Determination of rFVII Concentration in Cell Culture Supernatant Using VIISelect Resin and RP-HPLC-UV

化学 色谱法 高效液相色谱法 幼仓鼠肾细胞 细胞培养 重组DNA 墨盒 细胞 生物化学 基因 机械工程 遗传学 生物 工程类
作者
Mehdi Khodadadian,Nahid Zarezadeh,Hossein Behrouz,Zeinab Ahsani
出处
期刊:Current Pharmaceutical Analysis [Bentham Science]
卷期号:18 (10): 959-967
标识
DOI:10.2174/1573412918666220901155615
摘要

Background: Recombinant activated human coagulation factor VIIa (rFVIIa), a vitamin K-dependent serine protease, was originally developed by Novo Nordisk® for the treatment of patients with FVII deficiency as well as patients with hemophilia A and B with inhibitors against FVIII or FIX. The gene for human FVII is cloned and expressed in baby hamster kidney (BHK) cells, and the protein is secreted into the culture media, which is then converted to the active form during chromatographic purification steps. When secreted into the culture media, measuring the concentration levels of FVII is needed in order to monitor, control and optimize the production processes. However, because of the high complexity of such media, reliable analytical techniques are required for this purpose. Objective: This work focuses on the analytical application of VIISelect resin (GE Healthcare) as a highly selective adsorbent for cleanup and preconcentration of rFVII in culture supernatant before analysis by reversed-phase high-performance liquid chromatography (RP-HPLC). Method: Empty 1 ml SPE cartridges were packed with VIISelect resin. Four types of solutions were used for the sample preparation. The RP-HPLC separation was conducted on a C4 column with UV detection. Results: The method shows recoveries greater than 97% in culture medium with relative standard deviations (RSDs) of less than 2%. The limits of detection and quantification were 0.039 mg/L and 0.12 mg/L, respectively. Conclusion: The method showed better performance in terms of precision and accuracy for rFVIIa determination in cell culture supernatant compared to other techniques, like ELISA and SDSPAGE.
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