Application of octadecylsiloxane-coated fiber in solid-phase microextraction for determination of organophosphorus pesticide residues in vegetables
2006
Sasithorn Tantong(Chiang Mai University, Chiang Mai (Thailand). Faculty of Pharmacy. Dept. of Pharmaceutical Sciences) E-mail:[email protected] | Surapol Natakankitkul(Chiang Mai University, Chiang Mai (Thailand). Faculty of Pharmacy. Dept. of Pharmaceutical Sciences) | Prachya Kongtawelert(Chiang Mai University, Chiang Mai (Thailand). Faculty of Medicine. Dept. of Biochemistry) | Nuchnart Jonglakha(Royal Project Foundation, Chiang Mai (Thailand))
Recently, solid-phase microextraction (SPME) and gas chromatography (GC) has been recognized as another suitable method which can solve all the mentioned problems. In this study, SPME was prepared by hydrolysis and polycondensation with octadecylsiloxane (ODS) on fused silica fiber. The efficiency of extraction by ODS SPME was compared with available commercial SPME fibers and the standard GC-FPD analytical method. Results showed that the optimum conditions for analysis of OPPs using SPME/GC with DB-1 capillary column at 30 m * 0.32 mm I.D., 1 micro m film thickness, the optimum temperature program started with 80 deg C for 30 sec then increased to 300 deg C after injection at the rate of 30 deg C/min, the temperatures of GC injector port and PFPD detector were 250 deg C and 300 deg C. One gram of blended vegetable sample in 200 ml of ultrapure water had been shaken for 2 hrs and centrifuged for 2 min, then using ODS fiber to immerse in 1 ml of the aqueous extract for 30 min at room temperature. The analytes were desorbed for 4 mins at GC injector port. The optimum conditions were then used for determining the following insecticides: chlorpyriphos, methylparathion, profenofos and prothiofos standard mixtures spiked in vegetable samples. The percentage recoveries were 99.80 percent, 101.51 percent, 104.03 percent and 106.52 percent with RSD 9.42 percent, 6.46 percent, 7.73 percent and 3.96 percent respectively. The detection limits were 5.00, 40.00, 5.00 and 50.00 micro g/l, respectively. The precision of the insecticide determination using ODS was not significantly different from using commercial coated fibers. The ODS SPME developed in this study was found to be as effective as polyacralate (PAC) (1.43-5.56 percentRSD). Analysis of mevinphos, methylparathion, prothiofos and profenofos spiked in tomato samples using ODS SPME/GC-PFPD compared with using AOAC, was not found to be statistically different in percentage of recoveries. It can be concluded that the development of ODS SPME/GC-PFPD in this study was suitable for analysis of organophosphorus insecticides: the method is simple, uses less time, no complicate extraction and without using organic solvent.
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