Bracco Imaging SpA, Centro Ricerche Bracco, Via Ribes 5, 10010, Colleretto Giacosa, Turin, Italy.
Bracco Imaging SpA, Centro Ricerche Bracco, Via Ribes 5, 10010, Colleretto Giacosa, Turin, Italy.
Anal Biochem. 2023 Sep 15;677:115251. doi: 10.1016/j.ab.2023.115251. Epub 2023 Jul 18.
In recent years, significant progress has been made in the development of fluorescent contrast agents for clinical applications. For the development of a fluorescent probe, it is crucial to evaluate its safety profile, including biodistribution. Specific methods need to be developed for the absolute quantification of fluorescent probes in tissue specimens from animals administered with test compounds in the framework of biodistribution/efficacy/toxicity studies. Here, we describe a new method for the absolute quantification of fluorescent probes in tissue specimens from animals administered with compounds that have absorption and emission wavelength in the Near-Infrared region (600-800 nm). The protocol is based on the standard addition approach in order to minimize the interference of the matrix on the analyte signal causing inaccuracy in the absolute determination of the concentration. The measurement of the fluorescence intensity is done via a microplate reader. The method has been fully validated and applied for the quantification of a fluorescence-guided surgery targeted contrast agent in a Good Laboratory Practice (GLP) biodistribution study. Results clearly demonstrate that this procedure is fully applicable in a preclinical setting and that it overcomes common issues associated with fluorescence signal quantification in tissue extracts.
近年来,在临床应用的荧光对比剂的开发方面取得了重大进展。对于荧光探针的开发,评估其安全性概况至关重要,包括生物分布。在生物分布/功效/毒性研究中,需要为在给予试验化合物的动物的组织标本中绝对定量荧光探针开发特定的方法。在这里,我们描述了一种用于绝对定量在近红外区域(600-800nm)中具有吸收和发射波长的化合物给予的动物的组织标本中的荧光探针的新方法。该方案基于标准添加方法,以最大程度地减少基质对分析物信号的干扰,从而导致浓度的绝对测定不准确。荧光强度的测量通过微孔板读数器进行。该方法已全面验证,并应用于在良好实验室规范(GLP)生物分布研究中定量荧光引导手术靶向对比剂。结果清楚地表明,该程序完全适用于临床前环境,并且克服了与组织提取物中的荧光信号定量相关的常见问题。