Department of Biomedical Engineering, Yale University, New Haven, CT 06511.
Department of Surgery, Yale School of Medicine, New Haven, CT 06511.
Proc Natl Acad Sci U S A. 2020 Feb 18;117(7):3502-3508. doi: 10.1073/pnas.1915450117. Epub 2020 Feb 3.
Accurate analysis of blood concentration and circulation half-life is an important consideration for any intravenously administered agent in preclinical development or for therapeutic application. However, the currently available tools to measure these parameters are laborious, expensive, and inefficient for handling multiple samples from complex multivariable experiments. Here we describe a robust high-throughput quantitative microscopy-based method to measure the blood concentration and circulation half-life of any fluorescently labeled agent using only a small (2 µL) amount of blood volume, enabling additional end-point measurements to be assessed in the same subject. To validate this method, we demonstrate its use to measure the circulation half-life in mice of two types of fluorescently labeled polymeric nanoparticles of different sizes and surface chemistries and of a much smaller fluorescently labeled monoclonal antibody. Furthermore, we demonstrate the improved accuracy of this method compared to previously described methods.
准确分析血药浓度和循环半衰期是临床前开发或治疗应用中任何静脉内给予药物的重要考虑因素。然而,目前可用的测量这些参数的工具繁琐、昂贵且效率低下,无法处理来自复杂多变量实验的多个样本。在这里,我们描述了一种强大的高通量定量显微镜方法,仅使用少量(2 µL)血量即可测量任何荧光标记试剂的血药浓度和循环半衰期,从而能够在同一对象中评估其他终点测量。为了验证这种方法,我们证明了它在测量两种不同大小和表面化学性质的荧光标记聚合物纳米粒子以及一种更小的荧光标记单克隆抗体在小鼠体内的循环半衰期中的用途。此外,我们证明了与以前描述的方法相比,该方法具有更高的准确性。