Transport interactions

Reaction and Transport Interactions. The importance of the various design and operating variables largely depends on relative rates of reaction and transport of reactants to the reaction sites. If transport rates to and from reaction sites are substantially greater than the specific reaction rate at meso-scale reactant concentrations, the overall reaction rate is uncoupled from the transport rates and increasing reactor size has no effect on the apparent reaction rate, the macro-scale reaction rate. When these rates are comparable, they are coupled, that is they affect each other. In these situations, increasing reactor size alters mass- and heat-transport rates and changes the apparent reaction rate. Conversions are underestimated in small reactors and selectivity is affected. Selectivity does not exhibit such consistent impacts and any effects of size on selectivity must be deterrnined experimentally. 

Tukker, G., Houston, J. B., Huang, S.-M., Optimizing drug development strategies to assess drug metabolism/ transporter interaction potential — toward a consensus, Clin. Pharmacol. Ther. 2001, 70, 103-114. 

The Local Environment Determines the Nature of Substrate-Transporter Interactions... 

Therefore, if is necessary to have good interaction between the diffusion layers and fhe FF plafes—nof only from a mass transport standpoint but also to maintain optimal electrical and thermal conductivity between them. Section 4.4.4 explained in detail measurement techniques to determine the electrical resistance in diffusion layers. It is important to note that most of fhose methods can also be implemented in order to calculate the contact resistance between the DLs and the FF plates. In this subsection, we will focus mostly on mass transport interactions between these two components. 

Medication Transportation interactions. Recall that carrier proteins in the bloodstream escort medications and that over 80% of the circulating concentration of most psychiatric medicines is bound to serum proteins. When there are not enough protein binding sites to go around, however, the biologically active free fraction of the drug is increased. 

What Is a Side Effect This chapter picks up where Chapters 1 and 2 left off. As we discussed in the earlier chapters, all medications, psychiatric and otherwise, have multiple effects. One takes a medication to achieve a therapeutic effect. Occasionally, a single medication may have more than one therapeutic effect. All other effects are side effects. Different medications may have differing therapeutic and side effects depending on the intended use. For example, trazodone and quetiapine are often prescribed to aid in sleep, and in this instance sedation is the desired effect, yet when used as an antidepressant and antipsychotic, respectively, the sedation is often an unwanted effect. Psychotropic medications typically have multiple effects. First, they usually interact with more than one nerve cell protein, be it a transporter or a receptor. Quite often, one of the medication s receptor or transporter interactions produces the therapeutic effect. The other interactions tend to not be involved in the therapeutic effect and only serve to produce side effects. Sometimes a neurotransmitter will have multiple different receptor types, but the medication interacts with... 

In silico methods for unraveling the mechanistic complexities of intestinal absorption metabolism-efflux transport interactions. Drug Metabolism and Disposition. 

Tucker T, Houston JB, Huang S-M. Optimizing drug development strategies to assess drug metabolism/transporter interaction potential—toward a consensus. Clin Pharmacol Ther 2001 70, 103 Br J Clin Pharmacol 2001 52, 107 Eur J Pharm Sci 2001 13, 417 Pharm Res 2001 18, 1071. 

For the detailed study of reaction-transport interactions in the porous catalytic layer, the spatially 3D model computer-reconstructed washcoat section can be employed (Koci et al., 2006, 2007a). The structure of porous catalyst support is controlled in the course of washcoat preparation on two levels (i) the level of macropores, influenced by mixing of wet supporting material particles with different sizes followed by specific thermal treatment and (ii) the level of meso-/ micropores, determined by the internal nanostructure of the used materials (e.g. alumina, zeolites) and sizes of noble metal crystallites. Information about the porous structure (pore size distribution, typical sizes of particles, etc.) on the micro- and nanoscale levels can be obtained from scanning electron microscopy (SEM), transmission electron microscopy ( ), or other high-resolution imaging techniques in combination with mercury porosimetry and BET adsorption isotherm data. This information can be used in computer reconstruction of porous catalytic medium. In the reconstructed catalyst, transport (diffusion, permeation, heat conduction) and combined reaction-transport processes can be simulated on detailed level (Kosek et al., 2005). 

To model mass and energy transport in monolith systems, several approaches are discussed, leading from a representative channel spatially ID approach to 2D (1D+1D) modeling explicitly including washcoat diffusion. Correlations are given to describe heat and mass transfer between bulk gas phase and catalytic washcoat. For the detailed study of reaction-transport interactions in the porous catalytic layer, the spatially 3D model of the computer-reconstructed washcoat section can be employed. 

FLAVONOID-AUXIN TRANSPORT INTERACTION AND MODULATION OF PLANT GROWTH... 

Liu, H., and G. Amy. 1993. Modeling partition and transport interactions between natural organic matter and PAHs in groundwater. Environmental Science and Technology 27 1553. 

Sharom FJ. The P-glycoprotein multi drug transporter interactions with membrane lipids, and their modulation of activity. Biochem Soc Trans 1997 25(3) 1088-1096. 

Trap-Controlled Hopping. In trap-controlled hopping, the scenario described for trap-controlled band mobility applies. However, the microscopic mobility is associated now with carriers hopping in a manifold of localized states. Overall temperature and field dependence reflects the complicated convolution of the temperature and field dependence of both the microscopic mobility and the trap kinetic processes. Glearly, the observed behavior can now range from nondispersive to anomalously dispersive behavior as before, depending on the energy distribution of transport-interactive traps. 

Henry LK, Field JR, Adkins EM, Parnas ML, Vaughan RA, Zou MF, Newman AH, Blakely RD. Tyr-95 and Ile-172 in transmembrane segments 1 and 3 of human serotonin transporters interact to establish high affinity recognition of antidepressants. J. Biol. Chem. 2006 281 2012-2023. 

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