超连续谱
材料科学
激光器
纳米载体
光学
荧光寿命成像显微镜
显微镜
荧光
穿透深度
激发
波长
光谱学
光电子学
纳米技术
物理
量子力学
光子晶体光纤
纳米颗粒
作者
Pierre Volz,Robert Brodwolf,Christian Zoschke,Rainer Haag,Monika Schäfer‐Korting,Ulrike Alexiev
标识
DOI:10.1515/zpch-2017-1050
摘要
Abstract We report here on a custom-built time-correlated single photon-counting (TCSPC)-based fluorescence lifetime imaging microscopy (FLIM) setup with a continuously tunable white-light supercontinuum laser combined with acousto-optical tunable filters (AOTF) as an excitation source for simultaneous excitation of multiple spectrally separated fluorophores. We characterized the wavelength dependence of the white-light supercontinuum laser pulse properties and demonstrated the performance of the FLIM setup, aiming to show the experimental setup in depth together with a biomedical application. We herein summarize the physical-technical parameters as well as our approach to map the skin uptake of nanocarriers using FLIM with a resolution compared to spectroscopy. As an example, we focus on the penetration study of indocarbocyanine-labeled dendritic core-multishell nanocarriers (CMS-ICC) into reconstructed human epidermis. Unique fluorescence lifetime signatures of indocarbocyanine-labeled nanocarriers indicate nanocarrier-tissue interactions within reconstructed human epidermis, bringing FLIM close to spectroscopic analysis.
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