Machonis Philip R, Jones Matthew A, Kwik-Uribe Catherine
J AOAC Int. 2014 Jan-Feb;97(1):166-72. doi: 10.5740/jaoacint.13-034.
Recently, a multilaboratory validation (MLV) of AOAC Official Method 2012.24 for the determination of cocoa flavanols and procyanidins (CF-CP) in cocoa-based ingredients and products determined that the method was robust, reliable, and transferrable. Due to the complexity of the CF-CP molecules, this method required a run time exceeding 1 h to achieve acceptable separations. To address this issue, a rapid resolution normal phase LC method was developed, and a single-laboratory validation (SLV) study conducted. Flavanols and procyanidins with a degree of polymerization (DP) up to 10 were eluted in 15 min using a binary gradient applied to a diol stationary phase, detected using fluorescence detection, and reported as a total sum of DP 1-10. Quantification was achieved using (-)-epicatechin-based relative response factors for DP 2-10. Spike recovery samples and seven different types of cocoa-based samples were analyzed to evaluate the accuracy, precision, LOD, LOQ, and linearity of the method. The within-day precision of the reported content for the samples was 1.15-5.08%, and overall precision was 3.97-13.61%. Spike-recovery experiments demonstrated recoveries of over 98%. The results of this SLV were compared to those previously obtained in the MLV and found to be consistent. The translation to rapid resolution LC allowed for an 80% reduction in analysis time and solvent usage, while retaining the accuracy and reliability of the original method. The savings in both cost and time of this rapid method make it well-suited for routine laboratory use.
最近,针对AOAC官方方法2012.24用于测定可可基成分和产品中可可黄烷醇和原花青素(CF-CP)的多实验室验证(MLV)确定该方法稳健、可靠且可转移。由于CF-CP分子的复杂性,该方法需要超过1小时的运行时间才能实现可接受的分离。为了解决这个问题,开发了一种快速分离正相液相色谱方法,并进行了单实验室验证(SLV)研究。使用二元梯度应用于二醇固定相,在15分钟内洗脱聚合度(DP)高达10的黄烷醇和原花青素,采用荧光检测进行检测,并报告为DP 1-10的总和。使用基于(-)-表儿茶素的DP 2-10相对响应因子进行定量。分析加标回收样品和七种不同类型的可可基样品,以评估该方法的准确性、精密度、检测限、定量限和线性。样品报告含量的日内精密度为1.15-5.08%,总体精密度为3.97-13.61%。加标回收实验表明回收率超过98%。将该SLV的结果与之前在MLV中获得的结果进行比较,发现是一致的。向快速分离液相色谱的转变使分析时间和溶剂用量减少了80%,同时保留了原方法的准确性和可靠性。这种快速方法在成本和时间上的节省使其非常适合常规实验室使用。