Hu Jiajie, Li Xinrui, Li Meng, Shang Yazhuo, He Yifan, Liu Honglai
Key Laboratory for Advanced Materials, School of Chemistry & Molecular Engineering, East China University of Science and Technology, Shanghai, 200237, China.
Key Laboratory for Advanced Materials, School of Chemistry & Molecular Engineering, East China University of Science and Technology, Shanghai, 200237, China.
Colloids Surf B Biointerfaces. 2020 Jun;190:110922. doi: 10.1016/j.colsurfb.2020.110922. Epub 2020 Feb 29.
Air pollution has become increasingly serious. Fine particulate matter (PM2.5) is the most well-known air pollutant, which leads to some common respiratory diseases when inhaled into the lungs to certain concentration. However, there is a lack of research on the process of dynamically monitoring the real-time effect of nanoparticles on the pulmonary surfactant monolayer. In this study, the DPPC/DPPG monolayer is prepared by the Langmuir method to simulate the lung surfactant monolayer during respiration and the carbon nanoparticles are introduced to the monolayer under different surface pressures to simulate the real dynamic process of inhaling nanoparticles during breathing. The effect of carbon nanoparticles on the surface behavior of DPPC/DPPG monolayer in real-time was examined in details by a combination of surface pressure (π)-area (A) isotherms, compressibility modulus (C)-surface pressure (π) isotherms and the Brewster angle microscopy (BAM). The results have shown that the introduction of carbon nanoparticles under different surface pressures affects the properties of lipid monolayers. The added carbon nanoparticles under lower surface pressure are easy to penetrate the lipid molecules to inhibit monolayer phase transition. When the carbon nanoparticles are introduced to the monolayer under higher surface pressure, they tend to self-aggregate to reduce the monolayer stability rather than interact with lipid tail chains. This work not only confirms the exotic hydrophobic carbon nanoparticles retain in the DPPC/DPPG monolayer irreversibly and affect the surface behavior of monolayer during respiration, but also opens a new idea for real-time monitoring of the effects of PM2.5 on lung health.
空气污染日益严重。细颗粒物(PM2.5)是最广为人知的空气污染物,当吸入肺部达到一定浓度时会引发一些常见的呼吸道疾病。然而,目前缺乏对纳米颗粒对肺表面活性剂单层实时效应进行动态监测过程的研究。在本研究中,采用朗缪尔方法制备了二棕榈酰磷脂酰胆碱/二棕榈酰磷脂酰甘油(DPPC/DPPG)单层,以模拟呼吸过程中的肺表面活性剂单层,并在不同表面压力下将碳纳米颗粒引入该单层,以模拟呼吸过程中吸入纳米颗粒的真实动态过程。通过表面压力(π)-面积(A)等温线、压缩模量(C)-表面压力(π)等温线和布鲁斯特角显微镜(BAM)相结合的方法,详细研究了碳纳米颗粒对DPPC/DPPG单层表面行为的实时影响。结果表明,在不同表面压力下引入碳纳米颗粒会影响脂质单层的性质。在较低表面压力下添加的碳纳米颗粒容易穿透脂质分子以抑制单层相变。当在较高表面压力下将碳纳米颗粒引入单层时,它们倾向于自聚集以降低单层稳定性,而不是与脂质尾链相互作用。这项工作不仅证实了外来的疏水性碳纳米颗粒不可逆地保留在DPPC/DPPG单层中,并在呼吸过程中影响单层的表面行为,还为实时监测PM2.5对肺部健康的影响开辟了新思路。