[Validation of surgical masks during COVID19 emergency: activities at the University of Napoli Federico II].

IF 0.4 Q3 Medicine
Andrea D'Anna, Francesco Di Natale, Gianluigi De Falco, Ernesto Di Maio, Daniele Tammaro, Fabiana Quaglia, Francesca Ungaro, Chiara Cassiano, Paola Salvatore, Roberta Colicchio, Elena Scaglione, Chiara Pagliuca, Luca Fontana, Ivo Iavicoli
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引用次数: 0

Abstract

Summary: During COVID-19 pandemic crisis, Italian Government has approved Law Decree no. 18 of 17 march 2020, in which art. 15 allows enterprises to produce, import and commercialize surgical masks notwithstanding the current rules of product certification. It is just required that the interested enterprises send to the Italian National Institute of Health a selfcertification in which they declare the technical characteristics of the masks and that masks are produced according to the safety requirements. In this context, a technical-scientific unit was established at the University of Napoli Federico II to provide interested enterprises with state-of-the-art consultancy, testing and measurement services, adhering to rigorous scientific protocols. Characterization tests were carried out on 163 surgical masks and/or materials for their construction and they have enabled the identification of pre-screening criteria to simplify the procedure for evaluating surgical masks using methods for assessing the filtration efficiency of particles and aerosols. Based on experimental results, it has been observed that a filtration efficiency for particles with sizes larger that 650 nm (PFE>650) exceeding 35% might guarantees a bacterial filtration efficiency (BFE) higher than 95% while BFE values higher than 98% are obtained when the PFE>650 is larger than 40%. PFE measurement is extremely simpler with respect to BFE, the latter being time-consuming and requiring specific equipment and methods for its realization. Many tested materials have shown the capability to assure high filtration efficiencies but Spundonded-Meltblown-Spunbonded (SMS), that are layers of non-woven fabric with different weights of Meltblown, can simultaneously guarantee high particle filtration efficiencies with pressure drop values (breathability) in the limits to classify the surgical masks as Type II/IIR. In fact, the fabric products analyzed so far have not been able to simultaneously guarantee adequate BFE and breathability values. On the contrary, Spunbonds of adequate weights can virtually verify both requirements and accredit themselves as possible materials for the production of surgical masks, at least of Type I. Further studies are needed to verify the possibility of producing low-cost, reusable surgical masks that could meet the criteria of circular economy.

[covid - 19紧急情况下外科口罩的验证:那不勒斯费德里科大学II的活动]。
摘要:在2019冠状病毒病大流行危机期间,意大利政府批准了第19号法令。2020年3月17日第18条,其中。第15条允许企业生产、进口和商业化医用口罩,不受现行产品认证规则的限制。只需要感兴趣的企业向意大利国家卫生研究院提交一份自我认证,声明口罩的技术特性,并声明口罩是按照安全要求生产的。在这方面,在那不勒斯费德里科二世大学成立了一个技术科学单位,为有兴趣的企业提供最先进的咨询、测试和测量服务,遵守严格的科学协议。对163个外科口罩和/或其构造材料进行了特性测试,这些测试能够确定预筛选标准,从而简化使用评估颗粒和气溶胶过滤效率的方法评估外科口罩的程序。实验结果表明,对于大于650 nm的颗粒(PFE>650),过滤效率超过35%可以保证细菌过滤效率(BFE)大于95%,而当PFE>650大于40%时,细菌过滤效率(BFE)大于98%。相对于BFE, PFE测量非常简单,后者耗时且需要特定的设备和方法来实现。许多经过测试的材料已经显示出确保高过滤效率的能力,但是纺喷-熔喷-纺粘(SMS),即具有不同重量的熔喷非织造布层,可以同时保证高颗粒过滤效率,并且压降值(透气性)在将外科口罩分类为II/IIR型的限制范围内。事实上,迄今为止所分析的织物产品还不能同时保证足够的BFE和透气性值。相反,重量足够的纺粘剂实际上可以验证这两项要求,并将自己视为生产外科口罩的可能材料,至少是第一类。需要进一步研究,以验证生产符合循环经济标准的低成本、可重复使用的外科口罩的可能性。
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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来源期刊
Giornale italiano di medicina del lavoro ed ergonomia
Giornale italiano di medicina del lavoro ed ergonomia PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH-
CiteScore
0.80
自引率
0.00%
发文量
10
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