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Development and validation of a high-performance liquid chromatography method with post-column derivatization for the detection of aflatoxins in cereals and grains

机译:柱后衍生高效液相色谱法在谷物中检测黄曲霉毒素的开发与验证

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摘要

A novel, reliable and rapid high-performance liquid chromatography (HPLC) method with post-column derivatization was developed and validated. The HPLC method was used for the simultaneous determination of aflatoxin B1 (AFB1), B-2 (AFB(2)), G(1) (AFG (1)) and G2 (AFG(2)) in various cereals and grains. Samples were extracted with 80:20 (v/v) methanol:water and purified using C 18 (40-63 mu m) solid -phase extraction cartridges. AFs were separated using a LiChroCART RP-18 (5 m, 250 x 4.0 mm(2)) column. The mobile phase consisted of methanol:acetonitrile:buffer (17.5:17.5:65 v/v) (pH 7.4) delivered at the flow rate of 1.0 mL min I. The fluorescence of each AF was detected at lambda(ex) = 365 nm and 'em = 435 nm. All four AFs were properly resolved within the total run time of 20 min. The established method was extensively validated as a final verification of the method development by the evaluation of selectivity (AFB1, AFB2, AFG1 and AFG2), linearity (R-2 >= 0.9994), precision (average SD < 2.79), accuracy (relative mean error < 5.51), robustness (p < 0.0080), ruggedness (p < 0.0100) and average recoveries (89.2-97.8%). The limits of quantification of AFB 1, AFB2, AFG1 and AFG2 were 0.080, 0.073, 0.062 and 0.066 ng CI, respectively. Finally, the developed method was applied for the analysis of AFs in 45 samples comprising rice (n = 20), wheat (n = 15) and maize (n = 10). The results showed that 65% of rice, 20% of wheat and 80% of maize samples were found contaminated with AFs. Thus, according to the achieved results, it is suggested that the newly developed HPLC method could be effectively applied for the routine analysis of the AFs in different cereals and grains.
机译:建立并验证了一种新颖,可靠,快速的柱后衍生化高效液相色谱(HPLC)方法。 HPLC方法用于同时测定各种谷物和谷物中的黄曲霉毒素B1(AFB1),B-2(AFB(2)),G(1)(AFG(1))和G2(AFG(2))。用80:20(v / v)甲醇:水萃取样品,并使用C 18(40-63μm)固相萃取柱纯化。使用LiChroCART RP-18(5 m,250 x 4.0 mm(2))色谱柱分离AF。流动相由甲醇:乙腈:缓冲液(17.5:17.5:65 v / v)(pH 7.4)组成,流速为1.0 mL min I.在λ(ex)= 365 nm处检测到每个AF的荧光'em = 435 nm。在20分钟的总运行时间内,所有四个AF均已正确解决。通过评估选择性(AFB1,AFB2,AFG1和AFG2),线性(R-2> = 0.9994),精密度(平均SD <2.79),准确度(相对),已建立的方法被广泛验证为方法开发的最终验证平均误差<5.51),稳健性(p <0.0080),坚固性(p <0.0100)和平均回收率(89.2-97.8%)。 AFB 1,AFB2,AFG1和AFG2的定量限分别为0.080、0.073、0.062和0.066 ng CI。最后,将开发的方法用于分析包括稻米(n = 20),小麦(n = 15)和玉米(n = 10)的45个样品中的AF。结果表明,发现AF污染了65%的大米,20%的小麦和80%的玉米样品。因此,根据获得的结果,建议新开发的HPLC方法可以有效地用于常规谷物和谷物中AF的常规分析。

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