Improved methodology for assaying brassinosteroids in plant tissues using magnetic hydrophilic material for both extraction and derivatization

• Published in: Plant methods 2014-11, Vol.10 (1), p.39-39, Article 39
• Main Authors: Ding, Jun, Wu, Jian-Hong, Liu, Jiu-Feng, Yuan, Bi-Feng, Feng, Yu-Qi
• Format: Article
• Language: English
• Subjects: Analysis; Analytical methods; Brassica napus; brassinosteroids; Chromatography; Cytokinins; derivatization; growth and development; hydrophilicity; Liquid chromatography; Mass spectrometry; Methodology; Methods; microextraction; Plant growth; plant hormones; Plant tissues; Sample preparation; Silica; solid phase extraction; Titanium dioxide
• ISSN: 1746-4811; 1746-4811
• DOI: 10.1186/1746-4811-10-39

BACKGROUND: Brassinosteriods (BRs) are a group of important phytohormones that have major effects on plant growth and development. To fully elucidate the function of BRs, a sensitive BR assay is required. However, most of the previously reported methods are tedious and time-consuming due to multiple pretreatment steps. Therefore, it is of great significance to develop a method to increase the throughput and detection sensitivity of BR analysis. RESULTS: We established a novel analytical method of BRs based on magnetic solid phase extraction (MSPE) combined with in situ derivatization (ISD). TiO₂-coated magnetic hollow mesoporous silica spere(TiO₂/MHMSS) was served as a double identity- a microextraction sorbent and “microreactor” for the capture and derivatization of BRs in sequence. BRs were first extracted onto TiO₂/MHMSS through hydrophilic interaction. The BR-adsorbed TiO₂/MHMSS was then employed as a “microreactor” for the derivatization of BRs with 4-(N,N-dimethyamino)phenylboronic acid (DMAPBA). The MSPE-ISD method was simple and fast, which could be accomplished within 10 min. Furthermore, the derivatives of BRs showed better MS response because they were incorporated with tertiary amino groups. Uniquely, endogenous BRs were detected in only 100 mg fresh weight plant tissue. CONCLUSION: Our proposed MSPE-ISD method for the determination of endogenous BRs is rapid and sensitive. It can be applied to the analysis of endogenous BRs in 100 mg fresh plant tissue (Brassica napus L. (B. napus L)). The proposed strategy for plant sample preparation may be extended to develop analytical methods for determination of a wide range of analytes with poor MS response in other complex sample matrices.