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基于数字全息显微镜的硅藻壳体蚀刻成像与定量分析

Imaging and Quantitative Analysis on the Etching of Diatom Frustules via Digital Holographic Microscopy.

作者信息

Lugo Maria Christine, Saito Makoto, Kitamura Masaki, Ide Yuki, Koide Shinji, Mayama Shigeki

机构信息

Department of Physics, Tokyo University of Science, 1-3 Kagurazaka, Shinjuku, Tokyo 162-8601, Japan.

Tokyo Diatomology Lab, 2-3-2 Nukuikitamachi, Koganei, Tokyo 184-0015, Japan.

出版信息

ACS Biomater Sci Eng. 2024 Feb 12;10(2):1106-1111. doi: 10.1021/acsbiomaterials.3c01349. Epub 2023 Dec 28.

Abstract

Frustules, whose length spans from a few micrometers to more than a hundred micrometers, have been the subject of various modifications to improve their physical properties because of their complex porous silica structure. However, three-dimensional measurements of these changes can be challenging because of the complex 3D architecture and limitations of known methods. In this study, we present a new method that applies digital holographic microscopy (DHM) to analyze controlled etched frustules and observe real-time degradation of frustules at the single-cell level. Frustules obtained from sp. diatoms were etched in 1 N NaOH for 5 min at 25 and 60 °C, respectively, and the frustule's valve was analyzed using DHM. DHM uses a combination of holography and tomography to reconstruct a 3D refractive index image of the frustule. Measurements of the width, volume, and surface area are achieved. Results showed that at 60 °C of etching, a significant difference with the unetched frustule was observed for all measurements but with high fluctuation values. Finally, real-time observation of the degradation of the frustule is observed when immersed in a high concentration of NaOH. This is the first time the real-time etching of the frustule is observed at the single-cell level. This research provides an easy estimation of the 3D measurements of frustules that may provide new fundamental information and applications.

摘要

硅藻壳的长度从几微米到一百多微米不等,由于其复杂的多孔二氧化硅结构,人们对其进行了各种改性以改善其物理性能。然而,由于其复杂的三维结构和已知方法的局限性,对这些变化进行三维测量可能具有挑战性。在本研究中,我们提出了一种新方法,该方法应用数字全息显微镜(DHM)来分析受控蚀刻的硅藻壳,并在单细胞水平上观察硅藻壳的实时降解。分别从 sp.硅藻中获得的硅藻壳在 1 N NaOH 中于 25 和 60 °C 下蚀刻 5 分钟,并使用 DHM 分析硅藻壳的瓣膜。DHM 结合了全息术和层析成像来重建硅藻壳的三维折射率图像。实现了对宽度、体积和表面积的测量。结果表明,在 60 °C 蚀刻时,所有测量值与未蚀刻的硅藻壳相比均有显著差异,但波动值较高。最后,当浸入高浓度 NaOH 中时,可以观察到硅藻壳降解的实时过程。这是首次在单细胞水平上观察到硅藻壳的实时蚀刻。这项研究提供了一种对硅藻壳三维测量的简便估计方法,可能会提供新的基础信息和应用。

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