obtained in the presence of silica for some compounds. An explanation of the enhancement is given that also allows one to predict the “chromatographic” behavior of new compounds or mixtures. The binding strength is divided into categories of weakly bound, singly bound and multiply bound. Carboxylates, sulfonates, and diols are found to be particularly strongly bound and to diffuse up to 2½ orders of magnitude more slowly in the presence of silica. 相似文献
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Celecoxib (clxb) is an important drug for treatment of rheumatoid arthritis and osteoarthritis by specifically inhibiting the enzyme cyclooxygenase-2 (COX-2). Clxb is a type 2 drug characterized by low water solubility (<5 mug/ml) and fast transmembrane transport. The present formulations require high dosage since the transmembrane transport fluctuates and is very difficult to control. Dissolving the drug within an oil phase was not practical since its dissolution was very small and its dispersion in water was impossible. In our recent studies, we learned to construct U-type phase diagrams and to formulate reverse microemulsions (oil-based concentrates) that are progressively and fully dilutable with aqueous phase. In the present study, we solubilized clxb in nanostructures of reverse micelles of U-type nonionic microemulsions that consisted of R(+)-limonene, alcohol, propylene glycol (PG), and hydrophilic surfactant (Tween 60). The solubilization capacity of the drug in these systems is many times higher than in either the oil or the aqueous phase. The clxb solubilized microemulsions are fully diluted with aqueous phase without phase separation. The solubilization capacity decreases as the water content increases. Electrical conductivity, viscosity, and self-diffusion (SD) coefficients of the microemulsion components were measured along a suitable water dilution line. The three major microemulsion regions were detected and the transitions between the W/O to bicontinuous phase and from this phase to the O/W droplets were identified (at 30 and 70 wt% aqueous phase, respectively). From the SD coefficients, it was found that the drug is initially solubilized at the interface of the W/O droplets and there are no significant structural changes. The transition to a bicontinuous phase occurs at the same water content as in the empty (i.e., without drug) system. From the viscosity profiles, we concluded that the drug affects the structure of the bicontinuous phase as reflected in the water content at which the oil-continuous network is destroyed and full inversion occurs (50 vs 55 wt% in the drug-loaded system). Upon further dilution the drug remains solubilized at the interface and is oriented with its hydrophilic part facing the water, and is strongly affects the inversion to O/W droplets. From Small Angle X-ray Scattering (SAXS) measurements we learned that the drug effects the structure of microemulsion droplets and forms "ill-defined structures," probably less spherical. Yet, the overall droplet sizes at the high dilutions did not change very much. 相似文献
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Nissim Garti Moshe Frenkel Rosi Shwartz 《Journal of Dispersion Science and Technology》2013,34(3):237-252
Multiple emulsions of water in oil in water (W/O/W) have been used as a novel technique to overcome unpleasant taste of drugs. The drug is dissolved in the inner water phase and is released throughout the oil phase in the presence of synthetic gastric juice Yield of preparation and stability have been studied using various sets of different inner (emulsifier I) and outer (emulsifier II)emulsifiers Combination of anionic-nonionic emulsifiers yielded optimal results: High yield of preparation, high stability and complete release of the drug in synthetic gastric juice. 相似文献
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Janna GurfinkelAbraham Aserin Nissim Garti 《Colloids and surfaces. A, Physicochemical and engineering aspects》2011,392(1):322-328
In an attempt to form HII mesophases at room temperature we prepared lyotropic liquid crystals with two surfactants of the same lipophilic tails (glycerol monooleate, GMO, and oleyl lactate, OL) but differing in the size and charge of the headgroups.Increasing OL concentration significantly affected the hydration of the headgroups and subsequently the lipids packing. At low OL content the cubic mesophase was formed, while at higher OL contents the formation of hexagonal mesophase was favored. It was assumed that OL competed on the water binding, tuning the headgroups’ curvature and the packing parameter inducing the formation of reverse hexagonal mesophase. It was detected that cubic mesophase transformed upon heating to hexagonal structures. The hexagonal mesophases, which were formed both immediately after preparation and after aging, remained stable at elevated temperatures.α-Chymotrypsinogen was solubilized into the obtained LLCs at relatively high concentration (up to 1 wt%). The lattice parameter of the host LLCs exhibited a decrease as a function of the protein content. This process was assigned to partial dehydration of the GMO polar moieties in favor to CTA hydration.Generally speaking, the present study indicated that adding anionic to nonionic lipid is highly beneficial to gain additional compositional and structural characteristics of LLCs. 相似文献
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Multiple emulsions are emulsions within emulsions, stabilized traditionally by monomeric emulsifiers both at the inner and outer interface. 相似文献