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在钙/磷比率测定中ZAF校正因子的局限性:与使用扫描电子显微镜和能量色散X射线微分析对骨碎片进行分析相关的重要法医学考量

Limitations of ZAF correction factors in the determination of calcium/phosphorus ratios: important forensic science considerations relevant to the analysis of bone fragments using scanning electron microscopy and energy-dispersive x-ray microanalysis.

作者信息

Payne C M, Cromey D W

机构信息

Department of Pathology, College of Medicine, University of Arizona, Tucson.

出版信息

J Forensic Sci. 1990 May;35(3):560-8.

PMID:2348174
Abstract

A series of calcium phosphate standards having calcium/phosphorus (Ca/P) molar ratios of 0.50, 1.00, 1.50, and 1.67, respectively, was prepared for bulk specimen analysis using scanning electron microscopy (SEM) and energy-dispersive X-ray microanalysis (EDXA). The standards were mounted on carbon planchettes as either pure crystals or crystals embedded in epoxy resin. Ten different samples of each embedded and non-embedded standard were analyzed in a JEOL 100 CX electron microscope interfaced with a Kevex 8000 EDXA system using a lithium-drifted silicon detector and a multichannel analyzer. The Ca/P ratios were determined by calculating both net peak intensities without matrix corrections and atomic kappa-ratios using the MAGIC V computer program with ZAF correction factors for quantitative analysis. There was such extensive absorption of phosphorus X-rays in standards embedded in an epoxy matrix that the observed Ca/P ratios were statistically compatible with four different standards ranging in theoretical Ca/P ratios from 1.0 to 1.67. Although the non-embedded crystals showed a greater separation in the Ca/P ratios, both methods of preparation produced serious flaws in analysis. Direct application of the discovery of this caveat to the identification of suspected bone fragments for forensic science purposes is discussed.

摘要

制备了一系列磷酸钙标准品,其钙/磷(Ca/P)摩尔比分别为0.50、1.00、1.50和1.67,用于使用扫描电子显微镜(SEM)和能量色散X射线微分析(EDXA)进行大块标本分析。这些标准品以纯晶体或嵌入环氧树脂的晶体形式安装在碳平板上。使用配备锂漂移硅探测器和多通道分析仪的Kevex 8000 EDXA系统,在JEOL 100 CX电子显微镜中对每种嵌入和未嵌入的标准品的十个不同样品进行分析。Ca/P比通过使用具有ZAF校正因子的MAGIC V计算机程序计算未经基体校正的净峰强度和原子κ比来确定,用于定量分析。嵌入环氧树脂基体中的标准品中磷X射线有如此广泛的吸收,以至于观察到的Ca/P比在统计学上与理论Ca/P比从1.0到1.67的四种不同标准品相符。尽管未嵌入的晶体在Ca/P比上显示出更大的差异,但两种制备方法在分析中都产生了严重缺陷。讨论了将这一注意事项的发现直接应用于法医学目的的疑似骨碎片鉴定。

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