University of Belgrade, Faculty of Pharmacy, Department of Drug Analysis, Vojvode Stepe 450, 11 152, Belgrade, Serbia.
University of Würzburg, Institute for Pharmacy and Food Chemistry, 97074, Würzburg, Germany.
J Pharm Biomed Anal. 2021 Jan 30;193:113711. doi: 10.1016/j.jpba.2020.113711. Epub 2020 Oct 22.
Binding between cyclodextrin (CD) cavity and guest molecule in Reversed Phase High-Performance Liquid Chromatography (RP-HPLC) is dynamic process. In general, increasing CD concentration is inducing inclusion complex formation, leading to reduction of analyte's retention time. Consequently, the shortness in retention time is a measure of complex stability in HPLC. However, under certain experimental conditions, the retention of some analytes could be prolonged even when concentration of CD in the mobile phase is increased. In order to reveal the cause of this unexpected retention behavior, the present study was carried on. The model mixture consisted of risperidone, olanzapine and their related impurities, while β-CD was selected among CDs, as in the previous study. In order to achieve fast equilibrium between free analyte and β-CD-analyte complex, β-CD was not added to the mobile phase, but only to the sample. Detection was performed with Corona Charged Aerosol Detector (CAD), suitable for non-chromophoric β-CD. When analyzing olanzapine impurity B-β-CD sample, three peaks were detected, namely free β-CD, β-CD-analyte complex and free analyte. The complex stability constant was calculated employing a modification of the Benesi-Hildebrandt equation and CAD has proven to be useful in complex stability constants assessment if retention of free analyte and β-CD-analyte complex is distinguished. For all other analytes only two peaks could be detected, because free analyte and formed complex are eluting at the same retention time. Under such circumstances, the authors proposed the methodology for calculating stability constants and confirmed its applicability to studied model mixture.
在反相高效液相色谱(RP-HPLC)中,环糊精(CD)空腔与客体分子的结合是一个动态过程。通常,增加 CD 浓度会诱导包合复合物的形成,导致分析物保留时间的缩短。因此,保留时间的缩短是 HPLC 中复合物稳定性的衡量标准。然而,在某些实验条件下,即使在流动相中 CD 浓度增加的情况下,某些分析物的保留时间也可能延长。为了揭示这种意外保留行为的原因,进行了本研究。模型混合物由利培酮、奥氮平及其相关杂质组成,而β-CD 是在以前的研究中从 CD 中选择的。为了实现游离分析物和β-CD-分析物复合物之间的快速平衡,β-CD 未添加到流动相中,而仅添加到样品中。使用适合非生色性β-CD 的 Corona 带电气溶胶检测器(CAD)进行检测。当分析奥氮平杂质 B-β-CD 样品时,检测到三个峰,分别为游离β-CD、β-CD-分析物复合物和游离分析物。通过修改 Benesi-Hildebrandt 方程计算了复合物稳定常数,并且如果能够区分游离分析物和β-CD-分析物复合物的保留,则 CAD 已被证明在复合物稳定常数评估中是有用的。对于所有其他分析物,只能检测到两个峰,因为游离分析物和形成的复合物在相同的保留时间洗脱。在这种情况下,作者提出了计算稳定性常数的方法,并证实其适用于所研究的模型混合物。