Collaborative Research in Biophotonics: Towards high-resolution, label-free molecular imaging in deep tissue via stimulated Raman excitation and ultrasound detection

生物光子学合作研究：通过受激拉曼激发和超声检测实现深层组织的高分辨率、无标记分子成像

• 批准号: 1250363
• 负责人: Vladislav Yakovlev
• 金额: $ 20万
• 依托单位: Texas A&M Engineering Experiment Station
• 依托单位国家: 美国
• 项目类别: Continuing Grant
• 财政年份: 2012
• 资助国家: 美国
• 起止时间: 2012-01-01 至 2015-08-31
• 项目状态: 已结题
• 来源: https://www.nsf.gov/awardsearch/showAward?AWD_ID=1250363&HistoricalAwards=false
• 关键词: Collaborative; Research; Biophotonics; Towards; resolution

1066776/1066562Zhang/YakovlevThe grand challenge of optical tissue imaging is the ability to penetrate deeply into tissue while preserving molecular specificity and high spatial resolution. The proposed project tackles this grand challenge by developing a novel imaging modality based on stimulated Raman excitation and detection of the nonlinearly induced photoacoustic waves. Referred to as stimulated Raman photoacoustic microscopy, the proposed modality combines chemical specificity through the molecularly selective stimulated Raman excitation with the deep penetration and high-resolution photoacoustic imaging. Compared with existing spontaneous and nonlinear Raman microscopic imaging, the maximum imaging depth is expected to be extended by at least one order of magnitude. Compared with existing photoacoustic imaging, the much needed molecular specificity is achieved without resorting to extrinsic molecular labeling.This project will extend the existing knowledge on how advanced spectroscopic tools can be successfully used for biomedical imaging. It lays the foundation to develop a stand-alone molecular imaging microscope, capable of providing high-resolution deep tissue imaging without external labels. In the proposed research, the mechanism of the photoacoustic generation under the stimulated Raman excitation will be investigated. The investigations focus on how the elastic scattering in tissue will affect the proposed imaging modality. Monte Carlo simulations will model the effect of dual wavelength, short-pulse light propagation in scattering medium. These results will direct the design of the optimal optical illumination geometry in the future prototyping of the proposed microscope. Quantitative experimental studies will be carried out following the guidance of the theoretical estimation and Monte Carlo simulation. The sensitivity of the photoacoustic detection will be improved by matching the signal bandwidth and employing novel ultrasonic detectors. In non-scattering media, the sensitivity of stimulated Raman photoacoustic detection will be experimentally quantified in the presence of background linear optical absorption, whose effect will be mitigated by wavelength and/or time-delay modulation.

1066776/1066562 Zhang/YakovlevThe grand challenge of optical tissue imaging is the ability to penetrate deep into tissue while preserving molecular specificity and high spatial resolution.该项目通过开发一种基于受激拉曼激发和非线性诱导光声波检测的新型成像模式来应对这一重大挑战。被称为受激拉曼光声显微镜，所提出的模式相结合的化学特异性，通过分子选择性的受激拉曼激发与深穿透和高分辨率的光声成像。与现有的自发和非线性拉曼显微成像相比，最大成像深度有望扩展至少一个数量级。与现有的光声成像技术相比，该技术不需要借助外部分子标记就能实现所需的分子特异性，这将扩展先进的光谱工具如何成功地用于生物医学成像的现有知识。它为开发一种独立的分子成像显微镜奠定了基础，能够在没有外部标记的情况下提供高分辨率的深层组织成像。本研究将探讨受激拉曼激发下的光声产生机制。调查的重点是如何在组织中的弹性散射将影响拟议的成像模式。蒙特卡罗模拟将模拟双波长，短脉冲光在散射介质中的传播效果。这些结果将指导在未来的原型所提出的显微镜的最佳光学照明几何形状的设计。在理论估算和蒙特卡罗模拟的指导下，进行定量的实验研究。光声探测的灵敏度将通过匹配信号带宽和采用新型的超声探测器来提高。在非散射介质中，受激拉曼光声检测的灵敏度将在存在背景线性光吸收的情况下实验量化，其影响将通过波长和/或时间延迟调制来减轻。