开发用于癌症治疗实时荧光显微镜的无线图像传感器

Rozhan Rabbani;Hossein Najafiaghdam;Micah Roschelle;Efthymios Philip Papageorgiou;Biqi Rebekah Zhao;Mohammad Meraj Ghanbari;Rikky Muller;Vladimir Stojanović;Mekhail Anwar
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摘要

我们介绍了一种毫米大小的超声波供电无透镜 CMOS 图像传感器,这是无线荧光显微镜技术的一个进步。获取组织内的生物信息有可能为包括癌症治疗在内的多种疾病的诊断和治疗提供指导。目前的临床成像技术在连续获取图像方面存在局限性,而且缺乏无线兼容性,而这种信息与临床成像技术相结合,可以改善对组织深层多细胞集群的连续检测。拟议的平台包含一个 2.4×4.7 平方毫米的集成电路(IC)(台积电 0.18 微米制造)、一个微型激光二极管(μLD)、一个压电陶瓷和片外存储电容器。集成电路由一个基于电容跨阻放大器的 36×40 像素阵列、通过超声波进行的无线电源管理和通信以及激光驱动器组成,全部由一个有限状态机控制。压电陶瓷从 2 厘米深的声波中获取能量,为集成电路供电,并通过反向散射每帧传输 11.5 kb。在充电过程中,片外电容器会储存电荷,以便在成像过程中提供 78 mW μLD 的高功率。通过对 CD8 T 细胞(癌症免疫反应的指标)的分布进行成像,证明了成像前端的概念,体内外功能性免疫系统(BL6 小鼠)淋巴结对结直肠癌的免疫反应与荧光显微镜的结果一致。在 32 毫秒曝光时间和 389 毫秒超声反向散射条件下检测美国空军分辨率目标上 140 μm 的特征,验证了系统的整体性能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Toward a Wireless Image Sensor for Real-Time Fluorescence Microscopy in Cancer Therapy
We present a mm-sized, ultrasonically powered lensless CMOS image sensor as a progress towards wireless fluorescence microscopy. Access to biological information within the tissue has the potential to provide insights guiding diagnosis and treatment across numerous medical conditions including cancer therapy. This information, in conjunction with current clinical imaging techniques that have limitations in obtaining images continuously and lack wireless compatibility, can improve continual detection of multicell clusters deep within tissue. The proposed platform incorporates a 2.4 × 4.7 mm 2 integrated circuit (IC) fabricated in TSMC 0.18 µm, a micro laser diode (µLD), a single piezoceramic and off-chip storage capacitors. The IC consists of a 36 × 40 array of capacitive trans-impedance amplifier-based pixels, wireless power management and communication via ultrasound and a laser driver all controlled by a Finite State Machine. The piezoceramic harvests energy from the acoustic waves at a depth of 2 cm to power up the IC and transfer 11.5 kbits/frame via backscattering. During Charge-Up, the off-chip capacitor stores charge to later supply a high-power 78 mW µLD during Imaging . Proof of concept of the imaging front end is shown by imaging distributions of CD8 T-cells, an indicator of the immune response to cancer, ex vivo, in the lymph nodes of a functional immune system (BL6 mice) against colorectal cancer consistent with the results of a fluorescence microscope. The overall system performance is verified by detecting 140 µm features on a USAF resolution target with 32 ms exposure time and 389 ms ultrasound backscattering.
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