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首页> 外文期刊>Journal of AOAC International >Method for the determination of catechin and epicatechin enantiomers in cocoa-based ingredients and products by high-performance liquid chromatography: first action 2013.04.
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Method for the determination of catechin and epicatechin enantiomers in cocoa-based ingredients and products by high-performance liquid chromatography: first action 2013.04.

机译:高效液相色谱法测定可可基成分和产品中儿茶素和表儿茶素对映体的方法:初审2013.04。

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摘要

Single-laboratory validation data previously published in the Journal of AOAC INTERNATIONAL 95(2), 500-507 (2012) was reviewed by the Stakeholder Panel on Strategic Food Analytical Methods Expert Review Panel (ERP) at the AOAC INTERNATIONAL Mid-Year Meeting held on March 12-14, 2013 in Rockville, MD. The ERP determined the data presented met the established standard method performance requirement and approved the method as AOAC Official First Action on March 14, 2013. Using high-performance liquid chromatography (HPLC), flavanol enantiomers, (+)- and (-)-epicatechin and (+)- and (-)-catechin, are eluted isocratically using ammonium acetate and methanol mobile phase. The mobile phase is applied to a modified beta -cyclodextrin chiral stationary phase and the flavanols detected by fluorescence. Using several cocoa-based matrices, recoveries for the four enantiomers ranged from 82.2-102.1% at a 50% spike level, and 80.4-101.1% at a 100% spike level. Precision was determined to be 1.46-3.22% for (-)-epicatechin, 3.66-6.90% for (+)-catechin, 1.69-6.89% for (-)-catechin. (+)-Epicatechin was not detected in any of the samples used for this work, so precision could not be determined for this molecule.
机译:战略食品分析方法利益相关者小组在AOAC INTERNATIONAL年中会议上对先前在AOAC INTERNATIONAL 95(2),500-507(2012)杂志上发表的单实验室验证数据进行了审查将于2013年3月12日至14日在马里兰州罗克维尔市举行。 ERP确定提供的数据符合既定标准方法性能要求,并于2013年3月14日将该方法批准为AOAC官方第一个行动。使用高效液相色谱(HPLC),黄烷醇对映体,(+)-和(-)-使用乙酸铵和甲醇流动相等度洗脱表儿茶素和(+)-和(-)-儿茶素。将流动相应用于修饰的β-环糊精手性固定相,并通过荧光检测黄烷醇。使用几种基于可可的基质,四种对映体的回收率在50%峰值水平下为82.2-102.1%,在100%峰值水平下为80.4-101.1%。 (-)-表儿茶素的精密度确定为1.46-3.22%,(+)-儿茶素的精密度为3.66-6.90%,(-)-儿茶素的精密度为1.69-6.89%。在用于该工作的任何样品中均未检测到(+)-表儿茶素,因此无法确定该分子的精密度。

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