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用于单细胞操作的加工多芯光纤镊子的制造与表征

Fabrication and characterization of machined multi-core fiber tweezers for single cell manipulation.

作者信息

Anastasiadi Georgia, Leonard Mark, Paterson Lynn, Macpherson William N

出版信息

Opt Express. 2018 Feb 5;26(3):3557-3567. doi: 10.1364/OE.26.003557.

Abstract

Optical tweezing is a non-invasive technique that can enable a variety of single cell experiments; however, it tends to be based on a high numerical aperture (NA) microscope objective to both deliver the tweezing laser light and image the sample. This introduces restrictions in system flexibility when both trapping and imaging. Here, we demonstrate a novel, high NA tweezing system based on micro-machined multicore optical fibers. Using the machined, multicore fiber tweezer, cells are optically manipulated under a variety of microscopes, without requiring a high NA objective lens. The maximum NA of the fiber-based tweezer demonstrated is 1.039. A stable trap with a maximum total power 30 mW has been characterized to exert a maximum optical force of 26.4 pN, on a trapped, 7 μm diameter yeast cell. Single cells are held 15-35 μm from the fiber end and can be manipulated in the x, y and z directions throughout the sample. In this way, single cells are controllably trapped under a Raman microscope to categorize the yeast cells as live or dead, demonstrating trapping by the machined multicore fiber-based tweezer decoupled from the imaging or excitation objective lens.

摘要

光镊是一种非侵入性技术,可用于进行各种单细胞实验;然而,它往往基于高数值孔径(NA)的显微镜物镜来传输镊取激光并对样品成像。这在捕获和成像时都会给系统灵活性带来限制。在此,我们展示了一种基于微加工多芯光纤的新型高NA镊取系统。使用这种加工过的多芯光纤镊子,细胞可以在各种显微镜下进行光学操控,而无需高NA物镜。所展示的基于光纤的镊子的最大NA为1.039。已对一个最大总功率为30 mW的稳定陷阱进行了表征,该陷阱对一个被捕获的直径为7μm的酵母细胞施加的最大光学力为26.4 pN。单细胞被保持在距离光纤末端15 - 35μm处,并且可以在整个样品中在x、y和z方向上进行操控。通过这种方式,单细胞在拉曼显微镜下被可控地捕获,以将酵母细胞分类为活细胞或死细胞,这证明了基于加工过的多芯光纤的镊子的捕获与成像或激发物镜是解耦的。

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