Pharmaceutical Analysis, Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, 3000 Leuven, Belgium.
Molecules. 2022 Aug 18;27(16):5266. doi: 10.3390/molecules27165266.
A new, simple and sensitive ion chromatography (IC) method for the determination of sodium, potassium, magnesium, calcium and chloride in a parenteral nutrition (PN) solution was developed and validated. Before sample analysis, a sample pretreatment by calcination was applied which could totally remove interference from other constituents of the PN solution. Methanesulfonic acid (MSA) and sodium hydroxide were used as the mobile phase for the determination of cations and anions, respectively. The calibration curves showed good correlation between analyte peak area and concentration (r2 > 0.999). Detection limits ranged from 0.0001 to 0.02 mg/L and quantification limits from 0.0002 to 0.06 mg/L. Relative standard deviation (RSD) values for repeatability and inter-day precision did not exceed 1.0% and the recoveries for all analytes were between 99.1−101.1%. The robustness was verified by using an experimental design.
建立并验证了一种用于测定肠外营养液中钠、钾、镁、钙和氯的新型、简单、灵敏的离子色谱法。在样品分析前,采用煅烧法进行样品预处理,可完全消除肠外营养液中其他成分的干扰。甲磺酸(MSA)和氢氧化钠分别用作阳离子和阴离子的流动相。校准曲线表明分析物峰面积与浓度之间具有良好的相关性(r2>0.999)。检测限范围为 0.0001 至 0.02 毫克/升,定量限范围为 0.0002 至 0.06 毫克/升。重复性和日间精密度的相对标准偏差(RSD)值不超过 1.0%,所有分析物的回收率在 99.1-101.1%之间。通过实验设计验证了稳健性。