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Phase solubility profile types

The physicochemical properties and dissolution profile of zaleplon -cyclo-dextrin (jSCD) inclusion complex were investigated. The phase solubility profile of Zaleplon with /1CD was classified as AL-type. Stability constant with 1 1 molar ratio was calculated from the phase solubility diagram and... [Pg.354]

The effects of various formulation factors on the in vitro release characteristics of spherical polymethylmethacrylate implants were studied. Physical and mathematical models were proposed to describe the in vitro release profiles. The in vitro release data could be described by a biexponential equation of the following type fraction of tobramycin remaining in the implant at time t=Aerai+BQ, where a, and P represent the rate constants for the initial rapid and subsequent slow phases of release. The influence of drug loading, volume of dissolution medium, implant size and type of cement and the incorporation of water-soluble additives on the release profiles and a and P rate constants is described. [Pg.171]

A number of different approaches, all of which have both advantages and shortcomings, have been proposed for the analysis of water-soluble dyes. The separation of colours has been carried out using ion-exchange resins, reverse-phase HPLC coupled with ion-pair reagents and reverse-phase HPLC at low pH where the ionisation of the dyes is suppressed. The last of these is the technique used at RSSL and is also the method recommended by Wadds (1984). It offers the simplest approach to this type of analysis and a typical HPLC profile of... [Pg.261]

DMTA is a very interesting tool for characterizing heterogeneous materials in which domains of distinct Tg values coexist. The most interesting cases involve modified thermosets of different types (see Chapter 8). Examples are the use of rubbers (e.g., liquid polybutadiene and random copolymers), or thermoplastics (e.g., polyethersulphone or polyetherimide in epoxy matrices or poly(vinyl acetate) in unsaturated polyesters), as impact modifier (epoxies), or low-profile additives (polyesters). The modifier-rich phase may be characterized by the presence of a new a peak (Fig. 11.10). But on occasions there may be superposition of peaks and the presence of the modifier cannot be easily detected by these techniques. If part of the added polymer is soluble in the thermoset matrix, its eventual plasticizing effect can be determined from the corresponding matrix Tg depletion, and the... [Pg.351]

The nature of the dissolution medium can profoundly affect the shape of a dissolution profile. The relative rates of dissolution and the solubilities of the two polymorphs of 3-(3-hydroxy-3-methylbutylamino)-5-methyl-a5-triazino[5,6-Z)7indole were determined in USP artificial gastric fluid, water, and 50% ethanol solution [69]. In the artificial gastric fluid, both polymorphic forms exhibited essentially identical dissolution rates. This behavior has been contrasted in Fig. 6 with that observed in 50% aqueous ethanol, in which Form II has a significantly more rapid dissolution rate than Form I. If the dissolution rate of a solid phase is determined by its solubility, as predicted by the Noyes-Whitney equation, the ratio of dissolution rates would equal the ratio of solubilities. Because this type of behavior was not observed for this triazinoindole drug, the different effects of the dissolution medium on the transport rate constant can be suspected. [Pg.311]

By suitably choosing the solubility, the concentration of the reactant and the rate of reaction, either the mass transfer coefficients, or the interfacial area or both groups of parameters can be deduced from the overall rate of absorption (lA). Generally but not always, a steady flow of each phase through the reactor is assumed. Indeed the competition between the phsyical and chemical kinetics at the level of mass transfer between gas and liquid (the mass transfer reaction regime where the reaction belongs) may allow for the choice of the type of gas-liquid contactor (I). This is clearly shown in Fig. I that represents schematically the concentration profiles for A and B on each side of the interface. [Pg.107]


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