Analysis of Organochlorine Pesticides in a Soil Sample by a Modified QuEChERS Approach Using Ammonium Formate

Miguel &#193;ngel Gonz&#225;lez-Curbelo

doi:10.3791/64901

JoVE Journal > Chemistry

Chimica

Analysis of Organochlorine Pesticides in a Soil Sample by a Modified QuEChERS Approach Using Ammonium Formate

Published: January 20, 2023

doi:

10.3791/64901

Miguel Ángel González-Curbelo¹

¹Departamento de Ciencias Básicas, Facultad de Ingeniería,Universidad EAN

Summary

The present protocol describes the utilization of ammonium formate for phase partitioning in QuEChERS, together with gas chromatography-mass spectrometry, to successfully determine organochlorine pesticide residues in a soil sample.

Abstract

Currently, the QuEChERS method represents the most widely used sample preparation protocol worldwide for analyzing pesticide residues in a broad variety of matrices both in official and non-official laboratories. The QuEChERS method using ammonium formate has previously proven to be advantageous compared to the original and the two official versions. On the one hand, the simple addition of 0.5 g of ammonium formate per gram of sample is sufficient to induce phase separation and achieve good analytical performance. On the other hand, ammonium formate reduces the need for maintenance in routine analyses. Here, a modified QuEChERS method using ammonium formate was applied for the simultaneous analysis of organochlorine pesticide (OCP) residues in agricultural soil. Specifically, 10 g of the sample was hydrated with 10 mL of water and then extracted with 10 mL of acetonitrile. Next, phase separation was carried out using 5 g of ammonium formate. After centrifugation, the supernatant was subjected to a dispersive solid-phase extraction clean-up step with anhydrous magnesium sulfate, primary-secondary amine, and octadecylsilane. Gas chromatography-mass spectrometry was used as the analytical technique. The QuEChERS method using ammonium formate is demonstrated as a successful alternative for extracting OCP residues from a soil sample.

Introduction

The need to increase food production has led to the intensive and widespread use of pesticides worldwide over the last few decades. Pesticides are applied to the crops to protect them from pests and increase crop yields, but their residues usually end up in the soil environment, especially in agricultural areas¹. Furthermore, some pesticides, such as organochlorine pesticides (OCPs), have a very stable structure, so their residues do not decompose easily and persist in the soil for a long time². Generally, the soil has a high capacity to accumulate pesticide residues, especially when it has a high content of organic matter³. As a result, the soil is one of the environmental compartments most contaminated by pesticide residues. As an example, one of the complete studies to date found that 83% of 317 agricultural soils from across the European Union were contaminated with one or more pesticide residues⁴.

Soil pollution by pesticide residues may affect non-target species, soil function, and consumer health through the food chain because of the high toxicity of the residues⁵^,⁶. Consequently, the evaluation of pesticide residues in soils is essential to assess their potential negative effects on the environment and human health, particularly in developing countries due to a lack of strict regulations on the use of pesticides⁷. This makes pesticide multi-residue analysis increasingly important. However, the rapid and accurate analysis of pesticide residues in soils is a difficult challenge due to the large number of interfering substances, as well as the low concentration level and the diverse physicochemical properties of these analytes⁴.

Of all the pesticide residue analysis methods, the QuEChERS method has become the quickest, easiest, cheapest, most effective, robust, and safest option⁸. The QuEChERS method involves two steps. In the first step, a microscale extraction based on partitioning via salting-out between an aqueous and an acetonitrile layer is performed. In the second step, a cleaning process is carried out employing a dispersive solid phase extraction (dSPE); this technique uses small amounts of several combinations of porous sorbents to remove matrix-interfering components and overcomes the disadvantages of conventional SPE⁹. Hence, the QuEChERS is an environmentally friendly approach with little solvent/chemical going to waste that provides very accurate results and minimizes potential sources of random and systematic errors. In fact, it has been successfully applied for the high-throughput routine analysis of hundreds of pesticides, with strong applicability in almost all types of environmental, agri-food, and biological samples⁸^,¹⁰. This work aims to apply and validate a new modification of the QuEChERS method that was previously developed and coupled to GC-MS to analyze OCPs in agricultural soil.

Protocol

1. Preparation of the stock solutions

NOTE: It is recommended to wear nitrile gloves, a lab coat, and safety glasses during the entire protocol.

Prepare a stock solution in acetone at 400 mg/L from a commercial mix of OCPs (see Table of Materials) at 2,000 mg/L in hexane:toluene (1:1) in a 25 mL volumetric flask. Table 1 shows each of the selected OCPs.
Prepare the subsequent stock solutions in acetone at concentrations of 50 mg/L, 1 mg/L, and 0.08 mg/L in 10 mL volumetric flasks, and store them in amber glass vials at −18 °C.
NOTE: The same solutions can be used throughout the work, but it is important to store them under these conditions just after each use.
Prepare the stock solutions in acetone at concentrations of 20 mg/L and 0.4 mg/L from a commercial standard of 4,4'-DDE-d8 at 100 mg/L in acetone in 10 mL volumetric flasks, and store in amber glass vials at −18 °C. Use 4,4'-DDE-d8 as an internal standard (IS).

2. Sample collection

Collect approximately 0.5 kg of the upper 10 cm layer of an agricultural soil in a glass container. The soil object of this study was collected in a traditional agricultural zone of potato crops.
NOTE: Surface sampling with a spatula was carried out. However, the depth of the soil could influence its physicochemical characteristics. Therefore, if the organic carbon content varies with the depth, it is necessary to take samples at different depths.
Take the soil sample to the laboratory, sift it with a 1 mm diameter sieve, and store it until analysis at 4 °C in an amber glass container.
NOTE: The same soil sample can be used throughout the work, but it is important to store it under these conditions just after each use.

3. Sample preparation via the modified QuEChERS method using ammonium formate

NOTE: Figure 1 shows a schematic representation of the modified QuEChERS method.

Weigh 10 g of the soil sample in a 50 mL centrifuge tube, and add 50 µL of the IS solution at 20 mg/L to yield 100 µg/kg. For recovery purposes, also add the pesticide solutions prepared in step 1.2 to yield 10 µg/kg, 50 µg/kg, and 200 µg/kg (n = 3 each).
Shake the tube using a vortex for 30 s to better integrate the spike into the sample.
Add 10 mL of water. Shake the tube using an automated shaker at 10 x g for 5 min.
Add 10 mL of acetonitrile. Shake the tube again at 10 x g for 5 min.
Add 5 g of ammonium formate (see Table of Materials), shake the tube vigorously for 1 min by hand, and centrifuge at 1,800 x g for 5 min.
Transfer 1 mL of the acetonitrile extract to a 2 mL centrifuge tube containing 150 mg of anhydrous MgSO₄, 50 mg of primary-secondary amine (PSA), and 50 mg octadecylsilane (C₁₈) (see Table of Materials) for clean-up purposes by dispersive-solid phase extraction (d-SPE)⁸, vortex for 30 s, and centrifuge at 1,800 x g for 5 min.
Transfer 200 µL of the extract to an appropriately labeled autosampler vial with a 300 µL fused insert, and perform an instrumental analysis using a GC-MS system (step 4).
NOTE: Matrix-matched calibration is carried out following the same steps as previously using blank extracts, but 5 mL of the supernatant is cleaned in 15 mL tubes in the d-SPE step (step 3.6) and the spike and IS solutions are not added until step 3.7. Add the calibration standard solutions in the autosampler vials to yield 5 µg/kg, 10 µg/kg, 50 µg/kg, 100 µg/kg, 200 µg/kg, and 400 µg/kg, evaporate to dryness, and add 200 µL of the matrix extracts.

4. Instrumental analysis by GC-MS

Perform the GC-MS analyses using a GC-MS system with a single quadrupole mass spectrometer and an electron ionization interface (−70 eV) (see Table of Materials).
Set the MS transfer line at 280 °C and the ion source at 230 °C.
Use a 5%-phenyl-methylpolysiloxane 30 m x 250 µm x 0.25 µm column (see Table of Materials) and ultrahigh purity He as the carrier gas at a 1.2 mL/min constant flow rate.
Maintain the GC oven at 60 °C initially for 2 min, then ramp up the temperature to 160 °C at 25 °C/min, and hold for 1 min. Then, increase the temperature to 175 °C at 15 °C/min, and hold for 3 min. Then, increase to 220 °C at 40 °C/min, and hold for 3 min. Again, increase to 250 °C at 30 °C/min, and hold for 2 min. Finally, take the temperature to 310 °C at 30 °C/min, and hold for 2 min. The total analysis time is 22.125 min.
Conduct a full autotune and an air and water check of the MS before each sequence.
1. Open the MassHunter acquisition software that controls all the parameters of the GC-MS system.
  NOTE: The instrument system includes the MassHunter acquisition software by default.
2. Open the "View" option on the toolbar, and click on Vacuum control, click on Tune, and click on Autotune. The autotune will end after a few minutes.
3. Open the "View" option, and click on Instrument control.
4. Click on Yes, and save the new tune file for the autotune.
5. Open the "View" option on the toolbar, and click on Vacuum control, click on Tune again, and click on Air & Water check. The air and water check will end after a few seconds.
6. Open the "View" option, and click on Instrument control.
7. Click on Yes, and save the new tune file for the air and water check.
Perform the injection using an autosampler (see Table of Materials) at 280 °C in the splitless mode, keeping the injection volume 1.5 µL. After 0.75 min of the injection, open the split at a 40 mL/min flow rate.
NOTE: Between injections, the 10 µL syringe must be washed three times with ethyl acetate and three times with cyclohexane. All the injections are in duplicate.
Analyze the analytes in selected ion monitoring (SIM) mode. This is the standard mode used in MS systems with a single quadrupole.
NOTE: Table 1 shows the retention times (min) and the quantification parameters based on using one quantitation and two identification ions for the OCPs and the IS. The quantitative analysis is based on the ratio of the peak area of the quantitation ion to the ion of IS.

5. Data acquisition

Open the MassHunter acquisition software that controls all the parameters of the GC-MS system.
Open the "Sequence" option on the toolbar, and edit the sequence, including the sample name, the vial number, the number of injections, the instrumental method, and the name of the file to be generated. Add as many rows as necessary.
Click on OK, and save the new sequence.
Open the "Sequence" option on the toolbar again, and click on Run Sequence in the dropdown menu. A new window will open to confirm the injection method and the folder where the samples will be saved. Click on Run Sequence again, and the injection will begin.

Representative Results

The full validation of the analytical method was performed in terms of linearity, matrix effects, recovery, and repeatability.

Matrix-matched calibration curves with spiked blank samples at six concentration levels (5 µg/kg, 10 µg/kg, 50 µg/kg, 100 µg/kg, 200 µg/kg, and 400 µg/kg) were used for the linearity assessment. The determination coefficients (R²) were higher than or equal to 0.99 for all the OCPs. The lowest calibration level (LCL) was set at 5 µg/kg, which meets the maximum permissible limit established at 10 µg/kg for monitoring purposes in food applications¹¹.

The matrix effect assessment was carried out by comparing the slopes of the OCP calibration curves in pure solvent and the matrix-matched calibration curves. The matrix effect was calculated using the following equation¹²:

Matrix effect (%) = (slope of the matrix-matched calibration curve − slope of the pure solvent-based calibration curve)/(slope of the pure solvent-based calibration curve) × 100.

Figure 2 shows the matrix effect distributions for the OCPs studied by applying a modified QuEChERS method using ammonium formate to soil samples. Positive matrix effect percentages correspond to a signal enhancement, while negative percentages mean that there is signal suppression. Specifically, (1) values ranging between −20% and 20% correspond to a soft matrix effect; (2) values ranging between −20% and -50% or between 20% and 50% correspond to a medium matrix effect; (3) and values higher than 50% or lower than −50% mean that there is a strong matrix effect. As observed, more OCPs suffered soft or medium matrix effects, while fewer OCPs suffered strong matrix effects.

The recovery and repeatability were evaluated by spiking blank samples with pesticides at three concentration levels (10 µg/kg, 50 µg/kg, and 200 µg/kg). Figure 3 shows the overall recovery values and relative standard deviation (RSD) values for all the pesticides and spiking levels (n = 9). As can be observed, the great majority of the OCPs studied presented average recovery percentages in the range of 70%-120%, with RSDs lower than 20%, except heptachlor, endrin, and β-endosulfan, which gave slightly higher average recoveries.

Figure 1: Representation of the modified QuEChERS method using ammonium formate to extract pesticide residues from the soil sample. Please click here to view a larger version of this figure.

Figure 2: Distribution of the matrix effects versus retention times (min) for the 17 OCPs. A soft matrix effect corresponds to values between −20% and 20%; a medium matrix effect corresponds to values ranging between −20% and −50% or between 20% and 50%; a strong matrix effect corresponds to values that are greater than 50% or less than −50%. Please click here to view a larger version of this figure.

Figure 3: Average recoveries for the 17 OCPs after spiking 10 µg/kg, 50 µg/kg, and 200 µg/kg (n = 9) in the soil sample. The number of analytes within the acceptable recovery (70%-120 %) and RSD (<20 %) range are provided, along with those labeled outside of that range. Please click here to view a larger version of this figure.

Analyte	Retention time (min)	Quantifier ion	Qualifier ion 1	Qualifier ion 2
α-BHC	11.35	181	219	111
β-BHC	11.90	181	219	109
Lindane	12.01	181	183	219
δ-BHC	12.39	181	219	111
Heptachlor	13.24	272	100	274
Aldrin	13.94	263	66	265
Heptachlor epoxide	14.86	353	355	81
α-Endosulfan	15.71	241	239	195
4,4'-DDE-d8 (IS)	16.09	254	184	326
4,4'-DDE	16.12	246	318	248
Dieldrin	16.18	79	263	81
Endrin	16.57	263	317	345
β-Endosulfan	16.73	195	241	159
4,4'-DDD	16.89	235	237	165
Endosulfan sulfate	17.61	387	227	272
4,4'-DDT	17.65	235	237	165
Endrin ketone	18.64	317	67	315
Methoxychlor	18.86	227	228	212

Table 1: Retention times (min) and quantification parameters for the GC-MS analysis of the OCPs. Alpha-benzenehexachloride (α-BHC); beta-benzenehexachloride (β-BHC); lindane; delta-benzenehexachloride (δ-BHC); heptachlor; aldrin; heptachlor epoxide; α-endosulfan; 4,4'-dichlorodiphenyldichloroethylene-d8 (4,4'-DDE-d8) (IS); 4,4'-dichlorodiphenyldichloroethylene (4,4'-DDE); dieldrin; endrin; β-endosulfan; 4,4'-dichlorodiphenyldichloroethane (4,4'-DDD); endosulfan sulfate; 4,4'-dichlorodiphenyltrichloroethane (4,4'-DDT); endrin ketone; methoxychlor.

Discussion

The original⁹ and the two official versions¹³^,¹⁴ of the QuEChERS method use magnesium sulfate together with sodium chloride, acetate, or citrate salts to promote acetonitrile/water mixture separation during extraction. However, these salts tend to be deposited as solids on the surfaces in the mass spectrometry (MS) source, which causes the need for increased maintenance of liquid chromatography (LC)-MS-based methods. In terms of overcoming these disadvantages, González-Curbelo et al.¹⁵ reported that the more volatile ammonium formate worked well to induce phase separation and the extraction of pesticide residues for both LC- and GC-tandem mass spectrometry (MS/MS). Subsequent studies have also used 0.5 g of ammonium formate per gram of sample to extract pesticide residues from various complex matrices¹⁶^,¹⁷^,¹⁸^,¹⁹. In addition, the use of ammonium formate has been shown to provide lower amounts of co-extracted material²⁰, which justifies its use for GC-MS-based methods. The present study, for the first time, reports this version to analyze pesticide residues in soils²¹.

The GC analysis of pesticide residues in complex matrices such as soils has some limitations because of the action of the co-extracted matrix components on the instrumental response of the pesticides, which causes inaccurate determination and lower sensitivity²²^,²³. Hence, several improvements have been made to minimize the matrix effect, including optimized clean-up steps²¹. Nevertheless, the matrix effect still takes place and should be corrected as much as possible. In this sense, matrix-matched calibration has been the main approach used because it is very practical in compensating for the enhancement of the chromatographic signal with respect to that of pure solvents²⁴. Thus, in this study, linearity was evaluated by building the calibration curves in pure acetonitrile and using soil extracts, and R² values higher than or equal to 0.99 for all the OCPs were obtained using both approaches. However, when both calibration curves were compared, appreciable matrix effects were found in the range of –49% to 191% (Figure 2). Although the number of pesticides that suffered a strong matrix effect was only 3 of 17 (endrin, endrin ketone, and methoxychlor), subsequent studies were carried out using the matrix-matched calibration curves to compensate for the matrix effects to a greater extent.

No maximum residue limits (MRLs) have been established for pesticide residues in soils, but an LCL of 5 µg/kg was set for all the OCPs, which is lower than the very demanding standard MRL set at 10 µg/kg by the international legislation for the analysis of pesticide residues in agri-food products (Regulation 396/2005)¹¹. In addition, the LCL of 5 µg/kg provided a signal-to-noise ratio (S/N) of around 10 for all the OCPs. The high sensitivity of this method is similar to or even better than that obtained in other studies that have also analyzed OCPs in soils using the QuEChERS method followed by GC-MS. For example, in one study, 34 OCPs were analyzed using the official version of the QuEChERS method that uses a citrate buffer, and the limits of quantification (LOQs) were equal to or higher than 7 µg/kg²⁵. In particular, the LOQ values of α-BHC, β-BHC, lindane, and δ-BHC were between 206 µg/kg and 384 µg/kg. In another work, lindane and dieldrin were analyzed using the same version of the QuEChERS method, and LOQ values of 42 µg/kg and 292 µg/kg were obtained, respectively²⁶. Likewise, another research work also determined aldrin and heptachlor using QuEChERS and GC-MS, with LOQ values of 13 and 23 µg/kg, respectively²⁷.

The recovery and reproducibility assessment was developed at three concentration levels (low, medium, and high) in triplicate (n = 9). For this purpose, the overall recovery values were determined by comparing the pesticide peak area/IS (4,4'-DDE-d8) peak area ratios obtained from the soil samples spiked at the beginning of the application of the QuEChERS method using ammonium formate with those of matrix-matched calibration. In all cases, each replicate was injected twice in the same sequence. It should be noted that using an IS, an isotopically labeled standard, allows for compensating for the possible losses of the pesticides that take place during the whole procedure, as well as the matrix effect and/or possible variability in the instrument. According to the results, most pesticides met the acceptability criteria of 70%-120% recovery values with RSD ≤20% at each spiking level²⁸, which demonstrated the effectiveness and repeatability of the method. Nevertheless, the overall recovery values (n = 9) were slightly higher than 120% for heptachlor (122%), endrin (121%), and β-endosulfan (130%), though they were consistent (RSDs <13%). In this sense, considering the overall recovery values at three spiking levels, an acceptability criterion of 30%-140% with RSD values ≤20% has been established²⁸.

In conclusion, the QuEChERS method using ammonium formate coupled with GC-MS can successfully determine OCPs in agricultural soil samples. It was shown in this study that the simple addition of 5 g of ammonium formate to induce phase separation between the water and acetonitrile layers ensured suitable extraction with high recoveries of the selected pesticides. However, the matrix effect continued to take place, so other approaches, such as the addition of analyte protectants, should be studied in subsequent works. In any case, this alternative to the official QuEChERS versions may be used to avoid the undesirable solids deposited in the analytical system due to the use of magnesium and sodium salts, especially in routine LC-MS-based analysis. In the latter case, it would be even more interesting since ammonium formate is an aid for ionization in positive electrospray ionization and may enhance the formation of ammonium adducts instead of sodium adducts.

Divulgazioni

The authors have nothing to disclose.

Acknowledgements

I would like to thank Javier Hernández-Borges and Cecilia Ortega-Zamora for their invaluable support. I also want to thank the Universidad EAN and the Universidad de La Laguna.

Materials

15 mL disposable glass conical centrifuge tubes	PYREX	99502-15
2 mL centrifuge tubes	Eppendorf	30120094
50 mL centrifuge tubes with screw caps	VWR	21008-169
5977B mass-selective detector	Agilent Technologies	1617R019
7820A gas chromatography system	Agilent Technologies	16162016
Acetone	Supelco	1006582500
Acetonitrile	VWR	83642320
Ammonium formate	VWR	21254260
Automatic shaker KS 3000 i control	IKA	3940000
Balance	Sartorius Lab Instruments Gmbh & Co	ENTRIS224I-1S
Bondesil-C18, 40 µm	Agilent Technologies	12213012
Bondesil-PSA, 40 µm	Agilent Technologies	12213024
Cyclohexane	VWR	85385320
EPA TCL pesticides mix	Sigma Aldrich	48913
Ethyl acetate	Supelco	1036492500
G4567A automatic sampler	Agilent Technologies	19490057
HP-5ms Ultra Inert (5%-phenyl)-methylpolysiloxane 30 m x 250 µm x 0.25 µm column	Agilent Technologies	19091S-433UI
Magnesium sulfate monohydrate	Sigma Aldrich	434183-1KG
Mega Star 3.R centrifuge	VWR	521-1752
Milli-Q gradient A10	Millipore	RR400Q101
p,p'-DDE-d8	Dr Ehrenstorfer	DRE-XA12041100AC
Pipette tips 2 – 200 µL	BRAND	732008
Pipette tips 5 mL	BRAND	702595
Pipette tips 50 – 1000 uL	BRAND	732012
Pippette Transferpette S variabel 10 – 100 µL	BRAND	704774
Pippette Transferpette S variabel 100 – 1000 µL	BRAND	704780
Pippette Transferpette S variabel 20 – 200 µL	BRAND	704778
Pippette Transferpette S variabel 500 – 5000 µL	BRAND	704782
Vials with fused-in insert	Sigma Aldrich	29398-U
OCPs		CAS registry number
α-BHC		319-84-6
β-BHC		319-85-7
Lindane		58-89-9
δ-BHC		319-86-8
Heptachlor		76-44-8
Aldrin		309-00-2
Heptachlor epoxide		1024-57-3
α-Endosulfan		959-98-8
4,4'-DDE-d8 (IS)		93952-19-3
4,4'-DDE		72-55-9
Dieldrin		60-57-1
Endrin		72-20-8
β-Endosulfan		33213-65-9
4,4'-DDD		72-54-8
Endosulfan sulfate		1031-07-8
4,4'-DDT		50-29-3
Endrin ketone		53494-70-5
Methoxychlor		72-43-5

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González-Curbelo, M. Á. Analysis of Organochlorine Pesticides in a Soil Sample by a Modified QuEChERS Approach Using Ammonium Formate. J. Vis. Exp. (191), e64901, doi:10.3791/64901 (2023).