新型生物传感器检测大脑深处的光

Brain-X Pub Date : 2023-03-21 DOI:10.1002/brx2.3
Lei Luo, Dandan Yang, Yu Yang
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引用次数: 0

摘要

近年来,生物传感器领域在荧光传感器的开发方面取得了重大进展,包括量子点、1上转换纳米颗粒、2和荧光蛋白,3用于监测生命系统中信息的生成。可以通过向这些传感器照射激光来观察这些传感器的荧光。然而,传统的荧光传感器对深层组织中的信号成像的能力有限,因为大多数光在穿透组织时被吸收或散射。为了应对这一挑战,Jasanoff领导的一个团队开发了一种新型传感器,可以将光转换为不受吸收或散射影响的磁信号。这使得光探测器的响应可以使用磁共振成像(MRI;图1)进行可视化。4这种传感器的开发对提高我们对深层组织信息处理的理解具有重大潜力。为了制造光敏MRI探针,将磁性颗粒封装在光响应性偶氮苯缀合的脂质体(称为light LisNRs)中。5通过调整脂质双层分子的组成和比例,这些脂质体纳米颗粒可以根据光暴露的类型从可渗透变为不可渗透。这种特性允许对Light LisNR的MRI对比度进行调制,并有助于优化可切换的纵向弛豫时间(T1)。具体地,在暴露于紫外线(UV)光时,light LisNRs变得对水更具渗透性,导致磁性颗粒和水之间的强相互作用,从而产生强MRI信号。相反,暴露于蓝光导致light LisNR变得不透水,导致缺乏可检测的MRI信号。优化后的Light LisNR可能用于绘制活体动物的光分布图。当这些纳米颗粒被注射到活体大鼠大脑中时,它们通过对流有效地在大脑中扩散,磁共振信号的变化就是明证。探针表现出非凡的光敏感性,这可以通过蓝色和紫外线照射下磁弛豫的变化来证明。与初始基线相比,探针对紫外线和蓝光的平均MRI信号表现出显著差异,并且在重复光周期期间观察到的光响应的时间特征是一致的。Light LisNRs在大鼠大脑中的稳定表现表明,它们适合于定量测量组织中的光强度分布。此外,研究人员使用了一个由光束扩展函数和均匀光子扩散项组成的混合模型来拟合实验数据,并生成了植入大脑纹状体附近的光纤发射的光分布的定量图。这些结果突出了优化的Light LisNR在绘制活体动物中的光分布图方面的潜力。总之,本研究描述了一种新型传感器的设计及其应用,阐明了光在光学不透明环境中的传播。该传感器利用脂质体渗透性的光调制来增强造影剂分子产生的对比度,从而改善MRI的可视化。这项工作的结果证明了Light LisNRs作为光子检测的通用工具的潜力,并突出了通过调整作用光谱、吸收截面和造影剂包装参数进行进一步优化的机会。这里概述的传感方法有望在未来开发能够检测光以外刺激的MRI探针,如大脑中的神经化学物质或其他分子物种。此外,该传感器可以作为一种有价值的工具,用于监测正在接受光疗法的患者,包括使用激光消融癌症细胞的光动力疗法。雷洛:概念化、形象化、写作——初稿;杨丹丹:写作——评论与评论;编辑;于洋:概念化、资金获取、写作评论与实践;编辑。作者声明没有利益冲突。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

New biosensors detect light deep inside the brain

New biosensors detect light deep inside the brain

In recent years, the field of biosensors has seen significant advances in the development of fluorescent sensors, including quantum dots,1 upconversion nanoparticles,2 and fluorescent proteins,3 to monitor the generation of information in living systems. The fluorescence of these sensors can be observed by shining a laser at them. However, conventional fluorescent sensors are limited in their ability to image signals in deep tissues because most of the light is absorbed or scattered as it penetrates the tissue. To address this challenge, a team led by Jasanoff developed a novel sensor that converts light into a magnetic signal that is unaffected by absorption or scattering. This allows the response of the light detector to be visualized using magnetic resonance imaging (MRI; Figure 1).4 The development of this sensor has significant potential to improve our understanding of information processing in deep tissues.

To fabricate the photosensitive MRI probe, magnetic particles were encapsulated in light-responsive azobenzene-conjugated liposomes (called Light-LisNRs).5 By adjusting the composition and proportion of the lipid bilayer molecules, these liposome nanoparticles can switch from being permeable to being impenetrable, depending on the type of light exposure. This property allowed modulation of the MRI contrast of the Light-LisNRs and facilitated the optimization of the switchable longitudinal relaxation time (T1). Specifically, upon exposure to ultraviolet (UV) light, the Light-LisNRs became more permeable to water, resulting in a strong interaction between the magnetic particles and water and thereby producing strong MRI signals. Conversely, exposure to blue light caused the Light-LisNRs to become impermeable to water, resulting in the lack of a detectable MRI signal.

The optimized Light-LisNRs could potentially be used to map light distribution in live animals. When these nanoparticles were injected into the living rat brain, they effectively diffused through the brain by convection, as evidenced by changes in the magnetic resonance signal. The probes exhibited exceptional light sensitivity, which could be demonstrated by changes in magnetic relaxation under blue and UV irradiation. Relative to the initial baseline, the probes showed significant differences in the mean MRI signals in response to UV and blue light, and the temporal characteristics of the light response observed during repeated photoperiods were consistent.

The steady performance of Light-LisNRs in the rat brain suggests that they are suitable for the quantitative measurement of the light intensity distribution in tissues. In addition, the researchers used a hybrid model consisting of a beam spreading function combined with a homogeneous photon diffusion term to fit the experimental data and produced a quantitative map of the distribution of light emitted by the optical fiber implanted near the brain's striatum. These results highlight the potential of the optimized Light-LisNRs in mapping the distribution of light in living animals.

In summary, this study describes the design of a novel sensor and its application elucidating light propagation in optically opaque environments. The sensor exploits the photomodulation of liposomal permeability to enhance the contrast produced by contrast agent molecules, leading to improved visualization in MRI. The results of this work demonstrate the potential of Light-LisNRs as a versatile tool for photon detection and highlight opportunities for further optimization through adjustments to action spectra, absorption cross sections, and contrast agent packaging parameters. The sensing approach outlined here holds promise for the future development of MRI probes capable of detecting stimuli beyond light, such as neurochemicals or other molecular species in the brain. In addition, the sensor may serve as a valuable tool for monitoring patients undergoing light-based therapies, including photodynamic therapy, which uses lasers to ablate cancer cells.

Lei Luo: Conceptualization, Visualization, Writing - Original draft; Dandan Yang: Writing - Reviewing & Editing; Yu Yang: Conceptualization, Funding Acquisition, Writing - Reviewing & Editing.

The authors declare no conflicts of interest.

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