Open AccessDifferentiation of fibrotic liver tissue using laser-induced breakdown spectroscopy
Author(s) -
E. Terán-Hinojosa,
H. Sobral,
Celia SánchezPérez,
Adolfo Pérez-García,
Nathalie Alemán-García,
Joselín Hernández-Ruiz
Publication year - 2017
Publication title -
biomedical optics express
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.362
H-Index - 86
ISSN - 2156-7085
DOI - 10.1364/boe.8.003816
Subject(s) - laser induced breakdown spectroscopy , cirrhosis , fibrosis , hepatic fibrosis , laser , extracellular matrix , pathology , materials science , biomedical engineering , liver biopsy , spectroscopy , optical coherence tomography , medicine , optics , biopsy , chemistry , radiology , physics , biochemistry , quantum mechanics
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.