论文标题
生物成像应用的量子光学相干显微镜
Quantum optical coherence microscopy for bioimaging applications
论文作者
论文摘要
量子光相干断层扫描(QOCT)是一种基于从自发参数下调(SPDC)源获得的光子对量子干扰的光学分段。与等效的经典光学相干断层扫描(OCT)系统相比,QOCT的承诺来自两个量子限制的优势:2轴向分辨率增强以及分散取消。但是,由于需要长期的获取时间,该技术远非与当前的OCT设备竞争。在这里,我们一方面展示了一种量子光学相干显微镜(QOCM)技术,该技术旨在克服以前的QOCT实施的某些局限性,另一方面,另一方面对其进行了对代表样品的测试,包括具有制成的横向横向图案和金属涂层生物学标本的玻璃层。我们使用共线SPDC源,以便整个发射的光子对通量可能有助于测量以及多模式检测设计。我们采用米歇尔森干涉仪,将样品作为干涉仪臂之一放置为末端摩尔,而不是QOCT实施中使用的更典型的Hong-ou-Mandel。为了探测生物样品,我们通过将显微镜物镜放置在样品臂中,从米歇尔(Michelson)转变为Linnik干涉仪。在我们的设置中,当惰轮使用多模式光纤收集时,信号光子由ICCD摄像机检测到,从而通过单个轴向采集序列导致全场横向重建。有趣的是,我们的设置允许同时发生的OCT和QOCT痕量获取,前者的数量更高,后者具有量子限制优势的好处。我们希望我们目前的结果将代表朝着Qoct的实际适用性迈出的重要一步,例如在临床环境中。
Quantum-optical coherence tomography (QOCT) is an optical sectioning modality based on the quantum interference of photon pairs, obtained from a spontaneous parametric downconversion (SPDC) source. The promise of QOCT derives from two quantum-conferred advantages when compared to equivalent classical optical coherence tomography (OCT) systems: a factor of 2 axial resolution enhancement, as well as dispersion cancellation. However, the technique is far from being competitive with current OCT devices due to the long required acquisition times. Here, we on the one hand demonstrate a quantum optical coherence microscopy (QOCM) technique that is designed to overcome some of the limitations of previous QOCT implementations, and on the other hand test it on representative samples, including glass layers with manufactured transverse patterns and metal-coated biological specimens. We use a collinear SPDC source, so that the entire emitted photon pair flux may contribute to the measurements, together with a multi-mode detection design. We employ a Michelson interferometer with the sample placed as end-mirror in one of the interferometer arms, instead of the more typical Hong-Ou-Mandel used in QOCT implementations. In order to probe biological samples we transition from a Michelson to a Linnik interferometer by placing a microscope objective in the sample arm. In our setup, while the idler photon is collected with a multi-mode fiber, the signal photon is detected by an ICCD camera, leading to full-field transverse reconstruction through a single axial acquisition sequence. Interestingly, our setup permits concurrent OCT and QOCT trace acquisition, the former with greater counts and the latter with the benefit of quantum-conferred advantages. We hope that our current results will represent a significant step forward towards the actual applicability of QOCT, e.g. in clinical settings.