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Red colored IgG4 caused by vitamin B12 from cell culture media combined with disulfide reduction at harvest

机译:来自细胞培养基的维生素B12引起的红色IgG4结合收获时的二硫化物还原

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摘要

While many antibody therapeutics are formulated at low concentration (~10–20 mg/mL) for intravenous administration, high concentration (> 100 mg/mL) formulations may be required for subcutaneous delivery in certain clinical indications. For such high concentration formulations, product color is more apparent due to the higher molecular density across a given path-length. Color is therefore a product quality attribute that must be well-understood and controlled, to demonstrate process consistency and enable clinical trial blinding. Upon concentration of an IgG4 product at the 2000 L manufacturing scale, variability in product color, ranging from yellow to red, was observed. A small-scale experimental model was developed to assess the effect of processing conditions (medium composition and harvest conditions) on final bulk drug substance (BDS) color. The model was used to demonstrate that, for two distinct IgG4 products, red coloration occurred only in the presence of disulfide reduction-mediated antibody dissociation. The red color-causing component was identified as vitamin B12, in the hydroxocobalamin form, and the extent of red color was correlated with the cobalt (vitamin B12) concentration in the final pools. The intensity of redness in the final BDS was modulated by changing the concentration of vitamin B12 in the cell culture media.
机译:尽管许多抗体治疗剂均以低浓度(〜10–20 mg / mL)配制用于静脉内给药,但在某些临床适应症中可能需要高浓度(> 100 mg / mL)的皮下给药制剂。对于这种高浓度制剂,由于在给定路径长度上具有更高的分子密度,因此产品颜色更加明显。因此,颜色是必须很好理解和控制的产品质量属性,以证明过程的一致性并能够进行临床试验致盲。在以2000 L的制造规模浓缩IgG4产品时,观察到产品颜色的变化,从黄色到红色。开发了一个小规模的实验模型,以评估加工条件(中等成分和收获条件)对最终原料药(BDS)颜色的影响。该模型用于证明,对于两种不同的IgG4产物,仅在二硫键还原介导的抗体解离的情况下才会出现红色。导致红色的成分被鉴定为羟考巴兰形式的维生素B12,红色程度与最终溶液中钴(维生素B12)的浓度相关。通过改变细胞培养基中维生素​​B12的浓度来调节最终BDS中的红色强度。

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