| Literature DB >> 17152070 |
Alexander Ehlers1, Iris Riemann, Martin Stark, Karsten König.
Abstract
In vivo and in vitro multiphoton imaging was used to perform high resolution optical sectioning of human hair by nonlinear excitation of endogenous as well as exogenous fluorophores. Multiphoton fluorescence lifetime imaging (FLIM) based on time-resolved single photon counting and near-infrared femtosecond laser pulse excitation was employed to analyze the various fluorescent hair components. Time-resolved multiphoton imaging of intratissue pigments has the potential (i) to identify endogenous keratin and melanin, (ii) to obtain information on intrahair dye accumulation, (iii) to study bleaching effects, and (iv) to monitor the intratissue diffusion of pharmaceutical and cosmetical components along hair shafts.Entities:
Mesh:
Year: 2007 PMID: 17152070 DOI: 10.1002/jemt.20395
Source DB: PubMed Journal: Microsc Res Tech ISSN: 1059-910X Impact factor: 2.769