Reduced graphene oxide as an efficient sorbent in microextraction by packed sorbent: Determination of local anesthetics in human plasma and saliva samples utilizing liquid chromatography-tandem mass spectrometry

被引:12
作者
Ahmadi, Mazaher [1 ]
Moein, Mohammad Mahdi [2 ,3 ]
Madrakian, Tayyebeh [1 ]
Afkhami, Abbas [1 ]
Bahar, Soleiman [4 ]
Abdel-Rehim, Mohamed [2 ,3 ,5 ]
机构
[1] Bu Ali Sina Univ, Fac Chem, Hamadan, Iran
[2] Karolinska Inst, Ctr Psychiat Res, Dept Clin Neurosci, SE-17176 Stockholm, Sweden
[3] Stockholm Cty Council, SE-17176 Stockholm, Sweden
[4] Univ Kurdistan, Fac Sci, Dept Chem, Sanandaj, Iran
[5] KTH Royal Inst Technol, Div Mat & Nanofys MNF, Stockholm, Sweden
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2018年 / 1095卷
关键词
Local anesthetics; Microextraction by packed sorbent; Reduced graphene oxide; LC-MS/MS; Plasma; Saliva; SOLID-PHASE EXTRACTION; GAS-CHROMATOGRAPHY; ONLINE MICROEXTRACTION; POLYSULFONE MEMBRANE; DRUGS; NANOMATERIALS; BIOANALYSIS; MEPS;
D O I
10.1016/j.jchromb.2018.07.036
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Herein, reduced graphene oxide (RGO) has been utilized as an efficient sorbent in microextraction by packed sorbent (MEPS). The combination of MEPS and liquid chromatography-tandem mass spectrometry has been used to develop a method for the extraction and determination of three local anesthetics (i.e. lidocaine, prilocaine, and ropivacaine) in human plasma and saliva samples. The results showed that the utilization of RGO in MEPS could minimize the matrix effect so that no interfering peaks at the retention times of the analytes or internal standard was observed. The high extraction efficiency of this method was approved by mean recoveries of 97.26-106.83% and 95.21-105.83% for the studied analytes in plasma and saliva samples, respectively. Intra- and inter-day accuracies and precisions for all analytes were in good accordance with the international regulations. The accuracy values (as percentage deviation from the nominal value) of the quality control samples were between - 2.1 to 13.9 for lidocaine, - 4.2 to 11.0 for prilocaine and between - 4.5 to - 2.4 for ropivacaine in plasma samples while the values were ranged from - 4.6 to 1.6 for lidocaine, from - 4.2 to 15.5 for prilocaine and from - 3.3 to - 2.3 for ropivacaine in human saliva samples. Lower and upper limit of quantification (LLOQ, ULOQ) were set at 5 and 2000 nmol L-1 for all of the studied drugs. The correlation coefficients values were >= 0.995. The limit of detection values were obtained 4 nmol L-1 for lidocaine and prilocaine, and 2 nmol L-1 for ropivacaine.
引用
收藏
页码:177 / 182
页数:6
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