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Application News No.L502 Supercritical Fluid Extraction / Chromatography Analysis of Residual Pesticides in Agricultural Products Using Nexera UC Off-Line SFE-GC/MS System LAAN-A-LC-E278 Since enforcement of the positive list system for residual pesticides in foods in 2006 in Japan, over 800 pesticides have been included in the system. Consequently, there is now a strong demand for effective analytical methods encompassing any sample pretreatment steps that are capable of inspecting large numbers of pesticides. Conventionally, analysis of residual pesticides in foods has involved pesticide extraction by a solvent extraction method before analysis by LC/MS or GC/MS. The problem with solvent extraction methods is that sample pretreatment requires a substantial amount of time and effort, and large quantities of organic solvents are used. Supercritical fluid extraction (SFE) that uses supercritical carbon dioxide as the extraction solvent provides good extraction efficiency, where the solvent is similar to gas in terms of low viscosity and high diffusivity, and similar to fluid in terms of high solubility. This allows for extraction within a short period of time. This extraction method is also less damaging to the environment since it uses a smaller amount of organic solvent compared to conventional solvent extraction methods. We introduce an example GC/MS analysis of pesticides extracted from an agricultural products using the Nexera UC off-line SFE system. Meanwhile, as shown in Fig. 2, sample preparation for the Nexera UC off-line SFE system only involves mixing 1 g of agricultural product pulverized in a mixer with 1 g of dehydrating agent*, then filling the extraction vessel with this mixture. This not only results in improved productivity and a reduced environmental burden, but also avoids human errors involved in the sample pretreatment process. Using a specially designed rack changer also allows for extraction of a maximum of 48 samples consecutively. * "Miyazaki Hydro-Protect" Patent No. 3645552 n Off-Line SFE System n Sample Preparation Fig. 1 shows the principle behind operation of the Nexera UC off-line SFE system. An extraction vessel filled with a sample is placed in the SFE unit, and is heated to 40 °C (Fig. 1 A). The extraction vessel is then filled with supercritical carbon dioxide, and the target components are extracted statically without pumping the liquid (Fig. 1 B). After static extraction, dynamic extraction is performed by pumping supercritical carbon dioxide through the extraction vessel (Fig. 1 C). After trapping the extract material in the trap column, eluate that contains the target components is then collected in the fraction collector (Fig. 1 D). The QuEChERS method that prioritizes simplicity and speed is widely used to pretreat agricultural products for residual pesticide analysis. While there is a special kit available for the QuEChERS method, sample preparation for this kit requires a large number of process steps including reagent addition, solvent extraction, purification by dispersive solid phase extraction, and centrifugal separation. Fig. 2 Sample Preparation Fig. 1 Flow of Off-Line SFE Extraction (A) (B) (C) (D) CO2 cylinder Collection tubes Solvent delivery pump CO2 pump SFE unit Back pressure regulator Column oven Fraction collector Trap column Pressure control ON Extraction vessel 15MPa Atmospheric pressure Modifier Eluate CO2 cylinder Collection tubes Solvent delivery pump CO2 pump SFE unit Back pressure regulator Column oven Fraction collector Trap column Pressure control ON Extraction vessel 15MPa Atmospheric pressure Modifier Eluate CO2 cylinder Collection tubes Solvent delivery pump CO2 pump SFE unit Back pressure regulator Column oven Fraction collector Trap column Pressure control ON Extraction vessel 15MPa Atmospheric pressure Modifier Eluate CO2 cylinder Collection tubes Solvent delivery pump CO2 pump SFE unit Back pressure regulator Column oven Fraction collector Trap column Pressure control OFF Extraction vessel Atmospheric pressure Atmospheric pressure Modifier Eluate Homogenize Add absorbent Mix Enclose in extraction vessel Homogenize Add solvent Stir Add reagent Stir Centrifuge Centrifuge Stir Add reagent Transfer supernatant Conventional (QuEChERS) Pretreatment Method Nexera UC Pretreatment Rack changer Mixing agricultural product with dehydrating agent
Application News No. L502 Table 1 Analytical Conditions n Analysis of Brown Rice A mixed standard solution of pesticides for GC/MS analysis (Hayashi Pure Chemical PL2005 Pesticide GC/ MS Mix I-VI, 7) was added to pulverized brown rice to a concentration of 100 ng/g, and SFE was performed using the conditions shown in Table 1. The extraction liquid obtained was made up to 2 mL using eluate, and analyzed by GC/MS. The MRM chromatogram obtained from GC/MS analysis is shown in Fig. 4. Good repeatability (relative standard deviation of quantitation concentration <10 %) and recovery (70-120 %) were obtained for the 301 components. Repeatability and recovery for the 301 pesticides are shown in Table 2. This system uses a very simple pretreatment process, and can perform automated extraction from a single sample in approximately 30 minutes. [SFE] Nexera UC SFE System Extraction : A) Supercritical fluid of CO2 Solvent B) Methanol Flowrate : 5 mL/min Extraction : 8 min (Static mode → Dynamic mode) Extraction Vessel Temp. : 40 ˚C BPR Pressure : 15 MPa Trap Column : Shim-pack VP-ODS (50 mm L. × 4.6 mm I.D., 5 μm) Elution Solvent : Acetone/Hexane = 50/50 (2 mL/min, 2 min) [GC-MS] GCMS-TQ8040 Column : Rxi ® -5Sil MS 30 m × 0.25 mm I.D., df = 0.25 μm Column Temp. : 50 ˚C (1 min) → (25 ˚C/min) → 125 ˚C → (10 ˚C/min) → 300 ˚C (15 min) Carrier Gas : He (Constant linear velocity mode) Linear Velocity : 47.2 cm/sec Injection Mode : Splitless (Sampling time 1.00 min) High Press Inj. : 250 kPa (1.5 min) Injection Volume : 1 μL Interface Temp. : 250 ˚C Ion Source Temp. : 200 ˚C MS Mode : MRM Loop Time : 0.3 sec Fig. 3 Recovery in Brown Rice Analysis Fig. 4 MRM Chromatogram of Extraction Liquid from Brown Rice Table 2 Repeatability and Recovery Compounds Repeatability (%RSD, n = 6) Recovery (%) 2-Phenylphenol 3.8 87.0 Acetochlor 5.9 93.1 Acrinathrin-1 6.8 73.8 Acrinathrin-2 3.1 100.6 Alachlor 3.6 88.7 Allethrin-3,4 5.9 102.0 Allidochlor 5.3 86.4 alpha-BHC 4.6 88.9 alpha-Endosulfan 9.5 98.7 Ametryn 4.1 86.3 Anilofos 4.7 86.3 Atrazine 4.8 86.7 Azaconazole 5.5 70.5 Azamethiphos 9.9 78.4 Compounds Repeatability (%RSD, n = 6) Recovery (%) Azinphos-ethyl 5.3 84.3 Azinphos-methyl 2.7 83.1 Benalaxyl 7.0 84.9 Benfluralin 5.2 90.1 Benfuresate 4.1 91.5 Benoxacor 3.2 90.8 beta-BHC 5.3 87.8 beta-Endosulfan 6.5 90.7 Bifenox 4.1 84.5 Bifenthrin 3.3 89.2 Biphenyl 3.5 80.5 Bromobutide 4.6 90.4 Bromophos 5.4 90.1 Bromophos-ethyl 6.0 86.6
Application News No. L502 Table 2 Repeatability and Recovery (continued) Compounds Repeatability (%RSD, n = 6) Recovery (%) Bromopropylate 4.1 90.9 Bromuconazole-1 3.7 80.5 Bromuconazole-2 5.3 77.1 Bupirimate 7.9 86.8 Buprofezin 6.6 88.8 Butachlor 6.4 91.6 Butafenacil 4.4 90.4 Butamifos 3.8 90.1 Butylate 4.6 84.7 Cadusafos 4.1 88.1 Cafenstrole 5.1 91.1 Captan 9.1 77.6 Carbofuran 4.7 83.3 Carbophenothion 2.9 91.5 Carfentrazone-ethyl 4.1 96.8 Chinomethionat 4.2 82.1 Chlomethoxyfen 5.8 89.8 Chlorbenside 3.9 81.1 Chlorbufam 4.2 84.7 Chlorethoxyfos 4.6 90.3 Chlorfenapyr 7.5 86.5 Chlorfenson 7.7 91.4 Chlorfenvinphos-(E) 4.4 91.2 Chlorfenvinphos-(Z) 6.5 88.7 Chlormephos 3.1 89.6 Chlorobenzilate 3.6 92.0 Chloroneb 6.0 95.0 Chlorothalonil 5.3 87.7 Chlorpropham 4.9 88.5 Chlorpyrifos 6.2 90.8 Chlorpyrifos-methyl 5.1 90.5 Chlorthiophos-2 9.5 88.4 Chlorthiophos-3 2.8 92.8 Chlozolinate 7.8 82.4 Cinidon-ethyl 4.3 88.8 Cinmethylin 9.9 94.5 Clomazone 4.2 88.6 Clomeprop 3.3 89.8 Crimidine 6.0 80.0 Cyanofenphos 4.7 91.8 Cyanophos 5.0 91.3 Cyflufenamid 8.4 89.6 Cyfluthrin-1 5.1 95.6 Cyfluthrin-2 3.5 94.6 Cyfluthrin-3 4.9 92.0 Cyfluthrin-4 6.0 90.8 Cyhalofop-butyl 4.2 93.4 Cyhalothrin-1 9.1 90.6 Cyhalothrin-2 4.5 94.4 Cypermethrin-1 2.8 99.0 Cypermethrin-2 3.7 96.6 Cypermethrin-3 3.7 93.2 Cypermethrin-4 8.4 93.2 Cyprodinil 4.0 80.9 delta-BHC 2.2 88.2 Deltamethrin-2 3.7 103.2 Dialifos 3.2 91.4 Di-allate-1 2.5 91.5 Di-allate-2 4.7 92.0 Diazinon 7.8 90.0 Dichlobenil 4.0 79.8 Dichlofenthion 5.2 92.1 Dichlofluanid 3.3 87.2 Dichlorvos 3.2 83.9 Diclobutrazol 5.2 87.0 Diclocymet-1 4.3 83.4 Diclocymet-2 5.1 82.2 Diclofop-methyl 4.4 91.0 Diethofencarb 4.8 83.8 Difenoconazole-1 5.5 74.0 Difenoconazole-2 5.2 72.4 Diflufenican 4.4 94.3 Dimepiperate 2.5 87.8 Dimethametryn 6.4 84.8 Dimethenamid 5.4 88.8 Dimethipin 9.9 70.9 Dimethylvinphos-(E) 4.5 86.8 Dimethylvinphos-(Z) 4.9 86.1 Diniconazole 2.3 80.6 Dioxabenzofos 4.4 91.5 Dioxathion 5.4 88.6 Dioxathion deg. 4.4 86.1 Compounds Repeatability (%RSD, n = 6) Recovery (%) Diphenamid 5.7 79.3 Diphenylamine 3.1 91.5 Disulfoton sulfone 5.2 85.0 Ditalimfos 3.2 90.1 Dithiopyr 5.1 90.9 Edifenphos 3.5 95.9 Endosulfan sulfate 6.9 95.4 EPN 3.8 88.0 Epoxiconazole 3.7 83.9 EPTC 4.3 81.6 Esprocarb 2.7 90.6 Ethalfluralin 5.3 93.3 Ethion 3.4 93.1 Ethofumesate 5.7 91.4 Ethoprophos 4.3 91.0 Etobenzanid 3.8 86.6 Etofenprox 3.8 89.7 Etoxazole 8.2 87.9 Etridiazole 3.8 85.3 Etrimfos 2.9 87.9 Famoxadone 5.4 71.2 Fenamidone 5.7 70.1 Fenchlorphos 6.0 92.1 Fenitrothion 6.9 88.7 Fenothiocarb 5.4 88.6 Fenoxanil 6.2 88.2 Fenoxaprop-ethyl 4.1 90.5 Fenoxycarb 6.9 84.4 Fenpropathrin 3.7 91.6 Fenpropimorph 4.7 76.8 Fenthion 3.6 79.5 Fenvalerate-1 5.2 88.4 Fenvalerate-2 4.2 95.0 Fipronil 8.3 86.7 Flamprop-methyl 6.6 85.7 Fluacrypyrim 6.8 97.0 Flucythrinate-1 4.0 92.8 Flucythrinate-2 3.7 95.7 Flufenpyr-ethyl 1.8 98.0 Flumiclorac-pentyl 5.8 91.8 Flumioxazin 9.4 75.0 Fluquinconazole 4.3 81.2 Flusilazole 5.5 86.8 Fluthiacet-methyl 3.8 79.5 Flutolanil 9.6 87.8 Fluvalinate-1 2.6 100.0 Fluvalinate-2 2.6 98.6 Folpet 5.3 87.7 Fonofos 3.8 91.7 Formothion 5.3 74.4 Fosthiazate-2 9.6 93.2 Furilazole 3.3 92.4 gamma-BHC 4.1 88.7 Halfenprox 2.3 85.4 Hexaconazole 8.9 85.6 Indanofan 7.9 86.5 Indoxacarb 3.7 95.7 Iprobenfos 4.4 89.5 Iprodione 2.5 92.7 Iprodione metabolite 3.1 106.2 Isazofos 3.7 94.2 Isocarbophos 6.6 84.0 Isofenphos 3.2 89.0 Isofenphos oxon 5.2 84.5 Isoprocarb 4.5 86.6 Isoprothiolane 7.5 86.1 Isoxadifen-ethyl 5.0 90.5 Isoxathion 6.7 93.2 Kresoxim-methyl 7.0 89.7 Leptophos 3.5 93.3 Malathion 3.2 93.0 MCPB-ethyl 3.5 90.3 Mecarbam 8.4 97.6 Mefenacet 4.5 75.1 Mefenpyr-diethyl 5.0 90.4 Mepronil 4.2 79.5 Metalaxyl 7.0 86.6 Methacrifos 5.9 92.3 Methidathion 4.5 86.0 Methoprene 8.8 109.6 Methoxychlor 3.1 90.6 Metolachlor 2.9 91.1
Application News No. For Research Use Only. Not for use in diagnostic procedures. The content of this publication shall not be reproduced, altered or sold for any commercial purpose without the written approval of Shimadzu. The information contained herein is provided to you "as is" without warranty of any kind including without limitation warranties as to its accuracy or completeness. Shimadzu does not assume any responsibility or liability for any damage, whether direct or indirect, relating to the use of this publication. This publication is based upon the information available to Shimadzu on or before the date of publication, and subject to change without notice. © Shimadzu Corporation, 2016 www.shimadzu.com/an/ L502 First Edition: Jan. 2016 Table 2 Repeatability and Recovery (continued) Compounds Repeatability (%RSD, n = 6) Recovery (%) Metominostrobin-(E) 9.6 72.4 Metribuzin 6.5 75.1 Mevinphos-1 9.9 92.3 Mevinphos-2 6.0 85.4 Molinate 3.8 86.0 Myclobutanil 5.9 75.7 Naled 6.1 72.8 Nitralin 4.5 94.2 Nitrofen 8.1 88.9 Nitrothal-isopropyl 2.4 90.2 Oxabetrinil 3.4 91.7 Oxadiazon 3.9 94.7 Oxpoconazole 6.4 74.7 Oxpoconazole-formyl deg. 9.9 88.9 Oxyfluorfen 8.9 88.3 Paclobutrazol 7.5 72.6 Parathion 6.3 90.1 Parathion-methyl 5.1 90.4 Penconazole 4.7 85.0 Pendimethalin 5.1 86.9 Pentoxazone 4.2 95.6 Permethrin-1 4.8 89.0 Permethrin-2 4.0 88.8 Phenothrin-1 7.4 93.1 Phenothrin-2 2.5 90.2 Phenthoate 2.4 91.7 Phorate 4.1 75.9 Phosalone 3.5 88.1 Phosmet 4.2 84.5 Phosphamidon-1 8.6 75.8 Phosphamidon-2 6.6 70.8 Picolinafen 4.0 90.4 Piperonyl butoxide 3.8 89.2 Piperophos 3.5 88.9 Pirimiphos-methyl 5.7 90.8 Pretilachlor 5.6 89.8 Procymidone 7.0 91.6 Profenofos 5.6 94.1 Prohydrojasmon-1 5.5 87.7 Prohydrojasmon-2 8.7 88.6 Prometryn 3.0 86.8 Propachlor 4.4 88.0 Propargite-1 9.3 101.3 Propargite-2 9.5 94.5 Propazine 4.0 97.1 Propiconazole-1 6.7 89.4 Propiconazole-2 3.2 88.3 Propoxur 5.3 83.9 Propyzamide 4.2 81.6 Prothiofos 4.0 85.5 Pyraclofos 5.1 94.1 Pyraclostrobin 4.7 93.1 Pyraflufen-ethyl 4.7 92.7 Pyrazophos 4.2 92.8 Pyrazoxyfen 9.4 91.2 Pyributicarb 3.1 88.1 Pyridaben 3.1 86.1 Pyridaphenthion 5.4 84.2 Pyrifenox-(E) 5.9 85.2 Pyrifenox-(Z) 7.3 92.9 Pyrimethanil 6.0 83.9 Pyrimidifen 4.9 74.2 Pyriminobac-methyl-(E) 3.9 88.6 Pyriminobac-methyl-(Z) 5.2 88.6 Pyriproxyfen 5.7 92.1 Quinalphos 3.3 93.2 Quinoxyfen 3.2 87.1 Quintozene 6.0 90.3 Quizalofop-ethyl 3.0 86.9 Resmethrin-1 6.2 88.5 Resmethrin-2 3.3 86.1 Silafluofen 3.7 88.6 Compounds Repeatability (%RSD, n = 6) Recovery (%) Simazine 5.2 74.9 Simeconazole 6.1 79.1 Simetryn 5.0 74.1 Spirodiclofen 4.6 94.1 Sulfotep 3.9 92.9 Sulprofos 4.8 74.5 Swep 5.3 83.6 Tebufenpyrad 3.6 88.8 Tebupirimfos 4.6 89.4 Tecnazene 3.1 89.5 Tefluthrin 4.5 90.1 Terbucarb 4.0 87.6 Terbufos 3.8 77.9 Terbutryn 4.5 86.0 Tetrachlorvinphos 3.2 93.0 Tetraconazole 7.8 84.3 Tetradifon 5.9 89.5 Tetramethrin-1 6.9 93.8 Tetramethrin-2 4.3 90.9 Thenylchlor 3.5 87.3 Thifluzamide 5.9 84.6 Thiobencarb 3.5 85.6 Tolclofos-methyl 3.9 90.6 Tolfenpyrad 3.6 81.0 Tolylfluanid 5.8 91.1 Triadimefon 3.7 88.3 Triadimenol-1 6.2 70.8 Tri-allate 5.3 91.2 Triazophos 4.7 89.9 Tribufos 6.2 90.6 Trichlamide 5.2 85.3 Trifloxystrobin 5.9 90.7 Trifluralin 3.2 92.5 Vinclozolin 4.2 89.6 XMC 3.9 86.5 Xylylcarb 4.5 85.3 Zoxamide 3.6 82.6
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