Sarrut Morgan, Fekete Szabolcs, Janin-Bussat Marie-Claire, Colas Olivier, Guillarme Davy, Beck Alain, Heinisch Sabine
Univ Lyon, CNRS, Université Claude Bernard Lyon 1, Ens de Lyon, Institut des Sciences Analytiques, UMR 5280, 5 rue de la Doua, F-69100 VILLEURBANNE, France.
School of Pharmaceutical Sciences, University of Geneva, University of Lausanne, Bd d'Yvoy 20, 1211 Geneva 4, Switzerland.
J Chromatogr B Analyt Technol Biomed Life Sci. 2016 Oct 1;1032:91-102. doi: 10.1016/j.jchromb.2016.06.049. Epub 2016 Jun 28.
This paper is the second part of a two-part series dedicated to the development of an on-line comprehensive HICxRPLC-UV/MS method for the characterization of a commercial inter-chain cysteine-linked ADC (brentuximab vedotin, Adcetris(®)). The first part focused on the optimization of the chromatographic conditions. In the second part of this series of papers, the structural characterization of the Brentuximab Vedotin was extensively discussed. With the combination of HIC and RPLC-MS data, the average DAR was easily measured in HIC and, at the same time, the predominant positional isomers were identified in RPLC-MS in one single injection. It was also demonstrated that the retention data obtained in the first and second dimensions was particularly useful to assist ADC characterization through the identification of sub-units. Using this methodology, the presence of odd DARs (1, 3 and 5) and their relative abundance was assessed by a systematic evaluation of HIC x RPLC-UV/MS data for both commercial and stressed ADC samples. Finally, once the exhaustive characterization of ADC was completed, MS could be conveniently replaced by UV detection to quickly assess the conformity of different ADCs batches.
本文是一个两部分系列论文的第二部分,致力于开发一种在线综合HICxRPLC-UV/MS方法,用于表征一种商业化的链间半胱氨酸连接的ADC(本妥昔单抗,Adcetris®)。第一部分聚焦于色谱条件的优化。在本系列论文的第二部分,对本妥昔单抗的结构表征进行了广泛讨论。结合HIC和RPLC-MS数据,在一次进样中,可轻松在HIC中测定平均DAR,同时在RPLC-MS中鉴定主要的位置异构体。还证明,通过鉴定亚基,在第一维和第二维中获得的保留数据对于辅助ADC表征特别有用。使用该方法,通过对商业化和应激ADC样品的HIC x RPLC-UV/MS数据进行系统评估,评估了奇数DAR(1、3和5)的存在及其相对丰度。最后,一旦完成ADC的详尽表征,MS可方便地被UV检测取代,以快速评估不同ADC批次的一致性。