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Light Sci Appl. 2018 May 4;7:17179. doi: 10.1038/lsa.2017.179. eCollection 2018.
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Lissajous Scanning Two-photon Endomicroscope for In vivo Tissue Imaging.Lissajous 扫描双光子内窥显微镜用于活体组织成像。
Sci Rep. 2019 Mar 5;9(1):3560. doi: 10.1038/s41598-019-38762-w.
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Smart scanning for low-illumination and fast RESOLFT nanoscopy in vivo.智能扫描,用于体内低照明和快速 RESOLFT 纳米显微镜。
Nat Commun. 2019 Feb 1;10(1):556. doi: 10.1038/s41467-019-08442-4.
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A robust and versatile platform for image scanning microscopy enabling super-resolution FLIM.用于图像扫描显微镜的强大且多功能平台,可实现超分辨率 FLIM。
Nat Methods. 2019 Feb;16(2):175-178. doi: 10.1038/s41592-018-0291-9. Epub 2019 Jan 14.
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Quantitative spatial analysis of haematopoiesis-regulating stromal cells in the bone marrow microenvironment by 3D microscopy.通过三维显微镜对骨髓微环境中的造血调控基质细胞进行定量空间分析。
Nat Commun. 2018 Jun 28;9(1):2532. doi: 10.1038/s41467-018-04770-z.
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Multicolor quantitative confocal imaging cytometry.多色定量共聚焦成像细胞计量术。
Nat Methods. 2018 Jan;15(1):39-46. doi: 10.1038/nmeth.4503. Epub 2017 Nov 13.
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Fast wide-volume functional imaging of engineered in vitro brain tissues.快速大容量功能成像的工程体外脑组织。
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8
Enhanced volumetric imaging in 2-photon microscopy via acoustic lens beam shaping.基于声透镜光束整形的双光子显微镜增强体积成像。
J Biophotonics. 2018 Feb;11(2). doi: 10.1002/jbio.201700050. Epub 2017 Jul 25.
9
Quantitative mRNA imaging throughout the entire Drosophila brain.全果蝇大脑的定量 mRNA 成像。
Nat Methods. 2017 Jul;14(7):703-706. doi: 10.1038/nmeth.4309. Epub 2017 Jun 5.
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Smooth 2D manifold extraction from 3D image stack.从 3D 图像堆叠中提取平滑的 2D 流形。
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具有可调时空分辨率的体积利萨如共聚焦显微镜。

Volumetric Lissajous confocal microscopy with tunable spatiotemporal resolution.

作者信息

Deguchi Takahiro, Bianchini Paolo, Palazzolo Gemma, Oneto Michele, Diaspro Alberto, Duocastella Martí

机构信息

Nanoscopy & NIC@IIT, Center for Human Technologies, Istituto Italiano di Tecnologia, via E. Melen 83B, 16152 Genoa, Italy.

Enhanced Regenerative Medicine, Istituto Italiano di Tecnologia, via Morego 30, 16163 Genoa, Italy.

出版信息

Biomed Opt Express. 2020 Oct 13;11(11):6293-6310. doi: 10.1364/BOE.400777. eCollection 2020 Nov 1.

DOI:10.1364/BOE.400777
PMID:33282491
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7687945/
Abstract

Dynamic biological systems present challenges to existing three-dimensional (3D) optical microscopes because of their continuous temporal and spatial changes. Most techniques are rigid in adapting the acquisition parameters over time, as in confocal microscopy, where a laser beam is sequentially scanned at a predefined spatial sampling rate and pixel dwell time. Such lack of tunability forces a user to provide scan parameters, which may not be optimal, based on the best assumption before an acquisition starts. Here, we developed volumetric Lissajous confocal microscopy to achieve unsurpassed 3D scanning speed with a tunable sampling rate. The system combines an acoustic liquid lens for continuous axial focus translation with a resonant scanning mirror. Accordingly, the excitation beam follows a dynamic Lissajous trajectory enabling sub-millisecond acquisitions of image series containing 3D information at a sub-Nyquist sampling rate. By temporal accumulation and/or advanced interpolation algorithms, the volumetric imaging rate is selectable using a post-processing step at the desired spatiotemporal resolution for events of interest. We demonstrate multicolor and calcium imaging over volumes of tens of cubic microns with 3D acquisition speeds of 30 Hz and frame rates up to 5 kHz.

摘要

动态生物系统由于其持续的时空变化,给现有的三维(3D)光学显微镜带来了挑战。大多数技术在随时间调整采集参数方面较为僵化,例如在共聚焦显微镜中,激光束以预定义的空间采样率和像素驻留时间进行顺序扫描。这种缺乏可调性的情况迫使用户在采集开始前,基于最佳假设提供可能并非最优的扫描参数。在此,我们开发了体积型李萨如共聚焦显微镜,以实现具有可调采样率的无与伦比的3D扫描速度。该系统将用于连续轴向焦点平移的声学液体透镜与共振扫描镜相结合。因此,激发光束遵循动态李萨如轨迹,能够以亚奈奎斯特采样率在亚毫秒级采集包含3D信息的图像序列。通过时间累积和/或先进的插值算法,可使用后处理步骤以感兴趣事件所需的时空分辨率选择体积成像速率。我们展示了在数十立方微米体积上的多色和钙成像,3D采集速度为30 Hz,帧率高达5 kHz。