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抗EGFR/c-Met双特异性抗体药物的质量控制

武刚 徐刚领 黄子伊 魏思涵 杜加亮 俞小娟 崔永霏 倪永波 于传飞

山西医科大学学报2026,Vol.57Issue(1):97-104,8.
山西医科大学学报2026,Vol.57Issue(1):97-104,8.DOI:10.13753/j.issn.1007-6611.2026.01.013

抗EGFR/c-Met双特异性抗体药物的质量控制

Quality control of anti-EGFR/c-Met bispecific antibody drugs

武刚 1徐刚领 1黄子伊 2魏思涵 2杜加亮 1俞小娟 1崔永霏 1倪永波 1于传飞1

作者信息

  • 1. 中国食品药品检定研究院,药品监管科学全国重点实验室,国家卫生健康委生物技术产品检定方法及其标准化重点实验室,国家药品监督管理局生物制品质量研究与评价重点实验室,北京 102629
  • 2. 中国药科大学药学院
  • 折叠

摘要

Abstract

Objective To investigate and establish quality control methods for the critical quality attributes(CQAs)of anti-EGFR/c-Met bispecific antibody(BsAb).Methods The peptide mapping was used to identify the anti-EGFR/c-Met BsAb by reversed-phase ultra-high performance liquid chromatography(RP-UPLC)technology.Purity analysis was conducted using size exclusion chromatogra-phy(SEC),sodium dodecyl sulfate capillary electrophoresis(CE-SDS)and imaging capillary isoelectric focusing electrophoresis(icIEF).The contents of homodimeric impurities were analyzed by hydrophobic liquid chromatography(HIC).The contents of isomeri-zation and oxidation modifications were analyzed by multi-attribute method(MAM).Binding activity to the c-Met antigen was analyzed using time-resolved fluorescence resonance energy transfer assay(TR-FRET).Biological activity was determined by luciferase reporter gene assay(LRGA).Results The peptide mapping successfully identified all the characteristic peptides of the anti-EGFR/c-Met BsAb.The purity of anti-EGFR/c-Met BsAb was(99.24±0.00)%and(98.44±0.10)%by SEC and CE-SDS,respectively.The area per-centages of main peak,acidic peaks and basic peaks were(74.44±0.55)%,(22.91±0.28)%and(2.64±0.31)%by icIEF,respec-tively.The contents of homodimers were all below the limits of quantification(LOQ)by HIC.The contents of isomerization and oxida-tion modifications were(0.62±0.01)%and(2.35±0.03)%by MAM,respectively.Compared to the reference sample,the binding activity and the biological activity of anti-EGFR/c-Met BsAb were(99.00±10.78)%and(103.50±10.09)%,respectively.Conclusion Based on the physicochemical and biological characteristics of the anti-EGFR/c-Met BsAb,the quality control methods for its CQAs are successfully developed and validated,which ensures the clinical safety and efficacy of anti-EGFR/c-Met BsAb products from the perspective of quality controllability.

关键词

表皮生长因子受体/细胞间质上皮转换因子/双特异性抗体/关键质量属性/纯度分析/生物学活性

Key words

epidermal growth factor receptor(EGFR)/cellular mesenchymal epithelial transition factor(c-Met)/bispecific anti-body/critical quality attributes/purity analysis/biological activity

分类

医药卫生

引用本文复制引用

武刚,徐刚领,黄子伊,魏思涵,杜加亮,俞小娟,崔永霏,倪永波,于传飞..抗EGFR/c-Met双特异性抗体药物的质量控制[J].山西医科大学学报,2026,57(1):97-104,8.

基金项目

北京市科学技术委员会医药创新品种及平台培育项目(Z251100004625003) (Z251100004625003)

药品监管科学国家重点实验室项目(2024SKLDRS0204,2025SKLDRS0318) (2024SKLDRS0204,2025SKLDRS0318)

山西医科大学学报

1007-6611

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