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首页> 外文期刊>Analytical methods >Hollow fiber liquid based microextraction combined with high-performance liquid-chromatography for the analysis of lidocaine in biological and pharmaceutical samples
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Hollow fiber liquid based microextraction combined with high-performance liquid-chromatography for the analysis of lidocaine in biological and pharmaceutical samples

机译:中空纤维液微萃取结合高效液相色谱法分析生物和药物样品中的利多卡因

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This work presents a hollow fiber liquid—liquid—liquid microextraction (HF-LLLME) technique for extracting lidocaine from human plasma, urine and injection vial samples. It was combined with high-performance liquid-chromatography-ultraviolet detection (HPLC-UV). In this experiment, lidocaine was successively extracted from a sample donor phase into several microliters of an organic phase and then from the organic phase into an aqueous extract acceptor phase. The following separation and quantitative analyses were performed using HPLC/UV with 205 nm detection. Extraction conditions such as solvent selection, acceptor phase pH and donor phase pH, agitation rate, extraction time and salt addition effect were investigated and optimized. Under optimum conditions, a limit of detection (LOD) of 0.01 μg mL~(-1), a linear range of 0.05-2 ng mL~(-1) (n = 9) and a correlation of determination (R~2) of 0.9994 were obtained. The intra-day relative standard deviation based on three replicate determinations in one day for three days for 0.8 μg mL~(-1) was 8.2% and inter-day relative standard deviations (RSD%) based on five replicate measurements in one day for 0.8 μg mL~(-1) and 0.08 μg mL~(-1) were 2.01% and 6.90%, respectively. Extraction and determination of lidocaine in human plasma, urine and injection vial samples were successfully performed.
机译:这项工作提出了一种中空纤维液-液-液微萃取(HF-LLLME)技术,用于从人血浆,尿液和注射瓶样品中提取利多卡因。它与高效液相色谱-紫外线检测(HPLC-UV)结合使用。在该实验中,利多卡因连续从样品供体相中提取到几微升有机相中,然后从有机相中提取到水相提取物受体相中。使用HPLC / UV和205 nm检测进行以下分离和定量分析。研究和优化了萃取条件,如溶剂选择,受体相pH和供体相pH,搅拌速率,萃取时间和加盐效果。在最佳条件下,检出限(LOD)为0.01μgmL〜(-1),线性范围为0.05-2 ng mL〜(-1)(n = 9),测定的相关性(R〜2)获得0.9994。对于0.8μgmL〜(-1),基于一日三天重复测定的三天的日内相对标准偏差为8.2%,基于一天中五次重复测定的日间相对标准偏差(RSD%)为0.8μgmL〜(-1)和0.08μgmL〜(-1)分别为2.01%和6.90%。成功地进行了人血浆,尿液和注射瓶样品中利多卡因的提取和测定。

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