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细胞培养物对胶体颗粒的定量摄取。

Quantitative uptake of colloidal particles by cell cultures.

机构信息

(a)Department of Physics, Philipps University Marburg, Marburg, Germany; (b)Department for Clinical Science, Intervention and Technology (CLINTEC),Karolinska Institutet, Stockholm, Sweden.

(a)Department of Physics, Philipps University Marburg, Marburg, Germany.

出版信息

Sci Total Environ. 2016 Oct 15;568:819-828. doi: 10.1016/j.scitotenv.2016.05.213. Epub 2016 Jun 13.

Abstract

The use of nanotechnologies involving nano- and microparticles has increased tremendously in the recent past. There are various beneficial characteristics that make particles attractive for a wide range of technologies. However, colloidal particles on the other hand can potentially be harmful for humans and environment. Today, complete understanding of the interaction of colloidal particles with biological systems still remains a challenge. Indeed, their uptake, effects, and final cell cycle including their life span fate and degradation in biological systems are not fully understood. This is mainly due to the complexity of multiple parameters which need to be taken in consideration to perform the nanosafety research. Therefore, we will provide an overview of the common denominators and ideas to achieve universal metrics to assess their safety. The review discusses aspects including how biological media could change the physicochemical properties of colloids, how colloids are endocytosed by cells, how to distinguish between internalized versus membrane-attached colloids, possible correlation of cellular uptake of colloids with their physicochemical properties, and how the colloidal stability of colloids may vary upon cell internalization. In conclusion three main statements are given. First, in typically exposure scenarios only part of the colloids associated with cells are internalized while a significant part remain outside cells attached to their membrane. For quantitative uptake studies false positive counts in the form of only adherent but not internalized colloids have to be avoided. pH sensitive fluorophores attached to the colloids, which can discriminate between acidic endosomal/lysosomal and neutral extracellular environment around colloids offer a possible solution. Second, the metrics selected for uptake studies is of utmost importance. Counting the internalized colloids by number or by volume may lead to significantly different results. Third, colloids may change their physicochemical properties along their life cycle, and appropriate characterization is required during the different stages.

摘要

在最近的过去,涉及纳米和微米颗粒的纳米技术的使用已经大大增加。颗粒具有各种有益的特性,使其成为各种技术的吸引力。然而,胶体颗粒另一方面可能对人类和环境造成潜在危害。如今,胶体与生物系统相互作用的完全理解仍然是一个挑战。事实上,它们的摄取、作用以及最终的细胞周期,包括它们在生物系统中的寿命命运和降解,尚未完全理解。这主要是由于需要考虑多个参数的复杂性,以进行纳米安全研究。因此,我们将概述实现评估其安全性的通用指标的共同标准和思路。该综述讨论了包括生物介质如何改变胶体的物理化学性质、胶体如何被细胞内吞、如何区分内化与膜附着的胶体、胶体的细胞摄取与其物理化学性质之间可能的相关性以及胶体的胶体稳定性如何在细胞内化后发生变化等方面。总之,给出了三个主要陈述。首先,在典型的暴露情况下,只有与细胞相关的胶体的一部分被内化,而很大一部分仍附着在细胞的膜上。对于定量摄取研究,必须避免以仅附着但未内化的胶体形式出现的假阳性计数。附着在胶体上的对 pH 敏感的荧光染料可以区分胶体周围酸性的内体/溶酶体和中性的细胞外环境,这提供了一种可能的解决方案。其次,用于摄取研究的指标选择非常重要。通过数量或体积计数内化的胶体可能会导致显著不同的结果。第三,胶体可能会沿着它们的生命周期改变它们的物理化学性质,并且需要在不同的阶段进行适当的表征。

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