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使用静电纺丝纳米纤维评估呼出气生物材料特征化技术的更安全框架。

A safer framework to evaluate characterization technologies of exhaled biologic materials using electrospun nanofibers.

机构信息

Department of Biomedical Engineering, 5824 Stevenson Center, Vanderbilt University, Nashville, TN 37232, USA.

出版信息

Nanoscale. 2023 Sep 21;15(36):14822-14830. doi: 10.1039/d3nr01859h.

Abstract

Exhaled biologic material is the source for the spread of many respiratory tract infections. To avoid the high-level of biosafety required to manage dangerous pathogens, we developed a safer framework using the endogenous surrogate targets RNase P and as a means to sample exhaled biologics. Our exhalation collection scheme uses nanoscale fibrous poly(vinyl alcohol) substrates as facemask inserts. After a period of breathing or speaking, the inserts are removed and dissolved. RNase P RNA and DNA are extracted for quantification by multiplexed RT-qPCR. Both surrogate biomarkers were detected in all samples obtained during breathing for at least five minutes or speaking for one minute. Phrases repeated 30 times had the most copies with 375 ± 247 of and 54 ± 33 of RNase P. When the phrases were repeated just 5 times, the copies collected were still detectable but at a significantly lower level of 11 ± 5 for and 12 ± 9 for RNase P. These results demonstrate a collection and quantification framework that can be readily adapted to further characterize the exhalation of nanoscale biologic materials from healthy individuals, explore new collection designs safely, and serve as a method to incorporate sample controls for future pathogen exhalation studies.

摘要

呼出的生物材料是许多呼吸道感染传播的源头。为了避免管理危险病原体所需的高生物安全水平,我们开发了一种更安全的框架,使用内源性替代物靶标 RNase P 和 作为采样呼出生物标志物的手段。我们的呼气采集方案使用纳米纤维状聚(乙烯醇)作为口罩插入物。呼吸或说话一段时间后,将插入物取出并溶解。通过多重 RT-qPCR 提取 RNase P RNA 和 DNA 进行定量。在呼吸至少五分钟或说话一分钟期间获得的所有样本中均检测到这两种替代生物标志物。重复 30 次的短语具有最多的拷贝数,其中 有 375 ± 247,RNase P 有 54 ± 33。当短语仅重复 5 次时,仍可检测到收集的 拷贝数,但水平明显较低, 为 11 ± 5,RNase P 为 12 ± 9。这些结果表明,该采集和定量框架可以很容易地适应进一步表征健康个体呼出的纳米级生物材料,安全探索新的采集设计,并作为未来病原体呼出研究中纳入样本对照的方法。

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