结合
离子强度
寡核苷酸
化学
单克隆抗体
动态光散射
表面电荷
生物制药
胶体
静电学
相(物质)
离子键合
抗体-药物偶联物
溶剂
纳米颗粒
色谱法
静电
聚合物
生物物理学
静电相互作用
化学工程
纳米技术
化学物理
组合化学
分子间力
离子液体
活性成分
作者
Douglas D. Banks,Jon Cordia
标识
DOI:10.1021/acs.molpharmaceut.5c01126
摘要
Antibody oligonucleotide conjugates (AOCs) are quickly gaining traction as a new modality within the biopharmaceutical industry for their ability to precisely deliver gene expression modulating therapeutic oligonucleotides to specific tissues for the treatment of a range of genetic diseases. To realize their full pharmaceutical potential, high-concentration liquid formulations will need to be developed to minimize manufacturing costs and enable patient-centric subcutaneous routes of administration. Motivated by this goal, the current report details, to the best of our knowledge, the first systematic comparison of the pH and ionic strength dependence of the colloidal stabilities of a model AOC with the unconjugated monoclonal antibody (mAb) using a design of experiment approach. Similar to past investigations, protein-protein interactions of the mAb native state, as assessed by polyethylene glycol-induced liquid-liquid phase separation and dynamic light scattering experiments, were minimized at low pH and ionic strength solvent conditions, where long-range net electrostatic repulsion was highest. In contrast, the AOC was the least colloidally stable in these same solvent conditions, and higher solution viscosities were observed with increasing AOC concentration. The greater protein-protein intermolecular interactions of the AOC native state are believed to be caused by short-range attractive electrostatic interactions between the localized negative charge of the oligonucleotide and positive surface charge of the mAb. These interactions could be effectively minimized by raising solution pH and/or screening charge by increasing the ionic strength.
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