Graphical abstract<'/> Response surface methodology optimized dispersive liquid-liquid microextraction coupled with surface plasmon resonance of silver nanoparticles as colorimetric probe for determination of captopril
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Response surface methodology optimized dispersive liquid-liquid microextraction coupled with surface plasmon resonance of silver nanoparticles as colorimetric probe for determination of captopril

机译:响应面法优化的分散液-液微萃取结合银纳米颗粒的表面等离子体共振作为比色法测定卡托普利

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Graphical abstractDisplay OmittedHighlightsA novel and sensitive method was introduced for spectrophotometric determination of captopril.The sensing properties of label-free AgNPs were studied in a dispersive liquid–liquid microextraction method.A response surface methodology based on central composite design was developed to optimization.The LOD is better than other pre-extraction methods for captopril assay.AbstractA response surface methodology (RSM) based on central composite design was developed to optimize a novel method for the determination of trace levels of captopril by combination of dispersive liquid–liquid microextraction (DLLME) and surface plasmon resonance of silver nanoparticles (AgNPs). In this study AgNPs as a colorimetric sensor were synthesized in situ and used in a versatile DLLME method using carbon tetrachloride as extraction solvent and ethanol as disperser. The presence of captopril affected the production of AgNPs in the organic phase, thereby resulting in an increase of plasmon absorbance intensity of nanoparticles. The effect of different variables such as CTAB, sodium hydroxide and ascorbic acid concentration and also volume of extraction and disperser solvent was investigated and optimized by RSM at two steps. The calibration curve was linear in the range of 0.77–22.50nmolL−1of captopril, limit of detection was 0.51nmolL−1and the relative standard deviation for 11.54 and 19.23nmolL−1of captopril was 2.12 and 0.72%, respectively. The developed method was applied to the determination of the analyte in pharmaceutical, human serum and urine samples with good accuracy and excellent precision.
机译: 图形摘要 省略显示 重点 引入了一种新颖灵敏的分光光度法测定方法 采用分散液-液微萃取方法研究了无标签AgNPs的传感特性。 开发了基于中央复合设计的响应面方法进行优化。 在卡托普利测定中,LOD优于其他提取前方法。 摘要 < ce:abstract-sec id = “ abst0015 ” view = “ all ”> 基于的响应面方法(RSM)开发了中央复合设计以优化一种新方法od通过结合液-液微萃取(DLLME)和银纳米颗粒(AgNPs)的表面等离振子共振来测定卡托普利的痕量水平。在这项研究中,AgNPs作为比色传感器被原位合成,并用于以四氯化碳为萃取溶剂和乙醇为分散剂的多功能DLLME方法中。卡托普利的存在影响有机相中AgNP的产生,从而导致纳米粒子的等离激元吸收强度增加。通过RSM分两步研究和优化了不同变量(如CTAB,氢氧化钠和抗坏血酸浓度)以及萃取和分散剂溶剂体积的影响。校准曲线在卡托普利的0.77–22.50nmolL -1 范围内呈线性,检出限为0.51nmolL − 1 ,卡托普利的11.54和19.23nmolL − 1 的相对标准偏差是2.12和0.72%,分别。该方法用于测定药物,人血清和尿液中的分析物,具有较高的准确度和精密度。

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