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Determinant Multiplication

Model equations can be augmented with expressions accounting for covariates such as subject age, sex, weight, disease state, therapy history, and lifestyle (smoker or nonsmoker, IV drug user or not, therapy compliance, and others). If sufficient data exist, the parameters of these augmented models (or a distribution of the parameters consistent with the data) may be determined. Multiple simulations for prospective experiments or trials, with different parameter values generated from the distributions, can then be used to predict a range of outcomes and the related likelihood of each outcome. Such dose-exposure, exposure-response, or dose-response models can be classified as steady state, stochastic, of low to moderate complexity, predictive, and quantitative. A case study is described in Section 22.6. [Pg.536]

The most widely used method for determining multiplicities of carbon atoms is DEPT (Distortionless Enhancement by Polarization Transfer). This has generally replaced the classical method of recording off-resonance C spectra with reduced CH couplings from which the multiplicity could be read directly. [Pg.117]

In the wine industry, FTIR has become a useful technique for rapid analysis of industrial-grade glycerol adulteration, polymeric mannose, organic acids, and varietal authenticity. Urbano Cuadrado et al. (2005) studied the applicability of spectroscopic techniques in the near- and mid-infrared frequencies to determine multiple wine parameters alcoholic degree, volumic mass, total acidity, total polyphenol index, glycerol, and total sulfur dioxide in a much more efficient approach than standard and reference methods in terms of time, reagent, and operation errors. [Pg.497]

Determining multiple length scales in rocks), Nature 406, July 13, 178-181. [Pg.340]

HPLC has high-throughput capability when it can simultaneously determine multiple drugs and their metabolites or when coupled with a unique monolithic column or sample preparation technique. Some examples are summarized below. [Pg.302]

Determining multiple KIEs using natural abundance nmr spectroscopy 238... [Pg.144]

DETERMINING MULTIPLE KIEs USING NATURAL ABUNDANCE nmr SPECTROSCOPY... [Pg.238]

Ihis number v is the mean stoichiometric number of the rate-determining multiple steps. The mean stoichiometric number is thus represented by the energy average (afiiniiy average) of the stoichiometric niunbers v weighed with the step affinity 4gi in the respective rate-determining steps. [Pg.230]

Polarography is able to determine multiple analytes (cf. Figure 6.11). [Pg.160]

F. Du, X.-H. Zhu, H. Qiao, X. Zhang and W. Chen, Efficient in vivo P magnetization transfer approach for noninvasively determining multiple kinetic parameters and metabolic fluxes of ATP metabolism in the human brain. Magn. Reson. Med., 2007, 57, 103-114. [Pg.149]

The water-soluble vitamins are a highly diverse group of compounds with differing physicochemical properties. A single vitamin generally consists of several vitamers, or chemical species, each of which exhibits the same biological activity in vivo. Individual vitamers with the same biological functions often exhibit vastly different physicochemical properties. This necessitates unique extraction and separation procedures for each vitamin. As a result, each vitamin is considered individually in this chapter. A section on methods that determine multiple vitamins simultaneously is also included. [Pg.404]

Process monitoring, with on-line instruments that operate autonomously for extended periods of time, presents significant challenges and opportunities. The requirements for monitors will vary with the application they support. Where the monitor is set up to support a particular separation process, the analytical objectives may be to determine a single species. The technetium monitor described above, designed to support a technetium removal process, is such an example. On the other hand, some processes may seek to determine multiple actinides in a process stream. These actinides could be a selected group of the transuranic (TRU) elements, or the multiple isotopes of a particular actinide like plutonium. [Pg.553]

If less than about 100 nucleotides are to be sequenced the whole of each sample can be loaded onto the gel and electrophoresed until the xylene-cyanol dye marker (turquoise) has moved about a third of the way down the gel, (xylene-cyanol runs with fragments about 70 nucleotides long on an 8% gel). If sequences of 200 or more nucleotides are to be determined multiple loadings of the... [Pg.252]

This used to be a common way of distinguishing methyl, methylene and methine carbons. However, as can be seen in the spectrum above, it is not a clean experiment methylene carbons with non-equivalent protons attached often give particularly messy results ( 8.2.2). /-modulated spin-echoes, INEPT or DEPT provide much more reliable ways of determining multiplicities ( 3.3.2 and 8.5). [Pg.29]

The least-squares procedure just described is an example of a univariate calibration procedure because only one response is used per sample. The process of relating multiple instrument responses to an analyte or a mixture of analytes is known as multivariate calibration. Multivariate calibration methods have become quite popular in recent years as new instruments become available that produce multidimensional responses (absorbance of several samples at multiple wavelengths, mass spectrum of chromatographically separated components, and so forth). Multivariate calibration methods are very powerful. They can be used to determine multiple components in mixtures simultaneously and can provide redundancy in measurements to improve precision. Recall that repeating a measurement N times provides a Vn improvement in the precision of the mean value. These methods can also be used to detect the presence of interferences that would not be identified in a univariate calibration. [Pg.208]

Bhargava et al., submitted). Mice were injected subcutaneously (SC) with THC (10 milligrams per kilogram (mg/kg)) twice daily for 4 days. On day 5, analgesic and hypothermic responses to THC were determined. Multiple injections of THC resulted in the development of tolerance to both the analgesic and hypothermic effects of THC. [Pg.191]

In packed-bed, flow-through electrodes, concentration and potential variation within the bed can also give more than one steady state. The convective transport equation with axial dispersion, coupled with Ohm s law for the electrode potential, was solved recently (418) by polynomial expansion and orthogonal collocation within the bed, to determine multiplicity regions. [Pg.321]

Over the past decade, there has been considerable development in imaging type detectors for the measurement of ultraviolet (UV) and visible light. These new detectors have attracted the interest of a number of analytical spectroscopists. For absorption spectroscopy, analytical chemists have traditionally used such instruments as the photometer, which uses a narrow-band light source (for example the 254 nm emission line from a low pressure Hg lamp or a continuous source with a filter), a sample cell and a photomultiplier tube (FMT) as the detector. While useful for many specific applications, the single-wavelength photometer cannot determine multiple sample components simultaneously or provide a general absorbance characterization of the system. When information at multiple wavelengths is desired,... [Pg.57]

Malone B. 1970. Method for determining multiple residues of organic fumigants in cereal grain. J AOAC 53 742-746. [Pg.201]

A single solvent-solvent extraction step seldom satisfies the purification requirements for a GC determination multiple extractions are often needed for a more complete sample purification. However, such multiple extractions and transfers of a sample from one medium to another may result in further uncontrolled sample losses. Selective fractionations are used with advantage wherever some unique features of the analyzed molecules exist among the most typical approaches, researchers have extensively used ion-pairing extractions of various ionic samples and the digitonin or Girard separations of steroidal compounds. [Pg.104]

Certainly, one can fit each of the individual velocity versus substrate curves at each effector concentration and determine multiple K s and VmaxS for the process of activation. However, it may be more informative to fit all the data together to ascertain additional information regarding the phenomenon. In this case, equation (Eq. 4.11) may be used to estimate A and Vmax for the... [Pg.100]

There are two modes of operation, namely an automatic one started by Subtract and an interactive one launched by Start Interactive Mode. In the automatic mode, the difference spectrum with automatically determined multiplication factors is calculated from a least squares analysis over the displayed wavenumber range. The range of wavenumbers used is the largest range present in all spectra. The interactive mode allows you to set the multiplication factors manually. [Pg.81]


See other pages where Determinant Multiplication is mentioned: [Pg.30]    [Pg.187]    [Pg.269]    [Pg.15]    [Pg.26]    [Pg.59]    [Pg.295]    [Pg.5]    [Pg.121]    [Pg.29]    [Pg.140]    [Pg.261]    [Pg.266]    [Pg.55]    [Pg.413]    [Pg.288]    [Pg.243]    [Pg.458]    [Pg.176]    [Pg.122]    [Pg.235]    [Pg.238]    [Pg.515]   
See also in sourсe #XX -- [ Pg.589 ]




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Multiple Determinants

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