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Identification Screening

The advantage of the use of CE for identification screening is based on the high peak capacity of the system and the separation ability to identify substance mixtures. Due to variations in the electroosmotic flow, the migration times in CE are less stable as in a HPLC system. Therefore, the identification tests in CE are based on the principle of calculating the... [Pg.106]

Identification Screen Fraction, inch Proximate analysis, % A +2 B 2X1% c IVt x 1... [Pg.559]

Sensitive identification, screening, and quantitation of 18 compounds of interest were achieved in chromatographic separation in only 4.40 min. Accurate and reproducible results were obtained by using five different and carefully selected deuterated analogs on the basis of the chemical properties of the target analytes. The extraction efficiencies ranged from 74.3% to 105.7% and the limits of quantitation (LOQ) from 1 to 100 ng/ml. The method was fully validated and is applicable for sensitive, reliable, and quantitative determination of benzodiazepines, zaleplon, and zopi-clone, for example, in clinical and forensic toxicology [9]. [Pg.361]

Recent literature contains a multitude of examples of synthetic organic methodologies which have been optimized and applied to the solid-phase synthesis of combinatorial libraries [2]. In fact, the production of a number of these libraries has been realized on such systems as the Multipin SPOC [8], the DIVERSOMER [9] and the OntoBLOCK [10], All three apparatuses allow the automated production of spatially dispersed combinatorial libraries and facilitate the isolation, identification, screening and archiving of single compounds in distinct physical locations which are crucial factors during lead discovery and optimization. [Pg.21]

General screening for lead identification screening a diverse library is a sensible approach when little or nothing is known about the target or possible lead compounds. [Pg.76]

If you have networking installed, the next screen you will see will be the computer identification screen. This only applies if you have the Client for Microsoft Networks installed because, on Microsoft networks, each computer has to have a name and should belong to a workgroup (these concepts will also be discussed in Chapter 18). After entering the information for Computer Name and Workgroup parameters, click Next to continue to the next step in the installation. [Pg.541]

All activities were coordinated with state and local authorities as well as other federal agencies such as the Centers for Disease Control (CDC), the National Institute for Occupational Safety and Health (NIOSH), the Food and Drug Administration (FDA), and the Federal Emergency Management Agency (FEMA). Community relations played an important role in all activities conducted during the identification, screening, and cleanup of dioxin-contaminated sites. [Pg.37]

Target identification Screening Hit confirmation => lead Lead optimization Based on medical symptoms Using laboratory animals or cell cultures Use of second animal species Classical synthesis of 10 to 20 similar compounds, testing on laboratory animals Based on receptor hindii Using receptor hindii assays with st detection techniques Use of second assay type High throughput synthesis of 1000 to 100,000 compounds tested with HTS receptor hindii assays... [Pg.340]

The aim of discriminant analysis is to unambiguously determine the identity or quality of an unknown sample. There are two basic applications for spectroscopic discriminant analysis sample purity/quality and sample identification/screening. In the capacity of sample quality checking, discriminant analysis methods can replace many quantitative methods currently used. In effect, the algorithm gives an indication of whether the spectrum of the unknown sample matches the spectra from samples taken... [Pg.166]

Fig. Z Sample identification/screening application of spectroscopic discriminant analysis. The spectrum of the sample is compared to multiple models of different materials or different levels of quality of the same material. The models can predict the likelihood that the sample matches the training spectra they were constructed from, again giving a yes or no answer. Fig. Z Sample identification/screening application of spectroscopic discriminant analysis. The spectrum of the sample is compared to multiple models of different materials or different levels of quality of the same material. The models can predict the likelihood that the sample matches the training spectra they were constructed from, again giving a yes or no answer.
During hazard identification, screening of hazards is not recommended but based on consequences this may be done. It is important that all hazards need analysis but not at the same level. Screening will help in this regard. All screening shall be done on a real consequence basis on the assumption of effectiveness of control measures or... [Pg.148]


See other pages where Identification Screening is mentioned: [Pg.158]    [Pg.400]    [Pg.105]    [Pg.88]    [Pg.88]    [Pg.147]    [Pg.340]    [Pg.71]    [Pg.161]    [Pg.36]    [Pg.111]    [Pg.393]    [Pg.47]    [Pg.114]    [Pg.384]    [Pg.200]    [Pg.281]   


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Hazard identification screening tests

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Virtual screening lead identification

Virtual screening novel lead identification

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