Residues In Environmental Samples Research Articles

Multiplex electrochemical aptasensor for the simultaneous detection of linomycin and neomycin antibiotics

The escalating use of antibiotics across diverse sectors, including human healthcare, agriculture, and livestock, has led to their pervasive presence in the environment, raising concerns about their impact on ecosystems and human health. Traditional detection methods, reliant on high-performance liquid chromatography and immuno-assays, face challenges of complexity, cross-reactivity, and limited specificity. Aptamer-based biosensors offer a promising alternative, leveraging the specificity, stability, and cost-effectiveness of aptamers. Herein, we present a novel dual-screen-printed carbon electrode (SPCE) biosensor, modified with a nanocomposite of gold nanoparticles (AuNPs) and carbon nanofibers (CNFs), for the label-free electrochemical detection of lincomycin and neomycin antibiotics. Lincomycin and neomycin, two antibiotics of environmental concern due to their widespread usage and potential ecological impact, were simultaneously detected using square wave voltammetry. The aptasensors showed high sensitivity with detection limits of 0.02 pg/mL and 0.035 pg/mL for lincomycin and neomycin, respectively. The developed biosensor exhibited high selectivity and reproducibility in detecting both antibiotics. This multiplex biosensing platform offers a promising strategy for efficient and cost-effective monitoring of antibiotic residues in environmental samples, addressing the critical need for robust detection methods in environmental monitoring and public health surveillance.

Sensitive extraction of seven pesticide residues from environmental water with magnetic graphene oxide-based covalent organic framework

The use of pesticides has increased with the development of agriculture. However, due to the trace content and the matrix's inherent complexity in environmental water, development of rapid and sensitive detection method present significant challenges in the analysis of pesticide residues. The study synthesized magnetic graphene oxide (MGO) by combining superparamagnetic nanoparticles with the easy modification of graphene oxide (GO). Covalent organic frameworks (COFs) were then modified to have a large specific surface area. Finally, magnetic graphene oxide-based covalent organic frameworks, namely MGO-COFs, were obtained with a spherical structure and used as magnetic solid-phase extraction materials, which was successfully used to determine the seven pesticide residues in environmental samples in conjunction with high performance liquid chromatography. The method has a wide linear range for the tested pesticides, with satisfactory correlation coefficients (R ≥ 0.099) and low detection limits (0.3–1.21 μg L−1). The correlation coefficients for all seven pesticides were high (R2 ≥ 0.9996). The spiked recoveries, exhibiting a range of 91.3 to 109 %, demonstrated that the developed MGO-COF-MSPE-HPLC-UV method is simple, efficient, and suitable for the analysis and detection of seven pesticide residues in environmental water.

A homogenous fluorescence immunoassay based on a DNA-grafted labeling strategy of magnetic microspheres for multiple neonicotinoids monitoring

Given the detrimental impact on non-target pollinators, there is a high demand for monitoring multiple neonicotinoid residues in the environment. In this study, we proposed a novel physical-biological coupled multiplexing system (PBCMS) to achieve a homogeneous and high-performance indirect competitive suspension array technology (ic-SAT) for multiple neonicotinoids monitoring. First, hapten-decorated microspheres (HDMs) were prepared by ligating the streptavidin-modified microspheres with the biotinylated hapten, according to a novel molecularly-defined single-stranded DNA (ssDNA)-grafted labeling approach. Taking thiamethoxam (THX) and imidacloprid (IMI) as models, the binding properties of two anti-neonicotinoid antibodies were profiled by establishing fluorescence monoplex ic-SAT assays. Subsequently, two HDMs (2.8 and 5.0 μm) immobilized with THX and IMI haptens were synthesized and then implemented to fabricate a dualplex ic-SAT assay, while they were distinguished via a facile diameter-resolved decoding process through flow cytometry. Excitingly, the screening capacity of the dualplex ic-SAT assay was significantly expanded by employing antibodies with distinctive binding profiles. It enables the simultaneous monitoring of 7 representative neonicotinoid insecticides (THX, IMI, acetamiprid, clothianidin, thiacloprid, nitenpyram and imidaclothiz) and 4 major metabolites in a single test sample, with IC50 values ranging from 0.02 to 572.70 ng/mL. Furthermore, the dualplex ic-SAT assay was applied to honey, pollen and bee samples, demonstrating satisfactory recovery rates (74.1 %∼106.3 %) and nice agreement with LC-MS/MS analysis. In summary, the PBCMS offers an easy-to-implement, robust and cost-effective way for establishing user-defined ic-SAT, providing a powerful analytical tool to simultaneously monitor multiple neonicotinoid residues in environmental samples.

Analysis of carbamate and organophosphorus pesticide in agricultural irrigation water by Liquid Chromatography - Mass Spectrometry

So far, the ultra-trace concentration of pesticide residues in environmental samples has challenged many analytical techniques, which are used to detect simultaneously organophosphorus and carbamate with various polarities. In this study, the OASIS-HLB column was modified by the reagent 1,8-Dihydroxy-2-(4-sulfophenylazo)naphthalene-3,6-disulfonic to enhance the retention of polar pesticides. Both real irrigation water and distilled water samples were applied to validate the determination method of ten carbamates and thirty-eight organophosphorus pesticides all together using LC-MS. According to the results, the linear interval of the method ranged from 1.0 to 100 µg/L, the detection limit was as low as 5.0 µg/L, the relative standard deviations presented less than 8.0%, and the recoveries were ranging between 60% and 112%. Moreover, in the irrigation water samples which were collected in both dry and rainy seasons in ten stations around the agricultural area, five compounds were found, including fenamiphos, terbufos, aldicarb, propoxur, and methiocarb. In the midst of those sampling areas, the Environmental Impact Quotient Field Use Rating of detected pesticide residues presented a high value - 272 at one station, which indicates a high risk for the surrounding environment as well as the local people’s health.

Determination of three new herbicide residues in soil, sediment and water by liquid chromatography-tandem mass spectrometry

Herbicides play an important role in preventing and controlling weeds and harmful plants and are increasingly used in agriculture, forestry, landscaping, and other fields. However, the effective utilization rate of herbicides is only 20%-30%, and most herbicides enter the atmosphere, soil, sediment, and water environments through drift, leaching, and runoff after field application. Herbicide residues in the environment pose potential risks to ecological safety and human health. Therefore, establishing analytical methods to determine herbicide residues in environmental samples is of great importance. In this study, an analytical method based on liquid chromatography-tandem mass spectrometry (LC-MS/MS) in positive electrospray ionization mode (ESI+) was developed for the determination of isoxaflutole, metazachlor, and saflufenacil residues in soil, sediment, and water. The instrumental detection parameters, including electrospray ionization mode, mobile phase, and chromatographic column, were optimized. The mobile phases were methanol (A) and 0.1% formic acid aqueous solution (B). Gradient elution was performed as follows: 0-1.0 min, 60%A; 1.0-2.0 min, 60%A-90%A; 2.0-3.0 min, 90%A; 3.0-4.0 min, 90%A-60%A; 4.0-5.0 min, 60%A. The samples were salted after extraction with acetonitrile and cleaned using a C18 solid-phase extraction column. Different solid-phase extraction columns and leaching conditions were investigated during sample pretreatment. Working curves in the neat solvent and matrix were constructed by plotting the measured peak areas as a function of the concentrations of the analytes in the neat solvent and matrix. Good linearities were found for isoxaflutole, metazachlor, and saflufenacil in the solvent and matrix-matched standards in the range of 0.0005-0.02 mg/L, with r≥0.9961. The matrix effects of the three herbicides in soil, sediment, and water ranged from -10.1% to 16.5%. The limits of detection (LODs, S/N=3) for isoxaflutole, metazachlor, and saflufenacil were 0.05, 0.01, and 0.02 μg/kg, respectively. The limits of quantification (LOQs, S/N=10) for isoxaflutole, metazachlor, and saflufenacil were 0.2, 0.05, and 0.05 μg/kg, respectively. The herbicides were applied to soil, sediment, and water at spiked levels of 0.005, 0.1, and 2.0 mg/kg, respectively. The average recoveries for isoxaflutole, metazachlor, and saflufenacil in soil, sediment, and water were in the ranges of 77.2%-101.9%, 77.9%-105.1%, and 80.8%-107.1%, respectively. The RSDs for isoxaflutole, metazachlor, and saflufenacil were in the ranges of 1.4%-12.8%, 1.2%-7.7%, and 1.5%-11.5%, respectively. The established method was used to analyze actual samples collected from four different sites in Zhejiang Province (Xiaoshan, Taizhou, Dongyang, and Yuhang) and one site in Heilongjiang (Jiamusi). The proposed method is simple, rapid, accurate, stable, and highly practical. It can be used to detect isoxaflutole, metazachlor, and saflufenacil residues in soil, sediment, and water and provides a reference for monitoring the residual pollution and environmental behavior of herbicides.

A novel 3D-printed graphite/polylactic acid sensor for the electrochemical determination of 2,4,6-trinitrotoluene residues in environmental waters

Here, lab-made graphite and polylactic acid (Gpt-PLA) biocomposite materials were used to additively manufacture electrodes via the fused deposition modeling (FDM) technique for subsequent determination of the explosive 2,4,6-trinitrotoluene (TNT, considered a persistent organic pollutant). The surface of the 3D-printed material was characterized by SEM and Raman, which revealed high roughness and the presence of defects in the graphite structure, which enhanced the electrochemical response of TNT. The 3D-printed Gpt-PLA electrode coupled to square wave voltammetry (SWV) showed suitable performance for fastly determining the explosive residues (around 7 s). Two reduction processes at around −0.22 V and −0.36 V were selected for TNT detection, with linear ranges between 1.0 and 10.0 μM. Moreover, detection limits of 0.52 and 0.66 μM were achieved for both reduction steps. The proposed method was applied to determine TNT in different environmental water samples (tap water, river water, and seawater) without a dilution step (direct analysis). Recovery values between 98 and 106% confirmed the accuracy of the analyses. Additionally, adequate selectivity was achieved even in the presence of other explosives commonly used by military agencies, metallic ions commonly found in water, and also some electroactive camouflage species. Such results indicate that the proposed device is promising to quantify TNT residues in environmental samples, a viable on-site analysis strategy.

A facile rapid-response and on-site sensor for tetracycline detection in environmental water based on europium-doped carbonized polymer dots

With the increasing concerns about public safety and environmental protection, it is of great significance to establish a rapid and sensitive method to detect antibiotic residues in environmental samples. Herein, fluorescent carbonized polymer dots (CPDs) were synthesized and used for quantitative assay of tetracycline (TC) by chelating with europium ions (Eu3+). The green fluorescence of CPDs could be gradually quenched by TC via inner filter effect and static quenching mechanism, while the red emission of Eu3+ was remarkably enhanced through energy transfer and antenna effect. This ratiometric fluorescence Eu/CPDs-based sensor displayed a wide detection range of 0.05–56, 56–100 μM with a detection limit of 16.4 nM, and was triumphantly applied for TC analysis in water samples with high reliability and accuracy. Moreover, the polymeric structure in CPDs endowed the sensor with good long-term sensing stability up to 600 days. By integrating Eu/CPDs with portable capillary testing kit, a point-of-use device was constructed for facile determination of TC in river water samples with a short sample-to-answer analysis process in 2 min. Due to its easy operation, low-cost, and there is no pretreatment required, the capillary-based testing kit provides a new strategy for on-site and rapid detection of antibiotics in various environmental water samples.

Analysis of Residues in Environmental Samples

The state of the environment is very important for our lives and for that of future generations [...].

Review of Analytical and Sample Processing Technologies for Detecting Antibiotic Residues in Environmental Samples

Review of Analytical and Sample Processing Technologies for Detecting Antibiotic Residues in Environmental Samples

Rational effect of CuSe2 phase with octadecyl amine modified reduced graphene composite for dual-mode sensing of environmental hazardous anthelminthic drug in aquatic and biological samples

The increasing usage of antihelminthic drug mebendazole (MEB) in humans and livestock poses serious threat and is considered a significant environmental pollutant. Hence, monitoring the MEB residues in environmental samples, and human fluids is essential to decrease the ecological risk and improve the health of humans. In this work, copper selenide (CuSe2) nano/microspheres were hydrothermally synthesized and ultrasonically treated with rGO surface modified with ODA alkyl amine (rGO-ODA). The optical, structural, morphological, and functional analysis were performed which revealed the CuSe2 in marcasite phase, orthorhombic pattern with Pnnm space group, and substantial composite formation. The morphological studies revealed sphere structure of the CuSe2 and wrinkled sheets of rGO-ODA. A sensor that detects MEB using the cyclic voltammetry (CV), differential pulse voltammetry (DPV) and UV-Vis absorbance techniques was developed. For DPV analysis, the sensor exhibited a very low value for limit of detection 13.55 nM and a sensitivity of 9.4871 μA M−1cm−2. For UV-Vis, the sensor demonstrated a very low limit of detection 22.3 nM. The use of this sensor was validated in real-time analysis with aquatic and biological real samples. The results suggested > 90% of analyte recovery and enhanced efficiency for MEB detection with a potential for commercialization in future.

Molecularly Imprinted Polymer Modified Electrode Prepared by In Situ Polymerization for Specific Determination of Norfloxacin

Herein, a molecularly imprinted sensor was proposed via in situ polymerization technique for specifically sensing norfloxacin (NFX). The sensor indicates high stability due to the imprinting layer covalently conjugated on the surface of aminated glass carbon electrode. Emphasized, it shows excellent selectivity and specificity towards NFX ascribed to the unique characteristics of molecularly imprinted polymers (MIPs). Even in the presence of 10-fold concentration of its structural analog ciprofloxacin, there is no evident interference in the determination of NFX. Under optimized conditions, the oxidation current of square wave voltammetry (typically at +1.03 V vs Ag/AgCl) increases linearly with the concentration of NFX increasing in the ranges of 0.1–10 μM and 10−160 μM. And the limit of detection is 0.004 μM (based on a signal-to-noise ratio of 3). Average recoveries from (spiked) real water samples are between 99.63% and 103.20% with relative standard derivations less than 4.67% (n = 3) at three spiked levels, validated by independent assays of HPLC. This work provides a successful model for fast preparing MIP-based electrochemical sensors for detecting trace drug residues in environmental samples.

A nonenzymatic reduced graphene oxide-based nanosensor for parathion.

Organophosphate-based pesticides (e.g., parathion (PT)) have toxic effects on human health through their residues. Therefore, cost-effective and rapid detection strategies need to be developed to ensure the consuming food is free of any organophosphate-residue. This work proposed the fabrication of a robust, nonenzymatic electrochemical-sensing electrode modified with electrochemically reduced graphene oxide (ERGO) to detect PT residues in environmental samples (e.g., soil, water) as well as in vegetables and cereals. The ERGO sensor shows a significantly affected electrocatalytic reduction peak at −0.58 V (vs Ag/AgCl) for rapid quantification of PT due to the amplified electroactive surface area of the modified electrode. At optimized experimental conditions, square-wave voltammetric analysis exhibits higher sensitivity (50.5 μA·μM−1·cm−2), excellent selectivity, excellent stability (≈180 days), good reproducibility, and repeatability for interference-free detection of PT residues in actual samples. This electrochemical nanosensor is suitable for point-of-care detection of PT in a wide dynamic range of 3 × 10−11–11 × 10−6 M with a lower detection limit of 10.9 pM. The performance of the nanosensor was validated by adding PT to natural samples and comparing the data via absorption spectroscopy. PT detection results encourage the design of easy-to-use nanosensor-based analytical tools for rapidly monitoring other environmental samples.

Integrated ultrasound-assisted magnetic solid-phase extraction for efficient determination and pre-concentration of polycyclic aromatic hydrocarbons from high-consumption soft drinks and non-alcoholic beers in Iran.

In the present research, an ultrasound-assisted magnetic solid-phase extraction coupled with a gas chromatography-mass spectrometry hybrid system was developed for the extraction/determination of trace amounts of polycyclic aromatic hydrocarbons in high-consumption soft drinks and non-alcoholic beers in Iran using magnetite graphene oxide adsorbent. The magnetite graphene oxide was characterized by scanning electron microscope, transmission electron microscopy, Fourier-transform infrared spectroscopy, X-ray diffraction, and vibrating-sample magnetometer techniques. The highest extraction recovery (73.05%-95.56%) and enrichment factor (90.65-106.38) were obtained at adsorbent mass: 10mg, adsorption time: 30min, salt addition: sodium chloride 10% w/v, desorption time: 20min, eluent type: hexane: acetone (1:1, v/v), and desorption solvent volumes: 200 μl. Under optimum conditions, the linearity range for polycyclic aromatic hydrocarbons determination was 0.2-200ng/mlwith a coefficient of determination>0.993, the limit of detection=0.09-0.21ng/ml, the limit of quantitation=0.3-0.7ng/ml, and relative standard deviation<8.1%, respectively. Relative recoveries in spiked real samples ranged from 94.67 to 109.45% with a standard deviation<6.05%. The proposed method is effective, sensitive, and reusable and it is promising for the analysis of polycyclic aromatic hydrocarbons residues in environmental samples.

Natural deep eutectic solvent-decorated magnetic layered double hydroxide as a sorbent for the enrichment of organochlorine pesticides in environmental samples

A newly designed magnetic layered double hydroxide composite modified with a natural deep eutectic solvent derived from choline chloride and sucrose was synthesized and applied as a sorbent for the enrichment of organochlorine pesticides. The magnetic solid phase extraction (MSPE) procedure was optimized via a small central composite design and response surface methodology. The MSPE method was able to preconcentrate the organochlorine residues in environmental samples prior to GC–MS analysis. Good analytical performance of the proposed method was observed with an enrichment factor of up to 158 and low limits of detection in the ranges of 0.002–0.015 µg·L−1 and 0.03–0.10 ng·g−1 for water and soil, respectively. Satisfactory recoveries for spiked water and soil samples were obtained in the ranges of 80.9–104.7% (RSDs<7.9) and 88.8–104.1% (RSDs<7.3), respectively. This finding highlights the role of natural deep eutectic solvents as modifying agents for magnetic layered double hydroxides, which enhance the efficiency of extraction of the target analytes. The developed MSPE/GC–MS procedure was sensitive and reliable for the determination of trace organochlorine residues in environmental samples.

Synergetic combination of nano hexagons SnS2/Sulfur substituted graphitic carbon nitride: Evaluation of electrochemical sensor for the agricultural pollutant in environmental samples

• SnS 2 incorporated on the high defective sites of SGCN via ultrasonic dispersion. • This nanocomposite an displays excellent electroanalytical performance. • It is successfully implemented in the determination of agricultural pollutant CBZ. • An excellent candidate for the real-time applications in environmental samples. In the modern era, pesticide is highly formulated for huge harvest yield in agriculture. Nevertheless, improper disposal of pesticide residues from the industries has severely impacted living beings and poses a serious threat. Thus, researchers are keen to evaluate carbendazim’s complex chemical constituents in food samples through sensitive and selective detection. This study discusses nano hexagon-shaped tin sulfide (SnS 2 ) incorporated on the high defective sites of sulfur-doped graphitic carbon nitride (SGCN), a nanocomposite network prepared via ultrasonic dispersion. It displays low electron transfer resistance, high effective surface area, and excellent film electrode stability. A modified screen-printed carbon electrode (SPCE) was implemented to sense the carbendazim (CBZ) residues in environmental samples. Under the optimized conditions, the sensor presents a differential pulse voltammetry current response for CBZ concentration from 0.002 to 416 µmol. L -1 with a nanomolar detection (3 × 10 -8 mol. L -1 ). It also exemplifies high sensitivity (0.1366 µA µM −1 cm −2 ), selectivity, reproducibility, and long-term storage stability. Further, the proposed sensor was implemented to determine CBZ in apple, orange, cucumber, and carrot samples. Good recovery was found using the standard addition method that substantiates the excellent analytical performance of the proposed electrochemical sensor.

Amino-based magneto-polymeric-modified mixed iron hydroxides for magnetic solid phase extraction of phenol residues in environmental samples

Mixed iron hydroxides (MIHs) modified with different amino-based polymeric materials, including aminopropyltriethoxysilane, polydopamine, diaminobenzoic acid, polyaniline, and polyphenylenediamine, were comparatively investigated as sorbents for the extraction of phenol compounds. Polyphenylenediamine-modified mixed iron hydroxides (MIH@PPDA) showed high adsorption capability for most target analytes. Its ferromagnetic behavior, with a magnetization of 17.38 emu g−1, was sufficient for subsequent use in magnetic solid-phase extraction (MSPE). The functional groups, morphology, and magnetic properties of this magnetic nanomaterial were investigated using Fourier transform infrared spectroscopy, scanning electron microscopy, transmission electron microscopy, vibrating sample magnetometry, X-ray diffraction, and CHN analysis. High-performance liquid chromatography with a photodiode array detector was used to quantify phenol compounds. The experimental parameters affecting the efficiency of the entire MSPE process were optimized. Good linearity in the range of 0.5–1000 µg L−1 was obtained (depended on the compound). The detection and quantitation limits varied from 0.01 to 0.3 µg L−1 and 0.03 to 0.9 µg L−1, respectively. The enrichment factors for all phenol compounds were in the range of 80–285. The precision in terms of intra- and inter-day relative standard deviations were below 5.8% and 6.2%, respectively. The developed MSPE method was applied to analyze phenol compounds in diverse samples, including soil, drinking water, and fruit. Relative recoveries of 76.7–130.1% were obtained. The MIH@PPDA magneto-polymeric sorbent exhibits good stability and is reliable for a variety of phenol compounds.

Magnetic Mesoporous Carbon/β-Cyclodextrin-Chitosan Nanocomposite for Extraction and Preconcentration of Multi-Class Emerging Contaminant Residues in Environmental Samples.

This study reports the development of magnetic solid-phase extraction combined with high-performance liquid chromatography for the determination of ten trace amounts of emerging contaminants (fluoroquinolone antibiotics, parabens, anticonvulsants and β-blockers) in water systems. Magnetic mesoporous carbon/β-cyclodextrin–chitosan (MMPC/Cyc-Chit) was used as an adsorbent in dispersive magnetic solid-phase extraction (DMSPE). The magnetic solid-phase extraction method was optimized using central composite design. Under the optimum conditions, the limits of detection (LODs) ranged from 0.1 to 0.7 ng L−1, 0.5 to 1.1 ng L−1 and 0.2 to 0.8 ng L−1 for anticonvulsants and β-blockers, fluoroquinolone and parabens, respectively. Relatively good dynamic linear ranges were obtained for all the investigated analytes. The repeatability (n = 7) and reproducibility (n = 5) were less than 5%, while the enrichment factors ranged between 90 and 150. The feasibility of the method in real samples was assessed by analysis of river water, tap water and wastewater samples. The recoveries for the investigated analytes in the real samples ranged from 93.5 to 98.8%, with %RSDs under 4%.

Simultaneous determination of paracetamol and caffeine in aqueous samples by ultrasound‐assisted emulsification microextraction coupled with high‐performance liquid chromatography

AbstractToday, due to the growth of the pharmaceutical industry and the high consumption of drugs, monitoring of drug residues in environmental samples because of their destructive effects on the environment and humans is essential. In the present work, ultrasound‐assisted emulsification‐microextraction coupled with high‐performance liquid chromatography as a simple and fast method was applied for simultaneous determination of paracetamol and caffeine in the aqueous samples. Effective parameters on the extraction efficiencies of these analytes such as type and volume of extraction solvent, pH of sample solution, salt concentration, sonication, and centrifuging times were studied and optimized. Under the optimum conditions, the calibration graphs were linear in the range of 30.0–1100.0 ng/mL for paracetamol and 50.0–400.0 ng/mL for caffeine. The limits of detection were 9.7 and 15.2 ng/mL for paracetamol and caffeine, respectively. The proposed method was successfully applied for the determination of these drugs in different aqueous samples.

Determination of sulfa antibiotic residues in river and particulate matter by field-amplified sample injection-capillary zone electrophoresis.

In the present research, field-amplified sample injection-CZE (FASI-CZE) coupled with a diode array detector was established to determine trace level sulfa antibiotic. Sulfathiazole, sulfadiazine, sulfamethazine, sulfadimethoxine, sulfamethoxazole, and sulfisoxazole were selected as analytes for the experiments. The background electrolyte solution consisted of 70.0mmol/L borax and 60.0mmol/L boric acid (including 10% methanol, pH 9.1). The plug was 2.5mmol/L borax, which was injected into the capillary at a pressure of 0.5psi for 5s. Then the sample was injected into the capillary at an injection voltage of -10kV for 20s. The electrophoretic separation was carried out under a voltage of +19kV. The capillary temperature was maintained at 20˚C throughout the analysis, and six sulfonamides were completely separated within 35min. Compared with pressure injection-CZE, the sensitivity of FASI-CZE was increased by 6.25-10.0 times, and the LODs were reduced from 0.2-0.5 to 0.02-0.05μg/mL. The method was applied to the determination of sulfonamides in river water and particulate matter samples. The recoveries were 78.59-106.59%. The intraday and interday precisions were 2.89-7.35% and 2.77-7.09%, respectively. This provides a simpler and faster method for the analysis of sulfa antibiotic residues in environmental samples.

Fast and sensitive CG-MS/MS method for detection of some auxin herbicides residues in environmental samples

Fast and sensitive CG-MS/MS method for detection of some auxin herbicides residues in environmental samples