Department of Chemistry, Purdue University, 560 Oval Drive, West Lafayette, IN 47907-2084, USA.
Chemistry. 2011 Jan 24;17(4):1080-91. doi: 10.1002/chem.201002521. Epub 2011 Jan 5.
Biological imaging applications often employ molecular probes or nanoparticles for enhanced contrast. However, resolution and detection are still often limited by the intrinsic heterogeneity of the sample, which can produce high levels of background that obscure the signals of interest. Herein, we describe approaches to overcome this obstacle based on the concept of dynamic contrast: a strategy for elucidating signals by the suppression or removal of background noise. Dynamic contrast mechanisms can greatly reduce the loading requirement of contrast agents, and may be especially useful for single-probe imaging. Dynamic contrast modalities are also platform-independent, and can enhance the performance of sophisticated biomedical imaging systems or simple optical microscopes alike. Dynamic contrast is performed in two stages: 1) a signal modulation scheme to introduce time-dependent changes in amplitude or phase, and 2) a demodulation step for signal recovery. Optical signals can be coupled with magnetic nanoparticles, photoswitchable probes, or plasmon-resonant nanostructures for modulation by magnetomotive, photonic, or photothermal mechanisms, respectively. With respect to image demodulation, many of the strategies developed for signal processing in electronics and communication technologies can also be applied toward the editing of digital images. The image-processing step can be as simple as differential imaging, or may involve multiple reference points for deconvolution by using cross-correlation algorithms. Periodic signals are particularly amenable to image demodulation strategies based on Fourier transform; the contrast of the demodulated signal increases with acquisition time, and modulation frequencies in the kHz range are possible. Dynamic contrast is an emerging topic with considerable room for development, both with respect to molecular or nanoscale probes for signal modulation, and also to methods for more efficient image processing and editing.
生物成像应用通常采用分子探针或纳米颗粒来增强对比度。然而,分辨率和检测仍然常常受到样品固有异质性的限制,这会产生高水平的背景噪声,从而掩盖感兴趣的信号。在此,我们描述了基于动态对比概念的克服这一障碍的方法:通过抑制或去除背景噪声来阐明信号的策略。动态对比机制可以大大降低对比剂的加载要求,并且对于单探针成像可能特别有用。动态对比模式还与平台无关,可以增强复杂的生物医学成像系统或简单的光学显微镜的性能。动态对比分两个阶段进行:1)信号调制方案,引入幅度或相位的时变变化,2)信号恢复的解调步骤。光学信号可以与磁性纳米粒子、光致开关探针或等离子体共振纳米结构耦合,分别通过磁动、光子或光热机制进行调制。关于图像解调,许多在电子和通信技术中开发的信号处理策略也可以应用于数字图像的编辑。图像处理步骤可以像差分成像一样简单,或者可以通过使用互相关算法的多个参考点进行卷积反演。周期性信号特别适合基于傅里叶变换的图像解调策略;解调信号的对比度随采集时间增加而增加,并且可以达到 kHz 范围内的调制频率。动态对比是一个新兴的主题,在分子或纳米级探针的信号调制方面以及更有效的图像处理和编辑方法方面都有很大的发展空间。