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Activity, calibration curve

A volume equivalent to 0.25 mg of creatinine from 500 mL of urine of a healthy adult donor is analyzed as described above. The collection is then spiked with up to ten organic acids (1 mg/ml stock solutions), selected from those with an active calibration curve by GC-MS TIC, to mimic a concentration of 100 pg acid/mg creatinine. The spiked collection is aliquoted into screw-cap vials during continued mixing, then stored frozen. For GC-MS SIM analysis, all compounds listed in Table 3.1.5 are included in the abnormal control, at a concentration matching the fourth point of the calibration curve (1 1 molar ratio to the labeled internal standard, see Table 3.1.5). [Pg.147]

In most quantitative analyses we are interested in determining the concentration, not the activity, of the analyte. As noted earlier, however, the electrode s response is a function of the analyte s activity. In the absence of interferents, a calibration curve of potential versus activity is a straight line. A plot of potential versus concentration, however, may be curved at higher concentrations of analyte due to changes in the analyte s activity coefficient. A curved calibration curve may still be used to determine the analyte s concentration if the standard s matrix matches that of the sample. When the exact composition of the sample matrix is unknown, which often is the case, matrix matching becomes impossible. [Pg.487]

All packing materials produced at PSS are tested for all relevant properties. This includes physical tests (e.g., pressure stability, temperature stability, permeability, particle size distribution, porosity) as well as chromatographic tests using packed columns (plate count, resolution, peak symmetry, calibration curves). PSS uses inverse SEC methodology (26,27) to determine chromatographic-active sorbent properties such as surface area, pore volume, average pore size, and pore size distribution. Table 9.10 shows details on inverse SEC tests on PSS SDV sorbent as an example. Pig. 9.10 shows the dependence... [Pg.288]

Near-infrared spectroscopy is quickly becoming a preferred technique for the quantitative identification of an active component within a formulated tablet. In addition, the same spectroscopic measurement can be used to determine water content since the combination band of water displays a fairly large absorption band in the near-IR. In one such study [41] the concentration of ceftazidime pentahydrate and water content in physical mixtures has been determined. Due to the ease of sample preparation, near-IR spectra were collected on 20 samples, and subsequent calibration curves were constructed for active ingredient and water content. An interesting aspect of this study was the determination that the calibration samples must be representative of the production process. When calibration curves were constructed from laboratory samples only, significant prediction errors were noted. When, however, calibration curves were constructed from laboratory and production samples, realistic prediction values were determined ( 5%). [Pg.77]

Figure 3 Layout of competitive solid-phase antibody immunoassay format in an incubation step antigen (Ag) and labeled antigen (Ag-L) compete for the solid-phase antibodybinding sites (Ab) after the solid-phase antibodies are washed, the activity of the bound labeled antigen is measured, and a calibration curve constructed. The measured signal is inversely proportional to the antigen concentration. Figure 3 Layout of competitive solid-phase antibody immunoassay format in an incubation step antigen (Ag) and labeled antigen (Ag-L) compete for the solid-phase antibodybinding sites (Ab) after the solid-phase antibodies are washed, the activity of the bound labeled antigen is measured, and a calibration curve constructed. The measured signal is inversely proportional to the antigen concentration.
In this method, an entire calibration curve is measured for the primary ion in a constant background of interfering ion. aj(BG) is the activity of the constant interfering ion in the background. afiDL) is the low detection limit (LDL) of the Nernstian response curve of the electrode as a function of the primary-ion activity. In the mixed interference method the selectivity is calculated from the following equation ... [Pg.653]

From the calibration curve, the concentration of NAD+ in both the test and blank can be determined. Front the difference in the results the amount of NAD+ generated in 1 second can be calculated (mol 1 1 s l) and from this the enzyme activity in kalals per litre of sample ... [Pg.291]

Halohydrin dehalogenase activity was determined by monitoring halide liberation at 30 °C in tris-S04 buffer (50 mM, pH 8.0) containing 5 mM 1,3-dichloropropanol or 1,3-dibromopropanol as the substrate. All buffers used for activity assay were prepared with bidest water. From the incubation mixture, 0.5 ml samples were taken and mixed with 1.6 ml of H2O, 0.2 ml or halide reagent 1 and 0.2 ml of halide reagent II. Absorbances were read at 460 nm. A calibration curve of 0-1 mM of chloride or bromide was used to calculate the concentration of halide. The extinctions at 460 nm should be below 0.4 (for chloride) or 0.8 (for bromide). [Pg.200]

While this relationship is simple, it introduces more errors because the activity coefficient (or more normally, the mean ionic activity coefficient y ) is wholly unknown. While y can sometimes be calculated (e.g. via the Debye-Huckel relationships described in Section 3.4), such calculated values often differ quite significantly from experimental values, particularly when working at higher ionic strengths. In addition, ionic strength adjusters and TISABs are recommended in conjunction with calibration curves. [Pg.74]

Noncompetitive ELISA methods are based on sandwich assays in which an excess supply of immobilized primary antibody, the capture antibody, quantitatively binds the antigen of interest and an enzyme-labeled secondary antibody is then allowed to react with the bound antigen forming a sandwich. A color reaction product produced by the enzyme is then used to measure the enzyme activity that is bound to the surface of the microtiter plate. Sandwich ELISA (noncompetitive) methods yield calibration curves in which enzyme activity increases with increasing free antigen concentration. [Pg.214]

For those scientists who had to perform quantitation, the linearity of the A/D was also critical. Linearity is the condition in which the detector s response is directly proportional to the concentration or amount of a component over a specified range of component concentrations or amounts. It is imperative that the A/D not add any additional error or variability to the performance of the detector. The resulting calibration curve now becomes dependent on the combined linearity of the detector and the /VD. Accurate quantitation requires that the system is linear over the range of actual sample concentrations or amounts. Many pharmaceutical assays, like degradation and stability studies, require that the system be able to identify and quantitate very disparate levels of peaks. In many cases, this translates into a 3 to 4 order of magnitude difference between the main active component and the impurities that need to be quantitated. [Pg.585]

The lUPAC Commission for Analytical Nomenclature defines the calibration curve [138] as the dependence of the electromotive force of the given ISE -reference electrode cell on the logarithm of the activity or concentration of the given substance. It is recommended that the potential be plotted on the ordinate (the vertical axis) and the logarithmic function of the activity or concentration on the abscissa (the horizontal axis), with the concentration increasing from the left to the right. [Pg.78]

When the test component content in the samples varies over a wider interval, a calibration curve must be constructed. Calibration curves with ISEs are usually linear over several concentration orders (usually from about 10" m to about 10" m) and their slope is close to the theoretical Nernstian value. Both at high and at low concentrations with respect to the linear part, the caUbration dependence becomes curved and, eventually, independent of the test substance concentration (see fig. 5.1). The upper limit of the ISE response is mostly given by saturation of the active sites in the electrode membrane (for example ion-exchange sites), whereas the lower limit is determined by solubility of the... [Pg.102]

Cadmium in acidified aqueous solution may be analyzed at trace levels by various instrumental techniques such as flame and furnace atomic absorption, and ICP emission spectrophotometry. Cadmium in solid matrices is extracted into aqueous phase by digestion with nitric acid prior to analysis. A much lower detection level may be obtained by ICP-mass spectrometry. Other instrumental techniques to analyze this metal include neutron activation analysis and anodic stripping voltammetry. Cadmium also may be measured in aqueous matrices by colorimetry. Cadmium ions react with dithizone to form a pink-red color that can be extracted with chloroform. The absorbance of the solution is measured by a spectrophotometer and the concentration is determined from a standard calibration curve (APHA, AWWA and WEF. 1999. Standard Methods for the Examination of Water and Wastewater, 20th ed. Washington, DC American Public Health Association). The metal in the solid phase may be determined nondestructively by x-ray fluorescence or diffraction techniques. [Pg.143]


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Calibration curve

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