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采用示差折光(RI)检测的尺寸排阻高效液相色谱法定量分析聚乙二醇化蛋白偶联物中的游离聚乙二醇。

Quantitation of free polyethylene glycol in PEGylated protein conjugate by size exclusion HPLC with refractive index (RI) detection.

作者信息

Li Ning, Ziegemeier Daisy, Bass Laura, Wang Wei

机构信息

Department of Pharmaceutical Research and Development, Pfizer Global Biologics, St. Louis Laboratory, Pfizer Inc., St. Louis, MO 63017, USA.

出版信息

J Pharm Biomed Anal. 2008 Dec 15;48(5):1332-8. doi: 10.1016/j.jpba.2008.09.027. Epub 2008 Sep 26.

DOI:10.1016/j.jpba.2008.09.027
PMID:19019609
Abstract

In this study, size exclusion high performance liquid chromatography was evaluated for its application in separation and quantitation of free polyethylene glycol (PEG) and its PEGylated-protein-conjugate (PEG-conjugate). Although the large mass of the free PEG (2-fold greater than the protein) made separation difficult, chromatographic conditions were identified enabling resolution and quantitation of the free PEG, PEG-conjugate and non-PEGylated protein with Shodex Protein KW803 and KW804 columns in series and refractive index detection. The optimum resolution of 1.7 and 2.0 was achieved for the free PEG and PEG-conjugate as well as the free PEG and non-PEGylated protein using 20mM HEPES buffer at pH 6.5. Under this condition, the plot of log(10)MW of all the pertinent analytes against retention time showed a linear relationship with a correlation coefficient of 1. Limited assay performance evaluation demonstrated that the method was linear in the concentration range of 10 to 250 microg/mL of free PEG with correlation coefficients of > or = 0.99. When free PEG in this concentration range was spiked into PEG-conjugate samples at 1mg/mL, the recovery was in the range of 78%-120%. Detection and quantitation limits were determined to be, respectively, 10 and 25 microg/mL for free PEG. The R.S.D. for intra- and inter-day precision was 0.09% or less for retention time measurements and 2.9% or less for area count measurements. Robustness testing was performed by deliberately deviating +/-0.2 pH units away from the desired pH as well as by increasing the flow rate. These deviations resulted in no significant impact on area percent distribution of all species. However, separation was found to be sensitive to high ionic strength and buffer species.

摘要

在本研究中,对尺寸排阻高效液相色谱法在游离聚乙二醇(PEG)及其聚乙二醇化蛋白缀合物(PEG缀合物)的分离和定量分析中的应用进行了评估。尽管游离PEG的质量较大(比蛋白质大2倍)使得分离困难,但通过串联使用Shodex Protein KW803和KW804柱并采用示差折光检测,确定了能够分离并定量游离PEG、PEG缀合物和未聚乙二醇化蛋白的色谱条件。使用pH 6.5的20mM HEPES缓冲液时,游离PEG与PEG缀合物以及游离PEG与未聚乙二醇化蛋白的最佳分离度分别达到1.7和2.0。在此条件下,所有相关分析物的log(10)MW对保留时间的图谱呈现线性关系,相关系数为1。有限的分析性能评估表明,该方法在游离PEG浓度范围为10至250μg/mL时呈线性,相关系数≥0.99。当将此浓度范围内的游离PEG以1mg/mL的浓度加入PEG缀合物样品中时,回收率在78% - 120%范围内。游离PEG的检测限和定量限分别确定为10和25μg/mL。保留时间测量的日内和日间精密度的相对标准偏差(R.S.D.)为0.09%或更低,面积计数测量的R.S.D.为2.9%或更低。通过故意将pH值偏离所需pH值±0.2个单位以及增加流速进行稳健性测试。这些偏差对所有组分的面积百分比分布没有显著影响。然而,发现分离对高离子强度和缓冲液种类敏感。

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