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Fractional derivative technique functional derivatives

The GPC traces for the parent oligomer and several of the fractions derived from it are reproduced in Figure 10. The efficiency of this technique at producing difunctionalized fractions of narrow polydispersity is evident from Table III and Figure 10. The presence of two functional groups in these fractions was confirmed by comparing the determined by titration... [Pg.160]

The protonation equilibria for nine hydroxamic acids in solutions have been studied pH-potentiometrically via a modified Irving and Rossotti technique. The dissociation constants (p/fa values) of hydroxamic acids and the thermodynamic functions (AG°, AH°, AS°, and 5) for the successive and overall protonation processes of hydroxamic acids have been derived at different temperatures in water and in three different mixtures of water and dioxane (the mole fractions of dioxane were 0.083, 0.174, and 0.33). Titrations were also carried out in water ionic strengths of (0.15, 0.20, and 0.25) mol dm NaNOg, and the resulting dissociation constants are reported. A detailed thermodynamic analysis of the effects of organic solvent (dioxane), temperature, and ionic strength on the protonation processes of hydroxamic acids is presented and discussed to determine the factors which control these processes. [Pg.40]

Lennernas s group at Uppsala has performed extensive studies to confirm the validity of this in vivo experimental set-up at assessing the rate and the extent of drug absorption. Recovery of PEG 4000 (a non-absorbable marker) is more than 95%, which indicates that the absorption barrier is intact. In addition, maintenance of functional viability of the mucosa during perfusion has been demonstrated by the rapid transmucosal transport of D-glucose and L-leucine. Estimation of absorption half-lives from the measured Pefr agree well with half-lives derived from oral dose studies in humans (i.e. physiologically realistic half-lives). Human Peff estimates are well correlated with the fraction absorbed in humans, and served as the basis for BCS development, and hence the technique is ultimately the benchmark by which other in situ intestinal perfusion techniques are compared. The model has been extensively used to... [Pg.60]

Concentration techniques, applied to assign priority pollutants, function as an interface between the environment, chemical analysis, and bioassays. The transition of harmful pollutants in an environmental system to multicomponent concentrates derived from that system is the principal challenge of concentration techniques aimed at the assignment of organic priority pollutants. A compatible combination of chemical and biological methods must be used. These methods can vary from the development of analytical procedures based on the observed biological activity of fractions of an environmental concentrate to the toxicological... [Pg.49]

Euler-Euler models assume interpenetrating continua to derive averaged continuum equations for both phases. The probability that a phase exists at a certain position at a certain time is given by a phase indicator function, which, for steady-state processes, is equivalent to the volume of fraction of the correspondent phase (volume-of-fluid technique). The phase-averaging process introduces further unknowns into the basic conservation equations their description requires empirical and problem-dependent input (94). In principal, Euler-Euler models are applicable to all multiphase flows. Advantages and disadvantages of both methods are compared, e.g., in Refs. 95 and 96. [Pg.338]

Fractionation techniques have made it possible to recover active o -antitrypsin from blood. Use of this product for intravenous replacement therapy in deficient individuals has shown that it is possible to increase levels in the serum to those of PISZ heterozygotes who experience no increase in pulmonary disease over the general population. Pulmonary lavage of patients transfused with this product showed that functional (Xj-antitrypsin reaches the alveolar structures. The Food and Drug Administration has approved weekly administration of purified serum-derived oq-antitrypsin to PIZZ and PI null individuals with pulmonary disease. Although serum levels of oq-antitrypsin increase to those believed to be protective, it has not been possible to show clinical improvement. Furthermore, viral transmission via blood products is a significant risk factor. [Pg.51]

Clark et al. (40) developed what is a mathematically similar approach to Theil s, which was applied to both DPIs and pMDIs plus spacer and chambers. (Clark et al. deliberately avoided using data from pMDIs alone because of the difficulties associated with the ballistic nature of the plume.) The basis of the technique is the assumption that lung deposition is simply the inhaled dose minus that deposited in mouth and oropharynx. This approach does not require the application of a lung deposition model and is justified for most DPIs and pMDI since the fractions exhaled after a typical 5- to 10-s breath-hold are always close to zero. As an oral deposition function, Clark et al. chose to use the function proposed by Stahlhofen et al. and Rudolf et al., which is then numerically integrated with the size distribution derived from cascade impactor data to calculate oral deposition. Subtracting oral deposition from the inhaled dose allows calculation of the lung dose. Clark used gamma camera data from seven clinical studies, four DPI and three pMDI, to evaluate the approach. On analysis, it was seen that... [Pg.134]

For an overall description, the molecular motion is best divided into four major types. Type (1) is the vibrational motion of the atoms of the molecule about fixed positions, as described in Sect. 2.3.3. This motion occurs with small ampUmdes, typically a fraction of an angstrom (or 0.1 nm). Larger systems of vibrators have to be coupled, as discussed in Sect. 2.3.4 on hand of the Debye functions. The usual technique is to derive a spectrum of normal modes as described in Fig. A.6.4, based on the approximation of the motion as harmonic vibrators given in Fig. A.6.2. [Pg.121]


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See also in sourсe #XX -- [ Pg.57 , Pg.58 ]

See also in sourсe #XX -- [ Pg.57 , Pg.58 ]




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