Kyrish Matthew, Kester Robert, Richards-Kortum Rebecca, Tkaczyk Tomasz
Department of Bioengineering, Rice University, Houston, Texas 77005.
Proc SPIE Int Soc Opt Eng. 2010 Feb;7558:755807. doi: 10.1117/12.842744.
To reduce the number of invasive tissue biopsies and needle aspirations performed during cancer screenings, endo-microscopes can be used to image tissue in vivo. However, when optical fiber bundles are used to transmit the image, the resolution of such systems is limited by undersampling due to the spacing of the bundle's individual fibers for a given field of view. We propose a method to increase the sampling of an optical biopsy system and thereby improve the system's resolution. The method involves taking several images, shifting the object and fiber bundle slightly relative to each other from one image to the next. Multiple shifting patterns were evaluated to determine which provided the greatest increase in resolution. The shifted images are later realigned and recombined by a custom algorithm. By combining four shifted images of a USAF resolution target, we were able to measure an improvement in the resolution of the system from approximately 3.9 μm to 2.2 μm. When tested on cultured cells, a visible increase in detail was detectable. This technique can provide the basis for improving the diagnostic abilities of optical biopsy systems.
为了减少癌症筛查期间进行的侵入性组织活检和针吸活检的次数,可以使用内镜显微镜对体内组织进行成像。然而,当使用光纤束传输图像时,由于在给定视场下束中各根光纤的间距,此类系统的分辨率受到欠采样的限制。我们提出了一种增加光学活检系统采样率从而提高系统分辨率的方法。该方法包括拍摄多张图像,在相邻图像之间使物体和光纤束彼此相对轻微移动。评估了多种移动模式以确定哪种模式能带来最大的分辨率提升。随后通过定制算法对移位后的图像进行重新对齐和重组。通过组合美国空军分辨率靶标的四张移位图像,我们能够测得系统分辨率从约3.9μm提高到了2.2μm。在培养细胞上进行测试时,可以检测到细节明显增加。该技术可为提高光学活检系统的诊断能力提供基础。