Search results for "solid phase"

showing 10 items of 360 documents

Effect of the shampoo Ultra Clean on drug concentrations in human hair

2000

The influence of the special shampoo Ultra Clean (Zydot Unlimited, Tulsa, Oklahoma) on the results of hair analyses was investigated. Hair samples from persons (n = 14) with a known history of drug abuse were collected at autopsy. The hair samples were divided into separate strands which were analyzed both after washing with Ultra Clean and without treatment. Hair analyses were performed by methanol extraction under sonication, purification by solid phase extraction and GC/MS in SIM mode according to routine procedures for tetrahydrocannabinol (THC), cocaine, amphetamine, methylenedioxyamphetamine (MDA), methylenedioxymethamphetamine (MDMA), methylenedioxyethylamphetamine (MDE), heroin, 6-m…

Detection limitChromatographyChemistryCodeineHair PreparationsMDMAForensic MedicineDihydrocodeineShampooPathology and Forensic MedicineSubstance Abuse DetectionmedicineMorphineHumansSolid phase extractionTetrahydrocannabinolHairmedicine.drugInternational Journal of Legal Medicine
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On-line in-tube solid phase microextraction-capillary liquid chromatography method for monitoring degradation products of di-(2-ethylhexyl) phthalate…

2014

Abstract The main di-(2-ethylhexyl) phthalate (DEHP) degradation products, (2-ethylhexyl) phthalate (MEHP), diethyl phthalate (DEP) and dibutyl phthalate (DBP), have been tested. The proposed cost-effective method combines on-line, in-tube solid-phase micro extraction (IT-SPME) in in-valve configuration and capillary liquid chromatography with UV diode array detection (Cap-LC-DAD). Acidification of the samples at pH 3 improved markedly the estimation of MEHP. Aliquots of 4 mL of acidified water samples were directly processed. After sample loading, the analytes were desorbed with the mobile-phase and transferred to the monolithic capillary column. Satisfactory linearity and precision, absen…

Detection limitChromatographyChemistryDibutyl phthalateCapillary actionOrganic ChemistryExtraction (chemistry)Phthalic AcidsPhthalateGeneral MedicineSolid-phase microextractionDiethyl phthalateBiochemistryDibutyl PhthalateAnalytical Chemistrychemistry.chemical_compoundPlasticizersDiethylhexyl PhthalateSample preparationSolid Phase MicroextractionWater Pollutants ChemicalChromatography LiquidJournal of Chromatography A
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A solid-phase extraction and size-exclusion liquid chromatographic method for polyethylene glycol 25 p-aminobenzoic acid determination in urine: Vali…

2007

No previous publications about percutaneous absorption of polyethylene glycol 25 p-aminobenzoic acid (PEG-25 PABA) have been found in the literature and the expected levels to be found in human urine after sunscreens use are unknown. The method proposed here is suitable to determine PEG-25 PABA in the urine of sunscreens users in order to carry out studies on body accumulation/excretion. It is based on solid-phase extraction (SPE) with size-exclusion liquid chromatography determination. Solid-phase extraction allows the analyte to be retained and subsequently eluted for a clean-up, using a silica-based cartridge. The size-exclusion liquid chromatography of the eluted allows the rest of matr…

Detection limitChromatographyChemistryElutionExtraction (chemistry)Fluorescence spectrometryReproducibility of ResultsUrineBiochemistryPolyethylene GlycolsAnalytical ChemistryMatrix (chemical analysis)ExcretionSpectrometry FluorescenceChromatography GelHumansEnvironmental ChemistrySolid phase extraction4-Aminobenzoic AcidSunscreening AgentsSpectroscopyAnalytica Chimica Acta
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Determination of clenbuterol in urine by azo-dye precolumn derivatization and micellar liquid chromatography

1997

Clenbuterol has been determined in urine by solidphase extraction on a C18 cartridge, diazotization of the eluate with nitrite, coupling of the diazonium ion with 1-(naphthyl)ethylenediamine, and separation of the azo dye formed by HPLC with a C18 column and a micellar mobile phase containing 0.1 M sodium dodecyl sulphate, 12%n-butanol and 0.05 M citrate buffer, pH 3. Recoveries higher than 90% were obtained by mixing the samples with a 20% 0.2 M NaOH before extraction. Limits of detection of 51 and 6.7 ng L−1 were obtained with spectrophotometric and thermal lens spectrometric detection, respectively; respective repeatabilities were 3.1% (5 μg mL−1) and 5.6% (0.16 μg mL−1).

Detection limitChromatographyChemistryElutionOrganic ChemistryClinical BiochemistryExtraction (chemistry)Reversed-phase chromatographyBiochemistryHigh-performance liquid chromatographyAnalytical Chemistrychemistry.chemical_compoundMicellar liquid chromatographySolid phase extractionDerivatizationChromatographia
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Simultaneous detection of three antiviral and four antibiotic compounds in source-separated urine with liquid chromatography

2013

An analytical method for the simultaneous screening of three antiviral agents (nevirapine, zidovudine, lamivudine), four antibiotics (sulfamethoxazole, trimethoprim, ciprofloxacin, rifampicin) and one reference compound (carbamazepine) in human urine was developed. Separation was achieved with a Kinetex XB-C18 (75 × 4.6 mm, 2.6 μm) column after the extraction of pharmaceuticals from urine with SPE. Gradient elution with a mobile phase consisting of acetonitrile and 10 mM KH2 PO4 (pH 2.5), and diode array detection with monitoring at 210 and 264 nm was applied. The developed method was validated in terms of selectivity, linearity, stability and sensitivity. Repeatability (n = 3) and between-…

Detection limitChromatographyChemistryExtraction (chemistry)Filtration and SeparationRepeatabilityUrineHigh-performance liquid chromatographyTrimethoprimAnalytical ChemistryWastewatermedicineSolid phase extractionmedicine.drugJournal of Separation Science
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Sensitive determination of probenecid in urine samples by reversed-phase liquid chromatography and UV-visible detection using solid-phase extraction …

1993

This study describes a rapid method for the determination of probenecid in human urine by liquid chromatography with UV detection at 254 nm, after clean-up through a C8 solid-phase extraction column. Liquid chromatography was carried out on a C18-bonded phase using an acetonitrile-acetate buffer (pH=4) gradient elution. Ethacrynic acid was used as internal standard. The system has been applied to the determination of probenecid in the 0.10–100.0 μg/ml concentration range; the limit of detection was 5 ng/mL.

Detection limitChromatographyChemistryOrganic ChemistryClinical BiochemistryExtraction (chemistry)Reversed-phase chromatographyUrineBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryProbenecidPhase (matter)medicineSolid phase extractionmedicine.drugChromatographia
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Analysis of organic pollutants in water at trace levels using fully automated solid-phase extraction coupled to high-performance liquid chromatography

1997

A method has been developed for the determination of trace levels of 32 pesticides, 19 explosives and 16 polycyclic aromatic hydrocarbons (PAH) in water in three individual steps. Solid-phase enrichment (SPE) is coupled to high-performance liquid chromatography (HPLC) with a fully automated system. The organic pollutants are enriched on reusable cartridges packed with adsorbent materials: pesticides and explosives on a mixed bed of divinylbenzene-ethylvinylbenzene copolymers (LiChrolut EN®) and perfluorinated polyethylene (PolyF®), and polycyclic aromatic hydrocarbons on C18-modified silica (Zorbax® ODS1). Thermally assisted desorption (TAD) has been shown to increase the recovery of analyt…

Detection limitChromatographyChemistryOrganic ChemistryClinical BiochemistryReversed-phase chromatographyBiochemistryHigh-performance liquid chromatographyCapacity factorAnalytical ChemistryDesorptionSample preparationSolid phase extractionTheoretical plateChromatographia
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Solid-phase extraction on C18 in the trace determination of selected polychlorinated biphenyls in milk.

1995

The utility of solid-phase extraction with octadecylsilica for determining fifteen polychlorinated biphenyl (PCB) congeners from milk samples was examined. Recoveries higher than 80% and relative standard deviations better than 10% were obtained for PCBs from different kinds of milk (whole, skimmed, 2%, powdered, breast and evaporated). A comparison with other procedures was made. The described method provides better detection limits than those attainable with the liquid-liquid extractions currently used as standard methods, when capillary gas-liquid chromatography is used for the final determination. A study of the separation was also performed using six different fused-silica capillary co…

Detection limitChromatographyChromatography GasMilk HumanOrganic ChemistryExtraction (chemistry)food and beveragesPolychlorinated biphenylGeneral MedicineStandard methodsBiochemistryPolychlorinated BiphenylsAnalytical Chemistrychemistry.chemical_compoundMilkchemistryAnimalsSolid phase extractionJournal of chromatography. A
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COMPARATIVE STUDY OF C18- AND STYRENE-DIVINYLBENZENE-BASED SORBENTS FOR THE ENRICHMENT OF PHENOLS FROM WATER

2001

The potential of solid-phase extraction with C18- and styrene divinylbenzene-based sorbents for the preconcentration of phenols from water samples has been evaluated for a variety of phenols of different polarities: phenol, o-, m- and p-cresol, 2-chlorophenol, and 4-chloro-3-methylphenol. The extraction efficiencies have been calculated for different volumes of samples containing the analytes at different concentration levels. The UV limits of detection were of 1–5 ng/mL, for the method using Bond Elut C18 cartridges and sample volumes of 25 mL, and 0.05–0.1 ng/mL (except for 4-chloro-3-methylphenol) for the method using the polymeric sorbent Bond Elut PPL and 1000 mL of the samples. Possib…

Detection limitChromatographyClinical BiochemistryExtraction (chemistry)Pharmaceutical ScienceCresolDivinylbenzeneBiochemistryAnalytical ChemistryStyrenechemistry.chemical_compoundchemistrymedicineSample preparationSolid phase extractionPhenolsmedicine.drugJournal of Liquid Chromatography & Related Technologies
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Improved detection limit for ammonium/ammonia achieved by Berthelot's reaction by use of solid-phase extraction coupled to diffuse reflectance spectr…

2005

Abstract The proposed procedure is based on the extraction of the indothylmol blue into C 18 solid-phase extraction (SPE) membranes and direct quantification on the membrane surface by diffuse reflectance spectroscopy. The analytical performance of the proposed method has been evaluated for standard solutions of ammonium using reflectance values, R , as well as the Kubelka–Munk function, F ( R ). The results have been compared with those obtained by the conventional method, which uses UV–vis absorption spectroscopy with a sensor-based method. The described methodology provided satisfactory linearity and reproducibility within the ammonium concentration intervals 25–250 μg L −1 and 25–500 μg…

Detection limitChromatographyDiffuse reflectance infrared fourier transformExtraction (chemistry)Analytical chemistryStandard solutionBiochemistryAnalytical ChemistryAmmoniachemistry.chemical_compoundchemistryEnvironmental ChemistrySample preparationAmmoniumSolid phase extractionSpectroscopyAnalytica Chimica Acta
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