Matsuda Yutaka, Leung Monica, Okuzumi Tatsuya, Mendelsohn Brian
Ajinomoto Bio-Pharma Services, 11040 Roselle Street, San Diego, CA 92121, USA.
Ajinomoto Co., Inc., 1-1 Suzuki-cho, Kawasaki-ku, Kawasaki, Kanagawa 2108681, Japan.
Antibodies (Basel). 2020 May 18;9(2):16. doi: 10.3390/antib9020016.
In recent years, site-specific antibody drug conjugates (ADC)s have been in great demand because they have an expanded therapeutic index compared with conventional ADCs. AJICAP™ technology is a chemical conjugation platform to obtain site-specific ADCs through the use of a class of Fc-affinity compounds. Promising results from early technology development studies led to further investigation of AJICAP™ ADC materials to obtain site-specific and homogeneous drug antibody ratio (DAR) ADCs. Here we report site-specific conjugation followed by a preparative hydrophobic interaction chromatography (HIC) purification strategy to obtain purified "DAR = 1.0" and "DAR = 2.0" AJICAP™ ADC materials. Optimization of the mobile phase conditions and resin achieved a high recovery rate. In vitro biological assay demonstrated the target selective activity for purified homogeneous DAR ADCs. These results indicate the ability of a HIC purification strategy to provide "DAR = 1.0" and "DAR = 2.0" AJICAP™ ADCs with considerable potency and target selectivity.
近年来,位点特异性抗体药物偶联物(ADC)的需求量很大,因为与传统ADC相比,它们具有更宽的治疗指数。AJICAP™技术是一种化学偶联平台,通过使用一类Fc亲和化合物来获得位点特异性ADC。早期技术开发研究取得的有前景的结果促使对AJICAP™ ADC材料进行进一步研究,以获得位点特异性且药物抗体比(DAR)均一的ADC。在此,我们报告了一种位点特异性偶联方法,随后采用制备型疏水相互作用色谱(HIC)纯化策略,以获得纯化的“DAR = 1.0”和“DAR = 2.0”的AJICAP™ ADC材料。流动相条件和树脂的优化实现了高回收率。体外生物学测定证明了纯化的均一DAR ADC具有靶向选择性活性。这些结果表明,HIC纯化策略能够提供具有相当效力和靶向选择性的“DAR = 1.0”和“DAR = 2.0”的AJICAP™ ADC。