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Plasma three body systems

The effects of plasma environments on the spectral properties of exotic two-and three-body systems have been studied. Influence of the Debye plasma on the stability and spectral properties of spatially confined exotic systems like p+ x and [i+[i was investigated by Sil et al. [217] along the same line as was... [Pg.157]

The calculations have been further extended by Sil et al. [219] for analyzing the stability of exotic systems like ppp, ddp and ttp and also finding the behavior of the hadronic affinity under Debye plasma. An interesting feature emerges from this particular study, namely, a given two-body system becomes unstable at a screening parameter for which the corresponding three-body system is stable. This property depends very much on the... [Pg.158]

If opiates are such addictive and potentially lethal compounds, why does the body respond to them As with the cannabinoids (Chapter 7), it has been discovered that the body and brain possess numerous opiate-specific receptor sites. As many as nine receptor subtypes have been identified, with three of them being the most important p (mu), k (kappa) and 8 (delta). The finding that the distribution of opiate receptors did not parallel the distribution of any known neurotransmitter prompted the search for and identification of a number of endogenous compounds specific to these receptors. These enkephalins and endorphins are manufactured within the brain and other body systems (especially the gut and intestines) and form the body s natural response to pain. They appear to be produced in bulk chains of amino acids called polypeptides , with each active neurotransmitter being composed of around five amino acid molecules. These active neurotransmitters are subsequently cleaved from the larger polypeptides at times of demand for example, it has been demonstrated that the plasma levels of these active compounds rise during childbirth, traumatic incidents and vigorous physical exercise. [Pg.109]

Several empirical and semiempirical interatomic potentials have been developed for the Si H systembased on extensions and modifications of well-known potentials for Si including up to three-body interactions (StilUnger and Weber, 1985 Biswas and Hamann, 1985 Biswas et al., 1987 Mousseau and Lewis, 1991 Baskes, 1992). Recent atomic-scale simulation work of plasma-surface interactions in the PECVD of Si thin films has been based on an empirical description of interatomic interactions in the Si H system according to Tersoff s (1986, 1988, 1989) potential for Si, as extended by Ohira and co-workers (1994, 1995, 1996) to incorporate Si-H, H-H, and the corresponding three-body interactions. The extension of the potential to include the presence of hydrogen adopted the Tersoff parametrization to fit results of ab initio calculations for the structure and energetics of Sil 1., x <4, species in the gas phase (Ohira et al., 1994,1995,1996). A similar form of... [Pg.259]

Bergstrom et al. [63] used HPLC for determination of penicillamine in body fluids. Proteins were precipitated from plasma and hemolyzed blood with trichloroacetic acid and metaphosphoric acid, respectively, and, after centrifugation, the supernatant solution was injected into the HPLC system via a 20-pL loop valve. Urine samples were directly injected after dilution with 0.4 M citric acid. Two columns (5 cm x 0.41 cm and 30 cm x 0.41 cm) packed with Zipax SCX (30 pm) were used as the guard and analytical columns, respectively. The mobile phase (2.5 mL/min) was deoxygenated 0.03 M citric acid-0.01 M Na2HP04 buffer, and use was made of an electrochemical detector equipped with a three-electrode thin-layer cell. The method was selective and sensitive for mercapto-compounds. Recoveries of penicillamine averaged 101% from plasma and 107% from urine, with coefficients of variation equal to 3.68 and 4.25%, respectively. The limits of detection for penicillamine were 0.5 pm and 3 pm in plasma and in urine, respectively. This method is selective and sensitive for sulfhydryl compounds. [Pg.146]

This is the presence of excess fluid in the peritoneal cavity, leading to a swollen abdomen (Figure 4.3). The accumulation of ascitic fluid represents a state of sodimn excess in the body. Patients often present with hyponatraemia, but this is thought to be due to the dilutional effect of excess water rather than to low sodium. There are three theories of the cause of ascites formation. The underfill theory suggests that there is a reduction in circulating plasma volume as a result of accumulation in the splanchnic area due to vascular dilatation in portal hypertension. This activates the plasma renin, aldosterone and sympathetic nervous systems, which leads to sodium and water retention by the kidneys. [Pg.91]

The distribution of a compound in the human body can also be partially related to the absorption properties. There are specific transport systems that are expressed in certain tissues that can influence the distribution of the compound. For example, rosuvastatin, a new member of the statin family is transported by the OATP-C carrier system, which is selectively expressed in the liver, making this compound selectively distributed into this organ [27]. In general it is not possible to derive computational models for these selective transport systems since there is not yet enough experimental information and data to support the model building and validation. Nevertheless, there are three properties that are commonly used to describe the distribution of a compound in the human body the solubility, the unspecific binding of the compound to plasma proteins and the volume of distribution. [Pg.228]

Three common examples of buffers. Many medications are buffered to minimize digestive upset. Most body fluids, including blood plasma, contain very efficient namral buffer systems. Buffer capsules are used in laboratories to prepare solutions of specified pH. [Pg.800]


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See also in sourсe #XX -- [ Pg.155 , Pg.156 ]




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Three body systems, under plasma

Three-body system

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