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Trace analysis, Biochemical

Especially in the case of biochemical and environmental systems and generally in ultra trace analysis, SAM is frequently applied. By addition of standard solutions to the sample a similar behaviour of the calibration set and the sample is created provided that the analyte is added in form of... [Pg.172]

Plastic containers must be washed before use. Table 28-1 shows that manganese in blood serum samples increased by a factor of 7 when stored in unwashed polyethylene containers prior to analysis. In the most demanding trace analysis of lead at 1 pg/g in polar ice cores, it was observed that polyethylene containers contributed a measurable flux of 1 fg of lead per cm2 per day even after they had been soaked in acid for 7 months.4 Steel needles are an avoidable source of metal contamination in biochemical analysis. [Pg.645]

MS/MS) is the standard detector for bioanalytical assays and drug discovery screening, its use for routine assays of drug substances and products is still limited due to its high cost and lower precision. Nevertheless, LC/MS/MS methods are increasingly used for ultra trace analysis or screening of complex samples. Other detection options include conductivity detection for ionic species and electrochemical detection for neuroactive species in biochemical research. [Pg.199]

Capabilities of capillary GC extend well beyond the analysis of complex mixtures. The use of capillary columns is reflected in a more effective trace analysis, unique detection capabilities, and a more reliable GC/MS. While much important biochemical work has already been done with glass capillary columns, development of... [Pg.43]

Due to the rapidly growing importance of capillary columns in bioanalytical applications, special attention will now be devoted to sampling techniques associated with capillary GC. Small samples are typical for this type of chromatography and, consequently, a direct introduction of such samples is an apparent technological problem. In most biochemically interesting applications (typically, trace analysis problems), there is no general discrepancy between the demands of such analysis and the performance and sensitivity of capillary separation techniques. However, the manipulation of samples presents difficulties, as reliable methods for measurement, disposal, and introduction of nanoliter volumes are not readily available. Ironically, in many capillary GC applications, the solvent serves only as a sample vehicle we... [Pg.57]

Analysis Materials testing (X-ray examination) indicator and tracer methods radiochemical and biochemical labelling and trace analysis organic trace analysis (BCD) activation analysis... [Pg.28]

Concentration in Biochemical Trace Analysis Using Glass Capillary Gas Chromat o graphy... [Pg.68]

McKelvie, 2008). Detection methods have included UV/Vis spectroscopy (the largest number of applications for its robustness, versatility, simplicity, and low cost), luminescence and chemiluminescence (CL) (which offer low detection limits and high sensitivity, being therefore especially favored for biological, biochemical, and trace analysis), atomic absorption and emission spectroscopy (which benefit enormously from automated sample pretreatment, used for matrix removal and analyte accumulation), electrochemistry (pH, fluoride ion selective electrodes, stripping voltammetry and conductivity), turbidimetry, vibrational spectroscopy (Fourier transform infrared spectroscopy [FTIR] and Raman) and mass spectrometry. [Pg.41]

Dialysis and electrodialysis are techniques which are applicable to the separation of smaller ions and molecules, including ionic surfactants, from larger species. These methods have been used to separate sodium dodecylsulfate from biochemical media (106). Such separations must normally be run at surfactant concentrations below the critical micelle concentration, since the micelles are too large to pass through the dialysis membrane. A general difficulty in application to trace analysis is the loss of surfactant due to adsorption on the surface of the apparatus. Most often, the object of the experiment is the purification of a protein solution, rather than isolation of a pure solution of the surfactant. Dialysis has been used for the removal of hydrocarbon oil solvent from lubricating oil surfactants in micellar form. In this case, n-heptane was used as solvent at reflux temperature (107). [Pg.183]

Analytical Applications. Chemiluminescence and bioluminescence are useful in analysis for several reasons. (/) Modem low noise phototubes when properly instmmented can detect light fluxes as weak as 100 photons/s (1.7 x 10 eins/s). Thus luminescent reactions in which intensity depends on the concentration of a reactant of analytical interest can be used to determine attomole—2eptomole amounts (10 to 10 mol). This is especially useful for biochemical, trace metal, and pollution control analyses (93,260—266) (see Trace and residue analysis). (2) Light measurement is easily automated for routine measurements as, for example, in clinical analysis. [Pg.274]

Today it has become clear that the effect of trace elements in living systems, in food, and in the environment depends on the chemical form in which the element enters the system and the final form in which it is present. The form, or species, clearly governs its biochemical and geochemical behaviour. lUPAC (the International Union for Pure and Applied Chemistry) has recently set guidelines for terms related to chemical speciation of trace elements (Templeton et al. 2000). Speciation, or the analytical activity of measuring the chemical species, is a relatively new scientific field. The procedures usually consist of two consecutive steps (i) the separation of the species, and (2) their measurement An evident handicap in speciation analysis is that the concentration of the individual species is far lower than the total elemental concentration so that an enrichment step is indispensable in many cases. Such a proliferation of steps in analytical procedure not only increases the danger of losses due to incomplete recovery, chemical instability of the species and adsorption to laboratory ware, but may also enhance the risk of contamination from reagents and equipment. [Pg.75]

Burton, J. J. (1996), Trace elements in bone as palaeodietary indicators, in Orna, M. V. (ed.), Archaeological Chemistry - Organic, Inorganic and Biochemical Analysis, ACS, Washington, DC, pp. 327-333. [Pg.563]

By design, ANNs are inherently flexible (can map nonlinear relationships). They produce models well suited for classification of diverse bacteria. Examples of pattern analysis using ANNs for biochemical analysis by PyMS can be traced back to the early 1990s.4fM7 In order to better demonstrate the power of neural network analysis for pathogen ID, a brief background of artificial neural network principles is provided. In particular, backpropagation artificial neural network (backprop ANN) principles are discussed, since that is the most commonly used type of ANN. [Pg.113]

Surfactants are produced on very large or medium technical scales. Their analysis by manufacturers in products and their formulations sometimes may be complicated because of the great variety of surfactants [5]. After use as directed in aqueous systems they were discharged mainly with wastewaters. Their analysis in environmental samples then becomes quite difficult because analysis must be performed at trace concentrations with limited sample amounts after essential matrix-dependent pre-concentrations steps. In addition, homologues and isomers that exist for many surfactants, besides metabolites which are generated in biochemical processes, complicate their specific determination [6]. [Pg.256]

Figure 4.12 Analysis of biosynthetic human growth hormone by isocratic reversed-phase chromatography. To generate all possible degradation products, a production lot of HGH was exposed to 40°C. The profile of the unstressed HGH is shown in the upper trace. (Reproduced from R.M. Riggin, G.K. Dorulla, and DJ. Miner, Anal. Biochem., 167 199 [1987]. With permission from Elsevier Science.)... Figure 4.12 Analysis of biosynthetic human growth hormone by isocratic reversed-phase chromatography. To generate all possible degradation products, a production lot of HGH was exposed to 40°C. The profile of the unstressed HGH is shown in the upper trace. (Reproduced from R.M. Riggin, G.K. Dorulla, and DJ. Miner, Anal. Biochem., 167 199 [1987]. With permission from Elsevier Science.)...

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