Akers Walter J, Berezin Mikhail Y, Lee Hyeran, Achilefu Samuel
Washington University School of Medicine, Optical Radiology Laboratory, Department of Radiology, 4525 Scott Avenue, Saint Louis, Missouri 63110, USA.
J Biomed Opt. 2008 Sep-Oct;13(5):054042. doi: 10.1117/1.2982535.
Fluorescence lifetime (FLT) information is complementary to intensity measurement and can be used to improve signal-to-background contrast and provide environment sensing capability. In this study, we evaluate the FLTs of eight near-infrared fluorescent molecular probes in vitro in various solvent mediums and in vivo to establish the correlation between the in vitro and in vivo results. Compared with other mediums, two exponential fittings of the fluorescence decays of dyes dissolved in aqueous albumin solutions accurately predict the range of FLTs observed in vivo. We further demonstrate that the diffusion of a near-infrared (NIR) reporter from a dye-loaded gel can be detected by FLT change in mice as a model of controlled drug release. The mean FLT of the NIR probe increases as the dye diffuses from the highly polar gel interior to the more lipophilic tissue environment. The two-point analysis demonstrates an efficient in vitro method for screening new NIR fluorescent reporters for use as FLT probes in vivo, thereby minimizing the use of animals for FLT screening studies.
荧光寿命(FLT)信息是对强度测量的补充,可用于提高信号背景对比度并提供环境传感能力。在本研究中,我们在体外各种溶剂介质中以及在体内评估了八种近红外荧光分子探针的荧光寿命,以建立体外和体内结果之间的相关性。与其他介质相比,溶解在水性白蛋白溶液中的染料的荧光衰减的双指数拟合准确地预测了体内观察到的荧光寿命范围。我们进一步证明,作为可控药物释放模型,通过小鼠体内的FLT变化可以检测到近红外(NIR)报告分子从载有染料的凝胶中的扩散。随着染料从高极性凝胶内部扩散到亲脂性更强的组织环境中,NIR探针的平均FLT增加。两点分析证明了一种有效的体外方法,用于筛选新的NIR荧光报告分子以用作体内FLT探针,从而最大限度地减少用于FLT筛选研究的动物数量。