scholarly journals Rapid resolution liquid chromatography method for determination of malathion in pesticide formulation

2020 ◽  
Vol 32 (4) ◽  
pp. 256-259
Author(s):  
L. Velkoska-Markovska ◽  
B. Petanovska-Ilievska

This paper presents a new, simple, precise, and accurate rapid resolution liquid chromatography (RRLC) method for determination of an active ingredient malathion in the pesticide formulation. The analysis was performed on a Poroshell EC 120-C18 (50 mm × 3 mm, 2.7 μm) analytical column using isocratic elution with a mobile phase consisted of acetonitrile–water (50:50, v/v), a flow rate of 1 mL/min, a constant column temperature at 25 °C, and ultraviolet-diode array detection (UV-DAD) at 220 nm. The specificity, selectivity, linearity, precision, and accuracy were tested for the method validation according to the Collaborative International Pesticides Analytical Council (CIPAC) and Directorate General Health and Consumer Protection (SANCO) guidelines and all tested parameters were found within acceptance criteria. The obtained results indicated that the proposed method can be used for routine analysis of the active ingredient malathion in the pesticide formulation “Etiol tecni” following the CIPAC and SANCO rules. The run time of analysis under the stipulated chromatographic conditions was about 2.5 min, meaning that the proposed method requires a small volume (< 1.5 mL) of the organic solvent (acetonitrile) making it cost-effective.

2020 ◽  
Vol 15 (1) ◽  
pp. 27-32
Author(s):  
Pelin Kцseoğlu Yılmaz ◽  
Mehmet Akif Tokat

In this study, a new high performance liquid chromatography method with fluorescence detection was developed and validated for the simultaneous determination of methyl paraben, ethyl paraben, propyl paraben, isopropyl paraben, butyl paraben and benzyl paraben in cosmetics. Separations were achieved using a C18 guard column (2.1 Ч 10 mm, 3 µm) and a C18 analytical column (2.1 Ч 150 mm, 3 µm). Isocratic elution was applied with a mobile phase consisting of 45 % aqueous o-phosphoric acid solution (0.08 %) and 55 % methanol/water mixture (90 : 10 v/v). The excitation and the emission wavelengths were 254 and 310 nm, respectively. Column temperature was fixed at 40 єC. The linear range was 0.50-10.00 μg/mL for all of the parabens. Limits of detection and quantification were in the range of 0.29-0.32 μg/mL and 0.88-0.97 μg/ mL, respectively. Precision and accuracy values were calculated by analysis results of standard solutions at 0.50, 2.50 and 10.00 μg/mL. The developed and validated method was applied for simultaneous quantitative determination of six paraben species in cosmetic tonic and micellar water samples successfully.


2006 ◽  
Vol 835 (1-2) ◽  
pp. 131-135 ◽  
Author(s):  
Geetha Ramachandran ◽  
A.K. Hemanth Kumar ◽  
Soumya Swaminathan ◽  
P. Venkatesan ◽  
V. Kumaraswami ◽  
...  

2014 ◽  
Vol 6 (16) ◽  
pp. 6560-6564 ◽  
Author(s):  
Wuxiang Zhang ◽  
Yicong Su ◽  
Jiangu Shi ◽  
Maosheng Zhang ◽  
Bide Wu ◽  
...  

In this paper, a high performance liquid chromatography technique is established for quantification of paraquat in blood.


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