Report on fluorescence lifetime imaging using multiphoton laser scanning microscopy targeting sentinel lymph node diagnostics

被引:5
作者
James, Jeemol [1 ]
Kantere, Despoina [2 ]
Enger, Jonas [3 ]
Siarov, Jan [4 ]
Wennberg, Ann Marie [2 ]
Ericson, Marica B. [1 ]
机构
[1] Univ Gothenburg, Dept Chem & Mol Biol, Biomed Photon Grp, Gothenburg, Sweden
[2] Univ Gothenburg, Inst Clin Sci, Dept Dermatol & Venereol, Gothenburg, Sweden
[3] Univ Gothenburg, Dept Phys, Gothenburg, Sweden
[4] Univ Gothenburg, Dept Pathol, Gothenburg, Sweden
基金
瑞典研究理事会;
关键词
malignant melanoma; sentinel lymph node; multiphoton microscopy; fluorescence lifetime imaging; autofluorescence; HEMOGLOBIN FLUORESCENCE; MELANOMA; BIOPSY; TOMOGRAPHY; ACCURACY; CONTRAST; CANCER; FLIM;
D O I
10.1117/1.JBO.25.7.071204
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Significance: Sentinel lymph node (SLN) biopsy is an important method for metastasis staging in, e.g., patients with malignant melanoma. Tools enabling prompt histopathological analysis are expected to facilitate diagnostics; optical technologies are explored for this purpose. Aim: The objective of this exploratory study was to investigate the potential of adopting multi-photon laser scanning microscopy (MPM) together with fluorescence lifetime analysis (FLIM) for the examination of lymph node (LN) tissue ex vivo. Approach: Five LN tissue samples (three metastasis positive and two negative) were acquired from a biobank comprising tissues from melanoma patients. Tissues were deparaffinized and subjected to MPM-FLIM using an experimental MPM set-up equipped with a time correlated single photon counting module enabling FLIM. Results: The data confirm that morphological features similar to conventional histology were observed. In addition, FLIM analysis revealed elevated morphological contrast, particularly for discriminating between metastatic cells, lymphocytes, and erythrocytes. Conclusions: Taken together, the results from this investigation show promise for adopting MPM-FLIM in the context of SLN diagnostics and encourage further translational studies on fresh tissue samples. (C) The Authors. Published by SPIE under a Creative Commons Attribution 4.0 Unported License.
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页数:8
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