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J Biomed Opt. 2010 Mar-Apr;15(2):027011. doi: 10.1117/1.3374180.
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Fluorescence lifetime-based sensing and imaging.基于荧光寿命的传感与成像。
Sens Actuators B Chem. 1995 Oct;29(1-3):16-24. doi: 10.1016/0925-4005(95)01658-9. Epub 2000 Feb 4.
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Fluorescence spectroscopy of turbid media: Autofluorescence of the human aorta.浑浊介质的荧光光谱学:人体主动脉的自发荧光
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Fiber-optic bundle design for quantitative fluorescence measurement from tissue.用于从组织进行定量荧光测量的光纤束设计。
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Influence of the emission-reception geometry in laser-induced fluorescence spectra from turbid media.发射-接收几何结构对浑浊介质激光诱导荧光光谱的影响。
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Microscale enzymatic optical biosensors using mass transport limiting nanofilms. 2. Response modulation by varying analyte transport properties.使用传质受限纳米薄膜的微尺度酶促光学生物传感器。2. 通过改变分析物传输特性进行响应调制。
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8
Relationship between depth of a target in a turbid medium and fluorescence measured by a variable-aperture method.混浊介质中目标深度与可变孔径法测量的荧光之间的关系。
Opt Lett. 2002 Jan 15;27(2):104-6. doi: 10.1364/ol.27.000104.
9
Modeling of selective photon capture for collection of fluorescence emitted from dermally-implanted microparticle sensors.用于收集真皮植入微粒传感器发射荧光的选择性光子捕获建模。
Annu Int Conf IEEE Eng Med Biol Soc. 2007;2007:2972-5. doi: 10.1109/IEMBS.2007.4352953.
10
Microscale enzymatic optical biosensors using mass transport limiting nanofilms. 1. Fabrication and characterization using glucose as a model analyte.使用传质限制纳米膜的微尺度酶促光学生物传感器。1. 以葡萄糖作为模型分析物的制备与表征。
Anal Chem. 2007 Feb 15;79(4):1339-48. doi: 10.1021/ac061414z.

三维、多波长蒙卡模拟皮肤植入式发光传感器。

Three-dimensional, multiwavelength Monte Carlo simulations of dermally implantable luminescent sensors.

机构信息

Texas A&M University, Biomedical Engineering, College Station, Texas 77843-3120, USA.

出版信息

J Biomed Opt. 2010 Mar-Apr;15(2):027011. doi: 10.1117/1.3374180.

DOI:10.1117/1.3374180
PMID:20459285
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2874051/
Abstract

Dermally implanted luminescent sensors have been proposed for monitoring of tissue biochemistry, which has the potential to improve treatments for conditions such as diabetes and kidney failure. Effective in vivo monitoring via noninvasive transdermal measurement of emission from injected microparticles requires a matched optoelectronic system for excitation and collection of luminescence. We applied Monte Carlo modeling to predict the characteristics of output luminescence from microparticles in skin to facilitate hardware design. Three-dimensional, multiwavelength Monte Carlo simulations were used to determine the spatial and spectral distribution of the escaping luminescence for different implantation depths, excitation light source properties, particle characteristics, and particle packing density. Results indicate that the ratio of output emission to input excitation power ranged 10(-3) to 10(-6) for sensors at the upper and lower dermal boundaries, respectively, and 95% of the escaping emission photons induced by a 10-mm-diam excitation beam were confined within an 18-mm circle. Tightly packed sensor configurations yielded higher output intensity with fewer particles, even after luminophore concentration effects were removed. Most importantly, for the visible wavelengths studied, the ability to measure spectral changes in emission due to glucose changes was not significantly affected by absorption and scattering of tissue, which supports the potential to accurately track changes in luminescence of sensor implants that respond to the biochemistry of the skin.

摘要

已提出用于监测组织生物化学的经皮植入式发光传感器,这有可能改善糖尿病和肾衰竭等疾病的治疗效果。通过注射微颗粒的非侵入性透皮测量来实现有效的体内监测,需要一个匹配的光电系统来激发和收集发光。我们应用蒙特卡罗建模来预测皮肤中微颗粒的输出发光特性,以方便硬件设计。三维、多波长蒙特卡罗模拟用于确定不同植入深度、激发光源特性、颗粒特性和颗粒堆积密度下的逃逸发光的空间和光谱分布。结果表明,在上皮和真皮边界处的传感器的输出发射与输入激发功率的比值分别在 10(-3)到 10(-6)之间,并且由 10-mm 直径激发束诱导的 95%逃逸发射光子被限制在 18-mm 圆内。即使去除了发光体浓度的影响,紧密堆积的传感器配置也可以用更少的颗粒获得更高的输出强度。最重要的是,对于研究的可见波长,由于组织的吸收和散射,测量由于葡萄糖变化引起的发射光谱变化的能力没有受到显著影响,这支持了准确跟踪对皮肤生物化学做出反应的传感器植入物的发光变化的潜力。