Alcohol lipid solvent

It should be noted that all three are lethal, however, and so the acute toxicity of these compounds is not entirely due to C-40 substituent effects. Potency does follow the oxidation series from alcohol to aldehyde to acid vivo, suggesting that perhaps these substituents influence the degree of accessibility of each lipid-solvent soluble toxin to its membrane site of action. Being that the toxins in their natural forms are so soluble in non-polar solvents, and tend to bind to or solubilize in the lipid components of membrane... 

Figure 4. Cumulative yields of cholesterol and lipid extracted from beef tallow with SC-CO2 at 138 bar/40°C with and without 5% ethyl alcohol as solvent modifier.

Properties Colorless needles odorless sour taste. Mp 236C, sublimes above melting point, d 1.473. Soluble in water and alcohol insoluble in most lipid solvents, quite stable to heat and oxidation. A vasodilator in high concentration. Amounts of niacin are expressed in milligrams. 

Properties Orange-yellow crystals bitter taste. Mp 282C (decomposes). Slightly soluble in water and alcohols insoluble in lipid solvents stable to heat in dry form and in acid solution. Stable to ordinary... 

In the cat s adrenal cortex, Bennett found that yellow phenylhydra-zones and metallic silver both appeared predominantly in the outer portion of the zona fasciculata, the so-called spongy zone. These reactions failed to develop if the sections were previously extracted with acetone or ethyl alcohol at room temperature, indicating that the reactive compounds were readily soluble in such lipid solvents. In this same zone, the cells contained abundant small hpid droplets, as demonstrated with Sudan dyes or osmic acid. 

In the water-like solvent tert-butyl alcohol, a-tocopherol was found to prevent lipid oxidation, showing a distinct lag-phase for oxygen consumption. This was in contrast to quercetin or epicatechin, which were only weak retarders of lipid oxidation without any clear antioxidative effect. Quercetin or epicatechin, when combined with a-tocopherol, increased the lag-phase for oxygen consumption as seen for a-tocopherol alone. The stoichiometric factor for a-tocopherol, a-TOH, as chain-breaking antioxidant has the value n = 2 according to the well-established mechanism ... 

Lipids have been dehned on the basis of their stmctnre and solnbility. Lipids are natnrally occnrring componnds consisting of fatty acids and their derivatives, bile acids, pigments, vitamins, and steroids, as well as terpenoids, which are usually soluble in organic solvents such as benzene, chloroform, ether, and alcohol, etc., with variable solubility depending on the stmctnre of the lipid compound. 

Simple lipids such as CE, WE, EFA, cholesterol, alcohols, ketones, TG, DG, and MG are usually separated on silica gel plates. Depending on the complexity of the lipid material and the variety of lipid classes present in a single sample, either single-or multiple-solvent systems can be used (Figure 12.4a). Although benzene [45] or... 

The lipophilicity of a solute affects its permeability in lipid bilayers. Lipophilicity is usually expressed in terms of its partitioning between water and an organic solvent, such as olive oil [95], oleyl alcohol [96], ether [97], or octanol [98]. Partition coefficient (PC) of a compound is expressed as its concentration ratio between organic medium and water at equilibrium ... 

However, Emi et al. [50] have prepared LS with a method established in their laboratory using a solvent extraction. In particular, the method is based on the dissolution of the triglyceride (i.e., tripalmitin) and the cationic lipid in the organic solvent (i.e., dichloromethane), and on the addition of an aqueous polyvinyl alcohol (PVA)... 

Saponification (see Section 7.4) is carried out to extract more recalcitrant lipids, and the yields are higher than for conventional solvent extraction (Stern et al. 2000). 3 ml of 0.5 M methanolic NaOH is added to 0.1 g of the shard powder and heated at 70°C for 3 hours in a sealed glass vial. After cooling, the supernatant is acidified with HC1 and extracted with three aliquots of 3 ml //-hexane. The hexane will not mix with the methanolic solution (unlike the DCM MeOH used above), but will absorb the lipids and can be transferred into a new clean vial. The removal of excess hexane is carried out as above. Saponification will hydrolyze and methylate any ester functionalities, which removes the requirement to derivatize the samples (Section 7.4) unless other molecules are suspected of being present. However, any wax esters or triacylglycerols will also be hydrolyzed to their fatty acid methyl esters and alcohols therefore, if information on their composition is required, then conventional solvent extraction is recommended as a first step. For subsequent characterization of the lipid extract, see Chapter 7. 

Whatever the technique used, it is important to note that (i) only an equivalent viscosity can be determined, (ii) the response of a probe may be different in solvents of the same viscosity but of different chemical nature and structure, (iii) the measured equivalent viscosity often depends on the probe and on the fluorescence technique. Nevertheless, the relative variations of the diffusion coefficient resulting from an external perturbation are generally much less dependent on the technique and on the nature of the probe. Therefore, the fluorescence techniques are very valuable in monitoring changes in fluidity upon an external perturbation such as temperature, pressure and addition of compounds (e.g. cholesterol added to lipid vesicles alcohols and oil added to micellar systems). 

The general rules that should therefore be observed include the use of a blanket of nitrogen whenever possible and evaporation of solvents at the lowest feasible temperatures, which must not exceed 50°C. The addition of an antioxidant such as butylated hydroxytoluene (2,6-di-/-butyl-4-methylphenol) to the extraction solvents (0.1 g 1 ) might be necessary to prevent deterioration of unsaturated lipids but it is essential for storage of lipid extracts at about 0.1% of the weight of lipid. Inactivation of lipolytic enzymes may usually be achieved by addition of an alcohol such as methanol or, in some cases, isopropanol. The latter is recommended for some more stable enzymes sometimes found in plant tissues. Alternatively the plant may be briefly immersed in boiling water. 

The partition of different lipids between two immiscible solvents (countercurrent distribution) is useful for crude fractionation of lipid classes with greatly differing polarities. Repeated extractions in a carefully chosen solvent pair increase the effectiveness of the separation but in practice mixtures of lipids are still found in each fraction. A petroleum ether-ethanol-water system can be used to remove polar contaminants (into the alcoholic phase) when interest lies in the subsequent analysis of neutral glycerides, which may be recovered from the ether phase. Carbon... 

The procedure chosen for the preparation of lipid complexes of AmB was nanoprecipitation. This procedure has been developed in our laboratory for a number of years and can be applied to the formulation of a number of different colloidal systems liposomes, microemulsions, polymeric nanoparticles (nanospheres and nanocapsules), complexes, and pure drug particles (14-16). Briefly, the substances of interest are dissolved in a solvent A and this solution is poured into a nonsolvent B of the substance that is miscible with the solvent A. As the solvent diffuses, the dissolved material is stranded as small particles, typically 100 to 400 nm in diameter. The solvent is usually an alcohol, acetone, or tetrahydrofuran and the nonsolvent A is usually water or aqueous buffer, with or without a hydrophilic surfactant to improve colloid stability after formation. Solvent A can be removed by evaporation under vacuum, which can also be used to concentrate the suspension. The concentration of the substance of interest in the organic solvent and the proportions of the two solvents are the main parameters influencing the final size of the particles. For liposomes, this method is similar to the ethanol injection technique proposed by Batzii and Korn in 1973 (17), which is however limited to 40 mM of lipids in ethanol and 10% of ethanol in final aqueous suspension. 

Alcohols and acetone are the simplest kinds of membrane permeabilization agents. They act by dissolving membrane lipids, thus rendering the membrane permeable to antibodies (5). Because of their coagulant effects on proteins, these solvents can be used as a one-step fixative and permeant (18). 

Lipases are enzymes that catalyze the in vivo hydrolysis of lipids such as triacylglycerols. Lipases are not used in biological systems for ester synthesis, presumably because the large amounts of water present preclude ester formation due to the law of mass action which favors hydrolysis. A different pathway (using the coenzyme A thioester of a carboxylic acid and the enzyme synthase [Blei and Odian, 2000]) is present in biological systems for ester formation. However, lipases do catalyze the in vitro esterification reaction and have been used to synthesize polyesters. The reaction between alcohols and carboxylic acids occurs in organic solvents where the absence of water favors esterification. However, water is a by-product and must be removed efficiently to maximize conversions and molecular weights. 

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