Study of sample preparation, by acid digestion assisted by microwave radiation in a closed system, to determine inorganic contaminants in street cocaine samples by ICP OES and ICP MS

Z. Amorim, Maiara Pereira Machado Queiroz, Laura Oliveira Rebouças, Giacomina Possatti Lepaus, Christiane Feijó de Castro Porto, Eustaquio Vinícius Ribeiro De Castro, Maria Tereza Weitzel Dias Carneiro, G. Brandão
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Abstract

Knowledge of the inorganic composition of cocaine makes it possible to correlate the drug with its refinement and dilutions1, it is important to highlight that when aiming to study the adulteration/production of street cocaine it is interesting to carry out the total solubilization of the sample2. Thus, acid digestion using microwave radiation in a closed system is a widely used technique due to the speed and efficiency of digestion3. Thus, acid solubilization procedures and acid digestion assisted by radiation via microwaves of the sample were studied, varying the mass of the sample (0.050g, 0.100g, 0.200g and 0.500g) and concentration of the HNO3 solution (5%, 10% , 30%, 40% and 50% v/v). In order to verify whether the different sample preparation procedures and whether the final acidity interferes with the quantification of the analytes studied. ICP OES analysis was carried out on a high purity sample prepared by direct solubilization and digestion. The result of the intensities test for the elements Co, Cu, Mo, Pb and Zn, with final acidity of HNO3 2% or 4% v/v, demonstrated that samples prepared by direct solubilization or digested by microwaves, with final acidity of HNO3 2% v/v, presented very close intensity values for the elements analyzed, indicating that the types of sample preparation studied (solubilization or digestion) did not present significant interferences in the analysis by ICP OES.
研究在封闭系统中利用微波辐射辅助酸消化法制备样品,以通过 ICP OES 和 ICP MS 测定街头可卡因样品中的无机污染物
了解了可卡因的无机成分,就有可能将毒品与其提纯和稀释液联系起来1,必须强调的是,在研究街头可卡因的掺假/生产时,对样品进行完全溶解是很有意义的2。因此,在封闭系统中使用微波辐射进行酸解是一种广泛使用的技术,因为酸解速度快、效率高3。因此,我们研究了样品的酸溶解过程和通过微波辐射辅助的酸消解过程,并改变了样品的质量(0.050 克、0.100 克、0.200 克和 0.500 克)和 HNO3 溶液的浓度(5%、10%、30%、40% 和 50% v/v)。为了验证不同的样品制备程序和最终酸度是否会干扰所研究分析物的定量。对通过直接溶解和消化法制备的高纯度样品进行了 ICP OES 分析。对最终酸度为 HNO3 2% 或 4% v/v 的钴、铜、钼、铅和锌元素的强度测试结果表明,通过直接溶解法或微波消解法制备的样品(最终酸度为 HNO3 2% v/v)对所分析元素的强度值非常接近,这表明所研究的样品制备类型(溶解或消解)对 ICP OES 分析没有明显的干扰。
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