Kolb Thorsten, Albert Sahradha, Haug Michael, Whyte Graeme
Department of Physics, Friedrich-Alexander-Universität Erlangen-Nürnberg, Henkestrasse 91, 91052, Erlangen, Germany; Cluster for Engineering of Advanced Materials, Friedrich-Alexander-Universität Erlangen-Nürnberg, Henkestrasse 91, 91052, Erlangen, Germany.
J Biophotonics. 2015 Mar;8(3):239-46. doi: 10.1002/jbio.201300196. Epub 2014 Apr 14.
Flow cytometry provides a high throughput, multi-dimensional analysis of cells flowing in suspension. In order to combine this feature with the ability to resolve detailed structures in 3D, we developed an optofluidic device that combines a microfluidic system with a dual beam trap. This allows for the rotation of single cells in a continuous flow, around an axis perpendicular to the imaging plane. The combination of both techniques enables the tomographic reconstruction of the 3D structure of the cell. In addition this method is capable to provide detailed 3D structural data for flow cytometry, as it improves the reconstructed z-resolution of a standard microscopy system to produce images with isotropic resolution in all three axes.
流式细胞术可对悬浮流动的细胞进行高通量、多维度分析。为了将这一特性与解析三维精细结构的能力相结合,我们开发了一种光流体装置,它将微流体系统与双光束阱相结合。这使得单个细胞能够在连续流中绕垂直于成像平面的轴旋转。两种技术的结合能够对细胞的三维结构进行断层重建。此外,这种方法能够为流式细胞术提供详细的三维结构数据,因为它将标准显微镜系统的重建z分辨率提高,从而生成在所有三个轴上具有各向同性分辨率的图像。