首页> 外文会议>Genetically Engineered Probes for Biomedical Applications; Progress in Biomedical Optics and Imaging; vol.7, no.21 >Frequency domain fluorescent diffuse tomography of small animals with DsRed2-expressed tumors
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Frequency domain fluorescent diffuse tomography of small animals with DsRed2-expressed tumors

机译:患有DsRed2表达的肿瘤的小动物的频域荧光扩散层析成像

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The main applications of fluorescent proteins (FPs) are monitoring tumor growth, angiogenesis, metastases formation and effects of new classes of drugs. Different types of tomography allow fluorescence imaging of tumors located deep in human or animal tissue. These techniques were used for investigation of the distribution of near-infrared fluorescent probes, but only a few works are devoted to fluorescence tomography in visible light. In this work, preliminary results of the frequency domain fluorescent diffuse tomography (FD FDT) method in application to DsRed2 protein as a fluorescent agent are presented. For the first step of our experiments we utilized second harmonic generation of Nd:YAG laser (532 nm) modulated by low frequency (1 kHz) in the experimental setup. The transilluminative planar configuration was used in the setup. A series of model experiments has been conducted and show good agreement between theoretical and experimental fluorescence intensity. Post mortem experiments with capsules containing DsRed2 and scattering solution introduced into esophagus of rats to simulate tumor formation have been conducted. The results of these experiments show that sensitivity of the setup is sufficient to detect DsRed2 in concentrations similar to those in FP-expressed tumor, but the contrast is not enough high to separate fluorescence of DsRed2 and surrounding tissues. The setup can be significantly improved by utilizing high-frequency modulation (110 MHz using acousto-optical modulator) of the excitation light and precise phase measurements due to difference in fluorescence life-time of FPs and surrounding tissues. An algorithm of processing a fluorescent image based on calculating zero of maximum curvature was employed for detection of fluorescent inclusions boundaries in the image.
机译:荧光蛋白(FPs)的主要应用是监测肿瘤的生长,血管生成,转移灶的形成以及新型药物的作用。不同类型的断层扫描可以对位于人或动物组织深处的肿瘤进行荧光成像。这些技术用于研究近红外荧光探针的分布,但是只有少数工作致力于可见光下的荧光层析成像。在这项工作中,提出了频域荧光漫射层析成像(FD FDT)方法应用于DsRed2蛋白作为荧光剂的初步结果。对于实验的第一步,我们在实验设置中利用了低频(1 kHz)调制的Nd:YAG激光(532 nm)的二次谐波生成。在该设置中使用了透照式平面配置。已经进行了一系列的模型实验,显示出理论和实验荧光强度之间的良好一致性。进行了死后实验,将含有DsRed2的胶囊和散射溶液引入大鼠食道以模拟肿瘤形成。这些实验的结果表明,该装置的灵敏度足以检测DsRed2,其浓度与FP表达的肿瘤相似,但对比度不足以区分DsRed2和周围组织的荧光。通过利用激发光的高频调制(使用声光调制器为110 MHz)以及由于FP和周围组织的荧光寿命不同而进行的精确相位测量,可以显着改善设置。使用基于计算最大曲率零的处理荧光图像的算法来检测图像中的荧光夹杂物边界。

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