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本文引用的文献

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light dosimetry for HPPH-mediated pleural PDT.用于HPPH介导的胸膜光动力疗法的光剂量测定
Proc SPIE Int Soc Opt Eng. 2010 Mar 4;7551. doi: 10.1117/12.851514.
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A review of in-vivo optical properties of human tissues and its impact on PDT.人体组织的体内光学特性及其对 PDT 的影响综述。
J Biophotonics. 2011 Nov;4(11-12):773-87. doi: 10.1002/jbio.201100062.
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Implicit and explicit dosimetry in photodynamic therapy: a New paradigm.光动力疗法中的内隐和外显剂量学:一种新范例。
Lasers Med Sci. 1997 Oct;12(3):182-99. doi: 10.1007/BF02765099.
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Light distributions from point, line and plane sources for photochemical reactions and fluorescence in turbid biological tissues.用于浑浊生物组织中光化学反应和荧光的点、线和面光源的光分布。
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Optical properties of Intralipid: a phantom medium for light propagation studies.英脱利匹特的光学特性:用于光传播研究的模拟介质
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用于胸膜光动力疗法的光动力疗法剂量测定法

PDT dose dosimetry for pleural photodynamic therapy.

作者信息

Sharikova Anna V, Finlay Jarod C, Liang Xing, Zhu Timothy C

机构信息

Dept. of Radiation Oncology, University of Pennsylvania, 3400 Civic Center Blvd, Philadelphia, PA USA 19104.

出版信息

Proc SPIE Int Soc Opt Eng. 2013 Feb 2;8568. doi: 10.1117/12.2005198.

DOI:10.1117/12.2005198
PMID:25999645
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4437732/
Abstract

PDT dose is the product of the photosensitizer concentration and the light fluence in target tissue. Although existing systems are capable of measuring the light fluence , the concurrent measurement of photosensitizer in the treated tissue so far has been lacking. We have developed and tested a new method to simultaneously acquire light dosimetry and photosensitizer fluorescence data via the same isotropic detector, employing treatment light as the excitation source. A dichroic beamsplitter is used to split light from the isotropic detector into two fibers, one for light dosimetry, the other, after the 665 nm treatment light is removed by a band-stop filter, to a spectrometer for fluorescence detection. The light fluence varies significantly during treatment because of the source movement. The fluorescence signal is normalized by the light fluence measured at treatment wavelength. We have shown that the absolute photosensitizer concentration can be obtained by an optical properties correction factor and linear spectral fitting. Tissue optical properties are determined using an absorption spectroscopy probe immediately before PDT at the same sites. This novel method allows accurate real-time determination of delivered PDT dose using existing isotropic detectors, and may lead to a considerable improvement of PDT treatment quality compared to the currently employed systems. Preliminary data in patient studies is presented.

摘要

光动力疗法(PDT)剂量是光敏剂浓度与靶组织中光通量的乘积。尽管现有系统能够测量光通量,但迄今为止,仍缺乏对治疗组织中光敏剂的同步测量。我们开发并测试了一种新方法,通过同一个各向同性探测器,以治疗光作为激发源,同时获取光剂量测定和光敏剂荧光数据。使用一个二向色分束器将来自各向同性探测器的光分成两根光纤,一根用于光剂量测定,另一根在通过带阻滤波器去除665nm治疗光后,连接到光谱仪进行荧光检测。由于光源移动,治疗过程中光通量会显著变化。荧光信号通过在治疗波长处测量的光通量进行归一化。我们已经表明,通过光学性质校正因子和线性光谱拟合可以获得绝对光敏剂浓度。在进行PDT之前,立即在相同部位使用吸收光谱探头测定组织光学性质。这种新方法能够使用现有的各向同性探测器准确实时测定所给予的PDT剂量,与目前使用的系统相比,可能会显著提高PDT治疗质量。文中给出了患者研究的初步数据。