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  4. Human hepatocellular carcinoma diagnosis by multiphoton autofluorescence microscopy
 
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Human hepatocellular carcinoma diagnosis by multiphoton autofluorescence microscopy

Journal
Progress in Biomedical Optics and Imaging - Proceedings of SPIE
Journal Volume
7555
Pages
75551L
Date Issued
2010
Author(s)
Sun, T.-L.
Lee, Hsuan-Shu et al.  
Sung, M.-C.
Chen, H.-C.
Yang, C.-H.
Hovhannisyan, V.
Chiou, L.-L.
WEI-CHOU LIN  
GUAN-TARN HUANG  
Kim, K.-H.
So, P.T.C.
Lin, C.-J.
Lee, H.-S.
CHEN-YUAN DONG  
DOI
10.1117/12.843157
URI
https://www.scopus.com/inward/record.uri?eid=2-s2.0-77951702676&doi=10.1117%2f12.843157&partnerID=40&md5=e25e5db1dbae2d86f5db017eb6ba28d0
https://scholars.lib.ntu.edu.tw/handle/123456789/596166
Abstract
Conventionally, the diagnosis of hepatocellular carcinoma (HCC) is performed by qualitative examination of histopathological specimens, which takes times for sample preparation in fixation, section and stain. Our objective is to demonstrate an effective and efficient approach to apply multiphoton microscopy imaging the HCC specimens, with the advantages of being optical section, label-free, subcellular resolution, minimal invasiveness, and the acquisition of quantitative information at the same time. The imaging modality of multiphoton autofluorescence (MAF) was used for the qualitative imaging and quantitative analysis of HCC of different grades under ex-vivo, label-free conditions. We found that while MAF is effective in identifying cellular architecture in the liver specimens, and obtained quantitative parameters in characterizing the disease. Our results demonstrates the capability of using tissue quantitative parameters of multiphoton autofluorescence (MAF), the nuclear number density (NND), and nuclear-cytoplasmic ratio (NCR) for tumor discrimination and that this technology has the potential in clinical diagnosis of HCC and the in-vivo investigation of liver tumor development in animal models. ? 2010 Copyright SPIE - The International Society for Optical Engineering.
SDGs

[SDGs]SDG3

Other Subjects
Animal model; Autofluorescence; Cellular architecture; Clinical diagnosis; Ex-vivo; Hepatocellular carcinoma; Imaging modality; In-vivo; Invasiveness; Label free; Liver specimens; Liver tumors; Multi-photon microscopy; Multiphotons; Number density; Optical sections; Qualitative imaging; Quantitative analysis; Quantitative information; Quantitative parameters; Sample preparation; Subcellular resolution; Computer crime; Labels; Liver; Tumors; Diagnosis
Type
conference paper

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