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作 者:王静[1] 白璐[1] 谷艳[1] 项婧[1] 赵春杰[1]
出 处:《沈阳药科大学学报》2007年第11期695-699,共5页Journal of Shenyang Pharmaceutical University
摘 要:目的选择桂皮酸作为内标,建立HPLC法测定食品中山梨酸、苯甲酸、对羟基苯甲酸甲酯、对羟基苯甲酸乙酯、对羟基苯甲酸异丙酯、对羟基苯甲酸丙酯、对羟基苯甲酸丁酯。方法采用Dia—monsil(迪马)ODS(250mm×4.6mm,5μm)色谱柱,以乙腈、水(磷酸调pH:3)、四氢呋哺为流动相采用梯度洗脱,检测波长:254nm,流速:1.0mL·min^-1,样品用无水乙醇-水(体积比为85:15,磷酸调pH:2.5)提取。结果在上述条件下7种防腐剂可以达到基线分离,各组分对照曲线的线性相关性均大于0.9996,加样回收率:93.3%~100.5%,检出限:0.025~0.500gg。结论该方法适合食品中防腐剂的实际分析。Objective To develop a HPLC method for the determination of the contents of preservatives in cosmetic taking cinnamic acid as an internal standard. Therefore, the contents of sorbic acid, benzoic acid, methyl p-hydroxybenzoate, ethyl p-hydroxybenzoate, isopropyl p-hydroxybenzoate, propyl p-hydroxybenzoate and butyl p-hydroxybenzoate were evaluated. Methods The column was Diamonsil (Dikma) ODS (250.0 mm × 4.6 mm, 5μm) with acetonitrile, water(phosphate adjusted pH = 3) and tetrahydrofuran as the mobile phase. The way of gradient elution was adapted. The detection wavelength was set at 254 nm, The flow rate was 1.0 mL· min^- 1. Samples were extracted by ethanol-water ( V : V = 85 : 15, phosphate adjusted pH = 2.5). Results Under this condition, the peaks of seven preservatives were separated, the linear correlation coefficient was no less than 0. 999 6, the recoveries were 93.3% - 100.5%, detection limits were 0. 025 - 0. 500 μg. Conclusions This method is simple, accurate and sensitive. It can be applied for food analysis.
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