Dochow Sebastian, Fatakdawala Hussain, Phipps Jennifer E, Ma Dinglong, Bocklitz Thomas, Schmitt Michael, Bishop John W, Margulies Kenneth B, Marcu Laura, Popp Jürgen
Institute of Physical Chemistry and Abbe Center of Photonics, Friedrich-Schiller University Jena, Helmholtzweg 4, 07743, Jena, Germany.
Department of Biomedical Engineering, University of California, Davis, 451 E. Health Sciences Drive, Davis, CA 95616, USA.
J Biophotonics. 2016 Sep;9(9):958-66. doi: 10.1002/jbio.201500341. Epub 2016 Mar 22.
Fluorescence lifetime imaging (FLIm) and Raman spectroscopy are two promising methods to support morphological intravascular imaging techniques with chemical contrast. Both approaches are complementary and may also be used in combination with OCT/IVUS to add chemical specificity to these morphologic intravascular imaging modalities. In this contribution, both modalities were simultaneously acquired from two human coronary specimens using a bimodal probe. A previously trained SVM model was used to interpret the fluorescence lifetime data; integrated band intensities displayed in RGB false color images were used to interpret the Raman data. Both modalities demonstrate unique strengths and weaknesses and these will be discussed in comparison to histologic analyses from the two coronary arteries imaged.
荧光寿命成像(FLIm)和拉曼光谱是两种很有前景的方法,可通过化学对比来辅助形态学血管内成像技术。这两种方法互为补充,也可与光学相干断层扫描(OCT)/血管内超声(IVUS)联合使用,为这些形态学血管内成像模式增添化学特异性。在本研究中,使用双峰探头从两个人类冠状动脉标本中同时获取了这两种模式的数据。利用先前训练的支持向量机(SVM)模型来解读荧光寿命数据;使用RGB伪彩色图像中显示的积分带强度来解读拉曼数据。这两种模式都有各自独特的优缺点,将与所成像的两条冠状动脉的组织学分析结果进行对比讨论。