纳米医学
药物输送
共单体
化学
药品
结合
抗体
纳米技术
聚合物
组合化学
药理学
医学
材料科学
免疫学
纳米颗粒
单体
有机化学
数学分析
数学
作者
Pintu Kanjilal,Khushboo Singh,Rakha H. Das,J. J. Matte,S. Thayumanavan
出处
期刊:Biomacromolecules
[American Chemical Society]
日期:2023-07-21
卷期号:24 (8): 3638-3646
被引量:2
标识
DOI:10.1021/acs.biomac.3c00385
摘要
Antibody drug conjugates (ADCs) are poised to have an enormous impact on targeted nanomedicine, especially in many cancer pathologies. The reach of the current format of ADCs is limited by their low drug-to-antibody ratio (DAR) because of the associated physiochemical instabilities. Here, we design antibody polymer conjugates (APCs) as a modular strategy to utilize polymers to address ADC's shortcomings. We show here that conjugation of polymer-based therapeutic molecules to antibodies helps increase the DAR, owing to the hydrophilic comonomer in the polymer that helps in masking the increased hydrophobicity caused by high drug loading. We show that the platform exhibits cell targetability and selective cell killing in multiple cell lines expressing disease-relevant antigens, viz., HER2 and EGFR. The ability to use different functionalities in the drug as the handle for polymer attachment further demonstrates the platform nature of APCs. The findings here could serve as an alternative design strategy for the next generation of active targeted nanomedicine.
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