Ketoprofen surfactants

Table 7.23 shows the results for 47 specific PAMPA models tested at pION, according the the scheme in Fig. 7.58. The two columns on the right are the r2 values in the comparisons. The neutral-lipid models (1.0, 1A.0, 2.0, 3.0, and 4.0) at pH 7.4 do not explain the permeability trend indicated in the human jejunal permeabilities [56]. Octanol was least effective, with r2 0.01. This should not be too surprising, since we did note that the appearance of naproxen, ketoprofen, and piroxicam at the top of the HJP ordering was unexpected. Our expectations were based on the octanol-water lipophilicity scale, which clearly does not correlate with the HJP trend. Adding a sink condition to the 2% DOPC model (model 1.1) improves correlation (r1 increases from 0.33 to 0.53). The addition of cholesterol to the 2% DOPC/dodecane system made the model unstable to the surfactant-created sink condition. 

Mooney et al. [70] investigated the effect of pH on the solubility and dissolution of ionizable drugs based on a film model with total component material balances for reactive species, proposed by Olander. McNamara and Amidon [71] developed a convective diffusion model that included the effects of ionization at the solid-liquid surface and irreversible reaction of the dissolved species in the hydrodynamic boundary layer. Jinno et al. [72], and Kasim et al. [73] investigated the combined effects of pH and surfactants on the dissolution of the ionizable, poorly water-soluble BCS Class II weak acid NSAIDs piroxicam and ketoprofen, respectively. 

Crison, G. L. Amidon. pH and surfactant-facilitated in vitro solubilization and dissolution of ketoprofen, a class II drug. Implications for waiver of bioavailability and bioequivalence studies (Unpublished). 

Sheng and Amidon (2006) investigated the combined effed of pH and surfactant on the solubility and dissolution of ketoprofen. The solubility and dissolution rate enhancement were determined in buffers with pH range from 4.0 to 6.8 and sodium lauryl sulfate (SLS) concentration from... 

Alternatively, Huntington and Cormier used non-ionic surfactants, including dodecanol and 1,2-dodecanediol, to enhance the delivery of the anionic drug, ketoprofen. Because non-ionic surfactants are not directly affected by the applied electric field, their use may be preferred over ionic surfactants. 

Polyoxyethylene castor oil derivatives have been used experimentally as a surfactant for the controlled release matrix pellet formulation containing nanocrystalline ketoprofen, " and for the transdermal delivery of vinpocetin. " ... 

Sheng, J.J., Kasim, N.A., Chandrasekharan, R. and Amidon, G.L. (2006) Solubilization and dissolution of insoluble weak acid, ketoprofen effects of pH combined with surfactant European Journal of Pharmaceutical Sciences, 29 (3-4), 306. 

The pH of the reaction medium is another important factor for modulating both the activity and enantioselectivity of Lipase OF. The enzyme showed optimal hydrolysis activity at pH 4.0, while the enantioselectivity increased sharply with the decrease in medium pH from 4.0 to 2.2. Based on spectroscopic studies, the enhancement of the lipase activity and enantioselectivity at the lower pH could be attributed to the changes in the flexible and sensitive conformation of the lipase induced by tuning the biocatalyst microenvironment. Using a hybrid strategy by modulating pH and surfactant, enantiomer-enriched (5)-ketoprofen could be obtained with 95.5% ee and 39.1% yield from rac-ketoprofen chloroethyl ester (100 mM) at pH 2.5 in the presence of 0.5% (w/v) Tween-80 as a modulator. ... 

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