Application of instantaneous nebulization dispersive liquid-phase microextraction combined with HPLC for the determination of chalcone and isoflavone in traditional Chinese medicines.

A simple and rapid instantaneous nebulization dispersive liquid-phase microextraction method was developed, and combined with high-performance liquid chromatography for determination of the contents of seven analytes in traditional Chinese medicines. In this study, using the sprinkler device to achieve instantaneous synchronous dispersion and extraction, only one spray can rapidly achieve the concentration and enrichment of seven kinds of chalcone and isoflavones. The key factors affecting the extraction efficiency were optimized including the type and volume of extractant, the pH and salt concentration of the sample phase, and the number of dispersion. Under the optimal conditions, the enrichment factor of the target analytes ranged from 103.1 to 180.9, with good linearity and correlation coefficients above 0.9970. The limits of detection ranged from 0.02 to 0.15 ng/mL, with good accuracy (recoveries 91.1 to 108.9%) and precision (relative standard deviations 1.5-7.1%). This method has short extraction time (2 s), low organic solvent consumption and high enrichment effect, so it has a wide application prospects.

Ultrasound-assisted dispersive liquid-phase microextraction by solidifying L-menthol-decanoic acid hydrophobic deep eutectic solvents for detection of five fungicides in fruit juices and tea drinks.

An ecofriendly and efficient ultrasound-assisted deep eutectic solvents dispersive liquid-phase microextraction by solidifying the deep eutectic solvents-rich phase was developed to determine azoxystrobin, fludioxonil, epoxiconazole, cyprodinil, and prochloraz in fruit juices and tea drinks by high-performance liquid chromatography. A varieties of environmental hydrophobic deep eutectic solvents serving as extraction agents were prepared using L-menthol and decanoic acid as hydrogen-bond acceptor and hydrogen-bond donor, respectively. The deep eutectic solvents were ultrasonically dispersed in sample solutions, solidified in a freezer and easily harvested. The main variables were optimized by one-factor-at-a-time and response surface test. The new method performs well with relative recovery of 71.75-109.40%, linear range of 2.5-5000 µg/L (r ≥ 0.9968), detection limit of 0.75-8.45 µg/L, quantification limit of 2.5-25 µg/L,, and inter- and intraday relative standard deviations below 13.53 and 14.84%, respectively. As for the extraction mechanism, deep eutectic solvents were disposed into many fine particles in the solution and captured the analytes based on the changes of particle size and quantity in deep eutectic solvents droplets after extraction. The environmental method can successfully detect fungicide residues in real fruit juices and tea drinks.

Vortex-assisted dispersive liquid-phase microextraction for the analysis of main active compounds from Zi-Cao-Cheng-Qi decoction based on a hydrophobic deep eutectic solvent.

In this study, a vortex-assisted hydrophobic deep eutectic solvent dispersive liquid-phase microextraction was developed and used for the extraction and preconcentration of six main active compounds in Zi-Cao-Cheng-Qi decoction. The deep eutectic solvent, prepared by mixing tetrabutylammonium chloride and hexanoic acid at a molar ratio of 1:1, was added to the sample solution containing the analytes. In the absence of disperser, the extractant was rapidly dispersed into fine droplets by the aid of vortex and adequately contacted with the analytes. Some key parameters affecting the approach including extraction solvent type and volume, sample phase pH, extraction time, centrifugation time, and salt concentration were investigated and optimized. Under the optimum conditions, enrichment factors of the target analytes were in the range of 3-330. The calibration graphs were linear with a correlation coefficient (r) ≥ 0.9929. The detection limits were 0.3-0.9 ng/mL, and the satisfactory precisions (relative standard deviations, 0.5-8.9%) and accuracies (relative recoveries, 91.1-102.2%) were also obtained. The developed method was rapid (only 2 min), eco-friendly, effective, and easy to operate. And it has been successfully applied to simultaneous extraction, enrichment, and determination of the main active compounds in a traditional Chinese medicinal formula coupled with high-performance liquid chromatography.

Self-assembled supramolecular dispersive liquid-phase microextraction for concentration and determination of anthraquinone compounds in Rhubarb.

Self-assembled supramolecular dispersive liquid-phase microextraction combined with high-performance liquid chromatography was developed and introduced for simultaneous extraction and determination of the trace level rhein, chrysophanol, and physcion in Rhubarb. Compared with conventional dispersive liquid-phase microextraction, the proposed method used a self-assembled ternary supramolecular consisting of the mixed extraction solvent (heptanol and nonanol) and dispersant (acetone) to achieve high enrichment factors of target analytes. Several factors affecting performance were investigated and optimized, including the mixed extraction solvent, type and volume of the dispersant, the pH of sample phase, salt concentration, shaking time, volume of sample phase, centrifugation time, and rate. Meanwhile, the method mechanism of self-assembled supramolecular dispersive liquid-phase microextraction was analyzed and described. Under the optimized extraction conditions, the enrichment factors of rhein, chrysophanol, and physcion were 116.5, 325.9, and 356.1, respectively. Good linearities (r ≥ 0.9952) for all analytes, low limits of detection (less than 0.04 ng/mL), satisfactory precisions (0.1-8.9%), and accuracies (recoveries, 88.2-104.1%) were achieved. The experimental results showed that the approach was simple, fast, with short extraction time, high enrichment factors, good linearities, and low limits of detection.

Modified dispersive liquid-phase microextraction based on sequential injection solidified floating organic drop combined with HPLC for the determination of phenobarbital and phenytoin.

A modified dispersive liquid phase microextraction based on sequential injection solidified floating organic drop was developed for simultaneous separation/preconcentration of trace amounts of phenobarbital and phenytoin. The important factors affecting on the extraction recovery including pH, the volume of extraction solvent, ionic strength, and the number of injections were investigated and optimized by Box-Behnken design and desirability function. Under the optimum experimental conditions, the calibration graph was linear in the concentration range of 1.0-300.0 µg/L (r2  = 0.997) for phenobarbital and 2.0-400.0 µg/L (r2  = 0.996) for phenytoin. The limit of detection and limit of quantification were 0.35 and 1.2 µg/L for phenobarbital and 0.65 and 2.2 µg/L for phenytoin, respectively. The relative standard deviation for six replicate determinations at 10 µg/L was 3.3 and 4.1% for phenobarbital and phenytoin, respectively. The developed method was successfully applied to the determination of phenobarbital and phenytoin in urine and plasma samples.

Polytetrafluoroethylene physisorption-assisted emulsification microextraction as a cleanup and preconcentration step in the gas chromatography determination of aliphatic hydrocarbons in marine sediment samples.

For the first time, the application of polytetrafluoroethylene powder as an extractant phase collector or holder in liquid-phase microextraction has been developed. For this purpose, the analytical performances of two different ways of applying polytetrafluoroethylene powder in microextraction methods including polytetrafluoroethylene physisorption-assisted emulsification microextraction and dispersive liquid-phase microextraction via polytetrafluoroethylene extractant phase holders have been compared for analysis of aliphatic hydrocarbons in aqueous phases. Under the same conditions, the former showed better extraction efficiencies over the latter and as a result, it was applied as preconcentration and cleanup step in the analysis of aliphatic hydrocarbons in sediment samples followed by gas chromatography analysis. The linearity of the polytetrafluoroethylene physisorption-assisted emulsification microextraction method was obtained over a range of 3.7 and 2000 ng/g (R2 > 0.993). The relative standard deviations were less than 6.5% (n = 3). The limits of detection and quantification obtained by this method were 1.1-9.0 and 3.7-30 ng/g, respectively, indicating that satisfactory results were achieved by the procedure.

Syringe-to-syringe dispersive liquid-phase microextraction solidified floating organic drop combined with high-performance liquid chromatography for the separation and quantification of ochratoxin A in food samples.

A new, simple, and rapid syringe-to-syringe dispersive liquid-phase microextraction with solidified floating organic drop was used for the separation and preconcentration of ochratoxin A from grain and juice samples before its quantification using high-performance liquid chromatography and fluorescence detection. Factors influencing the microextraction efficiency of ochratoxin A, such as sample solution pH, type and volume of organic extractant, salt concentration, number of injections, and volume of the sample, were studied and optimized. Under the optimum properties, the calibration graph showed linearity in the range of 65.0-700.0 ng/L (coefficient of determination = 0.9991). The limit of detection was 20.0 ng/L. The inter-day and intra-day relative standard deviations were in the range of 5.0-8.5%. This method was successfully applied for the quantification of ochratoxin A in grain and juice samples.

Determination of three estrogens and bisphenol A by functional ionic liquid dispersive liquid-phase microextraction coupled with ultra-high performance liquid chromatography and ultraviolet detection.

A hydroxyl-functionalized ionic liquid, 1-hydroxyethyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide, was employed in an improved dispersive liquid-phase microextraction method coupled with ultra high performance liquid chromatography for the enrichment and determination of three estrogens and bisphenol A in environmental water samples. The introduced hydroxyl group acted as the H-bond acceptor that dispersed the ionic liquid effectively in the aqueous phase without dispersive solvent or external force. Fourier transform infrared spectroscopy indicated that the hydroxyl group of the cation of the ionic liquid enhanced the combination of extractant and analytes through the formation of hydrogen bonds. The improvement of the extraction efficiency compared with that with the use of alkyl ionic liquid was proved by a comparison study. The main parameters including volume of extractant, temperature, pH, and extraction time were investigated. The calibration curves were linear in the range of 5.0-1000 µg/L for estrone, estradiol, and bisphenol A, and 10.0-1000 µg/L for estriol. The detection limits were in the range of 1.7-3.4 µg/L. The extraction efficiency was evaluated by enrichment factor that were between 85 and 129. The proposed method was proved to be simple, low cost, and environmentally friendly for the determination of the four endocrine disruptors in environmental water samples.

Determination of estrogens in environmental water samples using 1,3-dipentylimidazolium hexafluorophosphate ionic liquid as extraction solvent in dispersive liquid-liquid microextraction.

In this work, the potential of a symmetric dialkyl-substituted ionic liquid (IL), 1,3-dipenthylimidazolium hexafluorophosphate ([PPIm][PF6 ]), as extraction solvent in dispersive liquid-liquid microextraction (DLLME) has been studied for the analysis of a group of three natural (estriol, 17ß-estradiol, and 17α-estradiol) and four synthetic (17α-ethynylestradiol, diethylstibestrol, dienestrol, and hexestrol) estrogenic compounds as well as one mycotoxin with estrogenic activity (zearalenone) in different types of water samples (Milli-Q, mineral, and wastewater). Separation, determination, and quantification were developed by HPLC-DAD and a fluorescence detector (FD) connected in series. Factors influencing the IL-DLLME procedure (sample pH, amount of IL, type and volume of disperser solvent, ionic strength, and assistance of vortex agitation) were investigated and optimized by means of a step-by-step approach. Once the optimum extraction conditions were established (10 mL of water at pH 8, 60 mg of [PPIm][PF6 ], 500 µL of ACN as disperser solvent and vortex agitation for 1 min), the calibration curves of the whole method (IL-DLLME-HPLC-DAD/FD) were obtained and precision and accuracy were evaluated. It was demonstrated that the developed methodology was repeatable, accurate, and selective with limits of detection in the 0.30-0.57 µg/L and 13.8-37.1 µg/L range for FD and DAD, respectively. Relative recovery values were higher than 85% for the different types of water samples and the Student's t test demonstrated that there were not significant differences between the added and the found concentration.

Dispersive liquid-phase microextraction in combination with HPLC for the enrichment and rapid determination of benzoylurea pesticides in environmental water samples.

Benzoylurea (BU) insecticides have contributed greatly to the output of crops. Their residue in the environment put serious threats on human health and environmental safety. In this study, we have established a new, rapid, and reliable method for the monitoring of typical BU insecticides such as diflubenzuron, flufenoxuron, triflumuron, and chlorfluazuron with dispersive liquid-liquid microextraction prior to HPLC. Chlorobenzene and ethanol were employed as the extraction solvent and disperser solvent, respectively. The possible parameters which would influence the extraction efficiency such as the kinds and volumes of extraction and disperser solvents, extraction time, sample pH, centrifuging time, and salting-out effect were optimized in detail. Under the optimal conditions, the linear range of proposed method was in the range of 1.0-70 µg/L. The detection limits varied from 0.24 to 0.82 µg/L and the precision of the method was <6.5% (RSD, n = 6). The proposed method was validated with real water samples and satisfactory spiked recoveries were achieved. All these results indicate that the proposed method is a low cost, easy to operate, efficient, and sensitive method for the analysis of BU insecticides in water samples.

An air-assisted dispersive liquid phase microextraction method based on a hydrophobic magnetic deep eutectic solvent for the extraction and preconcentration of melamine from milk and milk-based products.

In the current research, a fast and sustainable air-assisted hydrophobic magnetic deep eutectic solvent-based dispersive liquid phase microextraction followed by UV-Vis spectrophotometry measurements was optimized for the extraction and determination of melamine in milk and milk-based products. The central composite design was applied for the optimization of factors affecting the recovery of melamine. Quantitative extraction of melamine was achieved using hydrophobic magnetic deep eutectic solvents prepared from a mixture of octanoic acid, aliquat-336, and cobalt(II) chloride. The optimum conditions for extraction were found as follows: 6 extraction cycles, pH 8.2, extraction solvent volume 260 µL, and acetone volume 125 µL.Interestingly, a centrifugation step was not required to achieve phase separation. Under the optimum conditions, melamine was determined in the linear range of 3-600 ng mL-1, the limit of detection (3Sblank/m) of 0.9 ng mL-1, and the enrichment factor of 144. The validation of the method was investigated by the analysis of reference materials. Consequently, the method was successfully applied for the analysis of melamine residues in milk and milk-based products.

Development of an in-syringe gas-assisted density tunable solidification of floating organic droplet-based dispersive liquid phase microextraction method coupled with HPLC-MS/MS for monitoring amikacin in biological fluids.

A new sample preparation method named in-syringe gas-assisted density tunable dispersive liquid phase microextraction based on solidification of floating organic droplet has been introduced. This method was coupled with high-performance liquid chromatography-tandem mass spectrometry and used for the extraction and quantification of amikacin in plasma and exhaled breath condensate (EBC) samples of the patients receiving amikacin. In the proposed approach, an inert gas is bubbled into a syringe barrel containing aqueous solution of the analyte and a mixture of low density extraction solvent and volatile density modifier. Consequently, the density modifier is evaporated and the analyte is migrated into the released extractant droplets. Basic parameters affecting efficiency of the developed method were optimized. Under optimum conditions, the method limits of detection were 0.06 and 0.29 ng/mL in EBC and plasma, respectively. The extraction recoveries were 90% and 87% in EBC and plasma, respectively. Also, the obtained relative standard deviations were below 9.5% and 9.8% for EBC and plasma, respectively. Considering these results, the developed method provides a quick and efficient way to determine amikacin in patients' biological fluids and can be used widely in drug monitoring and clinical studies.

Strategies to improve the challenges of classic dispersive liquid-liquid microextraction for determination of the parabens in personal care products-One step closer to green analytical chemistry.

Gas flow-assisted dispersive liquid-phase microextraction based on deep eutectic solvent was used to determine parabens in personal care products such as mouthwash, lidocaine gel, aloe vera gel, and skin tonic. A homemade extraction device was innovated, in which by passing the stream of gas bubbles through the deep eutectic solvent a thin layer of the extraction phase is coated on the surface of the bubbles. The extraction is finally achieved when the bubbles are going up through the sample. The single-factor experiments and response surface methodology were applied to optimize the independent variables. The linear range of the method was 0.5 to 1000 µg L-1, the coefficient of determination for the goal analytes was higher than 0.9989, the instrumental limit of detections were in the range 0.2-0.3 µg L-1, and the instrumental limit of quantifications were in the range 0.5-1.1 µg L-1, the relative standard deviations were <5.2% for repeatability and <11.2% for intermediate precision, and the enrichment factors were 66 to 87 obtained under the optimized conditions. A spiking approach by means of standard material was used to estimate accuracy. The relative recoveries were in the range 95.8-105.2%. By using mentioned strategies, the organic waste and energy consumption reduced, toxic reagents replaced with safer ones, and operator safety enhanced. Accordingly, these benefits have been simultaneously attained and, the proposed method was one step closer to automation and sustainable analytical chemistry.

Homogenizer assisted dispersive liquid-phase microextraction for the extraction-enrichment of phenols from aqueous samples and determination by gas chromatography.

In this research, dispersive liquid-phase microextraction has been used for the extraction of some phenols including phenol, 3-methylphenol, 4-nitrophenol, 2-chlorophenol, tert-buthylphenol from aqueous samples, and then the analysis was done by the gas chromatography-flame ionization detector technique. For the first time, a laboratory homogenizer has been applied for dispersing of extracting organic solvent. To improve the chromatographic behavior, acetic anhydride was used as a derivatization reagent of the analytes. The effective parameters on the extraction and derivation process such as extraction solvent type and volume, amount and time of derivatization, sample pH and ionic strength, homogenization time and speed were investigated and optimized. The analytical performances of the method, such as linear dynamic range, repeatability, and detection limit were evaluated under the optimum condition. Under the optimal experimental conditions, the calibration plots were linear the range of 1-500 µg L-1 with the detection limits between 0.1-0.9 µg L-1, and the repeatability in the range of 2.6 to 10.0%. These values vary depend on the compounds. The proposed method was evaluated for the determination of the studied phenolic compounds in different real samples such as river water, tap water and industrial wastewater. The relative recoveries were between 90 and 111%.

Simultaneous extraction and determination of albendazole and triclabendazole by a novel syringe to syringe dispersive liquid phase microextraction-solidified floating organic drop combined with high performance liquid chromatography.

A syringe to syringe dispersive liquid phase microextraction-solidified floating organic drop was introduced and used for the simultaneous extraction of trace amounts of albendazole and triclabendazole from different matrices. The extracted analytes were determined by high performance liquid chromatography along with fluorescence detection. The analytical parameters affecting the microextraction efficiency including the nature and volume of the extraction solvent, sample volume, sample pH, ionic strength and the cycles of extraction were optimized. The calibration curves were linear in the range of 0.1-30.0 µg L(-1) and 0.2-30.0 µg L(-1) with determination coefficients of 0.9999 and 0.9998 for albendazole and triclabendazole respectively. The detection limits defined as three folds of the signal to noise ratio were found to be 0.02 µg L(-1) for albendazole and 0.06 µg L(-1) for triclabendazole. The inter-day and intra-day precision (RSD%) for both analytes at three concentration levels (0.5, 2.0 and 10.0 µg L(-1)) were in the range of 6.3-10.1% and 5.0-7.5% respectively. The developed method was successfully applied to determine albendazole and triclabendazole in water, cow milk, honey, and urine samples.

Gas-assisted dispersive liquid-phase microextraction using ionic liquid as extracting solvent for spectrophotometric speciation of copper.

Gas-assisted dispersive liquid-phase microextraction (GA-DLPME) has been developed for preconcentration and spectrophotometric determination of copper ion in different water samples. The ionic liquid 1-hexyl-3-methylimidazolium hexafluorophosphate and argon gas, respectively, were used as the extracting solvent and disperser. The procedure was based on direct reduction of Cu(II) to Cu(I) by hydroxylamine hydrochloride, followed by extracting Cu(I) into ionic liquid phase by using neocuproine as the chelating agent. Several experimental variables that affected the GA-DLPME efficiency were investigated and optimized. Under the optimum experimental conditions (IL volume, 50µL; pH, 6.0; acetate buffer, 1.5molL(-1); reducing agent concentration, 0.2molL(-1); NC concentration, 120µgmL(-1); Ar gas bubbling time, 6min; argon flow rate, 1Lmin(-1); NaCl concentration, 6% w/w; and centrifugation time, 3min), the calibration graph was linear over the concentration range of 0.30-2.00µgmL(-1) copper ion with a limit of detection of 0.07µgmL(-1). Relative standard deviation for five replicate determinations of 1.0µgmL(-1) copper ion was found to be 3.9%. The developed method was successfully applied to determination of both Cu(I) and Cu(II) species in water samples.

Solvent selection in ultrasonic-assisted emulsification microextraction: Comparison between high- and low-density solvents by means of novel type of extraction vessel.

There are numerous published reports about dispersive liquid phase microextraction of the wide range of substances, however, till now no broadly accepted systematic and purpose oriented selection of extraction solvent has been proposed. Most works deal with the optimization of available solvents without adequate pre-consideration of properness. In this study, it is tried to compare the performances of low- and high-density solvents at the same conditions by means of novel type of extraction vessel with head and bottom conical shape. Extraction efficiencies of seven basic pharmaceutical compounds using eighteen common organic solvents were studied in this work. It was much easier to work with high-density solvents and they mostly showed better performances. This work shows that although exact predicting the performance of the solvents is multifaceted case but the pre-consideration of initial selection of solvents with attention to the physiochemical properties of the desired analytes is feasible and promising. Finally, the practicality of the method for extraction from urine and plasma samples was investigated.

Green aspects, developments and perspectives of liquid phase microextraction techniques.

Determination of analytes at trace levels in complex samples (e.g. biological or contaminated water or soils) are often required for the environmental assessment and monitoring as well as for scientific research in the field of environmental pollution. A limited number of analytical techniques are sensitive enough for the direct determination of trace components in samples and, because of that, a preliminary step of the analyte isolation/enrichment prior to analysis is required in many cases. In this work the newest trends and innovations in liquid phase microextraction, like: single-drop microextraction (SDME), hollow fiber liquid-phase microextraction (HF-LPME), and dispersive liquid-liquid microextraction (DLLME) have been discussed, including their critical evaluation and possible application in analytical practice. The described modifications of extraction techniques deal with system miniaturization and/or automation, the use of ultrasound and physical agitation, and electrochemical methods. Particular attention was given to pro-ecological aspects therefore the possible use of novel, non-toxic extracting agents, inter alia, ionic liquids, coacervates, surfactant solutions and reverse micelles in the liquid phase microextraction techniques has been evaluated in depth. Also, new methodological solutions and the related instruments and devices for the efficient liquid phase micoextraction of analytes, which have found application at the stage of procedure prior to chromatographic determination, are presented.