Tandem solid phase extraction followed by online trapping-hydrophilic interaction chromatography-tandem mass spectrometry for sensitive detection of endogenous cytokinins in plant tissues.

INTRODUCTION Cytokinins (CKs) are a group of plant hormones that play pivotal roles at low concentration in plant growth, development and regulatory pathways. In order to study the function, metabolism and signal transduction of CKs, high performance analytical techniques are required for determination of their endogenous levels. OBJECTIVE To develop a highly sensitive, selective and reliable method for identification and quantification of CKs by employing a tandem solid phase extraction (SPE)-online trapping-hydrophilic interaction chromatography (HILIC)-MS/MS method. MATERIAL AND METHODS The extraction was performed firstly with tandem SPE containing a C(18) cartridge and a silica@C(8) /SO(3) H cartridge. After CKs were eluted from the silica@C(8)/SO(3) H cartridge, the desorption solvent was concentrated and redissolved in H(2)O and then injected into the online trapping-HILIC-MS/MS system with (Poly(MAA-co-EGDMA)) monolith as the trapping column. Subsequently, trapping, washing, desorption, separation and detection were accomplished automatically on the system. RESULTS Good linearities were obtained for eight cytokinins with correlation coefficients (R(2)) > 0.9964. The limits of detection (LOD; S:N = 3) for the targets ranged from 0.042 to 1.6 pg/mL. Reproducibility of the method was evaluated with intraday and interday relative standard deviations (RSDs) less than 13.4% and the recoveries ranged from 77.3% to 116.3%. The results showed that the LOD of the analytical method were at least one order of magnitude lower compared with other previously reported methods. Furthermore, only 20 mg of plant tissues were required for the quantitative analysis of the major CKs, which is, to the best of our knowledge, the smallest amount reported so far for the determination of endogenous CKs in plant tissues. CONCLUSION The tandem SPE-online trapping-HILIC-MS/MS method developed in current study provides a powerful tool for the convenient and highly sensitive quantification of the major CKs in plant tissue.

[1]  Francesca Blum,et al.  High performance liquid chromatography. , 2014, British journal of hospital medicine.

[2]  F. Wei,et al.  Simultaneous analysis of multiple endogenous plant hormones in leaf tissue of oilseed rape by solid-phase extraction coupled with high-performance liquid chromatography-electrospray ionisation tandem mass spectrometry. , 2011, Phytochemical analysis : PCA.

[3]  Fang Wei,et al.  Determination of cytokinins in plant samples by polymer monolith microextraction coupled with hydrophilic interaction chromatography-tandem mass spectrometry , 2010 .

[4]  Renxiao Wang,et al.  Quantitative analysis of cytokinins in plants by high performance liquid chromatography: electronspray ionization ion trap mass spectrometry. , 2010, Journal of integrative plant biology.

[5]  M. Strnad,et al.  Endogenous cytokinins in Cocos nucifera L. in vitro cultures obtained from plumular explants , 2010, Plant Cell Reports.

[6]  Xuemin Wang,et al.  Quantitative analysis of major plant hormones in crude plant extracts by high-performance liquid chromatography–mass spectrometry , 2010, Nature Protocols.

[7]  K. Shudo,et al.  Cytokinins , 2014, The arabidopsis book.

[8]  A. Das,et al.  Detection and quantification of some plant growth regulators in a seaweed-based foliar spray employing a mass spectrometric technique sans chromatographic separation. , 2010, Journal of agricultural and food chemistry.

[9]  T. Roitsch,et al.  Rapid Determination of Cytokinins and Auxin in Cyanobacteria , 2010, Current Microbiology.

[10]  E. Fukusaki,et al.  Development of a method for comprehensive and quantitative analysis of plant hormones by highly sensitive nanoflow liquid chromatography-electrospray ionization-ion trap mass spectrometry. , 2009, Analytica chimica acta.

[11]  M. Matsuoka,et al.  Highly sensitive and high-throughput analysis of plant hormones using MS-probe modification and liquid chromatography-tandem mass spectrometry: an application for hormone profiling in Oryza sativa. , 2009, Plant & cell physiology.

[12]  M. Strnad,et al.  Cytokinin profiling in plant tissues using ultra-performance liquid chromatography-electrospray tandem mass spectrometry. , 2008, Phytochemistry.

[13]  E. Ong,et al.  Determination of cytokinins in coconut (Cocos nucifera L.) water using capillary zone electrophoresis‐tandem mass spectrometry , 2006, Electrophoresis.

[14]  Qiong-Wei Yu,et al.  Determination of fluoroquinolones in eggs using in-tube solid-phase microextraction coupled to high-performance liquid chromatography , 2006, Analytical and bioanalytical chemistry.

[15]  M. Hajdúch,et al.  Batch immunoextraction method for efficient purification of aromatic cytokinins. , 2005, Journal of chromatography. A.

[16]  Yuqi Feng,et al.  Poly (methacrylic acid-ethylene glycol dimethacrylate) monolithic capillary for in-tube solid phase microextraction coupled to high performance liquid chromatography and its application to determination of basic drugs in human serum , 2004 .

[17]  G. Novikova,et al.  Cytokinin signalling systems , 1996, Plant Growth Regulation.

[18]  Y. Dekishima,et al.  A new method for enzymatic preparation of isopentenyladenine-type and trans-zeatin-type cytokinins with radioisotope-labeling , 2003, Journal of Plant Research.

[19]  J. Kopka,et al.  Comprehensive chemical derivatization for gas chromatography-mass spectrometry-based multi-targeted profiling of the major phytohormones. , 2003, Journal of chromatography. A.

[20]  M. Strnad,et al.  Quantitative analysis of cytokinins in plants by liquid chromatography–single-quadrupole mass spectrometry , 2003 .

[21]  P. Dobrev,et al.  Fast and efficient separation of cytokinins from auxin and abscisic acid and their purification using mixed-mode solid-phase extraction . , 2002, Journal of chromatography. A.

[22]  A. Székács,et al.  Immunoassays for plant cytokinins as tools for the assessment of environmental stress and disease resistance , 2000 .

[23]  P. Hernández,et al.  Voltammetry study of zeatin in a carbon fiber ultramicroelectrode. Determination by adsorptive stripping , 1997 .

[24]  E. Tillberg,et al.  Acetylation of Cytokinins and Modified Adenine Compounds: A Simple and Non-destructive Derivatization Method for Gas Chromatography–Mass Spectrometric Analysis , 1996 .

[25]  P. Hernández,et al.  Determination of Zeatin in plant extracts by square wave stripping polarography and differential pulse stripping polarography , 1995 .

[26]  C. Hocart,et al.  A procedure for quantification of cytokinins as free bases involving scintillation proximity immunoassay , 1995 .

[27]  B. Sotta,et al.  A biotin-avidin-based enzyme immunoassay to quantify three phytohormones: auxin, abscisic acid and zeatin-riboside , 1986 .

[28]  R. Bieleski THE PROBLEM OF HALTING ENZYME ACTION WHEN EXTRACTING PLANT TISSUES. , 1964, Analytical biochemistry.