Review: Clinical in vivo multiphoton FLIM tomography

被引:44
|
作者
Koenig, Karsten [1 ,2 ]
机构
[1] Saarland Univ, Dept Biophoton & Laser Technol, Campus A5-1, D-66123 Saarbrucken, Germany
[2] JenLab GmbH, Johann Hittorf Str 8, D-12489 Berlin, Germany
来源
基金
欧洲研究理事会;
关键词
TCSPC; FLIM; multiphoton microscopy; multiphoton tomography; skin; BASAL-CELL CARCINOMA; HUMAN SKIN; LASER TOMOGRAPHY; FLUORESCENCE MICROSCOPY; LIFETIME MEASUREMENTS; OPTICAL BIOPSY; AUTOFLUORESCENCE; RESOLUTION; QUANTIFICATION; SPECTROSCOPY;
D O I
10.1088/2050-6120/ab8808
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Fluorescence Lifetime Imaging (FLIM) in life sciences based on ultrashort laser scanning microscopy and time-correlated single photon counting (TCSPC) started 30 years ago in Jena/East-Germany. One decade later, first two-photon FLIM images of a human finger were taken with a lab microscope based on a tunable femtosecond Ti:sapphire laser. In 2002/2003, first clinical non-invasive two-photon FLIM studies on patients with dermatological disorders were performed using a novel multiphoton tomograph. Current in vivo two-photon FLIM studies on human subjects are based on TCSPC and focus on (i) patients with skin inflammation and skin cancer as well as brain tumors, (ii) cosmetic research on volunteers to evaluate anti-ageing cremes, (iii) pharmaceutical research on volunteers to gain information on in situ pharmacokinetics, and (iv) space medicine to study non-invasively skin modifications on astronauts during long-term space flights. Two-photon FLIM studies on volunteers and patients are performed with multiphoton FLIM tomographs using near infrared femtosecond laser technology that provide rapid non-invasive and label-free intratissue autofluorescence biopsies with picosecond temporal resolution.
引用
收藏
页数:11
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