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E-Cigarette Quality Control: Impurity and Nicotine Level Analysis in Electronic Cigarette Refill Liquids

机译:电子卷烟质量控制:电子烟补充液体中的杂质和尼古丁水平分析

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This work targets mainly the quality control of electronic cigarette liquids. It relies on an analytical control of a “32-product” sample made of several types of e-cigarette liquids taken from various supermarkets and tobacconist’s offices in Morocco. All along this study, we made sure to check both the conformity of the nicotine level indicated in the packaging of each product and the existence of any other components inside the product, especially toxic or unknown impurities. The method used for this study is known under the name of high-performance liquid chromatography. For statistical analysis, we used Student’s t-test for a single sample in order to analyze the relative differences between nicotine quantity reported in the product and the one measured during our experiment. Finally, we used linear regression test to determine the relationship between the nicotine level accuracy on the packaging and the level of toxic impurities in the products. The differences between the nicotine concentrations reported in the packages and the measured ones varied from ?100% to +3.3%. The study showed that 31% of analyzed products have an accurate indication of the level of nicotine on the packaging. However, 47% of the studied products showed more than 20% difference between measure and packaging indication. In all analyzed samples, the level of impurities altered from 0 to 32.6%. Furthermore, the level of the nicotine breakdown products did not exceed 2% of the nicotine content in pretty much all of the samples. The actual nicotine content of electronic cigarette refill liquids is not always as precise as what is stated on the packaging; in addition to the level of impurities detected in several brands and that exceeds the European Pharmacopoeia standards, some may even present a risk of causing toxicological damage.
机译:这项工作主要是电子烟液体的质量控制。它依赖于由各种类型的电子烟液体制成的“32-产品”样品的分析控制,从各种超市和摩洛哥的办事处采用。所有这项研究,我们肯定会检查每种产品包装中所示的尼古丁水平的一致性,以及产品内部的任何其他组分,尤其是毒性或未知的杂质。本研究用于该研究的方法是在高性能液相色谱的名称的。对于统计分析,我们使用了学生的单一样本的T检验,以分析产品中报告的尼古丁量与我们实验期间测量的相对差异。最后,我们使用了线性回归测试来确定尼古丁水平准确性与产品中有毒杂质的关系之间的关系。包装中报道的尼古丁浓度与测量的含量之间的差异变化,从Δ100%到+ 3.3%变化。该研究表明,31%的分析产品具有准确指示包装上的尼古丁水平。然而,47%的研究产品在测量和包装指示之间显示出超过20%的差异。在所有分析的样品中,杂质水平从0〜32.6%变化。此外,尼古丁分解产物的水平在几乎所有样品中都不超过尼古丁含量的2%。电子香烟填充液体的实际尼古丁含量并不总是精确,因为包装上的陈述是什么;除了在几个品牌中检测到的杂质水平,超过欧洲药典标准,有些人甚至可能呈现导致毒理学损害的风险。

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