首页> 外文期刊>Biomedical Chromatography: An International Journal Devoted to Research in Chromatographic Methodologies and Their Applications in the Biosciences >Molecularly imprinted polymer in microextraction by packed sorbent for the simultaneous determination of local anesthetics: Lidocaine, ropivacaine, mepivacaine and bupivacaine in plasma and urine samples
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Molecularly imprinted polymer in microextraction by packed sorbent for the simultaneous determination of local anesthetics: Lidocaine, ropivacaine, mepivacaine and bupivacaine in plasma and urine samples

机译:通过填充吸附剂在微萃取中分子印迹的聚合物,用于同时测定局麻药:血浆和尿液样品中的利多卡因,罗哌卡因,甲哌卡因和布比卡因

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This study presents the use of molecularly imprinted polymer (MIP) as packing material for microextraction by packed syringe (MEPS) to achieve higher extraction selectivity. Pentycaine was used as template for MIP. Development and validation of the determination of lidocaine, ropivacaine, mepivacaine and bupivacaine in human plasma and urine samples utilizing MIP-MEPS and liquid chromatography-tandem mass spectrometry (LC-MS/MS) were carried out. The MEPS MIP-cartridge could be used for 100 extractions before it was discarded. The extraction recovery ranged from 60 to 80%. The correlation coefficients values were >0.999 for all assays using lidocaine, ropivacaine, mepivacaine and bupivacaine in the calibration range 5-2000nmol/L. The accuracy of the studied compounds, given as a percentage variation from the nominal concentration values, ranged from -4.9 to 8.4% using plasma and urine samples. The between-batch precision, given as the relative standard deviation, at three different concentrations (quality control samples) was ranged from -4.7 to 14.0% and from 1.8 to 12.7% in plasma and urine, respectively. The lower limit of quantification and limit of detection of the studied substances were 5.0 and 1.0nm, respectively.
机译:这项研究提出了使用分子印迹聚合物(MIP)作为填充材料的包装注射器(MEPS)进行微萃取,以实现更高的萃取选择性。 Pentycaine被用作MIP的模板。使用MIP-MEPS和液相色谱-串联质谱(LC-MS / MS)进行了人类血浆和尿液样品中利多卡因,罗哌卡因,罗非卡因和布比卡因测定的开发和验证。 MEPS MIP弹药筒在丢弃前可用于100次提取。提取回收率范围为60%至80%。在5-2000nmol / L的校准范围内,所有使用利多卡因,罗哌卡因,甲哌卡因和布比卡因的测定的相关系数值均> 0.999。使用血浆和尿液样品,所研究化合物的准确度(与标称浓度值的百分比变化)为-4.9至8.4%。血浆和尿液中三种不同浓度(质量控制样品)的批间精密度(相对标准偏差)分别为-4.7至14.0%和1.8至12.7%。被研究物质的定量下限和检测限分别为5.0nm和1.0nm。

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