ABSTRACT
Marine chronometers, often considered precision instruments, proliferated in navigational practices during the nineteenth century. This paper examines their use in the hands of naval officers in the early-nineteenth century. It argues that both the instruments and their operators required careful management and regulation. In addition, officers learnt and adapted observatory practices relating to the process of data collection and management. Through these means, chronometric data was collected, organized, and reduced to negotiate accurate results.
ABSTRACT
Se presenta conceptos del saber hacer investigación científica asociada a la calidad de las mediciones, y dentro de ella sobre la calidad intrínseca de la medición de variables, dirigida a dos condiciones de la misma: la precisión y exactitud. Se describe formas de evaluación de la precisión como ser el coeficiente de variación y el error técnico de las mediciones. Por otro lado se describe formas de evaluación de la exactitud como son la regresión linear y el puntaje Z. También se sugieren y se describen las acciones y las herramientas para mejorar tanto la precisión como la exactitud. El análisis de agua enriquecida con oxido de deuterio, es una temática que fue tomada en cuenta por la Agencia Internacional de Energía Atómica (IAEA), Viena, Austria, en la gestión 2021, y se organizó una actividad mediante el "Estudio de Interlaboratorios, Oxido de Deuterio por FTIR 2021". El propósito fue asegurar la calidad integral en la capacidad construida en el uso de técnicas de isotopos estables para la evaluación del estado de salud y nutricional. Así mismo, evaluar la calidad de medición de la exactitud relativa sobre el enriquecimiento del agua con óxido de deuterio en 43 laboratorios a nivel internacional, grupo en cual se incluyó al Laboratorio de Biología Atómica (LABA) de la Unidad de Crecimiento y Desarrollo (UCREDE). Se utilizó la regresión linear y el puntaje Z para evaluar la exactitud. Se concluye que los resultados demostraron un muy buen rendimiento en exactitud relativa con los equipos FTIR que midieron el enriquecimiento de deuterio en muestras de agua.
Concepts of knowing how to do scientific research associated with the quality of measurements are presented, and within it on the intrinsic quality of the measurement of variables, aimed at two conditions of the same: precision and accuracy. Forms of precision evaluation are described, such as the coefficient of variation and the technical error of the measurements. On the other hand, forms of accuracy evaluation are described, such as linear regression and Z-score. Actions and tools to improve both precision and accuracy are also suggested and described. The analysis of water enriched with deuterium oxide is a topic that was taken into account by the International Atomic Energy Agency (IAEA), Vienna, Austria, in the 2021 management, and an activity was organized through the Interlaboratory Study, Deuterium Oxide by FTIR 2021. The purpose was to ensure comprehensive quality in the capacity built in the use of stable isotope techniques for the evaluation of health and nutritional status. Likewise, to evaluate the quality of measurement of the relative accuracy of the enrichment of water with deuterium oxide in 43 laboratories at the international level, a group that included the Atomic Biology Laboratory (LABA) of the Growth and Development Unit (UCREDE ). Linear regression and Z-score were used to assess accuracy. It is concluded that the results demonstrated a very good performance in relative accuracy with the FTIR equipment that measured deuterium enrichment in water samples.
Subject(s)
Water , Deuterium Oxide , Research , Nutritional Status , AltitudeABSTRACT
OBJECTIVE: Silibinin is an antioxidant agent and is shown to have anticancer effects in different cancers including lung, breast, colorectal, liver, prostate, and kidney. There are challenges in the clinical use of silibinin. The main limitation is low solubility, poor oral absorption, and extensive hepatic metabolism. We aim to develop a High-Performance Liquid Chromatography (HPLC) sensitive method for quantification of silibinin in aqueous samples to quantify its concentration in new formulations. A reverse-phase high-performance liquid chromatography (RP-HPLC) composed of C18 column as stationary phase and the mixture of methanol (90%) and water (10%) as mobile phase. The developed method was validated based on the established guidelines. RESULTS: The retention time for silibinin was seen in 2.97 min after injection. The calibration curve was drawn and the established method demonstrated a linear ranged from 10 to 100 µg/ml, with a correlation coefficient of 0.996. The sensitivity of the developed method was 10 µg/ml. The accuracy calculated in the range of 88-105.9% and the precision (as relative standard deviation) was between 2.7 and 10.9%. These results demonstrate that the developed method can be a fast and accurate method for quantification of silibinin in aqueous samples.
Subject(s)
Antineoplastic Agents, Phytogenic/analysis , Antioxidants/analysis , Chromatography, High Pressure Liquid/methods , Silybin/analysis , Calibration , Chromatography, High Pressure Liquid/standards , Limit of Detection , Linear Models , Reproducibility of ResultsABSTRACT
Purpose: To analyze factors which influence the precision & accuracy of target positions in Alderson Head phantom and(or) patients.Materials and Methods: A target position simulator was used to determine the precision and accuracy of target localization while Alderson head phantom used to determine the overall precision and accuracy through the treatment procedure.Results: The overall precision and accuracy through the treatment procedure was found to be 1.72?0.60mm, and its contribution from CT localizing step, which was 1.4?0.3mm。Conclusion: Since there are more factors related to patients' treatment, the precision and accuracy of simulating in Alderson phantom is the best estimate for patient treatment.
ABSTRACT
Choosing the right kind of samples from human subjects for trace element studies poses many difficult problems. First of all, due to practical considerations, specimens with clinical relevance are restricted to a few such as whole blood, hair, nail, urine, and faeces. Although autopsies provide access to collect various organs, their usefulness is restricted to monitoring type of activities and not for clinical diagnosis. Besides these basic differences one is also confronted with procuring "valid" samples for analysis. Validity refers to both analytical and biological aspects and the material collected should satisfy both the demands to make the specimen meaningful. In practice this is not a simple task because a number of presampling factors need to be taken into account. Significant situations among these are the biological variations, post mortem changes, intrinsic errors resulting from internal contaminations, etc. The impact of these factors alters the status of the sample and calls for adequate discription of the specimen. In the absence of a well defined sample protocol accurate characterization of the material will not be possible and renders the analytical effort worthless. Solutions to these problems should be sought at interdisciplinary level and effective team work is mandatory to make any meaningful progress in our endeavours to answer public health questions.
