[Qualitative and quantitative determination of caffeine in saliva by high performance liquid chromatography].

Przeglad lekarski Pub Date : 2016-01-01
Marta Napierała, Ewa Florek
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Abstract

The European Union drew attention to the increased consumption and the reports of adverse reactions to caffeine in recent years. The EU Commission in Regulation No. 536/2013 dated 11 June 2013 expressed concern about the caffeine content in the products. It is important to develop a simple and accurate methods for determining the level of caffeine in the biological material for accurate exposure assessment, as well as in the caffeinated products. The use of saliva as a diagnostic material is painless, non-invasive and does not require the participation of professional medical personnel. The compounds identified in saliva showed relatively high durability. The developed method for the determination of caffeine by high performance liquid chromatography with diode array detection (HPLC-DAD) after extraction of caffeine from saliva by solid phase extraction (SPE) is characterized by the linearity in the concentration range 50 - 2000 ng/mL. This method have low detection (12 ng/mL) and quantification (40 ng/mL) limits and high intra-day (4.87% for low concentration and 2.10% for high concentration) and inter-day (5.84% for low concentration and 2.43% for high concentration) repeatability.

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唾液中咖啡因的高效液相色谱定性定量测定
欧盟提请注意近年来咖啡因消费量的增加和对咖啡因不良反应的报道。欧盟委员会法规编号:2013年6月11日第536/2013号公告表达了对产品中咖啡因含量的担忧。开发一种简单而准确的方法来测定生物材料中的咖啡因水平,以进行准确的暴露评估,以及含咖啡因的产品。使用唾液作为诊断材料是无痛的,非侵入性的,不需要专业医务人员的参与。在唾液中发现的化合物显示出相对较高的耐久性。建立了用高效液相色谱-二极管阵列检测(HPLC-DAD)法测定唾液固相萃取(SPE)中咖啡因的浓度在50 ~ 2000 ng/mL范围内呈良好的线性关系。该方法检测限低(12ng/mL),定量限低(40 ng/mL),日内重复性高(低浓度4.87%,高浓度2.10%),日内重复性高(低浓度5.84%,高浓度2.43%)。
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