Suzuki Yuta, Wang Lihong V
Optical Imaging Laboratory, Department of Biomedical Engineering, Washington University in St. Louis , St. Louis, Missouri 63130, USA.
Appl Phys Lett. 2014 Nov 10;105(19):191108. doi: 10.1063/1.4901955. Epub 2014 Nov 11.
A technique to rapidly scan an optical focus inside a turbid medium is attractive for various biomedical applications. Time-reversed ultrasonically encoded (TRUE) optical focusing has previously demonstrated light focusing into a turbid medium, using both analog and digital devices. Although the digital implementation can generate a focus with high energy, it has been time consuming to scan the TRUE focus inside a sample. Here, by sweeping the frequencies of both ultrasound and light, we demonstrate a multiplex recording of ultrasonically encoded wavefronts, accelerating the generation of multiple TRUE foci. Using this technique, we obtained a 2-D image of a fluorescent target centered inside a turbid sample having a thickness of 2.4 transport mean free paths.
一种在混浊介质内部快速扫描光学焦点的技术对于各种生物医学应用具有吸引力。时间反转超声编码(TRUE)光学聚焦此前已通过模拟和数字设备展示了将光聚焦到混浊介质中。尽管数字实现方式能够产生高能量的焦点,但在样品内部扫描TRUE焦点一直很耗时。在此,通过扫描超声和光的频率,我们展示了超声编码波前的多路复用记录,加速了多个TRUE焦点的生成。使用该技术,我们获得了位于厚度为2.4个输运平均自由程的混浊样品内部中心的荧光目标的二维图像。