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Quantification of Four Isoflavones in Forages with UPLCA (R)-MS/MS, Using the Box-Behnken Experimental Design to Optimize Sample Preparation

机译:使用Box-Behnken实验设计优化样品制备的UPLCA(R)-MS / MS对饲料中四种异黄酮的定量

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A performant method for the simultaneous quantification of daidzein, genistein, formononetin, and biochanin A in forages using an UPLCA (R)-MS/MS was developed and fully validated. The ultrasound-assisted extraction and enzymatic hydrolysis used in the sample preparation step were optimized using the Box-Behnken experimental design. The optimal extraction conditions used for a representative mix of forage plants were 80 A degrees C, 10 min, and 55 % methanol, and for hydrolysis, they were 20 A degrees C, 18 h, and pH = 6. The chromatographic separation was achieved using an Acquity UPLCA (R) HSS T3 column, with a water/methanol linear gradient containing 0.01 % of formic acid at a 0.55 mL min(-1) flow rate. The four isoflavones were detected by ESI mass spectrometry in positive ion MRM mode. The method allows high throughput analyses of samples and showed an adequate linear regression model for all isoflavones over a range from 5 to 125 ng mL(-1). There were good intra- and inter-day precisions (a parts per thousand currency sign8.2 and a parts per thousand currency sign7.6 %) and accuracy (a parts per thousand currency sign11.4 and a parts per thousand currency sign7.1 %). The recovery rates were in an acceptable range of 70-120 %, except for biochanin A, where the rate was about 50 %. Good method repeatability was also observed, and there was no matrix effect or carryover problem. The sample extracts were stable for at least 6 days of storage at -21 and 6 A degrees C. The method proved to be sensitive, precise, and accurate for discriminating a wide variety of forages likely to be grazed by ruminants according to their isoflavone contents and to observe the impact of storage process on isoflavone content in forages.
机译:开发了一种高效方法,使用UPLCA(R)-MS / MS同时定量饲料中的大豆苷元,染料木黄酮,formononetin和生物chaninA。使用Box-Behnken实验设计优化了样品制备步骤中使用的超声辅助提取和酶促水解。用于代表性草料植物混合物的最佳提取条件是80 A摄氏度,10分钟和55%甲醇,水解条件是20 A摄氏度,18小时和pH =6。实现了色谱分离使用Acquity UPLCA HSS T3色谱柱,水/甲醇线性梯度洗脱,流速为0.55 mL min(-1)时,含有0.01%的甲酸。通过ESI质谱法在正离子MRM模式下检测到四种异黄酮。该方法可对样品进行高通量分析,并显示了适用于5至125 ng mL(-1)范围内所有异黄酮的线性回归模型。日间和日间精度(每千个货币符号8.2的一部分和每千个货币符号的7.6%)和准确性(每千个货币符号的11.4和每千个货币符号的7.1)具有良好的精度%)。回收率在70-120%的可接受范围内,除了生物松弛素A的回收率约为50%。还观察到了良好的方法可重复性,并且没有基质效应或残留问题。样品提取物在-21和6 A的温度下可稳定保存至少6天。该方法被证明是敏感,准确和准确的,可以根据其异黄酮含量来区分反刍动物可能吃草的各种草料并观察贮藏过程对草料中异黄酮含量的影响。

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