Samaei Saeed, Nowacka Klaudia, Gerega Anna, Pastuszak Żanna, Borycki Dawid
Institute of Physical Chemistry, Polish Academy of Sciences, Kasprzaka 44/52, 01-224 Warsaw, Poland.
Nalecz Institute of Biocybernetics and Biomedical Engineering, Polish Academy of Sciences, Ks. Trojdena 4, 02-109, Warsaw, Poland.
Biomed Opt Express. 2022 Oct 12;13(11):5753-5774. doi: 10.1364/BOE.472643. eCollection 2022 Nov 1.
Interferometric near-infrared spectroscopy (iNIRS) is an optical method that noninvasively measures the optical and dynamic properties of the human brain . However, the original iNIRS technique uses single-mode fibers for light collection, which reduces the detected light throughput. The reduced light throughput is compensated by the relatively long measurement or integration times (∼1 sec), which preclude monitoring of rapid blood flow changes that could be linked to neural activation. Here, we propose parallel interferometric near-infrared spectroscopy (πNIRS) to overcome this limitation. In πNIRS we use multi-mode fibers for light collection and a high-speed, two-dimensional camera for light detection. Each camera pixel acts effectively as a single iNIRS channel. So, the processed signals from each pixel are spatially averaged to reduce the overall integration time. Moreover, interferometric detection provides us with the unique capability of accessing complex information (amplitude and phase) about the light remitted from the sample, which with more than 8000 parallel channels, enabled us to sense the cerebral blood flow with only a 10 msec integration time (∼100x faster than conventional iNIRS). In this report, we have described the theoretical foundations and possible ways to implement πNIRS. Then, we developed a prototype continuous wave (CW) πNIRS system and validated it in liquid phantoms. We used our CW πNIRS to monitor the pulsatile blood flow in a human forearm . Finally, we demonstrated that CW πNIRS could monitor activation of the prefrontal cortex by recording the change in blood flow in the forehead of the subject while he was reading an unknown text.
干涉近红外光谱技术(iNIRS)是一种光学方法,可无创测量人脑的光学和动态特性。然而,原始的iNIRS技术使用单模光纤进行光收集,这降低了检测到的光通量。光通量的降低通过相对较长的测量或积分时间(约1秒)来补偿,这使得无法监测与神经激活相关的快速血流变化。在此,我们提出并行干涉近红外光谱技术(πNIRS)以克服这一限制。在πNIRS中,我们使用多模光纤进行光收集,并使用高速二维相机进行光检测。每个相机像素有效地充当一个单独的iNIRS通道。因此,来自每个像素的处理信号在空间上进行平均以减少总体积分时间。此外,干涉检测为我们提供了获取有关样品发射光的复杂信息(幅度和相位)的独特能力,通过8000多个并行通道,使我们能够仅用10毫秒的积分时间(比传统iNIRS快约100倍)来感知脑血流量。在本报告中,我们描述了πNIRS的理论基础和实现方法。然后,我们开发了一个连续波(CW)πNIRS系统原型,并在液体模型中对其进行了验证。我们使用我们的CW πNIRS监测人体前臂的搏动性血流。最后,我们通过记录受试者阅读未知文本时前额血流的变化,证明了CW πNIRS可以监测前额叶皮层的激活情况。