Multivariate optimization, in conjugation with matrix solid-phase dispersion and digital image detection, allows residual dye determination from shrimp samples

IF 5.2 Q1 CHEMISTRY, ANALYTICAL Advances in Sample Preparation Pub Date : 2024-02-01 DOI:10.1016/j.sampre.2024.100105
Jéssica Passos de Carvalho , Iare Soares Ribeiro , Marcos Vinícius de Sousa Pereira , Tatianny de Araujo Andrade , Jemmyson Romário de Jesus
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Abstract

Here, we report an optimization of the extraction of crystal violet and congo red dyes from shrimp samples, employing matrix solid phase dispersion and improved multivariate optimization. Three factors were evaluated: (i) adsorbent nature (neutral alumina, silica gel and C18); (ii) eluent strength (dimethylformamide, methanol and acetonitrile); and (iii) sample-adsorbent ratio (1:1; 1:5; and 1:10, m/m). Successful extraction of dyes was achieved using dimethylformamide as eluent, neutral alumina as adsorbent and sample:adsorbent ratio of 1:5 (m/m). Adsorption and kinetic studies suggest strong interaction between dye and adsorbent. Furthermore, employing digital image colorimetric detection, the study observed limit of detection (LOD) ranging between 3.8 to 29.8 µg L 1 and limit of quantification (LOQ) ranging between 12.3 to 90.3 µg L 1 with R2 > 0.9927 for both dyes, CV and CR, respectively. Notably, recovery was greater than 86 % with a relative standard deviation (RSD) inferior to 7 % (n = 3). These findings indicate the effectiveness of the improved multivariate optimization technique in conjunction with matrix solid-phase dispersion for successful extraction and quantification of dyes from shrimp samples, showing its potential for accurate and sensitive detection in similar analyses. The proposed method was compared with the gold method (UV/Vis spectroscopy) and the statistical treatment showed that the results of both methods are comparable.

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多变量优化与基质固相分散和数字图像检测相结合,可测定虾样品中的残留染料
在此,我们报告了利用基质固相分散和改进的多元优化技术从虾样品中萃取结晶紫和刚果红染料的优化方法。对三个因素进行了评估:(i) 吸附剂性质(中性氧化铝、硅胶和 C18);(ii) 洗脱液强度(二甲基甲酰胺、甲醇和乙腈);(iii) 样品与吸附剂的比例(1:1;1:5 和 1:10,m/m)。使用二甲基甲酰胺作为洗脱剂,中性氧化铝作为吸附剂,样品与吸附剂的比例为 1:5(m/m),成功萃取了染料。吸附和动力学研究表明,染料和吸附剂之间存在强烈的相互作用。此外,该研究采用数字图像比色法检测,观察到两种染料 CV 和 CR 的检测限(LOD)介于 3.8 至 29.8 µg L - 1 之间,定量限(LOQ)介于 12.3 至 90.3 µg L - 1 之间,R2 > 0.9927。值得注意的是,回收率大于 86%,相对标准偏差 (RSD) 小于 7%(n = 3)。这些研究结果表明,改进的多元优化技术与基质固相分散技术相结合,可成功地从虾样品中提取和定量染料,显示了其在类似分析中进行准确灵敏检测的潜力。将所提出的方法与金方法(紫外/可见光谱法)进行了比较,统计处理显示两种方法的结果具有可比性。
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