Kosmidis-Papadimitriou Alexandros, Qi Shaojun, Squillace Ophelie, Rosik Nicole, Bale Mark, Fryer Peter J, Zhang Zhenyu J
School of Chemical Engineering, University of Birmingham, Edgbaston, Birmingham B15 2TT, UK.
DoDxAct Ltd, Wells BA5 2LW, UK.
Interface Focus. 2021 Dec 10;12(1):20210044. doi: 10.1098/rsfs.2021.0044. eCollection 2022 Feb 6.
To evaluate the role of common substrates in the transmission of respiratory viruses, in particular SARS-CoV-2, uniformly distributed microdroplets (approx. 10 µm diameter) of artificial saliva were generated using an advanced inkjet printing technology to replicate the aerosol droplets and subsequently deposited on five substrates, including glass, polytetrafluoroethylene, stainless steel, acrylonitrile butadiene styrene and melamine. The droplets were found to evaporate within a short timeframe (less than 3 s), which is consistent with previous reports concerning the drying kinetics of picolitre droplets. Using fluorescence microscopy and atomic force microscopy, we found that the surface deposited microdroplet nuclei present two distinctive morphological features as the result of their drying mode, which is controlled by both interfacial energy and surface roughness. Nanomechanical measurements confirm that the nuclei deposited on all substrates possess similar surface adhesion (approx. 20 nN) and Young's modulus (approx. 4 MPa), supporting the proposed core-shell structure of the nuclei. We suggest that appropriate antiviral surface strategies, e.g. functionalization, chemical deposition, could be developed to modulate the evaporation process of microdroplet nuclei and subsequently mitigate the possible surface viability and transmissibility of respiratory virus.
为评估常见底物在呼吸道病毒传播,尤其是严重急性呼吸综合征冠状病毒2(SARS-CoV-2)传播中的作用,使用先进的喷墨打印技术生成人工唾液的均匀分布微滴(直径约10 µm),以复制气溶胶飞沫,随后将其沉积在包括玻璃、聚四氟乙烯、不锈钢、丙烯腈-丁二烯-苯乙烯和三聚氰胺在内的五种底物上。发现这些微滴在短时间内(少于3秒)蒸发,这与先前关于皮升微滴干燥动力学的报道一致。使用荧光显微镜和原子力显微镜,我们发现表面沉积的微滴核由于其干燥模式呈现出两种独特的形态特征,而干燥模式受界面能和表面粗糙度控制。纳米力学测量证实,沉积在所有底物上的核具有相似的表面附着力(约20 nN)和杨氏模量(约4 MPa),支持了所提出的核的核壳结构。我们建议可以开发适当的抗病毒表面策略,如功能化、化学沉积,以调节微滴核的蒸发过程,进而降低呼吸道病毒在表面的可能存活能力和传播性。