Sala Federico, Paiè Petra, Candeo Alessia, Ceccarelli Francesco, Osellame Roberto, Bassi Andrea, Bragheri Francesca
Istituto di Fotonica e Nanotecnologie, Consiglio Nazionale delle Ricerche, Piazza Leonardo da Vinci, 32, Milan, 20133, Italy.
Dipartimento di Fisica, Politecnico di Milano, Piazza Leonardo da Vinci, 32, Milan, 20133, Italy.
Sci Rep. 2025 Apr 8;15(1):11950. doi: 10.1038/s41598-025-93118-x.
In recent years imaging flow cytometry (IFC) is gaining increasing attention as it combines the characteristics of conventional flow cytometry with optical microscopy techniques, allowing for high-throughput, multi-parameter screening of single cell populations. In the field of biology, the always increasing demand for high content morphological and spatial information led to the development of systems for volumetric imaging. However, current 3D IFC systems are often limited by the incompatibility with available microfluidic devices or by instrumental complexity that might lead to optical misalignment or mechanical instabilities in day-by-day operation. To this end, here we demonstrate the importance of advancing the laser fabrication technique by reporting on a fully integrated optofluidic platform composed of a borosilicate glass chip encompassing reconfigurable integrated photonic circuits for patterned light generation, bonded to a fused silica glass chip incorporating cylindrical hollow lenses, for light-sheet illumination, perfectly aligned to a microchannel where the sample under investigation flows. The system is capable of high-resolution imaging flow cytometry by implementing structured light sheet microscopy in a heterogeneously integrated platform with unprecedented stability. All the components are realized by femtosecond laser irradiation followed by chemical etching. The extreme level of integration permitted by the advanced optimization of the laser fabrication technique allowed the reduction of the assembled components and the absence of moving parts, thus ensuring durable alignment as well as mechanical and thermal stability both in short and long-term operation of the device, for the automated fluorescence signal acquisition during the sample flow.
近年来,成像流式细胞术(IFC)越来越受到关注,因为它结合了传统流式细胞术的特点和光学显微镜技术,能够对单细胞群体进行高通量、多参数筛选。在生物学领域,对高含量形态学和空间信息的需求不断增加,促使了体积成像系统的发展。然而,目前的3D IFC系统往往受到与现有微流控设备不兼容的限制,或者受到仪器复杂性的限制,这可能导致日常操作中的光学对准误差或机械不稳定性。为此,我们在此展示了推进激光制造技术的重要性,报道了一个完全集成的光流控平台,该平台由一个硼硅酸盐玻璃芯片组成,其中包含用于产生图案光的可重构集成光子电路,与一个包含圆柱形空心透镜的熔融石英玻璃芯片键合,用于光片照明,与样品流动的微通道完美对准。该系统通过在具有前所未有的稳定性的异构集成平台上实施结构光片显微镜,能够进行高分辨率成像流式细胞术。所有组件均通过飞秒激光照射和化学蚀刻实现。激光制造技术的先进优化允许的极高集成度减少了组装组件的数量,并且没有移动部件,从而确保了在设备的短期和长期操作中都具有持久的对准以及机械和热稳定性,以便在样品流动期间自动采集荧光信号。