HOLLOW FIBER/SOLVENT BAR MICROEXTRACTION COUPLED WITH HIGH PERFORMANCE LIQUID CHROMATOGRAPHY FOR PRECONCENTRATION AND DETERMINATION OF TANSHINONES AND SALVIANOLIC ACIDS IN RADIX SALVIA MILTIORRHIZA

被引:17
作者
Ma, Wenyan [1 ]
Chen, Xuan [1 ]
Hu, Shuang [1 ]
Bai, Xiaohong [1 ]
Li, QingShan [1 ]
机构
[1] Shanxi Med Univ, Sch Pharm, Taiyuan 030001, Peoples R China
关键词
High-performance liquid chromatography; Hollow fiber solvent bar microextraction; Radix Salvia miltiorrhiza; Salvianolic acids; Tanshinones; PHASE MICROEXTRACTION; PLATELET-AGGREGATION; GAS-CHROMATOGRAPHY; SAMPLE PREPARATION; BACK-EXTRACTION; PESTICIDES; URINE; DRUGS;
D O I
10.1080/00032719.2013.836658
中图分类号
O65 [分析化学];
学科分类号
070302 [分析化学];
摘要
Hollow fiber solvent bar microextraction coupled with high-performance liquid chromatography was developed for the preconcentration and determination of active ingredients in Radix Salvia miltiorrhiza. These ingredients include dihydrotanshinone I, cryptotanshinone, tanshinone I, tanshinone IIA, salvianolic acid B, danshensu, and protocatechuic aldehyde. To evaluate the technique, seven compounds of varying polarity were used as model analytes, and a polyvinylidene fluoride hollow fiber (1.0cm) with octanol (2 mu L) was used as microextraction bar. The extraction conditions, including the identity of the hollow fiber, organic solvent, pH, salt addition, agitation speed, extraction time, and volume, were investigated and optimized. The extraction mechanism was analyzed and verified. The two main parameters, extraction recovery and enrichment factor, were obtained. Under the most favorable conditions, the enrichment factors of the analytes were 0.7-612, the limits of detection were below 1.11ngmL(-1), and the recoveries were between 95.4% and 101.3%. Thus, hollow fiber solvent bar microextraction is simple, rapid, and practical with a wide range of potential applications.
引用
收藏
页码:220 / 233
页数:14
相关论文
共 29 条
[1]
Bai XH, 2008, CHINESE J ANAL CHEM, V36, P182
[2]
Determination of the Migration of Bisphenol A from Polycarbonate by Dispersive Liquid-Liquid Microextraction Combined with High Performance Liquid Chromatography [J].
Cao, Jiangping ;
Liu, Shuhui ;
Bai, Weiwei ;
Chen, Jie ;
Xie, Qilong .
ANALYTICAL LETTERS, 2013, 46 (09) :1342-1354
[3]
Analysis of organochlorine pesticides in wine by solvent bar microextraction coupled with gas chromatography with tandem mass spectrometric detection [J].
Chia, KJ ;
Huang, SD .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2006, 20 (02) :118-124
[4]
Recent development in liquid phase microextraction for determination of trace level concentration of metals-A review [J].
Dadfarnia, Shayessteh ;
Shabani, Ali Mohammad Haji .
ANALYTICA CHIMICA ACTA, 2010, 658 (02) :107-119
[5]
Dispersive liquid-liquid microextraction based on the solidification of floating organic droplet for the determination of polychlorinated biphenyls in aqueous samples [J].
Dai, Liping ;
Cheng, Jing ;
Matsadiq, Guzalnur ;
Liu, Lu ;
Li, Jun-Kai .
ANALYTICA CHIMICA ACTA, 2010, 674 (02) :201-205
[6]
Investigation on ultrasound-assisted extraction of salvianolic acid B from Salvia miltiorrhiza root [J].
Dong, Juane ;
Liu, Yuanbai ;
Liang, Zongsuo ;
Wang, Weiling .
ULTRASONICS SONOCHEMISTRY, 2010, 17 (01) :61-65
[7]
Editorial Committee of Pharmacopoeia of People's Republic of China, 2010, PHARM PEOPL REP CHIN, P70
[8]
Development of a new dispersive liquid-liquid microextraction method in a narrow-bore tube for preconcentration of triazole pesticides from aqueous samples [J].
Farajzadeh, Mir Ali ;
Djozan, Djavanshir ;
Khorram, Parisa .
ANALYTICA CHIMICA ACTA, 2012, 713 :70-78
[9]
Three-phase hollow fiber liquid-phase microextraction based on two immiscible organic solvents for determination of tramadol in urine and plasma samples [J].
Ghambarian, Mahnaz ;
Yamini, Yadollah ;
Esrafili, Ali .
JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS, 2011, 56 (05) :1041-1045
[10]
Rapid and Simultaneous Study on Drug-Protein Binding of Four Furocoumarins by Hollow Fiber Liquid Phase Microextraction [J].
Hu, Shuang ;
Zhang, Yan Jie ;
Bai, Xiao Hong .
CHROMATOGRAPHIA, 2011, 74 (5-6) :503-506