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机构地区:[1]复旦大学附属眼耳鼻喉科医院药剂科,上海200031
出 处:《中国临床药学杂志》2016年第2期89-92,共4页Chinese Journal of Clinical Pharmacy
基 金:上海市科委基金项目(编号11DZ1972100)
摘 要:目的建立一种测定乙醇消毒液中乙醇含量的HPLC法。方法以甘油为内标,乙醇和甘油经对甲苯磺酰异氰酸酯(TSIC)衍生化后衍生化产物用HPLC法测定。色谱柱为Agilent C18(150mm×4.6mm,5μm),流动相为乙腈-磷酸缓冲液(0.01mol·L^-1 KH2P04,磷酸调pH至2.5)(35:65),检测波长227nm,流速1mL·min^-1,柱温25℃。结果在该条件下,乙醇在质量浓度2.5—200mg·L^-1内线性良好(r〉0.9995,n=7)。回收率为97%~103%(n=5),RSD〈3%(n=5)。衍生化产物在12h内稳定。测得样品中乙醇的标示量百分含量为90%~110%。结论经验证,该方法快速、简便、结果准确、重复性好,适合于乙醇消毒液中乙醇的含量测定。AIM To develop an HPLC method to analyze the content of ethanol in ethanol disinfection solution. METHODS Ethanol and glycerol (internal standard, IS) were derivatized with p-toluenesulfonyl isocyanate (TSIE) and analyzed by HPLC. The derivatized IS and derivatized ethanol were separated on an Agilent C18( 150 mm × 4.6 mm,5 μm) column, using a UV detector and the wavelength was 227 nm. The mobile phase was CH3CN- 0.01 mol·L-1KH2PO4 (adjusted to pH 2.5 with phosphoric acid)(35:65). The temperature of the column was 25 ℃ and the flow rate of the mobile phase was 1 mL· min- 1. RESULTS Ethanol had good linearity ( r 〉 0. 999 5, n = 7) in the range of 2.5 - 200 mg·L-1. The recovery values were between 97% and 103%, RSD 〈 3.0% (n = 5). The samples were stable in 12 h and qualified between 90% and 110% . CONCLUSION The method is proved to be simple, fast, accurate, reli- able and suitable for the quality control of ethanol in ethanol disinfection solution.
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