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纳米颗粒向细胞的特定呈现及其表面控制的摄取。

The defined presentation of nanoparticles to cells and their surface controlled uptake.

作者信息

Alberola Alicia Piera, Rädler Joachim O

机构信息

Fakultät für Physik and Center for NanoScience (CeNS), Ludwig-Maximilians-Universität, Geschwister Scholl Platz 1, D-80539 Munich, Germany.

出版信息

Biomaterials. 2009 Aug;30(22):3766-70. doi: 10.1016/j.biomaterials.2009.03.031. Epub 2009 Apr 16.

Abstract

New approaches and standardized test procedures to study the impact of nanoparticles (NPs) on living cells are urgently needed for the evaluation of potential hazards relating human exposure to NPs. Here we study semiconductor quantum dots (QDs) preparation on solid surfaces and the subsequent internalization by cells seeded on top of the NP layer. Controlled densities of NPs are adsorbed to solid surfaces coated with extra-cellular macromolecules. The fraction of QDs taken up by the cells is assessed by automated fluorescence microscopy z-scans. We find that NPs aggregate during the uptake process, forming clusters inside cells that are able to enter the cell nucleus. NP uptake is dependent on surface functionalization and can be hindered by increasing the strength of the adhesion force between NPs and the surface. Studying time dependent uptake, we show that particles are able to exit cells.

摘要

为了评估人类接触纳米颗粒(NPs)的潜在危害,迫切需要新的方法和标准化测试程序来研究NPs对活细胞的影响。在此,我们研究了在固体表面制备半导体量子点(QDs)以及随后接种在NP层上的细胞对其的内化过程。将可控密度的NPs吸附到涂有细胞外大分子的固体表面。通过自动荧光显微镜z扫描评估细胞摄取的量子点比例。我们发现NPs在摄取过程中聚集,在细胞内形成能够进入细胞核的簇。NP摄取取决于表面功能化,并且可以通过增加NPs与表面之间的粘附力强度来阻碍。通过研究时间依赖性摄取,我们表明颗粒能够从细胞中排出。

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