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Intermediate density

Endothelial-anchored enzyme in liver primarily responsible for hydrolysis of triglycerides and phospholipids in Intermediate Density Lipoproteins (IDL) and High Density Lipoproteins (HDL). [Pg.582]

Interleukins Intermediate Filaments Intermediate-density Lipoprotein (DDL) Intermittent Claudication Internalization... [Pg.1495]

Trio-beds (triple beds) This is an MB double compartment design with an intermediate-density inert resin added to physically split the cation/anion resins during regeneration to minimize leakage. [Pg.353]

Non-reactive ion-exchange resin. Commonly employed at a specific intermediate density to separate cation and anion resins in a mixed-bed demineralization plant, in order to limit contaminant leakage, especially from regenerants. [Pg.742]

A typical Ziegler-Natta catalyst is the complex prepared from titanium tetrachloride and triethylaluminium. It is fed into the reaction vessel first, after which ethylene is added. Reaction is carried out at low pressures and low temperatures, typically no more than 70 °C, with rigorous exclusion of air and moisture, which would destroy the catalyst. The poly(ethylenes) produced by such processes are of intermediate density, giving values of about 0.945 g cm. A range of relative molar masses may be obtained for such... [Pg.6]

Abbreviations HDL, high-density iipoproteins IDL, intermediate-density lipoproteins LDL, low-density lipoproteins VLDL, very low density lipoproteins. [Pg.206]

Reaction with lipoprotein lipase results in the loss of approximately 90% of the triacylglycerol of chylomicrons and in the loss of apo C (which remrns to HDL) but not apo E, which is retained. The resulting chy-lotnicron remnant is about half the diameter of the parent chylomicron and is relatively enriched in cholesterol and cholesteryl esters because of the loss of triacylglycerol (Figure 25-3). Similar changes occur to VLDL, with the formation of VLDL remnants or IDL (intermediate-density lipoprotein) (Figure 25-4). [Pg.208]

Figure 25-4. Metabolic fate of very low density lipoproteins (VLDL) and production of low-density lipoproteins (LDL). (A, apolipoprotein A B-100, apolipoprotein B-100 , apolipoprotein C E, apolipoprotein E HDL, high-density lipoprotein TG, triacylglycerol IDL, intermediate-density lipoprotein C, cholesterol and cholesteryl ester P, phospholipid.) Only the predominant lipids are shown. It is possible that some IDL is also metabolized via the LRP. Figure 25-4. Metabolic fate of very low density lipoproteins (VLDL) and production of low-density lipoproteins (LDL). (A, apolipoprotein A B-100, apolipoprotein B-100 , apolipoprotein C E, apolipoprotein E HDL, high-density lipoprotein TG, triacylglycerol IDL, intermediate-density lipoprotein C, cholesterol and cholesteryl ester P, phospholipid.) Only the predominant lipids are shown. It is possible that some IDL is also metabolized via the LRP.
Figure 26-6. Transport of cholesterol between the tissues in humans. (C, unesterified choiesterol CE, cho-iesteryi ester TG, triacyigiyceroi VLDL, very iow density iipoprotein iDL, intermediate-density iipoprotein LDL, iow-density iipoprotein HDL, high-density iipoprotein ACAT, acyi-CoA choiesteroi acyitransferase LCAT, iecithinxhoiesteroi acyitransferase A-i, apoiipoprotein A-i CETP, choiesteryi ester transfer protein LPL, lipoprotein iipase HL, hepatic iipase LRP, LDL receptor-reiated protein.)... Figure 26-6. Transport of cholesterol between the tissues in humans. (C, unesterified choiesterol CE, cho-iesteryi ester TG, triacyigiyceroi VLDL, very iow density iipoprotein iDL, intermediate-density iipoprotein LDL, iow-density iipoprotein HDL, high-density iipoprotein ACAT, acyi-CoA choiesteroi acyitransferase LCAT, iecithinxhoiesteroi acyitransferase A-i, apoiipoprotein A-i CETP, choiesteryi ester transfer protein LPL, lipoprotein iipase HL, hepatic iipase LRP, LDL receptor-reiated protein.)...
Fig. 9-4). Very low-density lipoprotein particles are released into the circulation where they acquire apolipoprotein E and apolipoprotein C-II from HDL. Very-low density lipoprotein loses its triglyceride content through the interaction with LPL to form VLDL remnant and IDL. Intermediate-density lipoprotein can be cleared from the circulation by hepatic LDL receptors or further converted to LDL (by further depletion of triglycerides) through the action of hepatic lipases (HL). Approximately 50% of IDL is converted to LDL. Low-density lipoprotein particles are cleared from the circulation primarily by hepatic LDL receptors by interaction with apolipoprotein B-100. They can also be taken up by extra-hepatic tissues or enter the arterial wall, contributing to atherogenesis.4,6... [Pg.177]

FIGURE 9. Endogenous lipoprotein metabolism. In liver cells, cholesterol and triglycerides are packaged into VLDL particles and exported into blood where VLDL is converted to IDL. Intermediate-density lipoprotein can be either cleared by hepatic LDL receptors or further metabolized to LDL. LDL can be cleared by hepatic LDL receptors or can enter the arterial wall, contributing to atherosclerosis. Acetyl CoA, acetyl coenzyme A Apo, apolipoprotein C, cholesterol CE, cholesterol ester FA, fatty acid HL, hepatic lipase HMG CoA, 3-hydroxy-3-methyglutaryl coenzyme A IDL, intermediate-density lipoprotein LCAT, lecithin-cholesterol acyltransferase LDL, low-density lipoprotein LPL, lipoprotein lipase VLDL, very low-density lipoprotein. [Pg.178]

Solids of different densities can be separated by immersing them in a fluid of intermediate density. The heavier solids sink to the bottom and the lighter float to the surface. Water suspensions of fine particles are often used as the dense liquid (heavy-medium). The technique is used extensively for the benefication (concentration) of mineral ores. [Pg.406]

Primary or genetic lipoprotein disorders are classified into six categories for the phenotypic description of dyslipidemia. The types and corresponding lipoprotein elevations include the following I (chylomicrons), Ha (LDL), lib (LDL + very low density lipoprotein, or VLDL), III (intermediate-density lipoprotein), IV (VLDL), and V (VLDL + chylomicrons). Secondary forms of hyperlipidemia also exist, and several drug classes may elevate lipid levels... [Pg.111]

The initial implementation of DFT employed the so-called local density approximation, LDA (or, if we have separate a and [i spin, the local spin density approximation, LSDA). The basic assumption is that the density varies only slowly with distance -which it is locally constant. Another way of visualizing the concept of LDA is that we start with a homogeneous electron gas and subsequently localize the density around each external potential - each nucleus in a molecule or a solid. That the density is locally constant is indeed true for the intermediate densities, but not necessarily so in the high- and low-density regions. To correct for this, it was rec-... [Pg.117]

At intermediate density, quarks and gluons are strongly interacting and gluons are therefore presumably screened. Then, QCD at intermediate density may be modeled by four-Fermi interactions and higher-order terms by massive gluons. [Pg.173]

For generic parameters of dense QCD, the gap is estimated to be 10 100 MeV at the intermediate density. The free energy of the BCS state is given as... [Pg.174]


See other pages where Intermediate density is mentioned: [Pg.128]    [Pg.446]    [Pg.302]    [Pg.407]    [Pg.378]    [Pg.51]    [Pg.478]    [Pg.478]    [Pg.491]    [Pg.132]    [Pg.1545]    [Pg.235]    [Pg.404]    [Pg.608]    [Pg.841]    [Pg.647]    [Pg.696]    [Pg.697]    [Pg.126]    [Pg.118]    [Pg.176]    [Pg.180]    [Pg.193]    [Pg.93]    [Pg.366]    [Pg.54]    [Pg.15]    [Pg.482]    [Pg.156]   


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