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Blood surfactants

Albertsson (Paiiition of Cell Paiiicle.s and Macromolecules, 3d ed., Wiley, New York, 1986) has extensively used particle distribution to fractionate mixtures of biological products. In order to demonstrate the versatility of particle distribution, he has cited the example shown in Table 22-14. The feed mixture consisted of polystyrene particles, red blood cells, starch, and cellulose. Liquid-liquid particle distribution has also been studied by using mineral-matter particles (average diameter = 5.5 Im) extracted from a coal liquid as the solid in a xylene-water system [Prudich and Heniy, Am. Inst. Chem. Eng. J., 24(5), 788 (1978)]. By using surface-active agents in order to enhance the water wettability of the solid particles, recoveries of better than 95 percent of the particles to the water phase were obsei ved. All particles remained in the xylene when no surfactant was added. [Pg.2015]

The selection of mix ingredients may depend heavily on the type of adhesive applieation equipment used. The main types of equipment for plywood and LVL are roll coaters, spray systems, eurtain coaters, and foam extruders. When foam extruders are used, animal blood and surfactants are usually added to the mill mix. For other application systems, resin producers typieally supply the non-filler additives as part of the resin eomposition. [Pg.894]

Figure 4 Stabilized bromine antimicrobials are produced by eosinophils, a type of mammalian white blood cell. Bacteria are captured by phagocytosis and contained intracellularly within vesicles called phagosomes. Granules release cationic surfactants, lytic enzymes, and eosinophil peroxidase into the phagosome in a process known as degranulation. Eosinophil peroxidase, an enzyme that is structurally similar to the bromoperoxidases found in seaweed (Figure I), selectively catalyzes oxidation of bromide to hypobromite by reducing hydrogen peroxide to water. The hypobromite immediately reacts with nitrogenous stabilizers such as aminoethanesulfonic acid (taurine) to form more effective and less toxic antimicrobial agents. Figure 4 Stabilized bromine antimicrobials are produced by eosinophils, a type of mammalian white blood cell. Bacteria are captured by phagocytosis and contained intracellularly within vesicles called phagosomes. Granules release cationic surfactants, lytic enzymes, and eosinophil peroxidase into the phagosome in a process known as degranulation. Eosinophil peroxidase, an enzyme that is structurally similar to the bromoperoxidases found in seaweed (Figure I), selectively catalyzes oxidation of bromide to hypobromite by reducing hydrogen peroxide to water. The hypobromite immediately reacts with nitrogenous stabilizers such as aminoethanesulfonic acid (taurine) to form more effective and less toxic antimicrobial agents.
Poloxamer 188 (Flocor) is being evaluated for vasoocclusive crisis. This surfactant returns RBCs to a nonadhesive state and blocks RBC aggregation to enhance blood flow in ischemic areas. [Pg.388]

The distribution of a chemical in tissue depends on the binding/par-titioning between circulatory blood and tissues, the transfer across biological membranes and the tissue-blood perfusion. After incorporation, contaminants are distributed from blood to high perfusion tissues (e.g. liver, kidney), then to low perfusion ones (skin, muscle) and finally to lipoidal tissues [2], establishing kinetically different compartments (internal organs > liver > head skin) and different times to equilibrium [18]. Surfactants (LAS, AS, AES, AEO and APEO) have been... [Pg.899]

Acridinium ester—labeled chemiluminescent probes have been utilized to detect the specific protein-coding transcripts and to distinguish between transcripts that code for the 190-kDa protein and the two closely related 210-kDa proteins. The assay is called the hybridization protection assay (D3). In this assay, RNA isolated from the patient s white blood cells is first amplified by PCR. The amplified product is incubated with the chemiluminescent probe. The unhybridized probe is removed by selective hydrolysis in sodium tetraborate buffer, containing surfactant Triton X-100 at pH 8.5, in an incubation step at 60°C for 6 min. After the sample is cooled to room temperature, the chemiluminescence of the hybridized probe is measured in a luminometer. The procedure is reported to detect one leukemic cell in a population of a million or more normal cells. It is also rapid, requiring less than 30 min. Its reliability has been attested to by correlation with results obtained on karyotypic and Southern blot analysis (D3). [Pg.32]

H-bonding potential Molecular weight/size PSA Intestinal metabolism Transport mechanisms Native surfactants Intestinal secretions, e.g. mucous, enzymes Intestinal blood/lymph flow Excipient effects... [Pg.37]

The influence of hydrophilic chain length and alkyl chain length of a series of alkyl ethers respectively) on the percentage change in blood glucose on administration rectally of insulin with the surfactants. The upper plot shows the results 30 minutes after administration and the lower plot results after 60 minutes. (Redrawn from data in Touitou et al, 1978). [Pg.196]

The answer is A. Lung surfactant reduces surface tension of the fluid lining the alveoli to increase pulmonary compliance and facilitate exchange of gases dissolved in that fluid from inspired air into the airway epithelial cells and eventually by diffusion into the blood. Although all the other options represent properties of water or solutions, they have nothing to do with the properties of surfactant. [Pg.8]


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See also in sourсe #XX -- [ Pg.461 , Pg.466 ]




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