共查询到20条相似文献,搜索用时 31 毫秒
1.
F A van der Hoorn F Boomsma A J Man in 't Veld M A Schalekamp 《Journal of chromatography. A》1989,487(1):17-28
We report a sensitive fluorimetric method, in which catecholamines are concentrated from plasma by liquid-liquid extraction and derivatized with the selective fluorescent agent 1,2-diphenylethyl-enediamine prior to chromatography. Optimal conditions for extraction, derivatization and chromatography were investigated. With alpha-methylnorepinephrine as internal standard, the chromatographic separations are complete within 6 min. Limits of detection are 0.3 pg for norepinephrine and epinephrine and 0.5 pg for dopamine. Coefficients of variation are low (3-7%). Comparison of plasma catecholamine values determined with this method and with an established method with electrochemical detection (n = 135) shows good correlation (r = 0.94-1.00), and regression lines are close to lines of identity. 相似文献
2.
Selective solid-phase extraction of catecholamines by the chemically modified polymeric adsorbents with crown ether 总被引:1,自引:0,他引:1
A simple and selective one-step solid-phase extraction procedure using chemically modified polymer resin (Amberlite XAD-4) with crown ether was investigated for the measurement of urinary catecholamines. After loading the urine samples (adjusted to pH 4) on the synthesized adsorbent cartridge, the column was washed with methanol followed by water and then the adsorbed catecholamines were eluted by 1.0 mL of 6.0 M acetic acid. The effectiveness of sample clean-up method was demonstrated by reversed-phase ion-pair high-performance liquid chromatography with electrochemical detection. Under optimal condition, the recoveries of epinephrine, norepinephrine, and dopamine from spiked urine sample were >86% for all catecholamines. The detection limits (n=5) for epinephrine, norepinephrine, and dopamine were 37, 52, and 46 nmol/L, respectively. 相似文献
3.
G. Cuisinaud N. Bernard C. Julien C. Rodriguez J. Sassard 《International journal of environmental analytical chemistry》2013,93(1-2):51-73
Abstract A new high-performance liquid chromatographic technique including the use of an automated column switching system has been developed for the study of dopamine, norepinephrine, epinephrine and serotonin and their related metabolites in biological samples. Through two runs, it has been possible to separate twenty derivatives and three internal standards which have to be added to samples prior to the extraction procedures. In each case, the column switching system allowed to obtain a clear separation of all the compounds, which will be of importance to avoid any expected interference from other endogenous substances, while decreasing the analysis time. By coupling on-line fluorimetric and electrochemical detections the specificity of the technique was enhanced, since the ratio of the responses of both detectors was an index of the purity of the peaks. In addition, fluorimetric detection was found of value to free the determination of some compunds from the effects of solvent front while electrochemical detection increased the sensitivity. Finally, the column switching system allowed a rapid cleaning of the columns between two analyses. A typical application to a human urine sample was shown. 相似文献
4.
G Alberts F Boomsma A J Man in 't Veld M A Schalekamp 《Journal of chromatography. A》1992,583(2):236-240
We report a reliable fluorimetric assay for the simultaneous determination of norepinephrine, epinephrine, dopamine and dobutamine in human plasma and urine, based on liquid-liquid extraction and derivatization with the fluorogenic agent 1,2-diphenylethylenediamine prior to chromatography. The method is sensitive (detection limit 0.3-0.8 pg injected) and reproducible (coefficients of variation 1-10%), and shows good accuracy (93-98%). The method should also be used when one only wants to measure the concentrations of the natural catecholamines, in order to avoid interference by metabolites of dobutamine and by the late-eluting dobutamine itself. 相似文献
5.
P. Rajec 《Journal of Radioanalytical and Nuclear Chemistry》1992,166(5):413-419
The determination of uranium by a fluorimetric method using a conventional spectrophotometer has been elaborated. The quenching effect of the matrix was reduced by separation with liquid-liquid extraction and emulsion liquid membrane extraction methods using D2EHPA as a selective extraction reagent. The method was employed for uranium determination in radioactive waste solutions and proved to be very fast and easy to perform. It was found that it is possible to determinate as low as 0.2 ppm of uranium in a 10 ml sample. 相似文献
6.
Residues of anti-hormones in biological materials are routinely determined at the ppb-level1 by specific detection through high-performance thin-layer chromatography with fluorimetric detection or capillary gas chromatography with electron-capture detection backed up by a selective single step extraction. 相似文献
7.
Sabbioni C Saracino MA Mandrioli R Pinzauti S Furlanetto S Gerra G Raggi MA 《Journal of chromatography. A》2004,1032(1-2):65-71
The comparison of two HPLC methods, one with electrochemical detection and the other with coulometric detection, for the simultaneous analysis of catecholamines and 4-hydroxy-3-methoxyphenylethylene glycol (MHPG) in human plasma is presented. The careful pre-treatment of plasma samples is based on an innovative two-step procedure by means of solid-phase extraction (SPE) which uses one single hydrophilic-lipophilic balance cartridge. The extraction yield values found were higher than 85% for epinephrine, norepinephrine and MHPG, and higher than 70% for dopamine. The assays carried out on real plasma samples with the coulometric system gave good results in terms of sensitivity (limits of quantitation: 0.10-0.15 ng ml(-1) for catecholamines, 0.6 ng ml(-1) for MHPG) and selectivity, while interference was sometimes found when using the amperometric system. Precision was also satisfactory, with relative standard deviation values for intermediate precision always lower than 6%. The HPLC method with coulometric detection coupled to a novel SPE procedure is thus suitable for the simultaneous determination of catecholamines and MHPG in plasma of volunteers subjected to experimental stress. 相似文献
8.
Lin Zhou Fengjun Shang Mila Pravda Jeremy D. Glennon John H. T. Luong 《Electroanalysis》2009,21(7):797-803
A sensitive and selective electrochemical method for the determination of dopamine using a combined electropolymerized permselective film of polytyramine and polypyrrole‐1‐propionic acid on a glassy carbon (GC) electrode was developed. The formation of a “layer‐by‐layer” film has allowed for selective detection of dopamine in the presence of 3,4‐dihydroxyphenylalanine (L‐DOPA), DOPAC, ascorbic acid, uric acid, epinephrine and norepinephrine. The modified electrodes exhibited a detection limit of 100 nM with linearity ranging from 5×10?6 to 5×10?5 M. No cleaning step was required during the course of repeated measurement. 相似文献
9.
Determination of catecholamines in urine using aminophenylboronic acid functionalized magnetic nanoparticles extraction followed by high‐performance liquid chromatography and electrochemical detection
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Liwei Jiang Yibang Chen Yanmei Luo Yueming Tan Ming Ma Bo Chen Qingji Xie Xubiao Luo 《Journal of separation science》2015,38(3):460-467
A new method was developed for the simultaneous determination of three catecholamines in urine using aminophenylboronic acid functionalized magnetic nanoparticles extraction followed by high‐performance liquid chromatography with electrochemical detection. Novel aminophenylboronic acid functionalized magnetic nanoparticles were prepared by multi‐step covalent modification, and characterized by transmission electron microscopy, Fourier‐transformed infrared spectroscopy, X‐ray diffraction, and vibrating sample magnetometry. With the help of the high affinity between the boronate and cis‐diol group, the particles were used for the highly selective separation and enrichment of three major catecholamines, norepinephrine, epinephrine, and dopamine. Effects of the pH of the feed solution, the extraction time, the composition of the buffer solution, the amount of the magnetic particles, the elution conditions, and the recycling of aminophenylboronic acid functionalized magnetic nanoparticles were explored. Under the optimized conditions, 13–17‐fold enrichment factors were obtained. The linear ranges were 0.01–2.0 μg/mL for the studied analytes. The limits of detection and quantification were in the range of 2.0–7.9 and 6.7–26.3 ng/mL, respectively. The relative recoveries were in the range of 92–108%, with intraday and interday relative standard deviations lower than 6.8%. This method was successfully applied to analysis of catecholamines in real urine. 相似文献
10.
A. A. Dutov D. A. Nikitin Z. Ts. Rinchinov P. P. Tereshkov P. P. Tsydendambaev A. A. Fedotova 《Russian Journal of Physical Chemistry A, Focus on Chemistry》2007,81(3):421-423
A HPLC method is proposed for determining neopterin in biological liquids. The method was realized using a standard chromatographic instrumentation. Neopterin was isolated from blood serum and urine by solid-phase extraction on cartridges containing 30 mg of supercrosslinked polystyrene. The separation was carried out on an Irica chromatograph (Japan) equipped with means of UV (350 nm) and fluorimetric (es350-em430 nm) detection. The degree of extraction was 96–113%, and the sensitivity of UV and fluorimetric detection was 0.1 and ~0.03 ng, respectively (at signal-to-noise ratio 3). It is shown that the method is suitable for use in routine clinical analysis of neopterin in biological liquids. 相似文献
11.
A method is described for the separation and automated fluorimetric determination of epinephrine and norepinephrine in brain tissue extracts without mutual interference. The catecholamines are isolated and purified by extraction from activated alumina. Oxidation and rearrangement to their fluorescent lutines is carried out on two separate AutoAnalyzer manifolds and fluorescence is read in an Aminco-Bowman spectrophotofluorimeter. The interference by one amine with the determination of the other is less than 1% for determination of epinephrine in the presence of an equimolar concentration of norepinephrine, and, conversely, less than 4% for determination of norepinephrine. This eliminates the need for solution of simultaneous equations, the results of which are often misleading when the ratio of one amine to the other in brain exceeds 10:1. This method can be useful for rapid screening of psychoactive compounds affecting central and peripheral adrenergic stores. 相似文献
12.
S K Salzman M S Sellers A L Beckman R Naidu G D Macewen 《Journal of chromatography. A》1985,343(2):285-301
Liquid chromatography with electrochemical detection was used for the determination of norepinephrine and epinephrine in human plasma samples obtained prior to, after, and six times during the course of spinal fusion surgery for the correction of scoliosis. The catecholamines were extracted from plasma by alumina adsorption and chromatographed isocratically using a reversed-phase, ion-pairing system. Data obtained are compared to those obtained intraoperatively by other authors using a radioenzymatic method, and the mechanism of sympathetic activation during surgery is discussed. Preliminary data using 3-micron particle size columns and dual-parallel electrochemical detection are presented. 相似文献
13.
The objective of this study was to develop a very sensitive and selective method for the determination of detajmium (4-3-diethylamino-2-hydroxypropyl-ajmaline), a sodium-channel-blocking drug with antiarrhythmic properties, in serum. A high-performance liquid chromatography (HPLC) method with solid-phase extraction and fluorimetric detection has been applied. Serum samples were diluted with phosphate buffer (pH 3.5) and the extraction of detajmium and ajmaline, which was used as an internal standard, was carried out with Oasis cartridges (Waters). The chromatographic separation was performed on a RP18 column. The limit of quantification for serum samples of detajmium was 1 ng/ml with good reproducibility (R.S.D. < 15%) and a linear response from 1 to 200 ng/ml. The described method is highly sensitive and specific for the determination of detajmium in serum of patients and volunteers. 相似文献
14.
《Analytical letters》2012,45(1):152-163
AbstractA simple, sensitive, and selective fluorimetric method is reported for the determination of β-carotene in various food samples. Three fluorescent dyes, including fluorescein (F), eosin B (EB), and Congo red (CR), were characterized in a series of measurements to optimize the analytical response for the reliable, suitable, and sustainable determination of β-carotene. 3′,6′-Dihydroxyspiro[isobenzofuran-1(3H),9′-[9H]xanthen]-3-one, commonly known as fluorescein, was selected for the fluorimetric determination of β-carotene using a phosphate buffer. Under the optimum experimental conditions, β-carotene was determined across a range from 0.54 to 536.87?mg L?1 with a detection limit equal to 0.47?mg L?1. The novel method was demonstrated to be easy to use, cost effective, rapid, and less complex compared to a standard protocol that involves a time-consuming extraction followed by an expensive HPLC determination. 相似文献
15.
The application of the matrix solid-phase dispersion (MSPD) process as sample treatment in connection with the electrochemical detection is studied for the first time. For this purpose, a novel methodology is introduced for the extraction of propham and maleic hydrazide herbicides from potatoes samples based in the MSPD process prior to their electrochemical detection. Potato samples disruption was done by blending them with C8 bonded-phase and selective herbicide extraction was achieved by successive treatment of the blended with 50 mM phosphate buffer pH 7.4 (for maleic hydrazide) and methanol (for propham). The extraction procedure efficiency was estimated using differential pulse voltammetry in potato samples spiked with the herbicides yielding recovery values of 98% and 68% for propham and maleic hydrazide, respectively. No significant adverse effect of the MSPD process was observed on the herbicides electrochemical signals. For comparison, recovery studies using HPLC with UV detection were carried out and a good correlation in the results obtained by using both techniques was observed. 相似文献
16.
《液相色谱法及相关技术杂志》2012,35(11):2161-2177
Abstract An improved reversed-phase liquid chromatography analysis with an electrochemical detector was developed to determine concurrently concentrations of the basic neurotransmitters, serotonin, dopamine, norepinephrine and epinephrine and their acidic metabolites. A combination of extraction procedures and a novel method of peak identification using applied potentials from 0.35 to 0.95 volts are described. 相似文献
17.
Yassine Benmassaoud Khaled Murtada Rachid Salghi Mohammed Zougagh ngel Ríos 《Molecules (Basel, Switzerland)》2021,26(9)
In this study, we combine magnetic solid phase extraction (MSPE), with the screen-printed carbon electrode (SPCE) modified by a molecular imprinted polymer (MIP) for sensitive and selective extraction and electrochemical determination of Rhodamine B in food samples. A magnetic solid phase extraction (MSPE) was carried out using magnetic poly(styrene-co-divinylbenzene) (PS-DVB) and magnetic nanoparticles (MNPs) synthetized on the surface of multiwalled carbon nanotubes (MWCNTs). An MIP was prepared on the surface of MWCNTs in the presence of titanium oxide nanoparticles (TiO2NPs) modifying the SPCE for the rapid electrochemical detection of Rhodamine B. The MIPs synthesis was optimized by varying the activated titanium oxide (TiO2) and multiwalled carbon nanotubes (MWCNTs) amounts. The MSPE and electrochemical detection conditions were optimized as well. The present method exhibited good selectivity, high sensitivity, and good reproducibility towards the determination of Rhodamine B, making it a suitable method for the determination of Rhodamine B in food samples. 相似文献
18.
A W Essink C P Lohuis J T Klein Elhorst W J Rutten 《Journal of chromatography. A》1991,570(2):419-424
A simple extraction system for the selective and quantitative isolation of apomorphine from human plasma is described. Apomorphine and N-n-propylnorapomorphine were isolated by complex formation between a borate group and the diol group of the apomorphines in an alkaline medium, this in combination with ion-pair formation. The reproducibility and linearity of this extraction method combined with high-performance liquid chromatography with electrochemical detection is excellent. The absolute mean recovery of apomorphine was 100%, the recovery of N-n-propylnorapomorphine was 98%. The detection limit of apomorphine in human plasma in the described system is approximately 0.5 ng/ml. 相似文献
19.
We have optimized a method for the determination of intracellular glutathione by high-performance liquid chromatography, using fluorimetric detection. To minimize artifacts and provide an accurate determination of intracellular glutathione, cell extracts were prepared using extraction conditions specifically designed to inhibit autoxidation and enzymatic degradation of glutathione. The sensitivity of the method was enhanced by adjusting the dansyl chloride derivatization reaction with regard to parameters such as pH, reaction time and dansyl chloride concentration. Both oxidized and reduced forms of glutathione were quantified using the refined method in extracts of oxidatively stressed J774A.1 mouse macrophage cells and reflected an expected shift in cellular redox status. 相似文献
20.
Sensitive analysis of blood for amodiaquine and three metabolites by high-performance liquid chromatography with electrochemical detection 总被引:2,自引:0,他引:2
D L Mount L C Patchen P Nguyen-Dinh A M Barber I K Schwartz F C Churchill 《Journal of chromatography. A》1986,383(2):375-386
A high-performance liquid chromatographic method using oxidative electrochemical detection has been developed for selective and sensitive quantification of the antimalarial drug amodiaquine and three of its metabolites in the blood of dosed individuals. The method requires only one extraction step and has detection limits of 1 ng/ml for amodiaquine and its metabolites desethylamodiaquine and bisdesethylamodiaquine and 3 ng/ml for 2-hydroxydesethylamodiaquine. Minor modification of the mobile phase preserves the chromatographic separation and allows ultraviolet spectroscopic detection, which, although appreciably less sensitive, permits monitoring of levels of amodiaquine and the three metabolites in blood and urine samples if an electrochemical detector is unavailable. Levels of amodiaquine and the three metabolites were determined for two volunteers undergoing a nine-week chemoprophylactic regimen in connection with travel to a malarious area. Data are included to compare the in vitro antimalarial activities against three strains of Plasmodium falciparum of amodiaquine and the three metabolites considered. 相似文献