首页> 外文期刊>Analytica chimica acta >Simultaneous liquid chromatographic determination of metals and organic compounds in pharmaceutical and food-supplement formulations using evaporative light scattering detection
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Simultaneous liquid chromatographic determination of metals and organic compounds in pharmaceutical and food-supplement formulations using evaporative light scattering detection

机译:使用蒸发光散射检测同时液相色谱法测定药物和食品补充制剂中的金属和有机化合物

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A novel method for the non-derivatization liquid chromatographic determination of metals (potassium,aluminium,calcium and magnesium) and organic compounds (ascorbate and aspartate) was developed and validated based on evaporative light scattering detection (ELSD).Separation of calcium,magnesium and aluminium was achieved by the cation exchange column Dionex CS-14 and an aqueous TFA mobile phase according to the following time program:0-6 min TFA 0.96 mL L-1,6-7 min linear gradient from TFA 0.96-6.4 mL L-1.Separation of potassium,magnesium and aspartate was achieved by the lipophilic C18 Waters Spherisorb column and isocratic aqueous 0.2 mL L-1 TFA mobile phase.Separation of sodium,magnesium,ascorbate and citrate was also achieved by the C18 analytical column,according to the following elution program:0-2.5 min aqueous nonafluoropentanoic acid (NFPA) 0.5mL L-1;2.5-3.5min linear gradient from 0.5mL L-1 NFPA to 1.0 mL L-1 TFA.In all cases,evaporation temperature was 70°C,pressure of the nebulizing gas (nitrogen) 3.5 bar,gain 11 and the flow rate 1.0 mL min-1.Resolution among calcium and magnesium was 1.8,while for all other separations was >3.2.Double logarithmic calibration curves were obtained within various ranges from 3-24 to 34-132 mu g mL-1,and with good correlation (r>0.996).Asymmetry factor ranged from 0.9 to 1.9 and limit of detection from 1.3 (magnesium) to 17 mu g mL-1 (ascorbate).The developed method was applied for the assay of potassium,magnesium,calcium,aluminium,aspartate and ascorbate in Pharmaceuticals and food-supplements.The accuracy of the method was evaluated using spiked samples (%recovery 95-105%,%R.S.D.< 2) and the absence of constant or proportional errors was confirmed by dilution experiments.
机译:建立了一种新的非衍生化液相色谱法测定金属(钾,铝,钙和镁)和有机化合物(抗坏血酸盐和天冬氨酸)的方法,并基于蒸发光散射检测(ELSD)进行了验证。钙,镁和钙的分离根据以下时间程序,通过阳离子交换柱Dionex CS-14和TFA水性流动相获得铝:0-6 min TFA 0.96 mL L-1,6-7 min来自TFA 0.96-6.4 mL L-的线性梯度1,亲脂性C18 Waters Spherisorb色谱柱和等度0.2 mL L-1 TFA流动相分离钾,镁和天门冬氨酸.C18分析柱分离钠,镁,抗坏血酸盐和柠檬酸盐以下洗脱程序:0-2.5分钟的九氟戊酸水溶液(mLPA)0.5mL L-1; 2.5-3.5min的线性梯度从0.5mL L-1 NFPA到1.0mL L-1 TFA。在所有情况下,蒸发温度均为70 °C,n的压力雾化气体(氮气)3.5 bar,增益11,流速1.0 mL min-1。钙和镁之间的分离度为1.8,而所有其他分离度均> 3.2。在3-24的不同范围内获得了双对数校准曲线到34-132μg mL-1且具有良好的相关性(r> 0.996)。不对称因子在0.9至1.9范围内,检出限在1.3(镁)至17μg mL-1(抗坏血酸盐)之间。用于药物和食品补充剂中钾,镁,钙,铝,天冬氨酸和抗坏血酸的测定。方法的准确性使用加标样品(%回收率95-105%,%RSD <2)和不存在时进行评估稀释实验确定了恒定误差或比例误差。

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