Kayaalp Nalbant Elif, Rounds Cody, Sadeghipour Negar, Meng Boyu, Folaron Margaret R, Haldar Chandrika, Strawbridge Rendall R, Samkoe Kimberley S, Davis Scott C, Tichauer Kenneth M
Biomedical Engineering, Illinois Institute of Technology, Chicago, IL.
Authors contributed equally.
Proc SPIE Int Soc Opt Eng. 2020 Feb;11219. doi: 10.1117/12.2545182. Epub 2020 Feb 19.
A paired-agent fluorescent molecular imaging strategy is presented as a method to measure drug target engagement in whole tumor imaging. The protocol involves dynamic imaging of a pair of targeted and control imaging agents prior to and following antibody therapy. Simulations demonstrated that antibody "drug target engagement" can be estimated within a 15%-error over a wide range of tumor physiology (blood flow, vascular permeability, target density) and antibody characteristics (affinity, binding rates). Experimental results demonstrated the first in vivo detection of binding site barrier, highlighting the potential for this methodology to provide novel insights in drug distribution/binding imaging.
一种双试剂荧光分子成像策略被提出,作为在全肿瘤成像中测量药物靶点结合的方法。该方案包括在抗体治疗前后对一对靶向和对照成像试剂进行动态成像。模拟表明,在广泛的肿瘤生理学(血流、血管通透性、靶点密度)和抗体特性(亲和力、结合速率)范围内,抗体“药物靶点结合”可在15%的误差范围内估计。实验结果首次在体内检测到结合位点屏障,突出了该方法在药物分布/结合成像中提供新见解的潜力。