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A novel method for removing polyethyleneimine from biopharmaceutical samples: improving assay sensitivity of residual DNA qPCR

机译:一种从生物制药样品中除去聚乙烯亚胺的新方法:提高残留DNA QPCR的测定敏感性

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摘要

Polyethyleneimine (PEI) is a flocculent that is widely used in the downstream purification of monoclonal antibodies. It is an in-process residual that is carried through the drug purification process and strongly inhibits residual DNA quantitation by real-time quantitative PCR assay. Very high sample dilutions (e.g., 1:10,000) can overcome the interference of PEI, but at the cost of DNA assay sensitivity. Diluting samples poses a significant risk to the assay sensitivity needed to satisfy regulatory requirements on the quantitation of residual genomic DNA present per dose (i.e., 10 ng/dose). Removing PEI while retaining DNA, by the use of sodium dodecyl sulfate, heparin and/or sarkosyl can overcome the interference of PEI and allow a more accurate quantitation of residual DNA.
机译:聚乙烯亚胺(PEI)是一种广泛应用于单克隆抗体的下游纯化的絮凝剂。 它是通过药物净化过程进行的过程中的残留物,并且通过实时定量PCR测定强烈抑制残留的DNA定量。 非常高的样品稀释度(例如,1:10,000)可以克服PEI的干扰,但是在DNA测定敏感性的成本下。 稀释样品对满足每剂量(即10ng /剂量)的残留基因组DNA的定量进行调控要求所需的测定灵敏度构成显着风险。 通过使用十二烷基硫酸钠,肝素和/或甲糖基来除去DNA的同时去除PEI,可以克服PEI的干扰并允许更准确地定量残留DNA。

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