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Differentiation of fibrotic liver tissue using laser-induced breakdown spectroscopy

机译:激光诱导击穿光谱法鉴别肝纤维化肝组织

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摘要

Hepatic cirrhosis is a major cause of morbidity and mortality worldwide due to hepatitis C, alcoholism and fatty liver disease associated with obesity. Assessment of hepatic fibrosis relies in qualitative histological evaluation of biopsy samples. This method is time-consuming and depends on the histopathologists’ interpretation. In the last decades, non-invasive techniques were developed to detect and monitor hepatic fibrosis. Laser-induced breakdown spectroscopy (LIBS) is a good candidate for a real-time, independent and fast technique to diagnose hepatic fibrosis. In this work LIBS was employed to characterize rat liver tissues with different stages of fibrosis. Depth profiling measurements were carried out by using a nanosecond Nd:YAG laser operated at the fundamental wavelength and an echelle spectrometer coupled with an ICCD camera. Due to the soft nature of the samples, plasma conditions largely change between consecutives shots. Thus, a theoretically supported procedure to correct the spectral line intensities was implemented. This procedure allows the reduction of the intensities’ dispersion from 67% to 12%. After the correction, the LIBS signal shows an enhancement in calcium intensity by a factor of three as the fibrosis progressed. Calcium is known to increase crosslinking of extracellular matrix proteins in the fibrous septa. Therefore, our result singles it out as a key participant in the hepatic fibrosis.
机译:由于丙型肝炎,酒精中毒和肥胖引起的脂肪肝疾病,肝硬化是全世界发病率和死亡率的主要原因。肝纤维化的评估依赖于活检样本的定性组织学评估。这种方法很耗时,取决于组织病理学家的解释。在过去的几十年中,开发了非侵入性技术来检测和监测肝纤维化。激光诱导击穿光谱法(LIBS)是一种实时,独立且快速的技术,可用于诊断肝纤维化。在这项工作中,LIBS用于表征具有不同纤维化阶段的大鼠肝脏组织。通过使用在基本波长下工作的纳秒Nd:YAG激光器和与ICCD相机耦合的echelle光谱仪进行深度轮廓测量。由于样品的柔软性质,在连续拍摄之间,等离子体条件会发生很大变化。因此,实施了理论上支持的校正光谱线强度的程序。这个程序可以将强度的分散度从67%降低到12%。校正后,随着纤维化的进展,LIBS信号显示钙强度增加了三倍。已知钙会增加纤维间隔中细胞外基质蛋白的交联。因此,我们的结果表明它是肝纤维化的关键参与者。

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