正相高效液相色谱法测定马拉硫磷及其残留

IF 1.7 4区 化学 Q3 CHEMISTRY, ANALYTICAL
L. Velkoska-Markovska, B. Petanovska-Ilievska
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引用次数: 1

摘要

农药制剂的质量影响着作物安全、环境和人类健康。因此,开发新的分析方法来测定农药制剂中的活性物质,以控制其质量,以及控制其在食品样品中的残留,以确保食品安全,始终是受欢迎的。建立了一种新的、简便、精密、准确的正相高效液相色谱法(NP-HPLC)测定市售乳油农药产品中活性成分马拉硫磷的方法,并进行了验证。分析是在LiChrosorb CN(250 x 4 毫米,5 μm)分析柱,流动相为正己烷和二氯甲烷(80/20,v/v),流速为1 mL/min,柱温恒定在25 220°C和紫外线二极管阵列检测 nm。多元相关系数R2≥0.9990,保留时间、峰面积和峰高的相对标准偏差(RSD≤1.14%),回收率范围为98.97~101.62%,表明该方法具有良好的线性、精密度和准确度。采用固相萃取法对苹果汁样品进行了初步制备,并成功地应用于苹果汁样品中马拉硫磷残留量的测定。对该方法的特异性、选择性、线性、基质效应、精密度和准确度进行了测试,以验证该方法的有效性。结果在可接受的范围内,表明该方法适用于农药制剂中马拉硫磷的常规测定,也适用于苹果汁样品中马拉硫磷残留量的测定。HPLC分析的运行时间约为6 最小。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Determination of malathion and its residues by normal-phase high-performance liquid chromatography method
The quality of pesticide formulations has an impact on the crop safety, environment and human health. Therefore, the development of new analytical methods for the determination of active substances in pesticide formulations in order to control their quality, as well as, their residues in food samples in order to ensure food safety, is always welcome. A new, simple, precise and accurate normal-phase high-performance liquid chromatography (NP-HPLC) method for determination of an active ingredient malathion in the commercial emulsifiable concentrate pesticide product has been developed and validated. The analysis was carried out on a LiChrosorb CN (250 x 4 mm, 5 μm) analytical column using isocratic elution with mobile phase consisted of n-hexane and dichloromethane (80/20, v/v), flow rate of 1 mL/min, constant column temperature at 25 °C and ultraviolet diode-array detection at 220 nm. The obtained values for multiple correlation coefficients (R2 ≥ 0.9990), relative standard deviation of retention times, peak areas and heights (RSD ≤ 1.14%), recoveries ranged from 98.97 to 101.62%, revealed that the developed method has a satisfactory linearity, precision and accuracy. Also, the developed method was successfully applied for determination of malathion residues in apple juice samples, after preliminary sample preparation using solid-phase extraction. Specificity, selectivity, linearity, matrix effect, precision and accuracy were tested in order to validation of this method. The obtained results were in acceptable ranges and indicated that the developed method is suitable for routine determination of malathion in the pesticide formulation, as well as for determination of malathion residues in apple juice samples. The run time of HPLC analysis was about 6 min.
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来源期刊
Acta Chromatographica
Acta Chromatographica 化学-分析化学
CiteScore
4.00
自引率
0.00%
发文量
55
审稿时长
2.3 months
期刊介绍: Acta Chromatographica Open Access Acta Chromatographica publishes peer-reviewed scientific articles on every field of chromatography, including theory of chromatography; progress in synthesis and characterization of new stationary phases; chromatography of organic, inorganic and complex compounds; enantioseparation and chromatography of chiral compounds; applications of chromatography in biology, pharmacy, medicine, and food analysis; environmental applications of chromatography; analytical and physico-chemical aspects of sample preparation for chromatography; hyphenated and combined techniques; chemometrics and its applications in separation science.
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