利用显微技术表征纳米生物界面:细胞系统成像与纳米颗粒系统成像同样重要。

Q3 Biochemistry, Genetics and Molecular Biology
Christie M Sayes, Henry Lujan
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引用次数: 1

摘要

纳米技术及其产业的快速发展提高了对处理、使用和处置纳米材料相关风险的理解需求。这些风险可以通过暴露测量和危害识别来评估。对产品、废物、人类或环境中的纳米材料进行量化的常见挑战之一是缺乏可用的测量浓度的工具。精细的工具和技术在复杂基质中定性检测纳米颗粒的能力已经得到证明。对于生物和生态测试系统,剂量可以表示为应用基质中的初始浓度、暴露过程中给药的浓度、靶器官的浓度和细胞水平的摄入浓度。每一种浓度测量都需要不同的工具集来进行准确的分析。显微镜技术的进步为报告在生物测试系统中纳米颗粒与类似大小的生物分子实体相互作用时发生的观察提供了新的机会。本协议概述了在基于细胞的系统中成像纳米材料的步骤。©2017 by John Wiley & Sons, Inc。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Characterizing the Nano-Bio Interface Using Microscopic Techniques: Imaging the Cell System is Just as Important as Imaging the Nanoparticle System.

The rapid growth of nanotechnology and its industries has elevated the need to understand the risks associated with handling, using, and disposing of nanomaterials. These risks can be assessed through exposure measurement and hazard identification. One of the common challenges associated with quantifying nanomaterials in products, waste, humans, or the environment is the lack of tools available to measure concentration. The ability of refined tools and techniques to qualitatively detect nanoparticles in complex matrices has been demonstrated. For biological and ecological tests systems, dose can be represented as initial concentration in the applied matrix, concentration administered during the route of exposure, concentration at the target organ, and intake concentration at the cellular level. Each of these concentration measurements requires different sets of tools to perform accurate analyses. Advances in microscopy techniques provide new opportunities for reporting observations occurring at the interaction of a nanoparticle with a biomolecular entity of similar size within a biological test(s) system. This protocol outlines the steps to image nanomaterials within cell-based systems. © 2017 by John Wiley & Sons, Inc.

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Current protocols in chemical biology
Current protocols in chemical biology Biochemistry, Genetics and Molecular Biology-Biophysics
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