Walther Rasmus, Krmar Jovana, Leistner Adrian, Svrkota Bojana, Otašević Biljana, Malenović Andjelija, Holzgrabe Ulrike, Protić Ana
Institute for Pharmacy and Food Chemistry, University of Würzburg, Am Hubland, 97074 Würzburg, Germany.
Department of Drug Analysis, Faculty of Pharmacy, University of Belgrade, Vojvode Stepe 450, 11 221 Belgrade, Serbia.
Pharmaceuticals (Basel). 2023 Mar 23;16(4):478. doi: 10.3390/ph16040478.
An alternative to the time-consuming and error-prone pharmacopoeial gas chromatography method for the analysis of fatty acids (FAs) is urgently needed. The objective was therefore to propose a robust liquid chromatography method with charged aerosol detection for the analysis of polysorbate 80 (PS80) and magnesium stearate. FAs with different numbers of carbon atoms in the chain necessitated the use of a gradient method with a Hypersil Gold C column and acetonitrile as organic modifier. The risk-based Analytical Quality by Design approach was applied to define the Method Operable Design Region (MODR). Formic acid concentration, initial and final percentages of acetonitrile, gradient elution time, column temperature, and mobile phase flow rate were identified as critical method parameters (CMPs). The initial and final percentages of acetonitrile were fixed while the remaining CMPs were fine-tuned using response surface methodology. Critical method attributes included the baseline separation of adjacent peaks (α-linolenic and myristic acid, and oleic and petroselinic acid) and the retention factor of the last compound eluted, stearic acid. The MODR was calculated by Monte Carlo simulations with a probability equal or greater than 90%. Finally, the column temperature was set at 33 °C, the flow rate was 0.575 mL/min, and acetonitrile linearly increased from 70 to 80% (/) within 14.2 min.
迫切需要一种替代耗时且容易出错的药典气相色谱法来分析脂肪酸(FAs)的方法。因此,目的是提出一种用于分析聚山梨醇酯80(PS80)和硬脂酸镁的带电荷气溶胶检测的稳健液相色谱法。链中碳原子数不同的脂肪酸需要使用以Hypersil Gold C柱和乙腈作为有机改性剂的梯度方法。基于风险的设计分析质量方法被用于定义方法可操作设计区域(MODR)。甲酸浓度、乙腈的初始和最终百分比、梯度洗脱时间、柱温和流动相流速被确定为关键方法参数(CMPs)。乙腈的初始和最终百分比被固定,而其余的CMPs使用响应面法进行微调。关键方法属性包括相邻峰(α-亚麻酸和肉豆蔻酸,以及油酸和岩芹酸)的基线分离以及最后洗脱化合物硬脂酸的保留因子。MODR通过概率等于或大于90%的蒙特卡洛模拟计算得出。最后,柱温设定为33℃,流速为0.575 mL/min,乙腈在14.2分钟内从70%线性增加到80%(/)。