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Carrier-bound systems

For the present, systems containing albumin-bound bilirubin appear to be of greatest practical value. The fraction of fully hydrated substrate can be known more accurately than with the other systems. Carrier-free systems or the addition of water-miscible solvents may be quite useful for specific purposes. Comparative studies with the three modes of substrate addition would be helpful to allow assessment of their merits. [Pg.252]

With UDP-glucuronic acid as the variable substrate and bilirubin at constant concentration, Michaelis-Menten kinetics were obeyed (A2, H2, HIO, P5, V2, W12). Rat liver microsomal preparations treated in different ways yielded apparent Km for UDP-glucuronic acid of 0.37-0.70 mM (A2, H2, HIO, V2), with albumin-bound bilirubin as the aglycon a higher value (1.66 mAf) was found in a carrier-free system (W12). These values probably do not represent Km for UDP-glucuronic acid at saturation with bilirubin (P5, V6). Under certain conditions of activation, cell extracts from livers of newborn and adult rats, wdicn tested with o-amino-... [Pg.255]

The aim was to achieve the same results with the Reflotron system as would have been obtained by employing a wet process. A certain concentration c of the substance to be analysed yields a certain reflection R when reacting with carrier-bound reagents. This relationship can be expressed by the functional curve... [Pg.340]

The method is based on the principle of enzyme immunoassay with fluorimet-ric detection and is termed radial partition immunoassay. This test can analyse macromolecules and haptens rapidly and with high sensitivity in a fully mechanised analysis system. The special feature of this test is the use of carrier-bound reagents on a so-called dry tab. [Pg.555]

Despite the advantages of enzymes immobilized on noncatalytic matrices, the yield and productivity of the reaction can be reduced simply due to the presence of the noncatalytic mass of the carrier. There has therefore been much interest in the development of carrier-free systems, in which enzyme molecules are linked to each other to form large complexes. These are inherently immobilized because individual enzyme molecules are no longer free to diffuse in solution, but they are largely undiluted by inert molecules and therefore retain a greater degree of activity than carrier-bound enzymes. This article discusses strategies for enzyme immobilization in carrier-based and carrier-free systems and considers some of their major applications. [Pg.1119]

Fig. 4. DNA synthesis. Phosphoramidite method of DNA synthesis, using a solid phase system. Coupling efficiency is measured by monitoring the DMTr cation, as in Fig. 3. R is a methyl or p-cyanoethyl group. is methyl, ethyl or isopropyl. Sa - spacer arm. The reactive phosphite is oxidized to a stable triester by aqueous iodine in the presence of lutidine. At the beginning of each new cycle, any unreacted, carrier-bound 5 -hydroxyl groups are acetylated with acetic anhydride, a process known as capping. Fig. 4. DNA synthesis. Phosphoramidite method of DNA synthesis, using a solid phase system. Coupling efficiency is measured by monitoring the DMTr cation, as in Fig. 3. R is a methyl or p-cyanoethyl group. is methyl, ethyl or isopropyl. Sa - spacer arm. The reactive phosphite is oxidized to a stable triester by aqueous iodine in the presence of lutidine. At the beginning of each new cycle, any unreacted, carrier-bound 5 -hydroxyl groups are acetylated with acetic anhydride, a process known as capping.
A theory for the mechanism of diffusion through a membrane using a fixed carrier covalently bound to the soHd matrix, was developed previously [Cussler et al., 1989]. The concept is that the solute molecule jumps from one carrier to the next in sequence. Facilitated diffusion can occur only if these chained carriers are reasonably close to each other and have some limited mobihty. The advantages of using a chained carrier in a soHd matrix vs. a mobile carrier in a Hquid membrane are that the stabihty is improved, there is no potential for solvent loss from the system, and the transport may actually be enhanced. Their theory is compared to that for the mobile carriers in the SLMS. For the fixed-carrier (chained) system. [Pg.81]

Carrier-bound drug systems designed to perform as described in Section VII. A should contain suitable cleavage sites permitting drug release. These release mechanisms depend crucially on the structural peculiarities of the type of drug incorporated into the conjugate. [Pg.149]

In low-dimensional systems, such as quantum-confined. semiconductors and conjugated polymers, the first step of optical absorption is the creation of bound electron-hole pairs, known as excitons [34). Charge photogcncration (CPG) occurs when excitons break into positive and negative carriers. This process is of essential importance both for the understanding of the fundamental physics of these materials and for applications in photovoltaic devices and photodctcctors. Since exciton dissociation can be affected by an external electric field, field-induced spectroscopy is a powerful tool for studying CPG. [Pg.138]

According to classical information theory, founded by Shannon [1948] (see also Shannon and Weaver [1949]), information is eliminated uncertainty about an occurrence or an object, obtained by a message or an experiment. Information is always bound up with signals. They are the carriers of information in the form of definite states or processes of material systems (Eckschlager and Danzer [1994] Danzer [2004]) see Sect. 3.1. [Pg.289]


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Carrier-bound systems strategy

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