Search results for " standard"

showing 10 items of 1548 documents

EP273 A new integrated pre-surgical diagnostic algorithm to define the local extent of disease in women with cervical cancer

2019

Introduction/Background Survival of patients with cervical cancer is strongly associated with the local extent of the primary disease. For this reason, the new FIGO staging system has given greater importance to instrumental investigations in the pre-surgical evaluation. The objective of this study is to develop an integrated diagnostic algorithm, including ultrasound (US), magnetic resonance imaging (MRI) and clinical examination under anaesthesia (CEUA), to better define the local extent of disease in patients with newly diagnosed cervical cancer, using histology as the referring gold standard. Methodology Patients with biopsy proven cervical cancer submitted to primary surgery from Janua…

Cervical cancermedicine.diagnostic_testParametrialbusiness.industryUltrasoundMagnetic resonance imagingPhysical examinationGold standard (test)medicine.diseaseTherapeutic approachBiopsymedicinebusinessAlgorithmePoster
researchProduct

Microscale synthesis of phosphatidyl-[3H]choline from 1,2-diacylglycerol. Assessment of isomerization by reversed-phase high-performance liquid chrom…

1995

The synthesis of rac-1-palmitoyl-2-oleoylglycero-3-phospho-[3H]choline of high specific activity was carried out on a microscale by making 7 mumol of rac-1-palmitoyl-2-oleoylglycerol react first with an equimolar amount of POCl3 and then of [3H]choline. After purification by thin-layer chromatography and normal-phase high-performance liquid chromatography and normal-phase high-performance liquid chromatography (HPLC), the yield of the synthesis of [3H]phosphatidylcholine (120 microCi/mumol) was 22%. rac-1-Palmitoyl-2-oleoylglycerol was purified before use by reversed-phase HPLC under conditions which were nonisomerizing and allowed the separation of 1,2- and 1,3-isomers of diacylglycerol. E…

Chromatography GasChromatographyOrganic ChemistryStereoisomerismCell BiologyReference StandardsBiochemistryHigh-performance liquid chromatographyDiglycerideschemistry.chemical_compoundchemistryPhosphatidylcholinePhosphatidylcholinesCholineChromatography Thin LayerMethanolAcetonitrileIsomerizationChromatography High Pressure LiquidCholine chlorideDiacylglycerol kinaseLipids
researchProduct

Determination of pyrethroid pesticide residues in fatty materials by solid-matrix dispersion partition, followed by mini-column size-exclusion chroma…

1999

The method studied uses a combination of a solid-matrix dispersion partition (SMDP) followed by high-performance size-exclusion chromatography on a minicolumn (HPmSEC) of 7.8 mm I.D. for the separation of pyrethroid (PYR) residues from fatty material. The solid-matrix dispersion extraction is carried out by absorbing a fat solution onto an Extrelut-3 cartridge (filled with a macroporous diatomaceous material) and extracting the PYR residues with acetonitrile. Up to 1 g of fatty material can be extracted with 15 ml acetonitrile. The small amount (mean +/- S.D. = 12.4 +/- 5.9 mg) of fatty material which is eluted into the acetonitrile is further removed by HPmSEC. PYR pesticide residues are c…

Chromatography GasChromatographyPesticide residueChemistryElutionOrganic ChemistrySize-exclusion chromatographyPesticide ResiduesTralomethrinGeneral MedicineReference StandardsBiochemistryAnalytical ChemistryFatsGel permeation chromatographychemistry.chemical_compoundColumn chromatographyPyrethrinsChromatography GelSolid phase extractionGas chromatographyChromatography High Pressure LiquidJournal of Chromatography A
researchProduct

Determination of organochlorine pesticide residues in honey from the central zone of Portugal and the Valencian community of Spain

2004

In this study nine organochlorine pesticide residues ([alpha]-, [beta]-, and [gamma]-hexachlorocyclohexane (HCH), hexachlorobenzene (HCB), aldrin, p,p'-DDE, p,p'-DDD, o,p'-DDT, and p,p'-DDT) in forty nine samples of honey collected from markets of Portugal and Spain during 2001 and 2002, respectively, were evaluated. For this evaluation, three analytical procedures were studied. The analytical procedure, based on LLE extraction with ethyl acetate followed by gas chromatography-electron-capture detection (GC-ECD) for quantification, and mass spectrometry (GC-MS) for confirmation, has been selected. Recoveries of spiked samples ranged from 68%, for [beta]-HCH, and 126% for p,p'-DDT, for forti…

Chromatography GasEthyl acetateOrganochlorineBiochemistryGas Chromatography-Mass SpectrometryAnalytical Chemistrychemistry.chemical_compoundElectrochemistryHydrocarbons ChlorinatedAldrinForty NinePesticidesDetection limitChromatographyPortugalPesticide residueOrganic ChemistryPesticide ResiduesReproducibility of ResultsHoneyGeneral MedicineHexachlorobenzeneReference StandardsPesticidechemistrySpainGas chromatography–mass spectrometryJournal of Chromatography A
researchProduct

Processing of Generator-Produced 68Ga for Medical Application

2007

The (68)Ge/(68)Ga generator provides an excellent source of positron-emitting (68)Ga. However, newly available "ionic" (68)Ge/(68)Ga radionuclide generators are not necessarily optimized for the synthesis of (68)Ga-labeled radiopharmaceuticals. The eluates have rather large volumes, a high concentration of H(+) (pH of 1), a breakthrough of (68)Ge, increasing with time or frequency of use, and impurities such as stable Zn(II) generated by the decay of (68)Ga, Ti(IV) as a constituent of the column material, and Fe(III) as a general impurity.We have developed an efficient route for the processing of generator-derived (68)Ga eluates, including the labeling and purification of biomolecules. Prec…

ChromatographyAqueous solutionElutionIon chromatographyGallium RadioisotopesFraction (chemistry)Hydrochloric acidEquipment DesignReference StandardsEquipment Failure Analysischemistry.chemical_compoundColumn chromatographychemistryGermanyIsotope LabelingAcetoneRadiology Nuclear Medicine and imagingRadionuclide GeneratorJournal of Nuclear Medicine
researchProduct

Immobilization of reagents by polymeric materials. Determination of metamizol

1992

Abstract A method for immobilization of inorganic reagents, based on the dispersion of the reagent into an unsaturated polyester solution is applied to immobilization of lead dioxide. The obtained solid is of application in a flow-injection manifold for indirect atomic absorption determination of metamizol in pharmaceutical formulations. The procedure gives a linear calibration graph up to 6 ppm of metamizol with a relative standard deviation of 1.6% (3.0 mg/l) and a sample throughput of 72 hr−1.

ChromatographyCalibration curveChemistryRelative standard deviationUnsaturated polyesterLead dioxideAnalytical Chemistrylaw.inventionchemistry.chemical_compoundlawReagentAtomic absorption spectroscopyDispersion (chemistry)Nuclear chemistryTalanta
researchProduct

Univariate method for background correction in liquid chromatography–Fourier transform infrared spectrometry

2007

An univariate method is proposed for background correction in on-line gradient liquid chromatography-Fourier transform infrared (LC-FTIR) spectrometry using acetonitrile:water as mobile phase components. The method is based on the calculation of the ratio of absorbances (AR) at two characteristic wavenumbers for each spectrum. This parameter is subsequently used to locate the most appropriated eluent spectrum within a reference spectra matrix (RSM) to be subtracted from each spectrum included in the sample chromatogram. To correct minor changes in eluent spectra intensity during the elution of analytes, a correction factor (Kf), defined as the ratio of the absorbance of the sample and the s…

ChromatographyChemistryElutionOrganic ChemistryAnalytical chemistryInfrared spectroscopyGeneral MedicineReference StandardsMass spectrometryBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryMatrix (chemical analysis)ChemometricsAbsorbanceDiuronSpectroscopy Fourier Transform InfraredAtrazineFourier transform infrared spectroscopyChromatography LiquidJournal of Chromatography A
researchProduct

Extraction of clenbuterol from calf urine using a molecularly imprinted polymer followed by quantitation by high-performance liquid chromatography wi…

2002

A method for the extraction of clenbuterol from calf urine samples using a molecularly imprinted polymer (MIP) has been developed. The aim was that the final extracts from the MIP should allow quantitation of clenbuterol down to 0.5 ng/mL urine using HPLC with UV detection. The MIP was produced using brombuterol as a template and the selectivity of the MIP, for clenbuterol, was tested against a non-imprinted polymer (produced without template) and was found to be high. After loading of 5 mL diluted centrifuged urine, selective binding was established in acetonitrile-acetic acid (98:2). For further elution of interferences, 0.5 M ammonium acetate buffer pH 5 and 70% acetonitrile in water was…

ChromatographyChemistryElutionOrganic ChemistryExtraction (chemistry)Molecularly imprinted polymerReproducibility of ResultsGeneral MedicineReversed-phase chromatographyReference StandardsSensitivity and SpecificityBiochemistryHigh-performance liquid chromatographyAnalytical ChemistryClenbuterolmedicineAnimalsCattleClenbuterolSpectrophotometry UltravioletSample preparationSolid phase extractionAdrenergic alpha-AgonistsChromatography High Pressure Liquidmedicine.drugJournal of Chromatography A
researchProduct

Determination of trichothecenes in chicken liver using gas chromatography coupled with triple-quadrupole mass spectrometry

2018

Abstract Chicken meat and edible offal are included in a wide number of preparations in the worldwide cuisine. Among the offal, the liver is one of the most consumed in some countries like Egypt since it is rich in proteins and is an economical source of many essential nutrients for humans. Mycotoxins, secondary toxic metabolites produced by fungi, have the potential to enter human food chain not only with cereal consumption but also through edible tissues from animals fed with mycotoxin-contaminated feed. Accordingly, a rapid method for the determination of eight trichothecenes in chicken liver was developed based on a quick, easy, cheap, effective, rugged and safe (QuEChERS) extraction an…

ChromatographyChemistryExtraction (chemistry)Relative standard deviation04 agricultural and veterinary sciencesQuechersTandem mass spectrometry040401 food sciencechemistry.chemical_compound0404 agricultural biotechnologyChicken LiverTriple quadrupole mass spectrometryGas chromatographyMycotoxinFood ScienceLWT
researchProduct

Determination of busulfan in human plasma using high-performance liquid chromatography with pre-column derivatization and fluorescence detection.

1999

A rapid, sensitive and reproducible high-performance liquid chromatographic assay for busulfan in human plasma was developed. After extraction of plasma samples with acetonitrile and methylene chloride, busulfan and the internal standard [1,5-bis(methanesulfonyloxy)pentane] were derivatized with 8-mercaptoquinoline to yield fluorescent compounds which were detected with a fluorescence detector equipped with filters of 360 nm (excitation) and 425 nm (emission). Calibration graphs showed a linear correlation (r>0.9990) over the concentration range of 20-2000 ng/ml. The recovery of busulfan from plasma standards was 70+/-5%. The detection and quantification limits for busulfan in plasma sample…

ChromatographyChemistryExtraction (chemistry)Reproducibility of ResultsGeneral ChemistryReference StandardsHigh-performance liquid chromatographyFluorescenceSensitivity and SpecificityFluorescence spectroscopyPentanechemistry.chemical_compoundSpectrometry FluorescenceCalibrationmedicineHumansDerivatizationQuantitative analysis (chemistry)Antineoplastic Agents AlkylatingBusulfanBusulfanChromatography High Pressure Liquidmedicine.drugJournal of chromatography. B, Biomedical sciences and applications
researchProduct