Search results for "Mace"

showing 10 items of 4713 documents

Innovative “Green” and Novel Strategies for the Extraction of Bioactive Added Value Compounds from Citrus Wastes—A Review

2017

Citrus is a major processed crop that results in large quantities of wastes and by-products rich in various bioactive compounds such as pectins, water soluble and insoluble antioxidants and essential oils. While some of those wastes are currently valorised by various technologies (yet most are discarded or used for feed), effective, non-toxic and profitable extraction strategies could further significantly promote the valorisation and provide both increased profits and high quality bioactives. The present review will describe and summarize the latest works concerning novel and greener methods for valorisation of citrus by-products. The outcomes and effectiveness of those technologies such a…

CitrusPharmaceutical Sciencecitrus wastes ; ultrasound ; pulsed electric fields ; microwaves ; high pressure ; supercritical CO2ReviewGarbageCitrus wastes; High pressure; Microwaves; Pulsed electric fields; Supercritical CO2; Ultrasound; Citrus; Fruit; Garbage; Green Chemistry Technology; Plant Extracts; Waste Products; Organic ChemistrymicrowavesLower energysupercritical CO2Analytical Chemistrylcsh:QD241-4410404 agricultural biotechnologylcsh:Organic chemistryDrug DiscoveryAdded valuePhysical and Theoretical ChemistryConventional techniqueWaste Products2. Zero hungercitrus wastesPlant Extractsultrasoundbusiness.industryOrganic ChemistryExtraction (chemistry)food and beveragesGreen Chemistry Technology04 agricultural and veterinary sciences040401 food scienceBiotechnologyhigh pressureWater solublepulsed electric fieldsChemistry (miscellaneous)FruitHigh pressureMolecular MedicineEnvironmental scienceBiochemical engineeringValorisationbusinessMolecules
researchProduct

Volatile Compounds of Lemon and Grapefruit IntegroPectin

2020

An HS-SPME GC-MS analysis of the volatile compounds adsorbed at the outer surface of lemon and grapefruit pectins obtained via the hydrodynamic cavitation of industrial waste streams of lemon and grapefruit peels in water suggests important new findings en route to understanding the powerful and broad biological activity of these new pectic materials. In agreement with the ultralow degree of esterification of these pectins, the high amount of highly bioactive &alpha

Citrusfood.ingredientPectinlemonPhytochemicalsPharmaceutical SciencegrapefruitArticleIndustrial wasteGas Chromatography-Mass SpectrometryAnalytical Chemistrylcsh:QD241-441chemistry.chemical_compoundAdsorptionfoodLinaloolCitrus paradisilcsh:Organic chemistryDrug Discoveryhydrodynamic cavitation?-terpineolFood sciencePhysical and Theoretical ChemistryIntegroPectinpectinResidue (complex analysis)LimoneneVolatile Organic CompoundsMolecular Structureapplied_chemistryOrganic Chemistrycircular economywaste citrus peelBiosynthetic PathwaysTerpineolchemistryChemistry (miscellaneous)FruitMolecular Medicineα-terpineolGas chromatography–mass spectrometryCitric acidCitrus paradisi
researchProduct

2014

The present review discusses the known synthetic routes to the lamellarin alkaloids published until 2014. It begins with syntheses of the structurally simpler type-II lamellarins and then focuses on the larger class of the 5,6-saturated and -unsaturated type-I lamellarins. The syntheses are grouped by the strategy employed for the assembly of the central pyrrole ring.

Class (set theory)Computer scienceStereochemistryDrug DiscoveryPharmaceutical ScienceTotal synthesisRing (chemistry)BioinformaticsPharmacology Toxicology and Pharmaceutics (miscellaneous)Marine Drugs
researchProduct

Multi-technique approach for qualitative and quantitative characterization of furazidin degradation kinetics under alkaline conditions

2016

Degradation of drug furazidin was studied under different conditions of environmental pH (11-13) and temperature (30-60°C). The novel approach of hybrid hard- and soft-multivariate curve resolution-alternating least squares (HS-MCR-ALS) method was applied to UV-vis spectral data to determine a valid kinetic model and kinetic parameters of the degradation process. The system was found to be comprised of three main species and best characterized by two consecutive first-order reactions. Furazidin degradation rate was found to be highly dependent on the applied environmental conditions, showing more prominent differences between both degradation steps towards higher pH and temperature. Complim…

Clinical BiochemistryAnalytical chemistryPharmaceutical ScienceHydantoin02 engineering and technologyDerivativeKinetic energy01 natural sciencesLeast squaresMass SpectrometrySpectral lineAnalytical ChemistryHydrolysischemistry.chemical_compoundUltraviolet visible spectroscopyDrug DiscoverySpectroscopyFuraginHydrolysis010401 analytical chemistryTemperatureHydrogen-Ion Concentration021001 nanoscience & nanotechnology0104 chemical sciencesKineticschemistryDegradation (geology)Spectrophotometry Ultraviolet0210 nano-technologyJournal of Pharmaceutical and Biomedical Analysis
researchProduct

Development and validation of a micellar liquid chromatographic method to determine three antitumorals in plasma

2017

Aim: A micellar liquid chromatographic method to determine several anticancer drugs (pazopanib, dabrafenib and regorafenib) in plasma was developed and validated by the guidelines of the EMA. Experimental: Plasma samples were directly injected, after a 1/5-dilution in a micellar solution. The drugs were resolved in <18 min using a C18 column. The mobile phase was an aqueous solution of 0.12 M SDS – 2% 1-pentanol, buffered at pH 7. The detection was performed by absorbance at 260 nm. Results: The values of the main validation parameters were: LOD (0.1–1 mg/l), calibration range (0.2–2 to 80 mg/l), accuracy (-12.5 to +11.7%) and precision (<11.9%). Conclusion: The procedure was conduct…

Clinical BiochemistryAntineoplastic Agents01 natural sciencesMicelleAnalytical ChemistryAbsorbance03 medical and health sciences0302 clinical medicineLimit of DetectionNeoplasmsCalibrationHumansGeneral Pharmacology Toxicology and PharmaceuticsMicellesDetection limitAqueous solutionChromatographyPlasma samplesChemistry010401 analytical chemistryGeneral MedicinePlasmaFactorial experiment0104 chemical sciencesMedical Laboratory TechnologyCase-Control Studies030220 oncology & carcinogenesisBlood Chemical AnalysisChromatography LiquidBioanalysis
researchProduct

Strategies to In Vitro Assessment of Major Human CYP Enzyme Activities by Using Liquid Chromatography Tandem Mass Spectrometry

2008

At the early stage of drug discovery, thousands of new chemical entities (NCEs) may be screened before a single candidate can be identified for development. Determining the role of CYP enzymes in the metabolism of a compound and evaluating the effect of NCEs on human CYP activities are key issues in pharmaceutical development as they may explain inter-subject variability, drug-drug interactions, non-linear pharmacokinetics and toxic effects. Reliable methods for determining enzyme activities are needed to characterize an individual CYP enzyme and to obtain a tool for the evaluation of its role in drug metabolism in humans. Different liquid chromatography tandem mass spectrometry methodologi…

Clinical BiochemistryDrug Evaluation PreclinicalIn Vitro TechniquesTandem mass spectrometrySubstrate SpecificityCytochrome P-450 Enzyme SystemPharmacokineticsTandem Mass SpectrometryIn vivoLiquid chromatography–mass spectrometryCytochrome P-450 Enzyme InhibitorsHumansPharmacokineticsEnzyme inducerChromatography High Pressure LiquidCytochrome P-450 Enzyme InhibitorsPharmacologyChromatographybiologyDrug discoveryChemistryPharmaceutical PreparationsBiochemistryEnzyme InductionHepatocytesMicrosomes Liverbiology.proteinDrug metabolismCurrent Drug Metabolism
researchProduct

Inhibition of activated STAT5 in Bcr/Abl expressing leukemia cells with new pimozide derivatives.

2014

STATs are transcription factors acting as intracellular signaling after stimulation with cytokines, growth factors and hormones. STAT5 is also constitutively active in many forms of cancers, including chronic myelogenous leukemia, acute lymphoblastic leukemia and Hodgkin's lymphoma. Recently, literature reported that the neuroleptic drug pimozide inhibits STAT5 phosphorylation inducing apoptosis in CML cells. We undertook an investigation from pimozide structure, obtaining simple derivatives with cytotoxic and STAT5-inhibitory activity, two of them markedly more potent than pimozide.

Clinical BiochemistryFusion Proteins bcr-ablPharmaceutical ScienceApoptosisBiochemistrySettore MED/15 - Malattie Del SangueCell LineStructure-Activity RelationshipPimozideSettore BIO/13 - Biologia Applicatahemic and lymphatic diseasesDrug DiscoverymedicineSTAT5 Transcription FactorCytotoxic T cellHumansPhosphorylationMolecular BiologyTranscription factorSTAT5Cell ProliferationbiologyDose-Response Relationship DrugMolecular StructureChemistrySTAT5 inhibitorsPimozideBCR/ABL expressing leukemia ApoptosisCell growth inhibitionOrganic ChemistryCell CyclePimozidemedicine.diseaseSettore CHIM/08 - Chimica FarmaceuticaLeukemiaApoptosisCancer researchbiology.proteinSettore BIO/14 - FarmacologiaMolecular MedicinePhosphorylationK562 Cellsmedicine.drugChronic myelogenous leukemia
researchProduct

The application of phospholipid removal columns and ultra-high performance liquid chromatography-tandem quadrupole mass spectrometry for quantificati…

2016

In this study a robust and sensitive method based on a proposed sample purification procedure, using zirconia-coated Phree™ columns and analysis by ultra-high performance liquid chromatography with triple quadrupole tandem mass spectrometry are presented for the assessment of multi-class antibiotics in farmed fish species. The sample preparation procedure benefited from combined precipitation of proteins and selective removal of phospholipids by Phree™ columns, resulting in a high sensitivity of the method (LOQ 0.3-9mgkg(-1)). The in-house validation results (precision, repeatability, decision limit CCα, detection capability CCβ, etc.) indicate that the elaborated method is fully suitable f…

Clinical BiochemistryPharmaceutical ScienceAquacultureTandem mass spectrometryMass spectrometry01 natural sciencesTrimethoprimAnalytical ChemistryTandem Mass SpectrometryDrug DiscoveryEnrofloxacinmedicinemedia_common.cataloged_instanceAnimalsSample preparationEuropean unionSpectroscopyChromatography High Pressure LiquidPhospholipidsmedia_commonEnrofloxacinChromatographyTandem010405 organic chemistryChemistry010401 analytical chemistryFishesReproducibility of ResultsRepeatabilityDrug Residues0104 chemical sciencesTriple quadrupole mass spectrometerAnti-Bacterial Agentsmedicine.drugFluoroquinolonesJournal of pharmaceutical and biomedical analysis
researchProduct

Comparison of several methods used for the determination of cephalosporins. Analysis of cephalexin in pharmaceutical samples

2002

The precision of UV absorbance of intact and acid degraded cephalosporins, ninhydrin, high performance liquid chromatography and iodometric methods used for analysis of cefoxitin, cefotaxime, cephazolin and cephalexin were compared. To obtain the calibration graphs the analytical signal used were: absorbance, first derivative absorbance, second derivative absorbance and H-point Standard Additions Method by using absorbance values at two selected wavelengths as analytical signal. These methods and calibration graphs were also used for the determination of cephalexin in pharmaceutical samples.

Clinical BiochemistryPharmaceutical ScienceCapsulesHigh-performance liquid chromatographyAnalytical ChemistryAbsorbancechemistry.chemical_compoundIodometrySpectrophotometryDrug Discoverypolycyclic compoundsmedicineChromatography High Pressure LiquidSpectroscopyAntibacterial agentSecond derivativeCephalexinChromatographymedicine.diagnostic_testChemistrydigestive oral and skin physiologyTitrimetryNinhydrinCephalosporinsSolutionsStandard additionNinhydrinIndicators and ReagentsSpectrophotometry UltravioletJournal of Pharmaceutical and Biomedical Analysis
researchProduct

Furosemide assay in pharmaceuticals by Micellar liquid chromatography: study of the stability of the drug.

2000

A simplified high-performance liquid chromatographic procedure is described for the determination of furosemide (4-chloro-N-furfuryl-5-sulphamoylanthranillic acid), which makes use of UV detection, a C18, reversed-phase column, and micellar mobile phases of sodium dodecyl sulphate (SDS) and 1-propanol at pH 3 buffered with phosphate system. The most adequate experimental conditions to handle furosemide solutions in the analytical laboratory are studied. The mixture of furosemide and its degradation products which are formed upon light exposition was resolved with a mobile phase of 0.04 M SDS-2% propanol. Separation of furosemide from its common impurities and the hydrolytic product, 4-chlor…

Clinical BiochemistryPharmaceutical ScienceDosage formMicellar electrokinetic chromatographyAnalytical ChemistryPropanolchemistry.chemical_compoundDrug StabilityFurosemideDrug DiscoverymedicineSodium dodecyl sulfateDiureticsSpectroscopyChromatography High Pressure LiquidMicellesChromatographyPhotolysisElutionHydrolysisFurosemideSodium Dodecyl SulfateHydrogen-Ion ConcentrationSolutionschemistryMicellar liquid chromatographyCalibrationIndicators and ReagentsSpectrophotometry UltravioletQuantitative analysis (chemistry)medicine.drugTabletsJournal of pharmaceutical and biomedical analysis
researchProduct