Reliable Quantification (reliable + quantification)

Distribution by Scientific Domains


Selected Abstracts


Investigation of a capillary electrophoretic approach for direct quantification of apolipoprotein A-I in serum

ELECTROPHORESIS, Issue 9 2003
Rainer Lehmann
Abstract In the present study a rapid, reproducible and robust capillary electrophoresis (CE) procedure for the quantification of apolipoprotein A-I (Apo A-I) in serum without pretreatment has been developed (total run time, 11 min). The coefficients of variation (CV; n = 10) for the relative peak area are 1.8% at a concentration of 145 mg/dL and 1.6% at 196 mg/dL; and for the inter-assay 8.9% at 161 mg/dL (10 consecutive days), i.e., similar to the CVs of a high-throughput immunonephelometric routine assay. The CV for the migration time is 0.4% (n = 20). The robustness of the CE approach was tested in patient samples with hemolysis, hyperbilirubinemia and hyperlipidemia. A comparison of 99 Apo A-I serum values with results of a fixed-time immunonephelometric routine assay showed a positive constant bias of 60% (mean) for the immunonephelometric values, no deviation from linearity, but significant deviations in several samples. Investigations on interferences in the CE analyses gave no evidence that CE failed. Our study shows that CE is amenable to a fast analysis and a reproducible and reliable quantification of Apo A-I level in sera of various clinical samples. [source]


Theoretical crack path prediction

FATIGUE & FRACTURE OF ENGINEERING MATERIALS AND STRUCTURES, Issue 1-2 2005
H. A. RICHARD
ABSTRACT In many practical cases, the crack growth leads to abrupt failure of components and structures. For reasons of a reliable quantification of the endangerment due to sudden fracture of a component, therefore, it is of enormous importance to know the threshold values, the crack paths and the growth rates for the fatigue crack growth as well as the limiting values for the beginning of unstable crack growth (fracture toughness). This contribution deals with the complex problem of a,however initiated,crack, that is subjected to a mixed-mode loading. It will present the hypotheses and concepts, which describe the superposition of Mode I and Mode II (plane mixed mode) as well as the superposition of all three modes (Mode I, II and III) for spatial loading conditions. Those concepts admit a quantitative appraisal of such crack situations and a characterization of possible crack paths. [source]


Dimensionality estimate of the manifold in chemical composition space for a turbulent premixed H2 + air flame,

INTERNATIONAL JOURNAL OF CHEMICAL KINETICS, Issue 6 2004
Shaheen R. Tonse
The dimensionality () of manifolds of active chemical composition space has been measured using three different approaches: the Hausdorff geometrical binning method, Principal Component Analysis, and the Grassberger-Procaccia cumulative distribution method. A series of artificial manifolds is also generated using a Monte Carlo approach to discern the advantages and limitations of the three methods. Dimensionality is quantified for different levels of turbulent intensity in a simulation of the interactions of a 2D premixed hydrogen flame with a localized region of turbulence superimposed over the cold region upstream of the flame front. The simulations are conducted using an adaptive mesh refinement code for low Mach number reacting flows. By treating the Ns species and temperature of the local thermo-chemical state as a point in multidimensional chemical composition space, a snapshot of a flame region is mapped into chemical composition space to generate the manifold associated with the 2-D flame system. An increase in was observed with increasing turbulent intensity for all three methods. Although each method provides useful information, the Grassberger-Procaccia method is subject to fewer artifacts than the other two thereby providing the most reliable quantification of . © 2004 Wiley Periodicals, Inc. Int J Chem Kinet 36: 326,336, 2004 [source]


Solvent effects in the hydrodechlorination of 2,4-dichlorophenol over Pd/Al2O3

AICHE JOURNAL, Issue 3 2010
Santiago Gómez-Quero
Abstract Solvent effects in the liquid phase (0.1 MPa; 303 K) hydrodechlorination (HDC) of 2,4-dichlorophenol have been established over Pd/Al2O3. In the absence of secondary reactions, catalyst deactivation, and transport limitations, a stepwise HDC yields 2-chlorophenol and phenol, where product selectivity was insensitive to the nature of the solvent. In contrast, the initial HDC rates exhibited a marked dependence on the reaction medium and increased in the order: benzene < THF < n -hexane < cyclohexane < alcohols < water. Higher rates result from the concomitant effect of an increase in the dielectric constant (,) and a decrease in the molar volume ( ) of the solvent, where the major (ca. 80%) contribution is due to ,. We attribute this response to the increased solvent capacity to stabilize the arenium intermediate at higher/lower ,/, an effect that extends to reaction in water + organic combinations. We provide, for the first time, a reliable quantification of solvent effects that can be potentially applied to other catalytic hydrogenolysis systems. © 2009 American Institute of Chemical Engineers AIChE J, 2010 [source]


High-resolution biomarker discovery: Moving from large-scale proteome profiling to quantitative validation of lead candidates

PROTEOMICS - CLINICAL APPLICATIONS, Issue 10-11 2008
Johannes A. Hewel
Abstract Diverse proteomic techniques based on protein MS have been introduced to systematically characterize protein perturbations associated with disease. Progress in clinical proteomics is essential for personalized medicine, wherein treatments will be tailored to individual needs based on patient stratification using noninvasive disease monitoring procedures to reveal the most appropriate therapeutic targets. However, breakthroughs await the successful development and application of a robust proteomic pipeline capable of identifying and rigorously assessing the relevance of multiple candidate proteins as informative diagnostic and prognostic indicators or suitable drug targets involved in a pathological process. While steady progress has been made toward more comprehensive proteome profiling, the emphasis must now shift from in depth screening of reference samples to stringent quantitative validation of selected lead candidates in a broader clinical context. Here, we present an overview of the emerging proteomic strategies for high-throughput protein detection focused primarily on targeted MS/MS as the basis for biomarker verification in large clinical cohorts. We discuss the conceptual promise and practical pitfalls of these methods in terms of achieving higher dynamic range, higher throughput, and more reliable quantification, highlighting research avenues that merit additional inquiry. [source]


Sensitive determination of acidic drugs and triclosan in surface and wastewater by ion-pair reverse-phase liquid chromatography/tandem mass spectrometry

RAPID COMMUNICATIONS IN MASS SPECTROMETRY, Issue 7 2004
José Benito Quintana
A new method is presented for the determination of 12 acidic pharmaceuticals (non-steroidal anti-inflammatory drugs and bezafibrate), including two metabolites from aqueous samples, together with triclosan as a personal care product. Ion-pair liquid chromatography (IP-LC) with electrospray ionisation tandem mass spectrometry (ESI-MS) in the negative ion mode was employed. The ion-pairing agent (tri- n -butylamine) increased the signal intensity for all acidic analytes and detection limits of 6,200,ng/L were obtained by multiple reaction monitoring. This allows analysis of wastewater samples by direct injection into the LC/MS system without the need for a preceding enrichment step. When combined with a solid-phase extraction (SPE) step, limits of quantification between 0.15 and 11,ng/L were obtained from 100-mL sample volumes, which is adequate for most applications. The occurrence of matrix effects was studied and standard addition was required for reliable quantification after SPE from wastewater. The method was finally applied to surface and wastewaters, with analyte concentrations ranging from below the detection limit up to 5.5,,g/L. Copyright © 2004 John Wiley & Sons, Ltd. [source]