Hendargo Hansford C, Bower Bradley A, Reinstein Alex S, Shepherd Neal, Tao Yuankai K, Izatt Joseph A
Biomedical Engineering Department, Duke University, Box 90281, Durham, NC, 27708, USA.
Opt Commun. 2011 Sep 1;284(19):4847-4851. doi: 10.1016/j.optcom.2011.06.001.
Spectral domain phase microscopy (SDPM) is an extension of spectral domain optical coherence tomography (SDOCT) that exploits the extraordinary phase stability of spectrometer-based systems with common-path geometry to resolve sub-wavelength displacements within a sample volume. This technique has been implemented for high resolution axial displacement and velocity measurements in biological samples, but since axial displacement information is acquired serially along the lateral dimension, it has been unable to measure fast temporal dynamics in extended samples. Depth-Encoded SDPM (DESDPM) uses multiple sample arms with unevenly spaced common path reference reflectors to multiplex independent SDPM signals from separate lateral positions on a sample simultaneously using a single interferometer, thereby reducing the time required to detect unique optical events to the integration period of the detector. Here, we introduce DESDPM and demonstrate the ability to acquire useful phase data concurrently at two laterally separated locations in a phantom sample as well as a biological preparation of spontaneously beating chick cardiomyocytes. DESDPM may be a useful tool for imaging fast cellular phenomena such as nervous conduction velocity or contractile motion.
光谱域相显微镜(SDPM)是光谱域光学相干断层扫描(SDOCT)的一种扩展技术,它利用具有共光路几何结构的基于光谱仪的系统的非凡相位稳定性,来解析样品体积内的亚波长位移。该技术已用于生物样品中的高分辨率轴向位移和速度测量,但由于轴向位移信息是沿横向维度串行获取的,因此它无法测量扩展样品中的快速时间动态。深度编码SDPM(DESDPM)使用多个带有间隔不均匀的共光路参考反射镜的样品臂,通过单个干涉仪同时对来自样品上不同横向位置的独立SDPM信号进行多路复用,从而将检测独特光学事件所需的时间减少到探测器的积分周期。在此,我们介绍DESDPM,并展示了在模拟样品以及自发跳动的鸡心肌细胞的生物制剂中,在两个横向分离的位置同时获取有用相位数据的能力。DESDPM可能是用于成像快速细胞现象(如神经传导速度或收缩运动)的有用工具。