8-acetoxy-trisulfopyrene as the first activatable fluorogenic probe for add-and-read assessment of Organic anion-transporting polypeptides, OATP1B1, OATP1B3, and OATP2B1.

Organic anion-transporting polypeptides, OATP1B1, OATP1B3, and OATP2B1 are multispecific membrane proteins mediating the hepatocellular uptake of structurally diverse endo- and exogenous compounds, including various kinds of drugs. Co-administration of OATP1B/2B1 substrates may lead to altered pharmacokinetics or even toxicity. Therefore, the study of the interaction with these OATPs is essential in drug development and is recommended by international regulatory agencies, the FDA, EMA, and PMDA. In general, radiolabeled indicators are used to measure drug interactions of OATPs, and, lately, fluorescent probes are also gaining wider application in OATP tests. However, all of the currently available methods (either radioactive or fluorescence-based) comprise multiple steps, including the removal of the indicator in the end of the experiment. Hence, they are not ideally suited for high-throughput screening. In the current study, in order to find an indicator allowing real-time assessment of hepatic OATP function, we searched for an activatable fluorogenic OATP substrate. Here, we show that 8-acetoxypyrene-1,3,6-trisulfonate (Ace), a fluorogenic derivative of the hepatic OATP substrate pyranine (8-hydroxypyrene-1,3,6-trisulfonate) enters the cells via OATP1B1/3 or OATP2B1 function. In living cells, Ace is then converted into highly fluorescent pyranine, allowing "no-wash" measurement of OATP function and drug interactions. Furthermore, we demonstrate that Ace can be used in an indirect assay termed as competitive counterflow suitable to distinguish between transported substrates and inhibitors of OATP1B1. The fluorescence-based methods described here are unique and open the way toward high-throughput screening of interactions between new molecular entities and OATPs.

A stable and sensitive enzyme-linked immunosorbent assay (ELISA) for the determination of metsulfuron-methyl residues in foods.

A hapten of metsulfuron-methyl was successfully designed and synthesized from 2-methylester-phenylsulfonamide and succinic anhydride, and the polyclonal antibody against metsulfuron-methyl was prepared by immunization procedure with the hapten-bovine serum albumin conjugate. A stable and sensitive direct competitive enzyme-linked immunosorbent assay (dcELISA) method had been developed under the optimal conditions. The sensitivity (IC50 ) was 37.03 ± 1.87 µg/L, and the detection line (IC15 ) was 1.57 ± 0.11 µg/L. Rice, wheat, oat, flaxseed, milk, and water were chosen to study the recovery test and the recovery rates were 83.11%-117.44% . The matrix effect was eliminated by a simple dilution of the sample extracts. The results from dcELISA were well agreement with the results from HPLC-MS. It was indicated that the developed method had good accuracy and stability. It could be applied for the detection of metsulfuron-methyl residues. It was worth mentioning that the antibody could recognize metsulfuron-methyl and tribenuron-methyl with cross-reactivities of 100% and 49.72%, respectively. In order to understand the cross-reactivity, molecular modeling including molecular alignment and electrostatic potential surfaces were introduced. It was found that the special group of metsulfuron-methyl played an important role, especially on C3 position of the phenyl group. PRACTICAL APPLICATION: A stable, sensitive, and low-cost dc ELISA method had been developed with good accuracy and applied in the determination of metsulfuron-methyl in foods. Molecular simulation was introduced to understand the specificity between the antibody and the analyst. It was a good method to study the cross-reactivity between the antibody and the analyst or analogue.

Residue and Dissipation Kinetics of Metsulfuron-Methyl Herbicide in Soil: A Field Assessment at an Oil Palm Plantation.

A field trial experiment was conducted to investigate the degradation of metsulfuron-methyl at two application dosages, 15 g a.i/ha and 30 g a.i/ha, at an oil palm plantation. Soil samples were collected at ‒1, 0, 1, 3, 7, 14, and 21 days after treatment (DAT) at the following depths: 0-10, 10-20, 20-30, 30-40, and 40-50 cm. The results showed rapid degradation of metsulfuron-methyl in the soil, with calculated half-life (t½) values ranging from 6.3 and 7.9 days. The rates of degradation of metsulfuron-methyl followed first-order reaction kinetics (R2 = 0.91-0.92). At the spray dosage of 15 g a.i/ha, metsulfuron-methyl residue was detected at up to 20-30 cm soil depth, at 3.56% to 1.78% at 3 and 7 DAT, respectively. Doubling the dosage to 30 g a.i/ha increased the metsulfuron-methyl residue in up to 30-40 cm soil depth at 3, 7, and 14 DAT, with concentrations ranging from 1.90% to 1.74%. These findings suggest that metsulfuron-methyl has a low impact on the accumulation of the residues in the soil at application dosages of 15 g a.i/ha and 30 g a.i/ha, due to rapid degradation, and the half-life was found to be 6.3 to 7.9 days.

Lipophilic G-Quadruplex Isomers as Biomimetic Ion Channels for Conformation-Dependent Selective Transmembrane Transport.

Transport selectivity is a challenge in the design of biomimetic transmembrane channels. In the present study, specific ion-dependent lipophilic G-quadruplexes displaying different conformations were designed for the construction of highly selective artificial transmembrane channels. The presence of Pb2+ and K+ ions prompted the folding of lipophilic PS2.M sequence into G-quadruplexes with antiparallel and parallel conformations. Membrane immobilization of the G-quadruplex channels restricted the reversible configurational changes between different topologies, which was confirmed by Förster resonance energy transfer (FRET) analysis. 8-Hydroxypyrene-1,3,6-trisulfonic acid (HPTS) transport assays revealed that Pb2+-stabilized antiparallel isomers, and K+-stabilized parallel isomers exhibited significant differences in the transmembrane transport. The former showed high Pb2+ transport activity (EC50 = 1.55 µM) and selectivity (Pb2+/K+ selectivity = 30.6), while the latter demonstrated high K+ transport activity (EC50 = 0.56 µM) and selectivity (K+/Pb2+ selectivity = 31.8). The cation selectivity of these channel mimics was also consistent with the outcomes of the conducted fluorescent probe assays. The results described herein provide a platform for effective development of conformation-dependent ion-selective biomimetic transmembrane channels. The G-quadruplex channels demonstrate high potential for application in the fields of molecular diagnostics, logic biocomputing, selective separation, and single-molecule biosensing.

Flooding performance evaluation of alkyl aryl sulfonate in various alkaline environments.

Alkaline-Surfactant-Polymer (ASP) flooding is an efficient chemical enhanced oil recovery (EOR) method gaining popularity in the industry. In this paper, the characteristics of three flooding systems with alkyl aryl sulfonate surfactants and a weak alkali concentration, strong alkali concentration and no alkali concentration were investigated. The emulsification, interfacial tension, viscosity, stability, adsorption resistance as well as the oil displacement effect for the flooding systems and simulated oil of the fourth plant of the Daqing Oilfield were measured. The results show that the three alkyl aryl sulphonates surfactants have different emulsification indexes with the weak and strong alkali concentrations possessing the best and worst indexes at 67.00% and 55.17% respectively, and the combination of surfactant and no alkali concentration with an emulsification index of 63.03%. The interfacial tension between the three flooding systems and the simulated oil of the fourth plant of Daqing Oilfield gets as low as 10-3 mN/m, and reduces as far as 10-4mN/m in certain points detected, all with good anti-dilution performance. In terms of interfacial tension stability, the three flooding systems are seen to reach ultra-low interfacial tension within 90 days. For viscosity stability, the addition of a strong alkali and a weak alkali further hydrolyzes the polymer, leading to an initial rise in viscosity and viscosity retention rates above 80%. In terms of adsorption resistance, ultra-low interfacial tension occurs adsorption is reduced by five times for the strong and weak alkali systems, and reduced by four times for the alkali-free system. These results show that all three combination flooding systems have good adsorption resistance. In the evaluation of oil displacement effect, the average chemical flooding recovery rate (33.83%) of the weak alkali-surfactant-polymer (ASP) system is nearly three percent higher (31.34%) than that of the surfactant-polymer (SP) system, and over seven percent higher (26.71%) than that of the strong ASP system.

Behavior and bioefficacy of tribenuron-methyl in wheat (Triticum astevum L.) under irrigated agro-ecosystem in India.

Possible bioaccumulation of pesticides in crop produce may cause ill effects on animals and humans. Tribenuron-methyl is a new post-emergence herbicide and is highly efficient to control the broad-leaf weeds in cereals, pasture, and plantation crops. There are scarce studies on its bioefficacy, sensitivity to weeds, tolerance to wheat, and persistence in crop produce, which are important information required before recommending an herbicide for use by the farmers. Weed control efficiency of an herbicide is dose-sensitive and site/soil-specific. Tribenuron-methyl (75% DF) was applied at 22.5 and 45.0 g a.i./ha along with the surfactant 300.12 mL/ha as a tank mixes after 30 days of sowing in wheat as post-emergence herbicide. The samples of wheat foliage, soil, and grains at harvest were processed and analyzed for residues by high-performance liquid chromatography using a UV detector at 240 nm. The study revealed that there was a significant reduction in weed population and dry matter accumulation due to tribenuron-methyl application at a higher dose (45.0 g/ha) compared to a lower dose (of 22.5 g/ha). The weed density was found to be from 16.1 to 44.3 no/m(2) for application rate of 22.5 g/ha while at the 45.0 g/ha application, the weed density was 5.3-5.9 as compared to untreated control, where 184.3-120.5 no/m(2) was observed. The yield varied from 4.30 to 4.80 t/ha as compared to 2.25-3.55 t/ha in unweeded control with the LSD value being 21.5-16.3 to 0.27-0.19. Residues were below detectable level (BDL, <0.005 mg/kg) of tribenuron-methyl since they were detected in wheat grains at 22.5 g a.i./ha rates. However, 0.012 µg/g residues were detected in wheat foliage at an application rate of 45.0 g a.i./ha. It can be concluded that it is safe to use tribenuron-methyl at 22.5 g a.i./ha on wheat crop as post-emergence herbicide.

Effect of organic carbon chemistry on sorption of atrazine and metsulfuron-methyl as determined by (13)C-NMR and IR spectroscopy.

Soil organic matter (SOM) content is the major soil component affecting pesticide sorption. However, recent studies have highlighted the fact that it is not the total carbon content of the organic matter, but its chemical structure which have a profound effect on the pesticide's sorption. In the present study, sorption of atrazine and metsulfuron-methyl herbicides was studied in four SOM fractions viz. commercial humic acid, commercial lignin, as well as humic acid and humin extracted from a compost. Sorption data was fitted to the Freundlich adsorption equation. In general, the Freundlich slope (1/n) values for both the herbicides were <1. Except for atrazine sorption on commercial humic acid, metsulfuron-methyl was more sorbed. Desorption results suggested that atrazine was more desorbed than metsulfuron-methyl. Lignin, which showed least sorption of both the herbicides, showed minimum desorption. Sorption of atrazine was best positively correlated with the alkyl carbon (adjusted R (2) = 0.748) and carbonyl carbon (adjusted R (2) = 0.498) but, their effect was statistically nonsignificant (P = 0.05). Metsulfuron-methyl sorption showed best positive correlation with carbonyl carbon (adjusted R (2) = 0.960; P = 0.05) content. Sorption of both the herbicides showed negative correlation with O/N-alkyl carbon. Correlation of herbicide's sorption with alkyl and carbonyl carbon content of SOM fractions suggested their contribution towards herbicide sorption. But, sorption of metsulfuron-methyl, relatively more polar than atrazine, was mainly governed by the polar groups in SOM. IR spectra showed that H-bonds and charge-transfer bonds between SOM fraction and herbicides probably operated as mechanisms of adsorption.

Dissipation kinetics and residues of florasulam and tribenuron-methyl in wheat ecosystem.

The dissipation kinetics and residual levels of florasulam and tribenuron-methyl in wheat field ecosystem were determined using a quick, easy, cheap, efficient, rugged and safe method (QuEChERS) with rapid resolution liquid chromatography tandem mass spectrometry (RRLC-MS/MS). The average recoveries of florasulam and tribenuron-methyl at three spiking levels in wheat plant, soil, wheat straw and wheat grain ranged from 72.8% to 99.2% with relative standard deviations (RSDs) were less than 10.1% and 82.5% to 103.8% with RSDs were less than 9.4%, respectively. The limits of quantification (LOQs) of florasulam and tribenuron-methyl for wheat plant, wheat straw, wheat grain and soil were 0.01, 0.01, 0.005, 0.005 mg kg(-1), respectively. The field trials results showed that the half-lives of florasulam were 2.76-10.83 d. Half-lives for tribenuron-methyl were found to be 1.27-5.37 d. The terminal residues in wheat grain were much lower than maximum residue limits (MRLs) set by China (0.01 mg kg(-1) for florasulam and 0.05 mg kg(-1) for tribenuron-methyl), which considered to be safe for human beings. These results will contribute to establishing the scientific basis of the dosage of florasulam and tribenuron-methyl for use in wheat field ecosystems.

Extraction and determination of sulfonylurea herbicides in water and soil samples by using ultrasound-assisted surfactant-enhanced emulsification microextraction and analysis by high-performance liquid chromatography.

An ultrasound-assisted surfactant-enhanced emulsification microextraction (UASEME) with low-density extraction solvents was developed for the extraction of sulfonylurea herbicides from water and soil samples prior to high-performance liquid chromatography coupled with ultraviolet detection (HPLC-UV). In this technique, a surfactant was used as emulsifier which could enhance the dispersion of water-immiscible extraction solvent into aqueous phase and was favorable for the mass-transfer of the analytes from aqueous phase to organic phase. The target analytes were extracted into an extraction phase (Aliquat-336 in 1-octanol) and dispersed in an aqueous solution. After extraction and phase separation, the organic solvent on top of the solution was withdrawn into a syringe and 20 µL of it was injected into a HPLC instrument for analysis. Influential factors in extraction were investigated and optimized. Under optimum experimental conditions, calibration curve was linear in the concentration range from 1 to 100 µg/L, with coefficients of estimation (R(2) values) varying from 0.9928 to 0.9952, and satisfactory repeatabilities (4.7

Application of a fully integrated photodegradation-detection flow-batch analysis system with an on-line preconcentration step for the determination of metsulfuron methyl in water samples.

This work presents the development of a fully automated flow-batch analysis (FBA) system as a new approach for on-line preconcentration, photodegradation and fluorescence detection in a lab-constructed mixing chamber that was designed to perform these processes without sample dispersion. The system positions the mixing chamber into the detection system and varies the instrumental parameters according to the required photodegradation conditions. The developed FBA system is simple and easily coupled with any sample pretreatment without altering the configuration. This FBA system was implemented to photodegrade and determine the fluorescence of the degradation products of metsulfuron methyl (MSM), a naturally non-fluorescent herbicide of the sulfonylurea׳s family. An on-line solid phase extraction (SPE) and clean up procedure using a C18 minicolumn was coupled to the photodegradation-detection mixing chamber (PDMC) that was located in the spectrofluorometer. An enrichment factor of 27 was achieved. Photodegradation conditions have been optimized by considering the influence of the elution solvent on both the formation of the photoproduct and on the fluorescence signal. Under optimal conditions, the calibration for the MSM determination was linear over the range of 1.00-7.20 µg L(-1). The limit of detection (LOD) was 0.28 µg L(-1); the relative standard deviation was 2.0% and the sample throughput for the entire process was 3h(-1). The proposed method was applied to real water samples from the Bahía Blanca׳s agricultural region (Bahía Blanca, Buenos Aires, Argentina). This method obtained satisfactory recoveries with a range of 94.7-109.8%.

Nanobiosensors exploiting specific interactions between an enzyme and herbicides in atomic force spectroscopy.

The development of sensitive methodologies for detecting agrochemicals has become important in recent years due to the increasingly indiscriminate use of these substances. In this context, nanosensors based on atomic force microscopy (AFM) tips are useful because they provide higher sensitivity with operation at the nanometer scale. In this paper we exploit specific interactions between AFM tips functionalized with the enzyme acetolactate synthase (ALS) to detect the ALS-inhibitor herbicides metsulfuron-methyl and imazaquin. Using atomic force spectroscopy (AFS) we could measure the adhesion force between tip and substrate, which was considerably higher when the ALS-functionalized tip (nanobiosensor) was employed. The increase was approximately 250% and 160% for metsulfuron-methyl and imazaquin, respectively, in comparison to unfunctionalized probes. We estimated the specific enzyme-herbicide force by assuming that the measured force comprises an adhesion force according to the Johnson-Kendall-Roberts (JKR) model, the capillary force and the specific force. We show that the specific, biorecognition force plays a crucial role in the higher sensitivity of the nanobiosensor, thus opening the way for the design of similarly engineered tips for detecting herbicides and other analytes.

Effect of fly ash on persistence, mobility and bio-efficacy of metribuzin and metsulfuron-methyl in crop fields.

Field evaluation of two fly ashes (40t/ha) on persistence, mobility and bioactivity of metribuzin and metsulfuron-methyl was studied in soybean and wheat crops, respectively. Metribuzin was applied as pre-emergence at 0.5kg/ha, while metsulfuron-methyl was applied post-emergence at 8g/ha. Results suggested that metribuzin in surface (0-15cm) soil of fly ash unamended plots reached below detectable limit in 60 days, while herbicide persisted till 112 days in surface soil of fly ash amended plots. No metribuzin leached down to subsurface (15-30cm) soil in fly ash amended plots, while traces of metribuzin (0.6-1.2µg/kg) were recovered in subsurface soil of fly ash unamended plot. Metsulfuron-methyl in surface soil persisted till 15 days in control and 20 days in fly ash amended plots and no metsulfuron-methyl leached down to subsurface soil. Fly ash amendment had no adverse effect on the bioactivity of herbicides and yield of soybean and wheat. The study suggested that fly ash amendment to soil can be exploited to retain applied herbicides in surface soil.

Determination of seven certified color additives in food products using liquid chromatography.

This study describes a new method for determining FD&C Blue No. 1, FD&C Blue No. 2, FD&C Green No. 3, FD&C Red No. 3, FD&C Red No. 40, FD&C Yellow No. 5, and FD&C Yellow No. 6 in food products. These seven color additives are water-soluble dyes that are required to be batch certified by the U.S. Food and Drug Administration (FDA) before they may be used in food and other FDA-regulated products. In the new method, the color additives are extracted from a product using one of two procedures developed for various product types, isolated from the noncolored components, and analyzed by liquid chromatography with photodiode array detection. The method was validated by determining linearity, range, precision, recovery from various matrices, limit of detection, limit of quantitation, and relative standard deviation for each color additive. A survey of 44 food products, including beverages, frozen treats, powder mixes, gelatin products, candies, icings, jellies, spices, dressings, sauces, baked goods, and dairy products, found total color additives ranging from 1.9 to 1221 mg/kg. FDA intends to use the new method for conducting a rigorous, comprehensive dietary exposure assessment of certified color additives in products likely to be consumed by children.

Nanobiosensors based on chemically modified AFM probes: a useful tool for metsulfuron-methyl detection.

The use of agrochemicals has increased considerably in recent years, and consequently, there has been increased exposure of ecosystems and human populations to these highly toxic compounds. The study and development of methodologies to detect these substances with greater sensitivity has become extremely relevant. This article describes, for the first time, the use of atomic force spectroscopy (AFS) in the detection of enzyme-inhibiting herbicides. A nanobiosensor based on an atomic force microscopy (AFM) tip functionalised with the acetolactate synthase (ALS) enzyme was developed and characterised. The herbicide metsulfuron-methyl, an ALS inhibitor, was successfully detected through the acquisition of force curves using this biosensor. The adhesion force values were considerably higher when the biosensor was used. An increase of ~250% was achieved relative to the adhesion force using an unfunctionalised AFM tip. This considerable increase was the result of a specific interaction between the enzyme and the herbicide, which was primarily responsible for the efficiency of the nanobiosensor. These results indicate that this methodology is promising for the detection of herbicides, pesticides, and other environmental contaminants.

Adsorption, desorption and mobility of metsulfuron-methyl in soils of the oil palm agroecosystem in Malaysia.

Laboratory experiments were conducted to evaluate adsorption, desorption and mobility of metsulfuron-methyl in soils of the oil palm agroecosystem consisting of the Bernam, Selangor, Rengam and Bongor soil series. The lowest adsorption of metsulfuron-methyl occurred in the Bongor soil (0.366 ml g(-1)), and the highest in the Bemam soil (2.837 ml g(-1). The K(fads) (Freundlich) values of metsulfuron-methyl were 0.366, 0.560, 1.570 and 2.837 ml g(-1) in Bongor, Rengam, Selangor and Bemam soil, respectively. The highest K(fdes) value of metsulfuron-methyl, observed in the Bemam soil, was 2.563 indicating low desorption 0.280 (relatively strong retention). In contrast, the lowest K(fdes) value of 0.564 was observed for the Bongor soil, which had the lowest organic matter (1.43%) and clay content (13.2%). Soil organic matter and clay content were the main factors affecting the adsorption of metsulfuron-methyl. The results of the soil column leaching studies suggested that metsulfuron-methyl has a moderate potential for mobility in the Bernam and Bongor soil series with 19.3% and 39%, respectively for rainfall at 200 mm. However, since metsulfuron-methyl is applied at a very low rate (the maximum field application rate used was 30 g ha(-1)) and is susceptible to biodegradation, the potential forground water contamination is low.

Sorption-desorption behavior of metsulfuron-methyl and sulfosulfuron in soils.

Sorption of metsulfuron-methyl and sulfosulfuron were studied in five Indian soils using batch sorption method. Freundlich adsorption equation described the sorption of herbicides with K(f) (adsorption coefficient) values ranging between 0.21 and 1.88 (metsulfuron-methyl) and 0.37 and 1.17 (sulfosulfuron). Adsorption isotherms were L-type suggesting that the herbicides sorption decreased with increase in the initial concentration of the herbicide in the solution. The K(f) for metsulfuron-methyl showed good positive correlation with silt content (significant at p = 0.01) and strong negative correlation with the soil pH (significant at p = 0.05) while sorption of sulfosulfuron did not correlate with any of the soil parameter. Desorption of herbicides was concentration dependent and, in general, sulfosulfuron showed higher desorption than the metsulfuron-methyl. The study indicates that these herbicides are poorly sorbed in the Indian soil types and there may be a possibility of their leaching to lower soil profiles.

Biodegradation of tribenuron methyl that is mediated by microbial acidohydrolysis at cell-soil interface.

Tribenuron methyl (TBM) is a member of the sulfonylurea herbicide family and is widely used in weed control. Due to its phytotoxicity to rotating-crops, concerns on TBM-pollution to soil have been raised. In this study, experimental results indicated that microbial activity played a key role in TBM removal from polluted soil. Twenty-six bacterial strains were isolated and their degradation of TBM was evaluated. Serratia sp. strain BW30 was selected and subjected to further investigation on its degradative mechanism. TBM degradation by strain BW30 was dependent on glucose that was converted into lactic or oxalic acids. HPLC-MS analysis revealed two end-products from TBM degradation, and they were identical to the products from TBM acidohydrolysis. Based on this observation, it is proposed that microbe-mediated acidohydrolysis of TBM was involved in TBM degradation in soil, and possible application of this observation in bioremediation of TBM-polluted soil is discussed.

Gas chromatographic method for residue analysis of metsulfuron methyl from soil.

Gas chromatographic method has been developed for the determination of metsulfuron methyl residues from soil. Due to the thermal unstability of this herbicide and its mono methyl derivative, it was derivatized to a dimethyl derivative using diazomethane. Structure of the derivatized product was confirmed by GC-MS. Time for methylation reaction was standardized and 24 h was found to be the optimum time in ethylacetate solvent. Using this method, recovery of metsulfuron methyl from soil was above 70%. Limit of detection (LOD) and limit of quantification (LOQ) of the method were 0.1 µg mL⁻¹ and 0.2 µg g⁻¹ respectively.

Monitoring of metsulfuron-methyl and its residues in an artificial pond.

The behavior of metsulfuron-methyl and its residues in an artificial pond was studied using a (14)C isotopic tracer technique. Throughout the experimental period, the majority of metsulfuron-methyl residues were sustained in the pond water. Furthermore, the metsulfuron-methyl residues were just found in the surface layer of the sediment, and the transfer distance of these residues had only reached 9-12 cm by the end of the experiment. The extract residues of metsulfuron-methyl in sediment were slightly higher than those of the bound residues (BR) during the initial experiment stage, while the BR dominated the surface sediment after 45 days. Finally, the metsulfuron-methyl residues could be combined with humus in the surface sediment, and the distribution of metsulfuron-methyl residues in fulvic acid was significantly higher than that in humic acid.

A simple and fast method for chlorsulfuron and metsulfuron methyl determination in water samples using multiwalled carbon nanotubes (MWCNTs) and capillary electrophoresis.

A new method to determine metsulfuron methyl (MSM) and chlorsulfuron (CS) in different water samples was developed. It consists in a solid phase extraction (SPE) procedure using multiwalled carbon nanotubes (MWCNTs) as sorbent material in combination with capillary zone electrophoretic determination. To carry out the pre-concentration step, a simple flow injection system was developed and optimized. Thus, 250 µL of aqueous solution containing methanol 50% (v/v) and acetonitrile 2% (v/v) as eluent, 10 mL of sample and a flow rate of 1.15 mL min(-1) were selected. The CE variables also were optimized. A rapid determination and good resolution of two herbicides were obtained within 9 min using a simple electrophoretic buffer (50 mmol L(-1) sodium tetraborate with 3% of methanol, pH=9.0). Under the optimum conditions, the calibration curves were linear between 0.5 and 6 µg L(-1) for MSM and CS with R(2)=0.995 and 0.997, respectively. The repeatability of the proposed method, expressed as relative standard deviation (RSD), varied between 4.1% and 5.4% (n=10) and the detection limits for MSM and CS were 0.40 and 0.36 µg L(-1), respectively. Good results were achieved when the proposed method was applied to spiked real water samples. The recoveries percentages of the two analytes were over the range 86-108%.