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Phase partition analysis

The use of DPH lifetimes for the analysis of phase separations and membrane properties has been described for mode) systems.n fl) In the case of both parinaric acids and DPH, one of the motivations for examining phase separation in a model lipid bilayer is the possibility that phase separations might be detectable in natural membranes. However, this technique has not been able to satisfactorily resolve lateral phase separations in natural membranes, either because they do not exist or because they are much more complex and even possibly transient in nature. Alternatively, it could be argued that if a probe could be found with the characteristics of trans-parinaric acid but perhaps with an even greater phase partitioning ability, then this approach might be reevaluated. [Pg.233]

Smith, E. (1967). Application of reverse phase partition chromatography to the analysis of testosterone propionate in oil injectables. J. Pharm. Sci., 56(5), 630-634. [Pg.177]

Recently, reversed-phase partition chromatography has become the method of choice for both qualitative and quantitative analysis of carotenoids. The stationary phases commonly used are those with C,8-bonded chains (ODS) their performances are influenced by the extent of endcap-... [Pg.830]

Phase Partition—A Method for Purification and Analysis of Cell Organelles ami... [Pg.257]

The aqueous polymer two-phase partition technique pioneered by Albertsson et al. [11] not only provides a method to separate right-side-out from inside-out vesicles (Section 2.2), but also allows the partial separation of appressed and non-appressed membrane fractions. The inside-out vesicles which partition to the lower phase were depleted in PS II activity [59]. Significantly, they were derived from the appressed membranes of the grana stacks as judged by electron microscopy [60] and their mode of formation [61], Futhermore, analysis of the Chl-protein content revealed a substantial depletion of PS I complex, and an enrichment of PS II complex and LHC II in the appressed membrane fraction [62]. In 1980, An-dersson and Anderson postulated that PS II and PS I are mainly laterally segregated, with PS I excluded from the appressed grana partitions, where most PS II-LHC II complexes are located [62,63] (Fig. 5). [Pg.284]

The quantitative analysis of the fat-soluble vitamins (A, E, D and K) and their esters by reversed-phase partition in water/alcohol solvents on Zipax columns has been reported [255]. The applicability of gas and high pressure liquid chromatography of vitamin A was discussed by Vecchi, Vesely and Oesterhelt [256] who concluded that HPLC was superior in this application. [Pg.148]

Lee et al. (2005) proposed a method for analysis of flavonols in grape by performing berry extraction with acidified methanol (0.01% of 12 N HC1). After filtration, the solvent is removed under vacuum and the residue is dissolved in a 0.1 M citric acid buffer with pH 3.5. First, polyphenols are fractionated on a reverse-phase Ci8 cartridge (e.g., Sep-Pak 5g), then on a Sephadex LH-20 3-g cartridge (a cross-linked dextran-based stationary phase used for gel permeation, normal-phase partition, and adsorption chromatography). Four fractions finally are recovered by ethyl acetate and methanol, as shown in the f >w diagram Fig. 6.5. [Pg.166]

Albertsson, P., Andersson, B., Larsson, C., and Akerlund, H., Phase Partition—A Method for Purification and Analysis of Cell... [Pg.353]

In the case of acidic glycolipids the relative proton affinity of chemicals can shift the balance for negative ionisation in favor of co-eluted compounds. Pre-analytical separation under acidic conditions serves also to reduce as much as possible the dispersion in the MS spectrum of the metabolite into multiple m/ z representing the various adducts of counterions Na, K, NH4, organic amines, ... which improves sensitivity of the test. Sulfatides are lost during the partition between the hexane and the methanol/water phase. The analysis of sulfatides involves the isolation of the glycosphingolipid fraction and the subsequent separation of sulfatides from neutral lipids by chromatography on DEAE-sephadex or DEAE-cellulose column (the variety of methods are referenced in the website CyberLipid (http //www.cyberlipid.org/). [Pg.582]

With the aid of gradient elution, a reversed phase partition method and an internal standard, considerable progress has been made in the quantitative determination of each constituent of the main component phenols present in technical CNSL and in natural cashew-nut shell liquid provided that relative molar response (RMR) factors are used. A typical quantitative HPLC analysis of the technical material indicated cardanol (67.8%), cardol (18.2%), 2-methylcardol (3.3%), minor constituents (3.3%) and polymeric material (7.4%). [Pg.526]

I able 28-3 lists a few typical examples of the multitude of uses of partition chromatography in various fields. A more complete picture of the many applications of this technique can be obtained by consulting review articles and b(K)ks. Figure 28-18 illustrates two of many thousands of applications of bonded-phase partition chromatography to the analysis of consumer and industrial materials. [Pg.835]

We now turn to processing situations in which heat effects are of primary importance examples include chemical reactors and separators that exploit phase partitioning. Thermodynamic analysis of these situations invoke the stuff equations in particular, steady-state heat effects are computed from (12.3.5). To obtain the partial molar enthalpies that appear in (12.3.5), we need enthalpies as functions of composition so in 12.4.1 we show how enthalpy-concentration diagrams can be constructed from volumetric equations of state applied to binary mixtures in phase equilibrium. Then we apply the energy balance (12.3.5) to multicomponent flash separators ( 12.4.2), binary absorbers ( 12.4.3), and chemical reactors ( 12.4.4). [Pg.555]

Experiments were carried out on a system composed of AOT, brine, and compressed liquid propane at 37°C [22], The effect of pressure on the partitioning of AOT for a system containing 1.7 wt% NaCl in the aqueous phase is shown in Fig. 6, and the pressure efifect on tVo in the propane phase is shown in Fig. 7. The addition of NaCl to the system was necessary to prevent the formation of an AOT liquid crystal phase. These data were obtained by withdrawing small samples from each phase for analysis. Similar data have also been... [Pg.288]

Method of Nobuhara et al. (1980). A simple and rapid method for the routine quantitative analysis of the six major alkaloids in gum opium by direct isocratic HPLC on a reversed phase partition mode column without using ion-pair reagents was successfully used by Nobuhara et al. (1980) under the following conditions ... [Pg.225]


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