Translocation and effects of ultrafine particles outside of the lung.

Alison Elder, Günter Oberdörster
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引用次数: 165

Abstract

Ultrafine, or nano-, particles (< 100 nm) have been associated in epidemiological, human clinical, and animal studies with adverse cardiopulmonary outcomes. Deposition of inhaled ultrafine particles in the respiratory tract is mainly governed by diffusion and is most efficient for alveolar regions of the lung, although deposition occurs in other regions, too. The nose is also a very efficient filter for smaller ultrafine (< 5 nm, diffusion) particles. Solid poorly-soluble ultrafine particles are not efficiently cleared via mucociliary or macrophage-mediated mechanisms and are, thus, likely to be taken up by epithelial cells and translocate to extrapulmonary sites (interstitium, lymph and blood circulation, neurons). These translocation processes are explored here as well potential consequences that result from exposure of extrapulmonary organs to inhaled ultrafine particles.

肺外超细颗粒的易位及其影响。
在流行病学、人类临床和动物研究中,超细或纳米颗粒(< 100 nm)与不良心肺预后相关。吸入的超细颗粒在呼吸道内的沉积主要受扩散控制,在肺的肺泡区最有效,尽管在其他区域也有沉积。对于更小的超细(< 5纳米,扩散)颗粒,鼻子也是一个非常有效的过滤器。固体难溶性超细颗粒不能通过粘膜纤毛或巨噬细胞介导的机制有效清除,因此很可能被上皮细胞吸收并转运到肺外部位(间质、淋巴和血液循环、神经元)。本文探讨了这些易位过程以及肺外器官暴露于吸入超细颗粒所导致的潜在后果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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