首页> 外文会议>Lasers in Surgery: Advanced Characterization, Therapeutics, and Systems X >Two-photon excitation laser scanning microscopy of porcine nasal septal cartilage following Nd:YAG laser-mediated stress relaxation
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Two-photon excitation laser scanning microscopy of porcine nasal septal cartilage following Nd:YAG laser-mediated stress relaxation

机译:Nd:YAG激光介导的应力松弛后猪鼻中隔软骨的双光子激发激光扫描显微镜

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Abstract: Laser irradiation of hyaline cartilage result in stable shape changes due to temperature dependent stress relaxation. In this study, we determined the structural changes in chondrocytes within porcine nasal septal cartilage tissue over a 4-day period using a two-photon laser scanning microscope (TPM) following Nd:YAG laser irradiation (lambda equals 1.32 micrometer) using parameters that result in mechanical stress relaxation (6.0 W, 5.4 mm spot diameter). TPM excitation (780 nm) result in induction of fluorescence from endogenous agents such as NADH, NADPH, and flavoproteins in the 400 - 500 nm spectral region. During laser irradiation diffuse reflectance (from a probe HeNe laser, $lambda equals 632.8 nm), surface temperature, and stress relaxation were measured dynamically. Each specimen received one, two, or three sequential laser exposures (average irradiation times of 5, 6, and 8 seconds). The cartilage reached a peak surface temperature of about 70 degrees Celsius during irradiation. Cartilage denatured in 50% EtOH (20 minutes) was used as a positive control. TPM was performed using a mode-locked 780 nm Titanium:Sapphire (Ti:Al203) beam with a, 63X, 1.2 N.A. water immersion objective (working distance of 200 mm) to detect the fluorescence emission from the chondrocytes. Images of chondrocytes were obtained at depths up to 150 microns (lateral resolution equals 35 micrometer $MUL 35 micrometer). Images were obtained immediately following laser exposure, and also after 4 days in culture. In both cases, the irradiated and non-irradiated specimens do not show any discernible difference in general shape or auto fluorescence. In contrast, positive controls (immersed in 50% ethanol), show markedly increased fluorescence relative to both the native and irradiated specimens, in the cytoplasmic region. !21
机译:摘要:由于温度依赖性应力松弛,激光照射透明软骨会导致形状稳定变化。在这项研究中,我们使用Nd:YAG激光辐照(λ等于1.32微米),并使用得到的参数,在两天的时间内使用两光子激光扫描显微镜(TPM)确定了猪鼻中隔软骨组织内软骨细胞的结构变化机械应力松弛(6.0 W,5.4毫米光斑直径)。 TPM激发(780 nm)导致在400-500 nm光谱区域内诱导来自内源性试剂(例如NADH,NADPH和黄素蛋白)的荧光。在激光辐照期间,动态测量了漫反射率(来自探测氦氖激光器的λ等于632.8 nm),表面温度和应力松弛。每个标本接受一,二或三次连续激光照射(平均照射时间为5、6和8秒)。在照射期间,软骨达到约70摄氏度的峰值表面温度。在50%乙醇中变性的软骨(20分钟)用作阳性对照。 TPM使用锁模的780 nm钛:蓝宝石(Ti:Al2O3)光束和63X,1.2 N.A.水浸物镜(工作距离为200 mm)执行,以检测软骨细胞发出的荧光。在高达150微米的深度(横向分辨率等于35微米×MUL 35微米)下获得软骨细胞的图像。激光曝光后以及培养4天后立即获得图像。在这两种情况下,受辐照和未经辐照的样品在总体形状或自发荧光方面均未显示任何可辨别的差异。相反,阳性对照(浸入50%乙醇中)相对于天然和辐射标本,在细胞质区域显示出显着增强的荧光。 !21

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