APPLICATION OF LIQUID CHROMATOGRAPHY WITH UV DETECTION FOR DETERMINATION OF PLANT GROWTH REGULATOR IN COMMON PLANT FERTILIZERS
Poster Aug 25, 2014
Borowczyk K., Wyszczelska-Rokiel M., Stachniuk J., Chwatko G., Glowacki R.
A simple and rapid HPLC-based method was developed for the determination of plant growth regulator in plant fertilizer samples. Plant hormones including indole-3-butyric acid (IBA) are structurally diverse compounds that play an important role in a variety of processes related to plant growth and development. As a minor component of the metabolome, phytohormones play a particular role in the regulation of cell division, enlargement and differentiation, organ formation, seed dormancy and germination [1, 2, 3]. In most cases phytohormones exist in plants either by endogenous secretion or exogenous treatment to achieve various enhanced agriculture characteristics during some critical growth stages. Besides, plant hormones could stimulate the human body or at least affect their immune cells . Therefore, it is necessary to develop a simple and effective methods to detect phytohormones in plant fertilizer samples.
The separation was carried out on Zorbax SB C18 column (4.6 x 150 mm, 5 μm), using acetonitrile/water containing 0.2% acetic acid, pH=2.65 (60:40, v/v) as the isocratic mobile phase at the flow-rate of 1.0 ml/min and column temperature 25 °C. The indole-3-butyric acid was determined with UV detection at λ = 280 nm. The analyte was eluted within 2.7 min. Validation experiments showed that the optimized method has good linearity within the range 1 – 50 nmol/ml, R2 = 0.9993 and high recovery (96.4 % - 114.4 %). The detection limit based on a signal-to-noise ratio was 0.15 nmol/ml. The results indicate that the novel method has advantages of convenience, good sensitivity, high efficiency, and can be useful for the determination of indole-3-butyric acid in common plant fertilizer samples (Clonex, Korzonek Z, Korzonek S).
In museum and archives’ collection environments, fungi are a critical artifact biodeterioration factor, whereas most infections are airborne. Typical fungal infections in museums, colonizing paper made documents, are caused by species of slow-growing Ascomycetes as well as mitosporic xerophilic fungi of the genera Aspergillus, Penicillium and Cladosporium.READ MORE