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Exact Measurement (exact + measurement)
Selected AbstractsMeasurement and correlation of microstructures: the case of foliation intersection axesJOURNAL OF METAMORPHIC GEOLOGY, Issue 3 2003A. R. Stallard Abstract Recent studies have used the relative rotation axis of sigmoidal and spiral-shaped inclusion trails, known as Foliation Inflexion/Intersection Axis (FIA), to investigate geological processes such as fold mechanisms and porphyroblast growth. The geological usefulness of this method depends upon the accurate measurement of FIA orientations and correct correlation of temporally related FIAs. This paper uses new data from the Canton Schist to assess the variation in FIA orientations within and between samples, and evaluates criteria for correlating FIAs. For the first time, an entire data set of FIA measurements is published, and data are presented in a way that reflects the variation in FIA orientations within individual samples and provides an indication of the reliability of the data. Analysis of 61 FIA trends determined from the Canton Schist indicate a minimum intrasample range in FIA orientations of 30°. Three competing models are presented for correlation of these FIAs, and each of the models employ different correlation criteria. Correlation of FIAs in Model 1 is based on relative timing and textural criteria, while Model 2 uses relative timing, orientation and patterns of changing FIA orientations, and Model 3 uses relative timing and FIA orientation as correlation criteria. Importantly, the three models differ in the spread of FIA orientations within individual sets, and the number of sets distinguished in the data. Relative timing is the most reliable criterion for correlation, followed by textural criteria and patterns of changing FIA orientations from core to rim of porphyroblasts. It is proposed that within a set of temporally related FIAs, the typical spread of orientations involves clustering of data in a 60° range, but outliers occur at other orientations including near-normal to the peak distribution. Consequently, in populations of FIA data that contain a wide range of orientations, correlation on the basis of orientation is unreliable in the absence of additional criteria. The results of this study suggest that FIAs are best used as semiquantitative indicators of bulk trends rather than an exact measurement for the purpose of quantitative analyses. [source] Comparison of particle sizing techniques in the case of inhalation dry powdersJOURNAL OF PHARMACEUTICAL SCIENCES, Issue 12 2001Cynthia Bosquillon Abstract The objectives of this work were (i) to validate electrical zone sensing and laser diffraction for the analysis of primary particle size in the case of inhalation dry powders and (ii) to study the influence of the aggregation state of the powder on the sizing techniques. Free-flowing dry powders were prepared by spray-drying with a combination of albumin, lactose, and dipalmitoylphosphatidylcholine. The replacement of lactose by mannitol, the removal of albumin, and the atomization at high relative humidity all increased powder cohesion. Automated measurements were compared with primary particle sizes collected by light and electron microscopy. The mass mode obtained by electrical zone sensing and the mass median diameter measured by laser diffraction following dispersion with compressed air at a pressure of 3 bar or following suspension in water and ultrasonic dispersion at a power of 60 W for 30 s each provided primary particle sizes close to microscopy measurements. However, these conditions only applied in the case of slightly to moderately aggregated powders. For strongly agglomerated powders, an exact measurement of the size was only collected by laser diffraction in the wet state combined with ultrasonic dispersion. Our study underlies how measurement of primary particle size highly depends on both powder material and proper particle dispersion. © 2001 Wiley-Liss, Inc. and the American Pharmaceutical Association J Pharm Sci 90:2032,2041, 2001 [source] Exposure to furry pets and the risk of asthma and allergic rhinitis: a meta-analysisALLERGY, Issue 7 2008B. Takkouche Background:, Exposure to pets has been implicated as a risk factor for asthma. However, this relation has been difficult to assess in individual studies because of the large potential of selection bias. We sought to examine the association between exposure to furry pets and asthma and allergic rhinitis by means of a meta-analysis. Methods:, We retrieved studies published in any language by searching systematically Medline (1966,March 2007), Embase, LILACS and ISI Proceedings computerized databases, and by examining manually the references of the original articles and reviews retrieved. We included cohort and case,control studies reporting relative risk estimates and confidence intervals of exposure to cats, dogs and unspecified furry animals and subsequent asthma and allergic rhinitis. We excluded cross-sectional studies and those studies that did not measure exposure but rather sensitization to pets. Results:, Thirty-two studies were included. For asthma, the pooled relative risk related to dog exposure was 1.14 (95% CI 1.01,1.29), that related to exposure to any furry pet was 1.39 (95% CI 1.00,1.95). Among cohort studies, exposure to cats yielded a relative risk of 0.72 (95% CI 0.55,0.93). For rhinitis, the pooled relative risk of exposure to any furry pet was 0.79 (95% CI 0.68,0.93). Conclusions:, Exposure to cats exerts a slight preventive effect on asthma, an effect that is more pronounced in cohort studies. On the contrary, exposure to dogs increases slightly the risk of asthma. Exposure to furry pets of undermined type is not conclusive. More studies with exact measurement of exposure are needed to elucidate the role of pet exposures in atopic diseases. [source] A unified approach to regression analysis under double-sampling designsJOURNAL OF THE ROYAL STATISTICAL SOCIETY: SERIES B (STATISTICAL METHODOLOGY), Issue 3 2000Yi-Hau Chen We propose a unified approach to the estimation of regression parameters under double-sampling designs, in which a primary sample consisting of data on the rough or proxy measures for the response and/or explanatory variables as well as a validation subsample consisting of data on the exact measurements are available. We assume that the validation sample is a simple random subsample from the primary sample. Our proposal utilizes a specific parametric model to extract the partial information contained in the primary sample. The resulting estimator is consistent even if such a model is misspecified, and it achieves higher asymptotic efficiency than the estimator based only on the validation data. Specific cases are discussed to illustrate the application of the estimator proposed. [source] Quantification of Chlamydia pneumoniae in cultured human macrophages and HL cells: comparison of real-time PCR, immunofluorescence and ELISA methodsAPMIS, Issue 1 2010KARI POIKONEN Poikonen K, Lajunen T, Silvennoinen-Kassinen S, Leinonen M, Saikku P. Quantification of Chlamydia pneumoniae in cultured human macrophages and HL cells: comparison of real-time PCR, immunofluorescence and ELISA methods. APMIS 2010; 118: 45,8. Chlamydia pneumoniae is an intracellular gram-negative bacterium, which replicates only in eukaryotic cells. Quantification of C. pneumoniae in cell culture is needed when studying e.g. the effect of drugs or host cell factors on infectivity and replication. Conventionally, this has been performed by immunofluorescence staining and microscopic counting of chlamydial inclusions. However, this method is usable only if the cell numbers do not fluctuate in cell culture vials and the inclusions are uniform. In macrophages, inclusions are often aberrant, their sizes vary, and multiple inclusions are also seen. Therefore, methods are needed to quantify exact amounts of C. pneumoniae in cells. Here, we describe a new method based on the real-time PCR quantification of chlamydial genomes adjusted to the number of human genomes in cultures. In human epithelial (HL) cell cultures, the C. pneumoniae inclusion numbers and the ratio of C. pneumonia genomes/human genome (Cpn/Hum) correlated significantly (r = 0.978, p < 0.001); thus with HL cells, both methods are usable. However, in macrophage cultures, the correlation was weaker (r = 0.133, p = 0.036) and we recommend PCR quantification for exact measurements. [source] | ||||||||||