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经皮给药后无定形纳米二氧化硅的全身分布、核内进入和细胞毒性。

Systemic distribution, nuclear entry and cytotoxicity of amorphous nanosilica following topical application.

机构信息

Department of Toxicology and Safety Science, Graduate School of Pharmaceutical Sciences, Osaka University, 1-6 Yamadaoka, Suita, Osaka 565-0871, Japan.

出版信息

Biomaterials. 2011 Apr;32(11):2713-24. doi: 10.1016/j.biomaterials.2010.12.042. Epub 2011 Jan 22.

Abstract

Currently, nanomaterials (NMs) with particle sizes below 100 nm have been successfully employed in various industrial applications in medicine, cosmetics and foods. On the other hand, NMs can also be problematic in terms of eliciting a toxicological effect by their small size. However, biological and/or cellular responses to NMs are often inconsistent and even contradictory. In addition, relationships among NMs physicochemical properties, absorbency, localization and biological responses are not yet well understood. In order to open new frontiers in medical, cosmetics and foods fields by the safer NMs, it is necessary to collect the information of the detailed properties of NMs and then, build the prediction system of NMs safety. The present study was designed to examine the skin penetration, cellular localization, and cytotoxic effects of the well-dispersed amorphous silica particles of diameters ranging from 70 nm to 1000 nm. Our results suggested that the well-dispersed amorphous nanosilica of particle size 70 nm (nSP70) penetrated the skin barrier and caused systemic exposure in mouse, and induced mutagenic activity in vitro. Our information indicated that further studies of relation between physicochemical properties and biological responses are needed for the development and the safer form of NMs.

摘要

目前,粒径小于 100nm 的纳米材料(NMs)已成功应用于医学、化妆品和食品等各个工业领域。另一方面,纳米材料由于其小尺寸,也可能引发毒理学效应。然而,生物和/或细胞对纳米材料的反应往往不一致,甚至相互矛盾。此外,纳米材料理化性质、吸收率、定位和生物反应之间的关系尚不清楚。为了通过更安全的纳米材料在医学、化妆品和食品领域开辟新的前沿,有必要收集纳米材料详细性质的信息,然后建立纳米材料安全性的预测系统。本研究旨在研究直径从 70nm 到 1000nm 的分散良好的无定形二氧化硅颗粒的皮肤穿透性、细胞定位和细胞毒性作用。我们的结果表明,粒径为 70nm 的分散良好的无定形纳米二氧化硅(nSP70)能够穿透皮肤屏障并在小鼠体内引起全身暴露,并在体外诱导致突变活性。我们的信息表明,为了开发和形成更安全的纳米材料形式,需要进一步研究理化性质与生物反应之间的关系。

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