首页|HPLC法检测保健品口服液中的盐酸左旋咪唑

HPLC法检测保健品口服液中的盐酸左旋咪唑

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目的:建立高效液相色谱法检测保健品口服液中盐酸左旋咪唑的方法.方法:采用C18-WR色谱柱(4.6 mm×250 mm,5 μm),流动相为乙腈-0.05 mol/L磷酸二氢钾溶液(用三乙胺调节pH=7)(25∶75,体积比),流速1.0 mL/min,检测波长210 nm,柱温30℃,进样量10 μL.结果:盐酸左旋咪唑在8.634~86.340 μg/mL时与峰面积线性关系良好(R=0.9997);低、中、高加标量对应的平均回收率分别为99.7%、99.2%和100.3%,RSD分别为1.40%、0.64%和0.78%,检测限为0.4317 μg/mL.随机对市售16批样品进行检测,均未检出盐酸左旋咪唑.结论:该方法简便、快速、准确,可用于保健品口服液中非法添加盐酸左旋咪唑的检测.
Determination of Levamisole Hydrochloride in Oral Solution of Health Care Products by HPLC
Objective:To establish an HPLC method for detecting levamisole hydrochloride in oral health products.Methods:Using a C18-WR chromatography column(4.6 mm×250 mm,5 μm),the mobile phase is acetonitrile-0.05 mol/L potassium dihydrogen phosphate solution(pH=7 adjusted with triethylamine)(25∶75,volume ratio),with a flow rate of 1.0 mL/min,detection wavelength of 210 nm,column temperature of 30℃,and injection volume of 10 μL.Results:The linear relationship between levamisole hydrochloride and peak area is good in the range of 8.634 μg/mL to 86.340 μg/mL(R=0.9997);the average recovery rates corresponding to low,medium,and high spiked quantities are 99.7%,99.2%,and 100.3%,respectively,with RSD of 1.40%,0.64%,and 0.78%,and detection limit of 0.4317 μg/mL.Randomly tested 16 batches of commercially available samples,but no levamisole hydrochloride is detected.Conclusion:This method is simple,fast,and accurate,and can be used for the detection of illegal addition of levamisole hydrochloride in oral health products.

oral solution of health care productslevamisole hydrochlorideHPLC

李晓茵、韦林、庄少珊、黄丽芹、吴淋富、郑晓渲、李聪聪

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汕尾市食品药品检验所,广东汕尾 516600

汕尾市高级技工学校,广东汕尾 516600

广东药科大学,广东中山 528458

保健品口服液 盐酸左旋咪唑 HPLC法

广东省市场监督管理局2020年度科技项目

2020CS08

2024

生物化工

生物化工

ISSN:
年,卷(期):2024.10(1)
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