Polymeric matrix, immobilization

The complex [Ir(ppy)2(dpt-NH2)]PF6 (175), dpt-NH2 4-ami no-3,5-bis(2-pyridyl)-477-1,2,-4-triazole, (176), has been synthesized and characterized319 A reversible, one-electron oxidation of (175) is assigned to removal of an electron from an Ir (/--based orbital. (175) luminesces at room temperature and 77 K. The complex (175), when immobilized in a polymeric matrix, acts as an... 

Immobilized cryptates. Like the crowns, cryptates have been immobilized on polymeric backbones. A typical system is given by (221) (Cinquini, Colonna, Molinari, Montanari Tundo, 1976). In this case, the polymeric matrix is polystyrene cross-linked with p-divinyl benzene and the cage is connected to this matrix via a long-chain aliphatic spacer group. This reagent is quite effective as a (triphase) transfer catalyst. 

Phase-Transfer Catalysts Immobilized into a Polymeric Matrix... 

The potentialities offered by chemical processes catalyzed by enzymes immobilized in a polymeric matrix are obvious and are now successfully utilized in various ways [6, 13, 16, 17, 40, 43,44, 50, 58, 61], This idea was introduced into electroanalytical chemistry by Clark and Lyons [9], who proposed a glucose electrode, with glucose oxidase immobilized between cuprophane membranes and with amperometric determination of the hydrogen peroxide formed by the reaction... 

The first synthesis of (3-lactams bound to a soluble/insoluble polyethylene glycol monomethylether polymeric matrix has been realized by standard reactions carried out on immobilized imines. From the polymer, [3-lactams were removed under acidic and basic conditions [76, 77]. The reactivity of the immobilized reagent was tested by synthesizing p-lactam from imines and an enolate 8a and the... 

The immobilization of enzymes may introduce a new problem which is absent in free soluble enzymes. It is the mass-transfer resistance due to the large particle size of immobilized enzyme or due to the inclusion of enzymes in polymeric matrix. If we follow the hypothetical path of a substrate from the liquid to the reaction site in an immobilized enzyme, it can be divided into several steps (Figure 3.2) (1) transfer from the bulk liquid to a relatively unmixed liquid layer surrounding the immobilized enzyme (2) diffusion through the relatively unmixed liquid layer and (3) diffusion from the surface of the particle to the active site of the enzyme in an inert support. Steps... 

Immobilized cells of S. clavuligerus NP1, entrapped on a polymeric matrix, were able to perform oxidative ring expansion of penicillin G into DAOG. Cells entrapped in polyethyleneimine barium alginate (1.5%) were able to sustain activity for at least four 2-hr cycles, whereas free resting cells were inactive after the second cycle. 

Novel microreactors with immobilized enzymes were fabricated using both silicon and polymer-based microfabrication techniques. The effectiveness of these reactors was examined along with their behavior over time. Urease enzyme was successfully incorporated into microchannels of a polymeric matrix of polydimethylsiloxane and through layer-bylayer self-assembly techniques onto silicon. The fabricated microchannels had cross-sectional dimensions ranging from tens to hundreds of micrometers in width and height. The experimental results for continuous-flow microreactors are reported for the conversion of urea to ammonia by urease enzyme. Urea conversions of >90% were observed. 

A biosensor utilizes a biological component to translate the concentration of a specific analyte of interest into a signal detectable by some chemical or physical means (7). Successful operation of a biosensor requires that the biological component and the signal it transduces be localized to and concentrated within a region in close proximity to the detection system. Immobilization of enzymes within a polymeric matrix ensures concentration and localization of the enzymic reaction, and creates a convective barrier, thus preventing dilution and convective removal of the product species before it is detected. Enzymes immobilized on or near the detection system are frequently used as the... 

Applications of polymerization in a supercooled state to the immobilization of various biofunctional components is reviewed. Those applications show advantages because in the low temperature biofunctional components such as proteins, drugs and cells are entrapped or adhered effectively in the polymerized matrix. The immobilized composites are used for biomedical and biochemical systems and processes, such as immuno-diagnosis, artificial organs, drug delivery systems and cell cultures. 

This book describes the science and practice behind the materials in foods that impart their desirable properties. The first part of the book describes those physicochemical aspects that intervene in the organization of food components from the molecular level to actual products and methods used to probe into foods at different length scales. The second part explains how food structures are assembled during processing in order to achieve desirable and recognizable properties. Processed foods are mostly metastable structures in which water, air, and lipids are immobilized as dispersed phases within a polymeric matrix of proteins, polysaccharides, or a fat crystal network. The last section of the book presents specific examples of how structures of familiar products are obtained by processing and describe some new developments. 

Entrapment methods of immobilization of bioreceptors utilized the lattice structure of particular base material. They include such methods as entrapment behind the membrane, covering the active surface of biosensors, entrapment within a self-assembled monolayers on the biosensor surface, as well as on freestanding or supported bilayer lipid membranes, and also entrapment within a polymeric matrix membranes, or within bulk material of sensor. All these mentioned methods are widely employed in design of biosensors. The essential condition of success of these methods of immobilization is preservation of sufficient mobility of substrate or products of biochemical reaction, involved in sensing mechanism, as matrix may act as a barrier to mass transfer with significant implications for... 

It was shown that polymeric matrices have their sensing response stability over several years.911 However, in fluorescent chemical sensors, photobleaching of matrix-immobilized organic dyes significantly hinders the applicability of such... 

Enzyme-antibody complex formation represents the simplest among the immunoaffinity immobilization procedures and the immunocomplexes can be readily formed simply by mixing of the enzyme solution with the antibody or even antiserum. Interestingly neither pure enzyme nor pure antibody may be required for the formation of immunocomplexes. Several early [14,36,39] and some recent studies [22,24,28] indicate high retention of catalytic activities by various enzymes in the immunocomplexes and marked stability enhancement against various forms of inactivation. The small particle dimensions of the enzyme-antibody complexes may however lead to their compact packing and consequently to slow flow-rates in the column reactors. Their usefulness can be however remarkably enhanced by entrapping the complexes in a polymeric matrix [60,61]. 

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