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首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Comparative HPLC methods for β-blockers separation using different types of chiral stationary phases in normal phase and polar organic phase elution modes. Analysis of propranolol enantiomers in natural waters.
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Comparative HPLC methods for β-blockers separation using different types of chiral stationary phases in normal phase and polar organic phase elution modes. Analysis of propranolol enantiomers in natural waters.

机译:在正常相和极性有机相洗脱模式下,使用不同类型的手性固定相进行HPLC分离β受体阻滞剂的比较方法。天然水中普萘洛尔对映体的分析。

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The enantioselectivities of β-blockers (propranolol, metoprolol, atenolol and pindolol) on four different types of chiral stationary phases (CSPs): Chiralpak AD-H, Lux Cellulose-1, Chirobiotic T and Sumichiral OA-4900 were compared using polar organic (PO) elution mode and normal phase (NP) elution mode. Method optimizations were demonstrated by modifying parameters such as organic modifier composition (ethanol, 2-propanol and acetonitrile) and basic mobile phase additives (triethylamine, diethylamine, ethanolamine, and buthylamine). In normal phase elution mode with Lux Cellulose-1, the four pairs of enantiomers can be separated in the same run in gradient elution mode. Additionally, a simple chiral HPLC-DAD method using a newly commercialized polysaccharide-based CSP by Phenomenex (Lux Cellulose-1) in NP elution mode for enantioselective determination of propranolol in water samples by highly selective molecularly imprinted polymers extraction was validated. The optimized conditions were a mobile phase composed by n-hexane/ethanol/DEA (70/30/0.3, v/v/v) at a flow rate of 1.0 mL min(-1) and 25 °C. The method is selective, precise and accurate and was found to be linear in the range of 0.125-50 μg mL(-1) (R(2)>0.999) with a method detection limit (MLD) of 0.4 μg mL(-1) for both enantiomers. Recoveries achieved with both enantiomers ranged from 97 to 109%.
机译:使用极性有机溶剂(CSP)分别比较了β受体阻滞剂(普萘洛尔,美托洛尔,阿替洛尔和品多洛尔)在四种不同类型的手性固定相(CSP)上的对映选择性: PO)洗脱模式和正相(NP)洗脱模式。通过修改参数(例如有机改性剂组成(乙醇,2-丙醇和乙腈)和碱性流动相添加剂(三乙胺,二乙胺,乙醇胺和丁胺))证明了方法的优化。在使用Lux Cellulose-1进行正相洗脱模式下,可以在梯度洗脱模式下同一运行中分离四对对映异构体。此外,还验证了一种简单的手性HPLC-DAD方法,该方法使用Phenomenex(Lux Cellulose-1)的新型商品化多糖基CSP在NP洗脱模式下通过高选择性分子印迹聚合物萃取对映体选择性测定水中的普萘洛尔。优化的条件是流动相由正己烷/乙醇/ DEA(70/30 / 0.3,v / v / v)组成,流速为1.0 mL min(-1)和25°C。该方法具有选择性,精确度和准确性,在0.125-50μgmL(-1)(R(2)> 0.999)范围内呈线性,方法检测限(MLD)为0.4μgmL(-1) )两种对映体。两种对映体的回收率在97%至109%之间。

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