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Solubility absorption

Experimental studies on the percutaneous absorption of hydrocortisone fail to reveal a significant increase in absorption when applied on a repetitive basis and a single daily application may be effective in most conditions. Ointment bases tend to give better activity to the corticosteroid than do cream or lotion vehicles. Increasing the concentration of a corticosteroid increases the penetration but not proportionately. For example, approximately 1% of a 0.25% hydrocortisone solution is absorbed from the forearm. A 10-fold increase in concentration causes only a fourfold increase in absorption. Solubility of the corticosteroid in the vehicle is a significant determinant of the percutaneous absorption of a topical steroid. Marked increases in efficacy are noted when optimized vehicles are used, as demonstrated by newer formulations of betamethasone dipropionate and diflorasone diacetate. [Pg.1300]

Note Moderately polar, weakly hydrogen bonding solvent, heavy liquid gradually decomposes to acquire a yellow color, air and light will accelerate this decomposition nonflammable commercial product is often stabilized by the addition of 3 to 4% (mass/mass) alcohols highly toxic by ingestion, inhalation, and skin absorption soluble in alcohols, organohalogen compounds, hydrocarbons, benzene, and many oils incompatible with many alkali and alkaline earth metals. Synonyms tribromomethane. [Pg.333]

Physical absorption Solubility Kt> 4 Optimize P and T Recycle the solvent... [Pg.65]

The focus before IND is on Tmax, Cmax and AUCs, while the complexity of pharmacokinetic characterization (like oral bioavailability, plasma half life, volume of distribution, mean residence time, absorption, solubility and concentration) is built up during clinical trials and on the basis of comparable human data. [Pg.766]

Pade V, Stavchansky S. Link between drug absorption solubility and permeability measurements in Caco-2 cells. J Pharm Sci 1998 Dec 87(12) 1604-1607. [Pg.164]

Because of this wide range of applications, much effort was dedicated to the design and synthesis of new molecules with optimized TPA efficiency in this context, the characteristics of the designed molecules (linear absorption, solubility, substituents...) will depend on the targeted application. The TPA response of moleciUes can be imderstood in the context of its TPA cross-section ajpA. which can be measmed using different techniques, such as nonlinear transmission, two-photon induced fluorescence and the Z-scan method although in a pure TPA process ajpA does not depend on the laser pulse duration, the nonlinear absorption can be more efficient in the nanosecond regime than in the femtosecond one, due to excited state reabsorption phenomena [34]. [Pg.151]

Studies to determine absorption, solubility, stability, and bioavailability are typically started after hits have been found. Text mining can be used here to determine appropriate test regimens and if pharmacodynamics and pharmacokinetics information is available for similar structure or on similar targets. [Pg.181]

D descriptors such as molecular weight, molar refractivity, as well as number of atoms and bonds have been used to model permeability, absorption, solubility, and toxicological effects. These kinds of descriptors are usually rather easy to interpret. [Pg.1017]

The use of the chemical and relevant regulatory information are then given and, when available, the physical properties are presented. These include melting point, boiling point, density or specific gravity, refractive index, uv absorption, solubility. Where available, acute toxicity data in various species are provided. Finally, the companies which manufacture or supply the product are given. It should be noted that almost all the data in this Book relate to pure compounds. [Pg.1188]

Oral absorption Solubility Permeability Ionization constant (pKa)... [Pg.372]

Chemical absorption usually has a much more favorable equilibrium relationship than physical absorption (solubility of most gases is usually very low) and is therefore often preferred. However, the Murphree efficiency is often quite low (10% is not unusual), and this must be taken into account. [Pg.469]

F. Generalize. Note that the gas concentration is considerably greater than the liquid concentratiom This situation is common for physical absorption (solubility is low). Chemical absorption is used to obtain more favorable equilibrium. The liquid flow rate required for physical absorption is often excessive. Thus, in practice, this type of operation uses chemical absorption. [Pg.487]

Absorption. Soluble arsenicals are readily absorbed from the gastrointestinal tract and throu the skin. [Pg.184]

Original units in Sada et al. [106] investigation are changed in Eq. (2.43), from molar to molal concentrations and a is the Bnnsen absorption (solubility) coefficient defined as the volirme of gas, rednced to standard conditions T=273.15 K andp= 101.325 kPa, which is absorbed by the imit volume of solvent. Solubilities of gases in pirre water, organic solvents and in electrolyte solutiorrs can be obtained from the literature [107-110]. [Pg.41]

Addition of hydroxyapatite modified with a silane coupling agent was introduced into PHBV by Tang et al. [255] in an effort to understand the influence of the bioceramic phase on water absorption, solubility, and biodegradation. They concluded that, compared to neat PHBV, diffusion coefficients for the bionanocomposites decreased, whereas the sorption coefficients and the solubility show an opposite tendency. In another work [256], the dynamic mechanical properties, thermal properties, and bioactivity of these bionanocomposite were examined, indicating that better mechanical properties and improved bioactivity were achieved with the introduction of hydroxyapatite. Moreover, thermal analysis revealed that when incorporating hydroxyapatite nanoparticles, the decomposition of PHBV was accelerated at the initial stage but retarded thereafter. [Pg.403]

Consider a simple experiment in which a clean solid surface (free of adsorbed liquid and vapour impurities) is immersed in an excess of pure liquid (Path 1 in Fig. 6.5). If thermal effects arising from absorption, solubility, and swelling of a solid may be eliminated, the whole enthalpy change on immersion is ascribed only to the interface. Sometimes the immersion of a solid in a liquid is accompanied by the formation of an electrical double layer. For mineral oxide-water systems [51, 52], the double-layer effects (i.e., generation of surface charge by protonation or deprotonation of some surface hydroxyl groups, and adsorption of counterions in the Stern or/and diffuse layers) are clearly secondary in comparison with the basic wetting (this contribution is 10-15 % of the total heat effect, at the most). [Pg.212]


See other pages where Solubility absorption is mentioned: [Pg.201]    [Pg.440]    [Pg.441]    [Pg.1185]    [Pg.265]    [Pg.383]    [Pg.56]    [Pg.168]    [Pg.39]    [Pg.85]   
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See also in sourсe #XX -- [ Pg.27 ]




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Absorption solubility-limited

Absorption yielding soluble complexes

Absorption, distribution, metabolism drug solubility

Gastrointestinal lipophilic drug absorption solubility

Intestinal drug absorption solubility

Lipophilic drug absorption solubility

Lipophilic drug absorption water-soluble prodrug

Liquid absorption solubility parameter

Solubility absorption and

Solubility drug absorption

Water-soluble drugs oral absorption

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