Method development for 14C-labeling of IgG antibodies in preparation for clinical trials

IF 2.5 4区 化学 Q3 CHEMISTRY, ANALYTICAL
Sooyoung Kim, Jae-Hwan Kwak, Jae-Kyung Jung, Soonsil Hyun
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Abstract

Carbon-14 (14C) labeling is a standard technology for tracing molecules and providing their pharmacokinetic profiles. However, its primary focus has been on small molecules, with limited application to biomacromolecules. Particularly in the development of new biological entities (NBE), the utilization of microdosing with a 14C-labeled biomacromolecule proves beneficial in the early stages of drug development, contributing to significant time and cost savings. This study investigates the 14C-labeling of antibody and explores the stability of 14C-labeled antibody under various storage conditions. In this study, the utilization of 14C-formaldehyde for labeling target antibodies at various molar ratios revealed a direct correlation between labeling efficiency and the quantity of 14C-formaldehyde applied: 1.5 mol/mol for 14C-labeled antibody with the use of 10 equivalents of 14C-formaldehyde, 3.8 mol/mol for 14C-labeled antibody with the use of 10 equivalents of 14C-formaldehyde, and 10.5 mol/mol for 14C-labeled antibody with the use of 60 equivalents of 14C-formaldehyde. All the reaction conditions exhibited no antibody degradation, as evidenced by the absence of a significant change in HPLC purity compared to the unlabeled antibody. Stability tests revealed that all groups maintained their purities over a 4-week period at both − 75 ± 10 °C and 5 ± 3 °C. Given safety concerns related to internal radiation exposure in potential human subjects during microdosing, this study established optimal conditions for employing 14C-labeled antibodies. Therefore, it is optimized that 10 equivalents of 14C-formaldehyde can be used for 14C-antibody labeling through reductive amination, storing the antibodies at 5 ± 3 °C, and assigning a storage period of 4 weeks. The findings from this study offer valuable insights into the effective application of 14C-labeling in microdosing studies, especially for larger molecules such as antibodies.
开发 14C 标记 IgG 抗体的方法,为临床试验做准备
碳-14(14C)标记是追踪分子和提供其药代动力学特征的标准技术。然而,该技术主要针对小分子,对生物大分子的应用有限。特别是在新生物实体(NBE)的开发过程中,使用 14C 标记的生物大分子进行微量给药证明有利于药物开发的早期阶段,可大大节省时间和成本。本研究对抗体的 14C 标记进行了研究,并探讨了 14C 标记抗体在各种储存条件下的稳定性。本研究利用不同摩尔比的 14C 甲醛标记目标抗体,发现标记效率与 14C 甲醛的用量直接相关:1.使用 10 个等量的 14C 甲醛标记 14C 标记抗体,标记效率为 1.5 摩尔/摩尔;使用 10 个等量的 14C 甲醛标记 14C 标记抗体,标记效率为 3.8 摩尔/摩尔;使用 60 个等量的 14C 甲醛标记 14C 标记抗体,标记效率为 10.5 摩尔/摩尔。与未标记的抗体相比,所有反应条件下的高效液相色谱纯度均无明显变化,证明抗体没有降解。稳定性测试表明,在 - 75 ± 10 °C 和 5 ± 3 °C 两种温度下,所有组别都能在 4 周内保持纯度。考虑到微量给药过程中可能对人体造成的内照射安全问题,本研究确定了使用 14C 标记抗体的最佳条件。因此,通过还原胺化,将 10 个等量的 14C 甲醛用于 14C 标记抗体,将抗体储存在 5 ± 3 °C,并指定储存期为 4 周,是最合适的方法。这项研究的结果为 14C 标记在微剂量研究中的有效应用提供了宝贵的见解,尤其是对抗体等大分子而言。
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来源期刊
Journal of Analytical Science and Technology
Journal of Analytical Science and Technology Environmental Science-General Environmental Science
CiteScore
4.00
自引率
4.20%
发文量
39
审稿时长
13 weeks
期刊介绍: The Journal of Analytical Science and Technology (JAST) is a fully open access peer-reviewed scientific journal published under the brand SpringerOpen. JAST was launched by Korea Basic Science Institute in 2010. JAST publishes original research and review articles on all aspects of analytical principles, techniques, methods, procedures, and equipment. JAST’s vision is to be an internationally influential and widely read analytical science journal. Our mission is to inform and stimulate researchers to make significant professional achievements in science. We aim to provide scientists, researchers, and students worldwide with unlimited access to the latest advances of the analytical sciences.
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