Discrimination of Polysorbate 20 by High-Performance Liquid Chromatography-Charged Aerosol Detection and Characterization for Components by Expanding Compound Database and Library

IF 6.1 1区 医学 Q1 PHARMACOLOGY & PHARMACY
Shi-Qi Wang, Xun Zhao, Li-Jun Zhang, Yue-Mei Zhao, Lei Chen, Jin-Lin Zhang, Bao-Cheng Wang, Sheng Tang, Tom Yuan, Yaozuo Yuan, Mei Zhang, Hian Kee Lee, Hai-Wei Shi
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引用次数: 0

Abstract

Analyzing polysorbate 20 (PS20) composition and the impact of each component on stability and safety is crucial due to formulation variations and individual tolerance. The similar structures and polarities of PS20 components make accurate separation, identification, and quantification challenging. In this work, a high-resolution quantitative method was developed using single-dimensional high-performance liquid chromatography (HPLC) with charged aerosol detection (CAD) to separate 18 key components with multiple esters. The separated components were characterized by ultra-high-performance LC-quadrupole time-of-flight mass spectrometry (UHPLC-Q-TOF-MS) with an identical gradient as the HPLC-CAD analysis. The polysorbate compound database and library were expanded over 7-time compared to the commercial database. The method investigated differences in PS20 samples from various origins and grades for different dosage forms to evaluate the composition-process relationship. UHPLC-Q-TOF-MS identified 1329 to 1511 compounds in 4 batches of PS20 from different sources. The method observed the impact of 4 degradation conditions on peak components, identifying stable components and their tendencies to change. HPLC-CAD and UHPLC-Q-TOF-MS results provided insights into fingerprint differences, distinguishing quasi products.

Abstract Image

用高效液相色谱法检测聚山梨醇酯 20,并通过扩展化合物数据库和资料库确定成分特征
由于配方的变化和个体耐受性,分析聚山梨醇酯 20(PS20)的成分以及每种成分对稳定性和安全性的影响至关重要。由于 PS20 成分的结构和极性相似,因此准确分离、鉴定和定量极具挑战性。本研究采用单维高效液相色谱法(HPLC)和带电气溶胶检测法(CAD)开发了一种高分辨率定量方法,用于分离 18 种含有多种酯的关键成分。分离出的成分采用超高效液相色谱-四极杆飞行时间质谱(UHPLC-Q-TOF-MS)进行表征,梯度与 HPLC-CAD 分析相同。与商业数据库相比,聚山梨醇酯化合物数据库和库扩大了 7 倍。该方法研究了不同产地、不同等级、不同剂型的 PS20 样品的差异,以评估成分与工艺的关系。UHPLC-Q-TOF-MS 在 4 批不同来源的 PS20 中鉴定出 1329 至 1511 种化合物。该方法观察了 4 种降解条件对峰值成分的影响,确定了稳定成分及其变化趋势。HPLC-CAD 和 UHPLC-Q-TOF-MS 的结果有助于深入了解指纹差异,区分准产品。
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来源期刊
Journal of Pharmaceutical Analysis
Journal of Pharmaceutical Analysis Chemistry-Electrochemistry
CiteScore
16.20
自引率
2.30%
发文量
674
审稿时长
22 weeks
期刊介绍: The Journal of Pharmaceutical Analysis (JPA), established in 2011, serves as the official publication of Xi'an Jiaotong University. JPA is a monthly, peer-reviewed, open-access journal dedicated to disseminating noteworthy original research articles, review papers, short communications, news, research highlights, and editorials in the realm of Pharmacy Analysis. Encompassing a wide spectrum of topics, including Pharmaceutical Analysis, Analytical Techniques and Methods, Pharmacology, Metabolism, Drug Delivery, Cellular Imaging & Analysis, Natural Products, and Biosensing, JPA provides a comprehensive platform for scholarly discourse and innovation in the field.
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