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一种基于微观动机的粒子渗透到肿胀生物网络中的模型。

A Microscopically Motivated Model for Particle Penetration into Swollen Biological Networks.

作者信息

Arzi Roni Sverdlov, Sosnik Alejandro, Cohen Noy

机构信息

Laboratory of Pharmaceutical Nanomaterials Science, Department of Materials Science and Engineering, Technion-Israel Institute of Technology, Haifa 3200003, Israel.

Mechanics of Soft Materials, Department of Materials Science and Engineering, Technion-Israel Institute of Technology, Haifa 3200003, Israel.

出版信息

Polymers (Basel). 2020 Aug 25;12(9):1912. doi: 10.3390/polym12091912.

DOI:10.3390/polym12091912
PMID:32854259
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7565132/
Abstract

Biological gels (bio-gels) are hydrated polymer networks that serve diverse biological functions, which often lead to intentional or unintentional exposure to particulate matter. In this work, we derive a microscopically motivated framework that enables the investigation of penetration mechanisms into bio-gels. We distinguish between two types of mechanisms: spontaneous (unforced) penetration and forced penetration. Using experimental data available in the literature, we exploit the proposed model to characterize and compare between the microstructures of respiratory, intestinal, and cervicovaginal mucus and two types of biofilms. Next, we investigate the forced penetration process of spherical and ellipsoidal particles into a locally quadrilateral network. The proposed framework can be used to improve and complement the analysis of experimental findings in vitro, ex vivo, and in vivo. Additionally, the insights from this work pave the way towards enhanced designs of nano-medicines and allow the assessment of risk factors related to the nano-pollutants exposure.

摘要

生物凝胶是水合聚合物网络,具有多种生物学功能,这常常导致有意或无意地接触颗粒物。在这项工作中,我们推导了一个基于微观的框架,用于研究进入生物凝胶的渗透机制。我们区分了两种类型的机制:自发(无外力)渗透和强制渗透。利用文献中可用的实验数据,我们运用所提出的模型来表征和比较呼吸道、肠道和宫颈阴道黏液以及两种生物膜的微观结构。接下来,我们研究球形和椭圆形颗粒进入局部四边形网络的强制渗透过程。所提出的框架可用于改进和补充体外、离体和体内实验结果的分析。此外,这项工作的见解为纳米药物的优化设计铺平了道路,并有助于评估与纳米污染物暴露相关的风险因素。

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本文引用的文献

1
Molecular and cellular cues governing nanomaterial-mucosae interactions: from nanomedicine to nanotoxicology.分子和细胞线索调控纳米材料-黏膜相互作用:从纳米医学到纳米毒理学。
Chem Soc Rev. 2020 Jul 21;49(14):5058-5100. doi: 10.1039/c8cs00948a.
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The health effects of ultrafine particles.超细颗粒对健康的影响。
Exp Mol Med. 2020 Mar;52(3):311-317. doi: 10.1038/s12276-020-0403-3. Epub 2020 Mar 17.
3
A microscopically motivated model for the swelling-induced drastic softening of hydrogen-bond dominated biopolymer networks.
一种微观驱动的模型,用于解释氢键主导的生物聚合物网络在溶胀诱导下的剧烈软化。
Acta Biomater. 2019 Sep 15;96:303-309. doi: 10.1016/j.actbio.2019.07.005. Epub 2019 Jul 15.
4
Influence of the viscosity of healthy and diseased human mucins on the motility of Helicobacter pylori.健康和患病的人粘蛋白的粘度对幽门螺杆菌运动性的影响。
Sci Rep. 2018 Jun 26;8(1):9710. doi: 10.1038/s41598-018-27732-3.
5
A slippery slope: On the origin, role and physiology of mucus.滑溜溜的山坡:黏液的起源、作用和生理学。
Adv Drug Deliv Rev. 2018 Jan 15;124:16-33. doi: 10.1016/j.addr.2017.10.014. Epub 2017 Nov 3.
6
Biological responses to nanomaterials: understanding nano-bio effects on cell behaviors.生物对纳米材料的反应:理解纳米生物效应对细胞行为的影响。
Drug Deliv. 2017 Dec;24(sup1):1-15. doi: 10.1080/10717544.2017.1375577.
7
The particle in the spider's web: transport through biological hydrogels.蜘蛛网上的颗粒:生物水凝胶中的传输。
Nanoscale. 2017 Jun 22;9(24):8080-8095. doi: 10.1039/c6nr09736g.
8
Nanoparticles that do not adhere to mucus provide uniform and long-lasting drug delivery to airways following inhalation.吸入后,不附着在黏液上的纳米颗粒为气道提供均匀且持久的药物输送。
Sci Adv. 2017 Apr 5;3(4):e1601556. doi: 10.1126/sciadv.1601556. eCollection 2017 Apr.
9
Inhaled Pollutants: The Molecular Scene behind Respiratory and Systemic Diseases Associated with Ultrafine Particulate Matter.吸入性污染物:与超细颗粒物相关的呼吸系统和全身性疾病背后的分子机制
Int J Mol Sci. 2017 Jan 24;18(2):243. doi: 10.3390/ijms18020243.
10
Recent Nanotechnology Approaches for Prevention and Treatment of Biofilm-Associated Infections on Medical Devices.用于预防和治疗医疗器械上生物膜相关感染的最新纳米技术方法。
Biomed Res Int. 2016;2016:1851242. doi: 10.1155/2016/1851242. Epub 2016 Oct 31.