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厚散射样品中的外差模式层析定量相位成像。

Epi-mode tomographic quantitative phase imaging in thick scattering samples.

作者信息

Ledwig Patrick, Robles Francisco E

机构信息

Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, Georgia 30332, USA.

出版信息

Biomed Opt Express. 2019 Jun 26;10(7):3605-3621. doi: 10.1364/BOE.10.003605. eCollection 2019 Jul 1.

Abstract

Quantitative phase imaging (QPI) is an important tool in biomedicine that allows for the microscopic investigation of live cells and other thin, transparent samples. Importantly, this technology yields access to the cellular and sub-cellular structure and activity at nanometer scales without labels or dyes. Despite this unparalleled ability, QPI's restriction to relatively thin samples severely hinders its versatility and overall utility in biomedicine. Here we overcome this significant limitation of QPI to enable the same rich level of quantitative detail in thick scattering samples. We achieve this by first illuminating the sample in an epi-mode configuration and using multiple scattering within the sample-a hindrance to conventional transmission imaging used in QPI-as a source of transmissive illumination from within. Second, we quantify phase via deconvolution by modeling the transfer function of the system based on the ensemble average angular distribution of light illuminating the sample at the focal plane. This technique packages the quantitative, real-time sub-cellular imaging capabilities of QPI into a flexible configuration, opening the door for truly non-invasive, label-free, tomographic quantitative phase imaging of unaltered thick, scattering specimens. Images of controlled scattering phantoms, blood in collection bags, cerebral organoids and freshly excised whole mouse brains are presented to validate the approach.

摘要

定量相成像(QPI)是生物医学中的一种重要工具,可用于对活细胞及其他薄的透明样本进行微观研究。重要的是,该技术无需标记或染料就能在纳米尺度上获取细胞和亚细胞结构及活性信息。尽管具备这种无与伦比的能力,但QPI对相对薄样本的限制严重阻碍了其在生物医学中的通用性和整体实用性。在此,我们克服了QPI的这一重大局限,以便在厚散射样本中实现同样丰富的定量细节水平。我们通过以下方式实现这一点:首先以落射模式配置照射样本,并利用样本内的多次散射——这是QPI中传统透射成像的一个障碍——作为来自样本内部的透射照明源。其次,我们通过基于焦平面上照射样本的光的总体平均角分布对系统传递函数进行建模,经由去卷积来量化相位。这项技术将QPI的定量、实时亚细胞成像能力整合到一个灵活的配置中,为对未改变的厚散射标本进行真正的非侵入性、无标记断层定量相成像打开了大门。文中展示了受控散射体模、采血袋中的血液、脑类器官和新鲜切除的完整小鼠大脑的图像,以验证该方法。

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Epi-mode tomographic quantitative phase imaging in thick scattering samples.厚散射样品中的外差模式层析定量相位成像。
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