Membrane transport mechanisms

This book provides a general introduction to membrane science and technology. Chapters 2 to 4 cover membrane science, that is, topics that are basic to all membrane processes, such as transport mechanisms, membrane preparation, and boundary layer effects. The next six chapters cover the industrial membrane separation processes, which represent the heart of current membrane technology. Carrier facilitated transport is covered next, followed by a chapter reviewing the medical applications of membranes. The book closes with a chapter that describes various minor or yet-to-be-developed membrane processes, including membrane reactors, membrane contactors and piezodialysis. 

Care should be exercised when attempting to interpret in vivo pharmacological data in terms of specific chemical—biological interactions for a series of asymmetric compounds, particularly when this interaction is the only parameter considered in the analysis (10). It is important to recognize that the observed difference in activity between optical antipodes is not simply a result of the association of the compound with an enzyme or receptor target. Enantiomers differ in absorption rates across membranes, especially where active transport mechanisms are involved (11). They bind with different affinities to plasma proteins (12) and undergo alternative metaboHc and detoxification processes (13). This ultimately leads to one enantiomer being more available to produce a therapeutic effect. 

The concentration boundary layer forms because of the convective transport of solutes toward the membrane due to the viscous drag exerted by the flux. A diffusive back-transport is produced by the concentration gradient between the membranes surface and the bulk. At equiUbrium the two transport mechanisms are equal to each other. Solving the equations leads to an expression of the flux ... 

FIGt 22-48 Transport mechanisms for separation membranes a) Viscous flow, used in UF and MF. No separation achieved in RO, NF, ED, GAS, or PY (h) Knudsen flow used in some gas membranes. Pore diameter < mean free path, (c) Ultramicroporoiis membrane—precise pore diameter used in gas separation, (d) Solution-diffusion used in gas, RO, PY Molecule dissolves in the membrane and diffuses through. Not shown Electro-dialysis membranes and metallic membranes for hydrogen. 

Bitter, J. G. A. (1991) Transport Mechanisms in Membrane Separation Processes, Plenum Press, New York. 

A different approach is the use of an ultrafiltration membrane with an immobilized chiral component [31]. The transport mechanism for the separation of d,l-phenylalanine by an enantioselective ultrafiltration membrane is shown schematically in Fig. 5-4a. Depending on the trans-membrane pressure, selectivities were found to be between 1.25 and 4.1, at permeabilities between 10 and 10 m s respectively (Fig. 5-4b). 

A number of studies have recently been devoted to membrane applications [8, 100-102], Yoshikawa and co-workers developed an imprinting technique by casting membranes from a mixture of a Merrifield resin containing a grafted tetrapeptide and of linear co-polymers of acrylonitrile and styrene in the presence of amino acid derivatives as templates [103], The membranes were cast from a tetrahydrofuran (THF) solution and the template, usually N-protected d- or 1-tryptophan, removed by washing in more polar nonsolvents for the polymer (Fig. 6-17). Membrane applications using free amino acids revealed that only the imprinted membranes showed detectable permeation. Enantioselective electrodialysis with a maximum selectivity factor of ca. 7 could be reached, although this factor depended inversely on the flux rate [7]. Also, the transport mechanism in imprinted membranes is still poorly understood. 

With the adequacy of lipid bilayer membranes as models for the basic structural motif and hence for the ion transport barrier of biological membranes, studies of channel and carrier ion transport mechanisms across such membranes become of central relevance to transport across cell membranes. The fundamental principles derived from these studies, however, have generality beyond the specific model systems. As noted above and as will be treated below, it is found that selective transport... 

Urry, D. W. On the Molecular Structure and Ion Transport Mechanism of the Gramicidin Transmembrane Channel. In Membranes and Transport, Vol. 2, (ed. Martonosi, A.), p. 285, Plenum Publishing Corporation, New York 1982... 

Additional cellular events linked to the activity of blood pressure regulating substances involve membrane sodium transport mechanisms Na+/K.+ ATPase Na+fLi countertransport Na+ -H exchange Na+-Ca2+ exchange Na+-K+ 2C1 transport passive Na+ transport potassium channels cell volume and intracellular pH changes and calcium channels. 

A number of genetic diseases that result in defects of tryptophan metabolism are associated with the development of pellagra despite an apparently adequate intake of both tryptophan and niacin. Hartnup disease is a rare genetic condition in which there is a defect of the membrane transport mechanism for tryptophan, resulting in large losses due to intestinal malabsorption and failure of the renal resorption mechanism. In carcinoid syndrome there is metastasis of a primary liver tumor of enterochromaffin cells which synthesize 5-hydroxy-tryptamine. Overproduction of 5-hydroxytryptamine may account for as much as 60% of the body s tryptophan metabolism, causing pellagra because of the diversion away from NAD synthesis. 

Biochemical studies of plasma membrane Na /H exchangers have been directed at two major goals (1) identification of amino acids that are involved in the transport mechanism and (2) identification and characterization of the transport pro-tein(s). To date, most studies have been performed on the amiloride-resistant form of Na /H" exchanger that is present in apical or brush border membrane vesicles from mammalian kidney, probably because of the relative abundance of transport activity in this starting material. However, some studies have also been performed on the amiloride-sensitive isoform present in non-epithelial cells. 

Taken together, these results indicate that similar to other proton-translocating membrane proteins, both types of Na /H exchangers contain critical sulfhydryl groups that are involved in the transport mechanism. These sulfhydryl groups do not appear to be present at the external transport site but may be involved in switching from an inactive to an activated state. 

Figure 20-48 shows Wijmans s plot [Wijmans et al.,/. Membr. Sci., 109, 135 (1996)] along with regions where different membrane processes operate (Baker, Membrane Technology and Applications, 2d ed., Wiley, 2004, p. 177). For RO and UF applications, Sj , < 1, and c > Cl,. This may cause precipitation, fouling, or product denatura-tion. For gas separation and pervaporation, Sj , >1 and c < ci. MF is not shown since other transport mechanisms besides Brownian diffusion are at work. 

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