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Balanced hydrophobic and hydrophilic

Although cholesterol is essentially insoluble in water, a soluble cholesterol derivative can be formed by reacting it with high levels of ethylene oxide.66,67 This ethoxylated product has balanced hydrophobic and hydrophilic properties. The increased hydrophilicity makes it useful as an oil-inwater emulsifier or as a stabilizer. Ethoxylated lanolin is used for viscosity regulation, pigment dispersion, and as a solubilizer. Less than 1% ethoxylated cholesterol is effective at reducing the viscosity of anionic lotions to make them easier to pour. Non-ionic systems require more ethoxylated cholesterol for this purpose 68... [Pg.314]

The tendency of nonionics to produce foam varies. Some, such as the block copolymers, are even used as defoamers. Their wetting, detergency and emulsifying properties also vary widely, depending to a large extent on the balance between the hydrophobic and hydrophilic (oxyethylene) portions. [Pg.30]

Figure 5. Cross-section balance between the hydrophobic and hydrophilic parts. Figure 5. Cross-section balance between the hydrophobic and hydrophilic parts.
Both synthetic and natural polymers have superstructures that influence or dictate the properties of the material. Many of these primary, secondary, tertiary, and quaternary structures are influenced in a similar manner. Thus, the primary structure is a driving force for the secondary structure. Allowed and preferred primary and secondary bondings influence structure. For most natural and synthetic polymers, hydrophobic and hydrophilic domains tend to cluster. Thus, most helical structures will have either a hydrophobic or hydrophilic inner core with the opposite outer core resulting from a balance between secondary and primary bonding factors and steric and bond angle constraints. Nature has used these differences in domain character to create the world around us. [Pg.314]

In this paper we apply basic solution thermodynamics to both the adsorption of single surfactants and the competitive adsorption of two surfactants on a latex surface. The surfactant system chosen in this model study is sodium dodecyl sulfate (SDS) and nonylphenol deca (oxyethylene glycol) monoether (NP-EO o) These two surfactants have very different erne s, i.e. the balance between their hydrophobic and hydrophilic properties are very different while both are still highly soluble in water. [Pg.226]

It depends on the solution properties, or the relative balance between the hydrophobic and hydrophilic properties of the surfactants at this temperature. This term reflects the relative gain in the free energy when the hydrocarbon part of the surfactants is transferred from the aqueous solution to a hydrocarbon environment (either the micelle interior or the surface layer). The reason for this free energy gain is that the surfactant molecules are oriented at the... [Pg.231]

A stable emulsion requires balancing of hydrophobic and hydrophilic components into a uniform suspension. The suspension may be a multicomponent system of emulsifiers, surfactants, stabilizers, and thickeners that are included only to make an aesthetically pleasing product — not for their clinical significance. [Pg.174]

The surface isotherms obtained with these hydrophobic modified polymers were interpreted in terms of hydrophobic and hydrophilic balance of the polymers. [Pg.173]

The surfactant selection determines the emulsion properties, such as stability, particle size, viscosity, and internal phase content. A correct balance between the hydrophobic and hydrophilic character of the emulsifier is necessary for minimizing the surfactant concentration at the resin-water interface. The surfactants used in resin emulsification can be ionic (in most cases anionic), nonionic, polymeric, or a combination of these. [Pg.80]

Figure 4.7. Vertical capillary forces acting on the hydrophobic faces pull the hexagons into the PFD/H20 interface. The dashed line indicates the level of the interface far from the objects, (a) Hexagons with an unbalanced distribution of vertical capillary forces float with a tilt relative to the plane of the PFD/H20 interface. The surface tension, yLL, can be separated into vertical, y L, and horizontal, components, (b, c) Hexagons with a balanced distribution of vertical capillary forces float parallel to the plane of the interface. Thick and thin lines indicate hydrophobic and hydrophilic... Figure 4.7. Vertical capillary forces acting on the hydrophobic faces pull the hexagons into the PFD/H20 interface. The dashed line indicates the level of the interface far from the objects, (a) Hexagons with an unbalanced distribution of vertical capillary forces float with a tilt relative to the plane of the PFD/H20 interface. The surface tension, yLL, can be separated into vertical, y L, and horizontal, components, (b, c) Hexagons with a balanced distribution of vertical capillary forces float parallel to the plane of the interface. Thick and thin lines indicate hydrophobic and hydrophilic...
This is an interesting series in that Ri is insulated from the ring consequently, any electronic influence of the substituent will have negligible influence on the ring. Our tentative conclusion from the above analysis is that Ri plays an important role in obtaining a drug that has the proper balance of hydrophobic and hydrophilic properties. The electronic effect of ring substituents was partly described in an earlier report (12). [Pg.281]

The model that emerges from this study consists of a receptor site which has the ability to accept electrons from an electron-donating drug. The association is similar to a Michaelis-Menten type hence, the biological reaction would have a relatively short half-life. In addition to these electronic considerations, a proper balance of hydrophobic and hydrophilic properties must be maintained. [Pg.282]

Low molecular weight antioxidants react with ROS in cell compartments which for some reasons are lack of antioxidant enzymes. Thus, suppression of bifurcate chain reactions of lipid peroxidation in hydrophobic core of cell membrane is mostly effectively performed by vitamin E (a-tocopherol). Interaction of lipid molecules with hydroxyl radical in the absence of vitamin E results in bifurcation of oxidative processes and formation of peroxyl and alcoxyl radicals. They are quickly accumulated in the restricted volume of the membrane and reaction began to be uncontrolled. a-Tocopherol interacts with peroxyl radicals with high affinity, reduces them and is then oxidized itself into relatively nonactive phenoxyl radical [8]. The latter can be accumulated within the bilayer until it will be returned to initial state by reduction by ascorbate [9]. Pair Vitamin E - Vitamin C is a good example of a mutual interaction between hydrophobic and hydrophilic low molecular weight antioxidants. Recently, tight relations were demonstrated for several natural antioxidants which interaction balances the red/ox state of the cell [3.5.10-12]. Figure 4 demonstrates such interaction between some of them. [Pg.158]

The amphiphilic nature of nonionic surfactants is often expressed in terms of the balance between the hydrophobic and hydrophilic portions of the molecule. An empirical scale of ffLB (hydrophile-lipophile balance) numbers has been devised (see Chapter 7, section 7.3.2). The lower the ffLB number, the more lipophilic is the compound and vice versa. ffLB values for a series of commercial nonionic surfactants are quoted in Tables 6.7 and 6.8. The choice of surfactant for medicinal use involves a consideration of the toxicity of the substance, which may be ingested in large amounts. The following surfactants are widely used in pharmaceutical formulations. [Pg.217]

VolSurf descriptors were designed to compress relevant MIF information into a few alignment-independent descriptors encoding information about molecular size and shape, the overall distribution of hydrophobic and hydrophilic regions and the balance between them (Table G7). [Pg.360]

The fine balance between hydrophobic and hydrophilic interactions, as well as major steric requirements, play important roles in the binding of inhibitors. Cyanide is the only ligand that may bind in a 2 1 ratio. It is likely that the bis-cyanide adduct has the same arrangement as the NCS —H2O derivative. The spin state of the bis-cyanide adduct is S = 2. ... [Pg.61]


See other pages where Balanced hydrophobic and hydrophilic is mentioned: [Pg.531]    [Pg.47]    [Pg.137]    [Pg.508]    [Pg.85]    [Pg.508]    [Pg.531]    [Pg.47]    [Pg.137]    [Pg.508]    [Pg.85]    [Pg.508]    [Pg.108]    [Pg.117]    [Pg.195]    [Pg.30]    [Pg.25]    [Pg.198]    [Pg.609]    [Pg.49]    [Pg.368]    [Pg.138]    [Pg.43]    [Pg.240]    [Pg.187]    [Pg.179]    [Pg.505]    [Pg.9]    [Pg.21]    [Pg.627]    [Pg.490]    [Pg.1319]    [Pg.11]    [Pg.11]    [Pg.58]    [Pg.178]    [Pg.209]    [Pg.358]    [Pg.225]    [Pg.58]   


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And hydrophobicity

Balance, hydrophile-hydrophobe

Hydrophilic and hydrophobic

Hydrophilicity and Hydrophobicity

Hydrophilicity-hydrophobicity

Hydrophilicity-hydrophobicity balance

Hydrophobic-hydrophilic

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