共查询到20条相似文献,搜索用时 12 毫秒
1.
Tahereh Sadeghcheh Mohammad Saber Tehrani Hakim Faraji Parviz Aberoomand Azar Masoumeh Helalizadeh 《Journal of separation science》2022,45(7):1362-1373
A sensitive method based on liquid chromatography combined with a diode array detector was developed and validated to simultaneously determine tamoxifen, and its active metabolites N-desmethyltamoxifen, 4-hydroxytamoxifen, and endoxifen in human plasma samples. The green and sustainable vortex-assisted dispersive liquid-phase microextraction technique based on the natural hydrophobic deep eutectic solvent was used for the extraction and preconcentration of the analytes. Chemometrics and multivariate analysis were used to optimize the independent variables including the type and volume of deep eutectic solvent, extraction time, and ionic strength. Under optimal conditions, calibration curves were linear in a suitable range with the lower limits of quantification (0.8–10.0 μg/L), which covered the relevant concentrations of the analytes in plasma samples for a clinical study. Intra- and interday precision evaluated at three concentrations for the analytes were lower than 8.2 and 12.1%, respectively. Accuracy was in the range of 94.9–104.7%. The applicability of the developed method on human plasma samples illustrated the range 45.1–72.8, 98.4–128.3, 0.9–1.2, and 2.7–6.1 μg/L for tamoxifen, N-desmethyltamoxifen, 4-hydroxytamoxifen, and endoxifen, respectively. The validated method can be effective for the pharmacokinetics, pharmacodynamics, and therapeutic drug monitoring studies of tamoxifen and its main metabolites in biological fluids. 相似文献
2.
低共熔液相微萃取-高效液相色谱法测定食用油中双酚AEI北大核心CSCD 总被引:2,自引:0,他引:2
建立了一种基于低共熔溶剂(DESs)的液液微萃取-高效液相色谱联用(LLME-HPLC)技术用于测定食用油中的双酚A(BPA)的方法,对比了3种DES和甲醇、乙二醇对食用油中BPA的萃取效率,研究了温度、萃取时间和萃取剂体积对萃取效率的影响。结果表明:氯化胆碱/乙二醇组成的DES萃取率最高;低共熔溶剂用量100μL,萃取温度25℃,萃取时间5 min时,萃取效率最高。BPA的检测限和定量限分别为0.10 mg/L和0.50 mg/L,加标回收率在86.3%~109.9%范围内,RSD小于6%。方法可用于食用油中BPA的检测。 相似文献
3.
One of the highlights of green chemistry is the development of techniques and procedures with low environmental impact. In the last years, deep eutectic solvents (DES) have become an important alternative to conventional organic solvents. For a period ionic liquids have provoked remarkable interest, but they have been displaced by DES because they show easier preparation methods, lower prices, many of them are biodegradable and compatible with biological systems. In addition, they show adjustable physicochemical properties, high thermal stability, low volatility and are compatible with water. In this paper is reviewed the state of the art of the use of DES paying special attention to the role of reaction media in organic synthesis. 相似文献
4.
Justyna Werner Karolina Kohut Robert Frankowski Agnieszka Zgoła-Grześkowiak 《Journal of separation science》2023,46(2):2200682
In this study, an efficient preconcentration method was presented that is based on dispersive liquid-liquid microextraction taking the advantage of newly synthesized phosphonium deep eutectic solvents used as extractants and ultrasound probe as a dispersing agent. The extracts obtained were analyzed by high-performance liquid chromatography. To optimize the five most important factors for the microextraction procedure a central composite design plan was used. Under optimal conditions (140 μl of extractant, 60 mg of NaCl, pH = 2.0, 120 s of extraction time with ultrasound probe as the dispersing agent, 16 min of centrifugation for phase separation), the proposed method allowed to achieve good precision with RSD between 3.2% and 9.7% at 1.0, 5.0 and 40.0 ng ml levels. The preconcentration factors were equal to 42, 39, and 41, and the limits of detection 0.128, 0.103, and 0.135 ng/ml for dicamba, 2-methyl-4-chlorophenoxyacetic acid, and 2-methyl-4-chlorophenoxypropionic acid, respectively. The proposed method was successfully applied for the determination of chlorophenoxy acid herbicides in water samples from drainage ditches with a good recovery in the range of 70%–93%. 相似文献
5.
Shuanggen Wu Changyong Cai Fenfang Li Zhijian Tan Shengyi Dong 《Angewandte Chemie (International ed. in English)》2020,59(29):11871-11875
Application of new strategies for supramolecular self‐assembly can significantly impact the properties and/or functions of supramolecular polymers. To realize a facial strategy for the development of solvent‐free supramolecular polymers in bulk, “deep eutectic solvents” were employed. Cyclodextrins and natural acids were used to prepare deep eutectic supramolecular polymers ( DESP s). Deep eutectic solvents have special characteristics that endow DESP s with unique macroscopic properties and excellent processability. DESP s exhibit supramolecular adhesion and temperature‐dependent behavior originating from the combined effects of deep eutectic solvents and supramolecular polymerization. Because DESP s are solvent‐free and display interesting macroscopic properties, they have potential as new adaptive materials. 相似文献
6.
Maryam Shahbodaghi Hakim Faraji Hamidreza Shahbaazi Mohsen Shabani 《Journal of separation science》2020,43(2):452-461
Based on the solidification of a hydrophobic deep eutectic solvent in air‐assisted liquid phase microextraction combined with gas chromatography and mass spectrometry, a green and sustainable microextraction technique was developed for extracting, separating, and detecting organophosphorus flame retardants in aqueous samples. In this study, some strategies were considered for overcoming or improving the challenges of conventional solvent microextraction procedures. In addition, a hydrophobic deep eutectic solvent with a freezing point near the ambient temperature was employed as an extraction phase, the dispersive solvent was substituted by the syringe pump process, and the centrifugation step was omitted by using salting‐out phenomenon. Further, the effect of the main independent variables was evaluated by using the chemometric methods in order to maximize the extraction efficiency of the procedure. Under optimal conditions, the calibration model was linear in the range of 0.01–25.0 µg/L. Limits of detection and quantitation were assessed at the concentration levels of 2–23 and 9–65 ng/L, respectively. The precision involving repeatability and reproducibility was evaluated by estimating the relative standard deviation, the levels of which were <6.6 and <8.7%, respectively. The applicability of the method was successfully evaluated by analyzing the target analytes in real aqueous samples, which illustrated satisfactory recoveries (95–104.61%). 相似文献
7.
《Journal of separation science》2018,41(14):2870-2877
A dispersive liquid–liquid microextraction method for the simultaneous determination of 11 pharmaceuticals has been developed. The method is based on a microextraction procedure applied to wastewater samples from different regions of Hungary followed by high‐performance liquid chromatography with mass spectrometry. The effect of the nature of the extractant, dispersive solvent, different additives, and extraction time were examined on the extraction efficiently of the dispersive liquid–liquid microextraction method. Under optimal conditions, the linearity for determining the pharmaceuticals was in the range of 1–500 ng/mL, with the correlation coefficients ranging from 0.9922 to 0.9995. The limits of detection and limits of quantification were in the range of 0.31–6.65 and 0.93–22.18 ng/mL, respectively. 相似文献
8.
深共融溶剂在有机合成中的应用 总被引:1,自引:0,他引:1
深共融溶剂是一种新型绿色溶剂,与传统的有机溶剂相比,其具有低蒸气压、 不易燃、 稳定性好、 无毒性、 生物降解性、 可回收和廉价易得等优点。深共融溶剂作为新型溶剂,应用前景广泛。本文综述了近几年其作为新型的反应介质或催化剂用于传统的有机合成反应的最新研究成果,主要从卤代反应、Diels-Alder反应、Knoevenagel缩合、Henry反应、Perkin反应、Paal-Knorr反应和Biginelli反应等方面对其进行综述,最后展望了深共融溶剂在有机反应中的发展前景。 相似文献
9.
Wentao Han Yang Yang Na Hang Wanning Zhao Pengfei Lu Songqing Li 《Journal of separation science》2022,45(6):1252-1261
In this study, switchable hydrophilic solvent-based dispersive liquid-liquid microextraction coupled with high-performance liquid chromatography was developed for the determination of four sulfonylurea herbicides in soils. For the first time, the sample pretreatment was achieved due to the similar acid-base status of sulfonylurea herbicides and switchable hydrophilic solvent. In the extraction step, sulfonylurea herbicides were extracted as anions and transferred to an alkaline solution with switchable hydrophilic solvent anions. In the concentration step, two types of anions were transformed to their molecular state after the aqueous solution was acidified. In addition, the dispersion and microextraction processes were completed efficiently with the simultaneous formation of analytes and extractants. The factors affecting the extraction performance were optimized. Under the optimized conditions, good linearity was observed for each herbicide with correlation coefficients ranging from 0.9952 to 0.9978. The limits of detection were in the range of 0.1–0.2 μg/g. Moreover, the relative recoveries of the sulfonylurea herbicides at spiking levels of 0.5, 1, and 1.5 μg/g in soil samples were between 75 and 111% (relative standard deviations: 0.4–11.4%). Therefore, the proposed method in this study could be successfully applied to the analysis of four types of sulfonylurea herbicides in soil samples. 相似文献
10.
In this study, a simple and green deep eutectic solvent based dispersive liquid‐liquid microextraction methodology had been proposed for the assessment of four macrolides in swine urine samples. Some important parameters including type and volume of extraction solvent and demulsifier solvent, sample pH, salt concentration affecting extraction efficiency were investigated. The quantitative recoveries were achieved at pH 9 and 20% (w/v) NaCl by using 0.3 mL of deep eutectic solvent consisting of choline chloride‐phenol (1:2, molar ratio) and 0.3 mL of tetrahydrofuran. Under optimal conditions, the linear ranges of four macrolides were 0.5–20.0 µg/L with correlation coefficient higher than 0.999. Limits of detection and quantification were in the ranges of 0.02–0.1 and 0.1–0.5 µg/L, respectively. The relative recoveries for macrolides in spiked swine urine samples ranged from 80 to 93% with relative standard deviations less than 6%. 相似文献
11.
Since its innovation in 2006, the dispersive liquid-liquid microextraction (DLLME) method has attracted the attention of analytical chemists in the field of sample preparation. This method has been successfully applied to determine trace amounts of pollutants in various matrices, but the restriction in the choice of suitable disperser and extraction solvents, and high disperser solvent consumption leading to decreased partition coefficients of the analytes between aqueous phase and extractant are its problems. To solve these drawbacks and develop environmentally friendly techniques, various alternatives for the conventional DLLME have been presented. The current review will begin with an introduction to the sample preparation, implementation of DLLME, and its advantages. Then, we focus on its drawbacks, which result mainly from the use of disperser solvent. Afterward, some of the most interesting approaches that have been employed and published until now are reviewed. Finally, an outlook on the future of these techniques will be given. 相似文献
12.
Eduarda S. Morais Dr. André M. Da Costa Lopes Dr. Mara G. Freire Dr. Carmen S. R. Freire Prof. Armando J. D. Silvestre 《ChemSusChem》2021,14(2):686-698
A deep analysis upon the chemical modifications of the cellulose and hemicelluloses fractions that take place during biomass delignification with deep eutectic solvents (DES) is lacking in literature, being this a critical issue given the continued research on DES for this purpose. This work intends to fill this gap by disclosing a comprehensive study on the chemical modifications of cellulose (microcrystalline cellulose and bleached kraft pulp) and hemicelluloses (xylans) during thermal treatment (130 °C) with cholinium chloride/lactic acid ([Ch]Cl/LA) at molar ratio 1 : 10, one of the best reported DES for biomass delignification. The obtained data revealed that [Ch]Cl/LA (1 : 10) has a negative impact on the polysaccharides fractions at prolonged treatments (>4 h), resulting on substantial modifications including the esterification of cellulose with lactic acid, shortening of fibers length, fibers agglomeration and side reactions of the hemicelluloses fraction (e. g., humin formation, lactic acid grafting). Wood delignification trials with [Ch]Cl/LA (1 : 10) at the same conditions also corroborate these findings. Moreover, the DES suffers degradation, including the formation of lactic acid derivatives and its polymerization. Therefore, short time delignification treatments are strongly recommended when using the [Ch]Cl/LA DES, so that a sustainable fractionation of biomass into high quality cellulose fibers, isolated lignin, and xylose/furfural co-production along with solvent recyclability could be achieved. 相似文献
13.
Prof. Roger A. Sheldon 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(37):12984-12999
In this Minireview, the state of the art in the use of ionic liquids (ILs) and deep eutectic solvents (DESs) as alternative reaction media for biocatalytic processes and biomass conversion is presented. Initial, proof‐of‐concept studies, more than a decade ago, involved first‐generation ILs based on dialkylimidazolium cations and non‐coordinating anions, such as tetrafluoroborate and hexafluorophosphate. More recently, emphasis has switched to more environmentally acceptable second‐generation ILs comprising cations, which are designed to be compatible with enzymes and, in many cases are derived from readily available, renewable resources, such as cholinium salts. Protic ionic liquids (PILs), prepared simply by mixing inexpensive amines and acids, are particularly attractive from both an environmental and economic viewpoint. DESs, prepared by mixing inexpensive salts with, preferably renewable, hydrogen‐bond donors such as glycerol and amino acids, have also proved suitable reaction media for biocatalytic conversions. A broad range of enzymes can be used in ILs, PILs and DESs, for example lipases in biodiesel production. These neoteric solvents are of particular interest, however, as reaction media for biocatalytic conversions of substrates that have limited solubility in common organic solvents, such as carbohydrates, nucleosides, steroids and polysaccharides. This has culminated in the recent focus of attention on their use as (co)solvents in the pretreatment and saccharification of lignocellulose as the initial steps in the conversion of second‐generation renewable biomass into biofuels and chemicals. They can similarly be used as reaction media in subsequent conversions of hexoses and pentoses into platform chemicals. 相似文献
14.
Dinis O. Abranches Liliana P. Silva Dr. Mónia A. R. Martins Prof. Simão P. Pinho Prof. João A. P. Coutinho 《ChemSusChem》2020,13(18):4916-4921
The mechanism of formation of betaine-based deep eutectic solvents (DES) is presented for the first time. Due to its polarity unbalance, it was found that betaine displays strong negative deviations from ideality when mixed with a variety of different organic substances. These results pave the way for a comprehensive design of novel deep eutectic solvents. A connection to biologically relevant systems was made using betaine (osmolyte) and urea (protein denaturant), showing that these two compounds formed a DES, the molecular interactions of which were greatly enhanced in the presence of water. 相似文献
15.
《Journal of separation science》2018,41(17):3424-3431
Ternary deep eutectic solvent magnetic molecularly imprinted polymers grafted on silica were developed for the selective recognition and separation of theophylline, theobromine, (+)‐catechin hydrate, and caffeic acid from green tea through dispersive magnetic solid‐phase microextraction. A new ternary deep eutectic solvent was adopted as a functional monomer. The materials obtained were characterized by FTIR spectroscopy, field emission scanning electron microscopy, transmission electron microscopy, NMR spectroscopy, and powder X‐ray diffraction. The practical recovery of the theophylline, theobromine, (+)‐catechin hydrate, and caffeic acid isolated with ternary deep eutectic solvent magnetic molecularly imprinted polymers in green tea were 91.82, 92.13, 89.96, and 90.73%, respectively, and the actual amounts extracted were 5.82, 4.32, 18.36, and 3.69 mg/g, respectively. The new method involving the novel material coupled with dispersive magnetic solid‐phase microextraction showed outstanding recognition, selectivity and excellent magnetism, providing a new perspective for the separation of bioactive compounds. 相似文献
16.
Catarina Florindo Prof. Luís C. Branco Prof. Dr. Isabel M. Marrucho 《ChemSusChem》2019,12(8):1481-1481
17.
Catarina Florindo Prof. Luís C. Branco Prof. Dr. Isabel M. Marrucho 《ChemSusChem》2019,12(8):1549-1559
Deep eutectic solvents (DESs) consist of a mixture of two or more solid components, which gives rise to a lower melting point compared to the starting materials. Until recently only hydrophilic DESs were available, and despite their revolutionary role in the alternative-solvents field, important issues in chemistry, and chemical engineering (such as water-related problems and the replacement of toxic volatile organic compounds) could not be tackled. Hydrophobic (deep)—here in parenthesis due to the different depths of the eutectic melting points—eutectic solvents are a subclass of DESs where both components are hydrophobic. The low toxicity, high biodegradability, and straightforward preparation without further purification steps of naturally occurring low-cost compounds are among the key advantages. Although research on hydrophobic DESs is scarce (the first report was only published in 2015), some interesting features and applications have been reported and deserve to be evaluated and comparisons established. This Minireview is divided into two parts: The first part provides a brief general introduction to DESs and the second part discusses the nomenclature using solid–liquid phase diagram analysis, chemical stability, thermophysical properties comparison, and finally the most important emerging fields of application. 相似文献
18.
19.
Andrew J. Maneffa Dr. Adrian B. Harrison Dr. Stewart J. Radford Dr. A. Steve Whitehouse Prof. James H. Clark Dr. Avtar S. Matharu 《ChemistryOpen》2020,9(5):559-567
Deep eutectic solvents (DES) are one of the most promising green technologies to emerge in recent years given their combination of environmentally friendly credentials and useful functionalities. Considering the continued search for new DES – especially those that exemplify the aforementioned characteristics, we report the preparation of DES based on natural analogues of l -ascorbic acid for the first time. The onset of eutectic melting occurred at temperatures far below the melting point of the individual components and resulted in the generation of glass forming fluids with glass transition temperatures, viscosities and flow behavior that are comparable to similar systems. This work expands the current array of DES that can be produced using naturally occurring components, which given their potential to be bio-derived, interesting physicochemical properties (e. g. propensity to supercool and vitrify) and apparent antibacterial nature, may provide utility within a range of applications. 相似文献
20.
Alba Sánchez-Condado Prof. Gabino A. Carriedo Prof. Alejandro Presa Soto María J. Rodríguez-Álvarez Prof. Joaquín García-Álvarez Prof. Eva Hevia 《ChemSusChem》2019,12(13):3134-3143
Despite their ubiquitous presence in synthesis, the use of polar organolithium reagents under environmentally benign conditions constitutes one of the greatest challenges in sustainable chemistry. Their high reactivity imposes the use of severely restrictive protocols (e.g., moisture- and oxygen-free, toxic organic solvents, inert atmospheres, low temperatures, etc.). Making inroads towards meeting this challenge, a new air- and moisture-compatible organolithium-mediated methodology for the anionic polymerization of different olefins (e.g., styrenes and vinylpyridines) was established by pioneering the use of deep eutectic solvents (DESs) as an eco-friendly reaction medium in this type of transformation. Fine-tuning of the conditions (sonication of the reaction mixture at 40 °C in the absence of protecting atmosphere) along with careful choice of components of the DES [choline chloride (ChCl) and glycerol (Gly) in a 1:2 ratio] furnished the desired organic polymers (homopolymers and random copolymers) in excellent yields (up to 90 %) and low polydispersities (IPD 1.1–1.3). Remarkably, the in situ-formed polystyril lithium intermediates exhibited a great resistance to hydrolysis in the eutectic mixture 1ChCl/2Gly (up to 1.5 h), hinting at an unexpected high stability of these otherwise highly reactive organolithium species in these unconventional reaction media. This unique stability can be exploited to create well defined block-copolymers. 相似文献

