Quantitative analysis of carbohydrate residues in dextran 40 from various sources: a comparative study using high-performance liquid chromatography coupled with a charged aerosol detector

IF 2.6 3区 化学 Q2 CHEMISTRY, ANALYTICAL
Shenggu Xie, Zhuyu Jin, Yan Huang and Qiaoqiao Huang
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Abstract

Dextran 40, a typical high molecular weight carbohydrate drug refined through fermentation, is widely used in the clinical field in an injectable form. The final product obtained through fermentation may contain by-products such as fructose and residual sucrose, which carry a risk of adverse reactions. Current quality standards do not effectively control for the possible presence of carbohydrate residues, and methods for detecting such residues are lacking. This gap in quality control exists in the vast majority of existing carbohydrate drugs. This study established and compared liquid chromatography methods equipped with three different detectors (RID, MS, and CAD), selecting a convenient, rapid, and efficient HILIC-CAD method. This method combines the high sensitivity of the HILIC-MS method with the high throughput of the HILIC-RID method, using porous silica as the stationary phase and a high-precision charged aerosol detector in tandem, achieving rapid separation and quantification of fructose and sucrose. Additionally, pretreatment optimization was conducted to eliminate the impact of dextran 40 on the detection of fructose and sucrose. The method was validated, showing good repeatability, recovery, robustness, and linearity, capable of quantifying carbohydrate residues at approximately 3.3 ppm. This study compared the residual levels of fructose and sucrose in dextran 40 obtained from different purification processes, analyzing key purification operations that influence the extent of carbohydrate residues. These findings provide a reference for optimizing the production process of dextran 40, ensuring the quality of the drug and public drug safety. Furthermore, the approach used in this study for detecting carbohydrate residues is applicable to the quality control of other carbohydrate drugs produced via fermentation.

Abstract Image

不同来源葡聚糖40中碳水化合物残基的定量分析:采用高效液相色谱与带电气溶胶检测器相结合的比较研究。
葡聚糖40是一种典型的经发酵精制而成的高分子量碳水化合物药物,以注射形式广泛应用于临床。通过发酵获得的最终产品可能含有副产品,如果糖和残留的蔗糖,它们有不良反应的风险。目前的质量标准不能有效地控制可能存在的碳水化合物残留物,并且缺乏检测这些残留物的方法。这种质量控制上的差距存在于绝大多数现有的碳水化合物药物中。本研究建立并比较了三种不同检测器(RID、MS和CAD)的液相色谱方法,选择了方便、快速、高效的HILIC-CAD方法。该方法结合了HILIC-MS法的高灵敏度和HILIC-RID法的高通量,采用多孔二氧化硅作为固定相和高精度带电气溶胶检测器串联,实现了果糖和蔗糖的快速分离和定量。并对预处理进行优化,消除葡聚糖40对果糖和蔗糖检测的影响。该方法经过验证,具有良好的重复性、回收率、稳健性和线性,能够定量约3.3 ppm的碳水化合物残留物。本研究比较了不同纯化工艺获得的葡聚糖40中果糖和蔗糖的残留水平,分析了影响碳水化合物残留程度的关键纯化操作。研究结果可为优化葡聚糖40的生产工艺,保证药品质量和公众用药安全提供参考。此外,本研究所采用的碳水化合物残留量检测方法也适用于其他通过发酵生产的碳水化合物药物的质量控制。
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来源期刊
Analytical Methods
Analytical Methods CHEMISTRY, ANALYTICAL-FOOD SCIENCE & TECHNOLOGY
CiteScore
5.10
自引率
3.20%
发文量
569
审稿时长
1.8 months
期刊介绍: Early applied demonstrations of new analytical methods with clear societal impact
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