张孝明, 马蚺, 吕丽静, 王绿音, 吕萍, 梁成罡, 李晶. 均相时间分辨荧光技术测定替度格鲁肽生物学活性J. 药学学报, 2025, 60(1): 211-217. DOI: 10.16438/j.0513-4870.2024-0513
引用本文: 张孝明, 马蚺, 吕丽静, 王绿音, 吕萍, 梁成罡, 李晶. 均相时间分辨荧光技术测定替度格鲁肽生物学活性J. 药学学报, 2025, 60(1): 211-217. DOI: 10.16438/j.0513-4870.2024-0513
ZHANG Xiao-ming, MA Ran, LÜ Li-jing, WANG Lü-yin, LÜ Ping, LIANG Cheng-gang, LI Jing. Determination of biological activity of teduglutide by a homogeneous time-resolved fluorescence methodJ. Acta Pharmaceutica Sinica, 2025, 60(1): 211-217. DOI: 10.16438/j.0513-4870.2024-0513
Citation: ZHANG Xiao-ming, MA Ran, LÜ Li-jing, WANG Lü-yin, LÜ Ping, LIANG Cheng-gang, LI Jing. Determination of biological activity of teduglutide by a homogeneous time-resolved fluorescence methodJ. Acta Pharmaceutica Sinica, 2025, 60(1): 211-217. DOI: 10.16438/j.0513-4870.2024-0513

均相时间分辨荧光技术测定替度格鲁肽生物学活性

Determination of biological activity of teduglutide by a homogeneous time-resolved fluorescence method

  • 摘要: 本研究成功构建了GLP-2R-HEK293细胞, 通过试验条件参数优化和方法学验证, 建立了基于均相时间分辨荧光免疫分析技术的替度格鲁肽体外生物学活性分析方法, 并用该方法开展了替度格鲁肽原液和注射用替度格鲁肽相对效价检测。研究表明, GLP-2R-HEK293细胞中cAMP含量与替度格鲁肽浓度存在量效关系且符合四参数模型。用该方法检测64%、80%、100%、125%、156%共5个相对效价浓度的替度格鲁肽, 验证结果符合《中华人民共和国药典》2020版四部通则9401的要求。分别对3批替度格鲁肽原液和3批制剂进行相对效价测定, 所得曲线线性、回归性和平行性均通过系统适用性要求, 6批样品的相对效价在83%~105%。本研究建立的替度格鲁肽生物学活性检测方法准确度高、精密度好、操作简便、耗时短, 可用于替度格鲁肽产品的质量控制。

     

    Abstract: In this study, we constructed a GLP-2R-HEK293 cell line and established a method for the determination of the in vitro biological activity of teduglutide based on HTRF, after optimizing experimental conditions and methodological verification. We also carried out relative potency detection of teduglutide pharmaceutical products using this method. The result showed that there was a quantitative-efficient relationship between the teduglutide activity and cAMP contents in GLP-2R-HEK293 cells, which conformed to four-parameter model. Method verification results of five concentrations of teduglutide (64%, 80%, 100%, 125% and 156%) met the requirements of the General Rules of Chinese Pharmacopoeia, 2020 edition, Volume Ⅳ (9401). We then analyzed the relative potency of three batches of teduglutide drug substances and three batches of drug products. The linearity, regression and parallelism of the obtained curves all fit the system suitability requirements. The relative potency of six batches of teduglutide was from 83% to 105%. In summary, the biological activity detection method established in this study was accurate, precise, simple and time-saving, which can be used for quality control of teduglutide pharmaceutical products.

     

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