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利用共轭涡旋相位调制增强荧光发射差异显微镜技术

Enhancement of fluorescence emission difference microscopy using conjugated vortex phase modulation.

作者信息

Zhu D, Liu W, Zhang Z, Zheng C, Chen Y, Li C, Kuang C, Fan J, Xu Y, Liu X, Hussain A

机构信息

State Key Laboratory of Modern Optical Instrumentation, College of Optical Science and Engineering, Zhejiang University, Hangzhou, China.

Key Laboratory of Instrumentation Science & Dynamic Measurement of Ministry of Education, North University of China, Taiyuan, China.

出版信息

J Microsc. 2018 Nov;272(2):151-159. doi: 10.1111/jmi.12756. Epub 2018 Sep 14.

Abstract

In this paper, we propose and demonstrate an improved fluorescence emission difference microscopy (FED) method, exploiting programmable phase modulation for image enhancement. The main novelty of the proposed approach lies in the matched size and intensity of two excitation spots. The proposed method improves the FED performance on image quality via artefact elimination. We demonstrate the feasibility of this method through theoretical studies and experimental tests. The experimental results of nanobeads and cells validate the practical performance of this method, which can enable reliable observations at superresolution in biomedical studies. LAY DESCRIPTION: In this paper, we propose a method to improve the imaging quality of regular fluorescence emission difference (FED) microscopy. In regular FED imaging, a solid and a doughnut excitation beam are successively used to acquire two images which are then subtracted with each other to improve the resolution of confocal microscopy. The doughnut beam can be generated by modulating the excitation beam with a vortex phase mask. Note that both of the excitation beam and the vortex phase mask must have the same handed direction in regular FED microscopy. However, some negative values may be produced and some information may be lost due to the subtraction process in regular FED imaging, which is mainly caused by the mismatched size and intensity of these two excitation spots. To address this issue, we propose conjugated FED (cFED) microscopy which additionally uses a conjugated vortex phase mask to modulate the solid beam to extend its focal spot size to be matched with the doughnut spot, which means the handed direction of the solid beam and the vortex phase mask is different. Besides, in order not to damage the resolution, the doughnut beam needs to be saturated to some degree. The experiment results show that, at the same resolution level, the negative values and the information loss in cFED image are all less than that of regular FED image.

摘要

在本文中,我们提出并演示了一种改进的荧光发射差异显微镜(FED)方法,该方法利用可编程相位调制来增强图像。所提出方法的主要新颖之处在于两个激发光斑的匹配尺寸和强度。该方法通过消除伪像提高了FED在图像质量方面的性能。我们通过理论研究和实验测试证明了该方法的可行性。纳米珠和细胞的实验结果验证了该方法的实际性能,这能够在生物医学研究中实现超分辨率下的可靠观察。通俗易懂的描述:在本文中,我们提出了一种提高常规荧光发射差异(FED)显微镜成像质量的方法。在常规FED成像中,先后使用实心和环形激发光束获取两幅图像,然后将它们相减以提高共聚焦显微镜的分辨率。环形光束可通过用涡旋相位掩模调制激发光束来产生。请注意,在常规FED显微镜中,激发光束和涡旋相位掩模必须具有相同的旋向。然而,由于常规FED成像中的相减过程,可能会产生一些负值并且会丢失一些信息,这主要是由这两个激发光斑的尺寸和强度不匹配导致的。为了解决这个问题,我们提出了共轭FED(cFED)显微镜,它额外使用一个共轭涡旋相位掩模来调制实心光束,以扩展其焦斑尺寸使其与环形光斑匹配,这意味着实心光束和涡旋相位掩模的旋向不同。此外,为了不损害分辨率,环形光束需要在一定程度上饱和。实验结果表明,在相同分辨率水平下,cFED图像中的负值和信息损失均小于常规FED图像。

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