Theunis Mart, Naessens Tania, Verhoeven Veronique, Hermans Nina, Apers Sandra
University of Antwerp, Natural Products & Food Research and Analysis (NatuRA), Universiteitsplein 1, B-2610 Antwerp, Belgium.
University of Antwerp, Research Group Primary and Interdisciplinary Care Antwerp (ELIZA), Universiteitsplein 1, B-2610 Antwerp, Belgium.
Food Chem. 2017 Nov 1;234:33-37. doi: 10.1016/j.foodchem.2017.04.136. Epub 2017 Apr 24.
A robust analytical method, using reversed phase high-performance liquid chromatography with diode array detection, was developed and validated for the quantification of monacolins in red yeast rice bulk products. Tests on the composition of the extraction solvent, extraction time and the number of repetitions of extraction were evaluated with the aim of complete extraction of the monacolins and minimal transitions between the monacolins during analysis. Monacolin K (acid form), monacolin K (lactone form) and minor monacolin peaks were separated on a C18 column (250×4.6mm, 5µm) using acetonitrile/0.1% trifluoroacetic acid as the mobile phase. For the calibration curve of monacolin K (lactone form), a linear correlation in the range 6-119µg/mL was found. The precision of the method for time and concentration gave a relative standard deviation of less than 5%, which was deemed acceptable. The recovery of the method was 98.75%.
开发并验证了一种稳健的分析方法,该方法采用反相高效液相色谱法并结合二极管阵列检测,用于定量红曲米散装产品中的莫纳可林。对萃取溶剂的组成、萃取时间和萃取重复次数进行了测试评估,目的是完全萃取莫纳可林,并在分析过程中使莫纳可林之间的转化最小化。使用乙腈/0.1%三氟乙酸作为流动相,在C18柱(250×4.6mm,5µm)上分离莫纳可林K(酸形式)、莫纳可林K(内酯形式)和次要的莫纳可林峰。对于莫纳可林K(内酯形式)的校准曲线,发现在6 - 119µg/mL范围内呈线性相关。该方法在时间和浓度方面的精密度给出的相对标准偏差小于5%,这被认为是可接受的。该方法的回收率为98.75%。