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采用紫外/可见分光光度法和二极管阵列高效液相色谱法对咖啡因标准物质纯度进行双重独立分析认证。

Certification of caffeine reference material purity by ultraviolet/visible spectrophotometry and high-performance liquid chromatography with diode-array detection as two independent analytical methods.

机构信息

Reference Materials Department, National Institute of Standards, El-Matbah, Haram, Giza, Egypt.

Department of Chemistry, Faculty of Science, Cairo University, Giza, Egypt.

出版信息

J Food Drug Anal. 2016 Oct;24(4):703-715. doi: 10.1016/j.jfda.2016.06.009. Epub 2016 Jul 30.

Abstract

Caffeine reference material certified for purity is produced worldwide, but no research work on the details of the certification process has been published in the literature. In this paper, we report the scientific details of the preparation and certification of pure caffeine reference materials. Caffeine was prepared by extraction from roasted and ground coffee by dichloromethane after heating in deionized water mixed with magnesium oxide. The extract was purified, dried, and bottled in dark glass vials. Stratified random selection was applied to select a number of vials for homogeneity and stability studies, which revealed that the prepared reference material is homogeneous and sufficiently stable. Quantification of caffeine purity % was carried out using a calibrated UV/visible spectrophotometer and a calibrated high-performance liquid chromatography with diode-array detection method. The results obtained from both methods were combined to drive the certified value and its associated uncertainty. The certified value of the reference material purity was found to be 99.86% and its associated uncertainty was ±0.65%, which makes the candidate reference material a very useful calibrant in food and drug chemical analysis.

摘要

全球范围内都有生产经过纯度认证的咖啡因标准物质,但文献中尚未发表有关其认证过程细节的研究工作。本文报告了纯咖啡因标准物质的制备和认证的科学细节。咖啡因是通过在去离子水中加热后用二氯甲烷从烘焙研磨过的咖啡中提取得到的,其中加入了氧化镁。提取物经过纯化、干燥,并装在深色玻璃瓶中。采用分层随机抽样的方法选择了多个小瓶进行均匀性和稳定性研究,结果表明所制备的参考物质是均匀的,并且足够稳定。使用经过校准的紫外/可见分光光度计和经过校准的带有二极管阵列检测的高效液相色谱法对咖啡因纯度的百分比进行定量。将两种方法的结果结合起来得出认证值及其相关不确定度。该参考物质的纯度认证值为 99.86%,其相关不确定度为±0.65%,这使得候选参考物质成为食品和药物化学分析中非常有用的校准标准物质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd18/9337290/13e3c350a4e4/jfda-24-04-703f1.jpg

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