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使用白光超连续谱源对龋坏和完好牙齿结构进行时间相关单光子计数荧光寿命共聚焦成像。

Time-correlated single-photon counting fluorescence lifetime confocal imaging of decayed and sound dental structures with a white-light supercontinuum source.

作者信息

McConnell G, Girkin J M, Ameer-Beg S M, Barber P R, Vojnovic B, Ng T, Banerjee A, Watson T F, Cook R J

机构信息

Centre for Biophotonics, Strathclyde Institute of Pharmacy and Biomedical Sciences, University of Strathclyde, 27 Taylor Street, Glasgow, G4 0NR, UK.

出版信息

J Microsc. 2007 Feb;225(Pt 2):126-36. doi: 10.1111/j.1365-2818.2007.01724.x.

Abstract

We report the demonstration of time-correlated single-photon counting (TCSPC) fluorescence lifetime imaging (FLIM) to ex vivo decayed and healthy dentinal tooth structures, using a white-light supercontinuum excitation source. By using a 100 fs-pulsed Ti:Sapphire laser with a low-frequency chirp to pump a 30-cm long section of photonic crystal fibre, a ps-pulsed white-light supercontinuum was created. Optical bandpass interference filters were then applied to this broad-bandwidth source to select the 488-nm excitation wavelength required to perform TCSPC FLIM of dental structures. Decayed dentine showed significantly shorter lifetimes, discriminating it from healthy tissue and hard, stained and thus affected but non-infected material. The white-light generation source provides a flexible method of producing variable-bandwidth visible and ps-pulsed light for TCSPC FLIM. The results from the dental tissue indicate a potential method of discriminating diseased tissue from sound, but stained tissue, which could be of crucial importance in limiting tissue resection during preparation for clinical restorations.

摘要

我们报告了使用白光超连续谱激发源,对离体的龋坏和健康牙本质牙齿结构进行时间相关单光子计数(TCSPC)荧光寿命成像(FLIM)的演示。通过使用具有低频啁啾的100飞秒脉冲钛宝石激光器泵浦一段30厘米长的光子晶体光纤,产生了皮秒脉冲白光超连续谱。然后将光学带通干涉滤光片应用于该宽带光源,以选择对牙齿结构进行TCSPC FLIM所需的488纳米激发波长。龋坏牙本质显示出明显更短的寿命,将其与健康组织以及坚硬、染色但未感染的材料区分开来。白光产生源为TCSPC FLIM提供了一种产生可变带宽可见光和皮秒脉冲光的灵活方法。牙齿组织的结果表明,这是一种区分患病组织与健康但染色组织的潜在方法,这在临床修复准备过程中限制组织切除可能至关重要。

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