Search results for "TRID"

showing 10 items of 753 documents

Magneto-Structural Correlations in μ-Halo Bridged Copper(II) Chains

1987

To design synthetic pathways to systems of desired properties is a growing challenge for inorganic chemist. Our current interest in this area is focused on copper(II) chemistry. Besides to advance in the understanding of the factors determining the conformation around copper(II) in the solid state, we intend to gain insight into the chemical and structural effects that govern exchange coupling interactions in condensed species. In this context, we have approached the synthesis and characterization of a wide set of pentacoordinated Cu(LIII)XY complexes (LIII=tridentate ligand, X=coordinating anion, Y=coordinating or non-coordinating anion) showing a great structural diversity (including mono…

CrystallographyTridentate ligandChemistryInorganic chemistStackingSolid-stateStructural diversitychemistry.chemical_elementCopperIon
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Efficacy and safety study of an eyelid gel after repeated nocturnal application in healthy contact lens users and non-users

2020

Purpose: To evaluate skin biocompatibility of a nighttime hydrating eyelid gel and possible ocular surface effects in contact lens users (CLU) and non-contact lens users (NCLU). The formulation is registered as a medical device as Tridocosahexaenoine-AOX® (TDHA-AOX) (a concentrated DHA triglyceride), containing also hyaluronic acid (HA). Methods: A prospective, randomized, masked clinical trial was performed with 62 participants of both sexes, aged 20–70 years, split into: (1) CLU (n = 30) and (2) NCLU (n = 32). All participants were instructed to apply a single dose of the moisturizing gel (containing TDHA-AOX and HA) nightly to the upper and inner eyelids of their right eye (RE) only, and…

DHA docosahexaenoic acidNon usersFBUT fluorescein break-up timeALA alpha linolenic acidTDAH-AOX tridocosahexaenoin-antioxidantNCLU non contact lens users0302 clinical medicineLC PUFAs long chain polyunsaturated fatty acidsMedicineCL contact lensesOS ocular surfaceHA hyaluronic acidOSDI ocular surface disease indexDE dry eyeCLU contact lens usersCLDEQ contact lens dry eye questionnaireVEGF vascular endothelial growth factorDocosahexaenoic acidBMC biomicroscopymedicine.anatomical_structureMedicamentosCytokinesOftalmologíaOriginal ArticleBCVA best corrected visual acuitymedicine.medical_specialtyOcular surface dysfunctionCorneal stainingContact LensesHyaluronic acidRE right eyeDEs dry eye syndrome03 medical and health sciencesOphthalmologyHumansAdverse effectbusiness.industryEyelidsEPA eicosapentaenoic acidAnatomía ocularIOP intraocular pressureeye diseasesClinical trialContact lensMOISTURIZING GEL030221 ophthalmology & optometryTearsLE left eyeEyelidsense organsbusiness030217 neurology & neurosurgeryOptometry
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Comparative sequence analysis of the Clostridium difficile toxins A and B.

1992

The six clones pTB112, pTB324, pTBs12, pCd122, pCd14 and pCd13 cover the tox locus of Clostridium difficile VPI 10463. This region of 19 kb of chromosomal DNA contains four open reading frames including the complete toxB and toxA genes. The two toxins show 63% amino acid (aa) homology, a relatedness that had been predicted by the cross-reactivity of some monoclonal antibodies (mAb) but that is in contrast to the toxin specificity of polyclonal antisera. A special feature of ToxA and ToxB is their repetitive C-termini. We define herein 19 individual CROPs (combined repetitive oligopeptides of 20-50 aa length) in the ToxB C-terminus, which are separable into five homologous groups. Comparison…

DNA BacterialSequence analysisBacterial ToxinsBlotting WesternMolecular Sequence DataRestriction MappingDNA RecombinantLocus (genetics)Cross ReactionsHomology (biology)EnterotoxinsBacterial ProteinsSequence Homology Nucleic AcidGene duplicationGeneticsAmino Acid SequenceMolecular BiologyGeneRepetitive Sequences Nucleic AcidGeneticsbiologyBase SequenceClostridioides difficileNucleic acid sequenceAntibodies MonoclonalNucleic Acid HybridizationMolecular biologyRecombinant ProteinsOpen reading framePolyclonal antibodiesbiology.proteinMoleculargeneral genetics : MGG
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Definition of the single integration site of the pathogenicity locus in Clostridium difficile.

1996

We determined the nucleotide sequence 3.8 kb upstream and 5.2 kb downstream of the toxin genes A and B of Clostridium difficile. Nine ORFs were discovered. Based on PCR-directed approaches, two were attributed to the pathogenicity locus (PaLoc). The other seven were found in every C. difficile isolate obtained from the human gastrointestinal tract, respectless of their toxinogenicity. The ORFs cdu1 and cdu2/2' upstream of the PaLoc displayed similarity to repressors of Gram-positive bacteria (cdu1), and to an Na+/H+ antiporter described for Enterococcus hirae (cdu2/2'). Downstream of the locus a putative ABC transporter (cdd2-4) was identified. With a set of three paired primers used in pol…

DNA BacterialSequence analysisBacterial ToxinsMolecular Sequence DataVirulenceLocus (genetics)BiologyEnterotoxinsOpen Reading FramesBacterial ProteinsSpecies SpecificityGeneticsHumansAmino Acid SequenceORFSGeneGeneticsBase SequenceSequence Homology Amino AcidVirulenceClostridioides difficileNucleic acid sequenceGeneral MedicineMolecular biologyIntestinesTerminator (genetics)DNA Transposable ElementsATP-Binding Cassette TransportersMobile genetic elementsGene
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Transcription analysis of the genes tcdA-E of the pathogenicity locus of Clostridium difficile.

1997

To analyse the transcription pattern of the five tcdA-E genes of the pathogenicity locus (PaLoc) of Clostridium difficile a protocol was established to purify RNA from strain VPI10463. Transcription analysis of the five tcdA-E genes showed that they were all transcribed. In the early exponential phase, a high level of tcdC and low levels of tcdA,B,D,E transcripts were detectable; this was inverted in the stationary phase, suggesting that TcdC might have a negative influence on transcription of the other genes. Three transcription initiation sites, one for tcdA and two for tcdB were determined by primer extension analysis. Readthrough transcripts from outside the locus were not obtainable, s…

DNA BacterialTranscription GeneticBacterial ToxinsMolecular Sequence DataLocus (genetics)Helix-turn-helixBiologymedicine.disease_causeBiochemistryPolymerase Chain ReactionPrimer extensionchemistry.chemical_compoundEnterotoxinsBacterial ProteinsTranscription (biology)medicineAmino Acid SequencePromoter Regions GeneticGeneDNA PrimersRegulation of gene expressionGeneticsBase SequenceSequence Homology Amino AcidVirulenceClostridioides difficileClostridium perfringensMolecular biologyDNA-Binding ProteinsRepressor ProteinschemistryGenes BacterialDNAEuropean journal of biochemistry
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Development and characterization of a thermal inkjet-based aerosol generator for micro-volume sample introduction in analytical atomic spectrometry

2011

A novel system for the introduction of liquid samples into analytical plasmas for atomic spectrometric analysis is presented in this manuscript for the first time. The proposed “drop-on-demand” (DOD) aerosol generator is based on the use of a modified thermal inkjet cartridge. This system employs a lab-built microcontroller, which allows accessing all parameters important for driving the dosing cartridge for the generation of pL-droplets from sample volumes in the μL range. The droplet generation frequency, thus the resulting liquid flow rate, is variable over a wide range from the generation of isolated droplets up to a theoretical flow rate of approximately 2 mL min−1, with parallel opera…

Detection limitCartridgeNebulizerChemistryAnalytical chemistryCalibrationFigure of meritAtomic spectroscopyStandard solutionSpectroscopyAnalytical ChemistryVolumetric flow rateJournal of Analytical Atomic Spectrometry
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Study of passive sampling of polycyclic aromatic hydrocarbons in gas phase using Amberlite XAD resins as filling materials of semipermeable membranes

2013

Abstract In this work, a study was performed to evaluate the use of Amberlite XAD resins (XAD-2, XAD-4 and XAD-16), for the first time, as filling materials for low-density polyethylene membranes, which will be inserted as passive samplers for polycyclic aromatic hydrocarbons (PAHs) in gas phase. The use of samplers deployed for 48 h evidenced a relative capability to retain the compounds under study. A detailed study was performed to evaluate the recovery of analytes from the sampler through microwave-assisted extraction by using acetonitrile. A clean-up step using alumina-C18 cartridges was necessary before determination of the PAHs by high performance liquid chromatography with fluoresce…

Detection limitCartridgechemistry.chemical_compoundMembraneChromatographychemistryExtraction (chemistry)AmberlitePolyethyleneAcetonitrileHigh-performance liquid chromatographySpectroscopyAnalytical ChemistryMicrochemical Journal
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Flow injection Fourier transform infrared determination of caffeine in coffee

1999

Abstract A fully automatized procedure has been developed for the Fourier transform infrared (FT-IR) spectroscopic determination of caffeine in coffee samples. The method involves the on-line extraction of caffeine with CHCl3. Samples, weighed inside empty PTFE cartridges of 0.5 cm internal diameter (i.d.) and 1.5 ml volume, were humidified with four drops of 0.25 M NH3. The cartridge was installed in a flow manifold, in which samples were extracted in a closed-flow system with 1 ml CHCl3 during 6 min. Four hundred microliters of the extract were introduced in a microflow cell and absorbance measured as a function of time at 1659 cm−1, with a baseline established between 1900 and 830 cm−1, …

Detection limitFlow injection analysisChromatographyAnalytical chemistryStandard solutionAbsorbanceCartridgechemistry.chemical_compoundsymbols.namesakeFourier transformchemistrysymbolsSample preparationCaffeineSpectroscopyVibrational Spectroscopy
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Calibration of LA-ICP-MS via standard addition using dried picoliter droplets

2020

A novel microanalytical calibration approach for quantitative spatially resolved analysis of thin layered materials with laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) is presented. This method relies on standard addition via the generation of dried pL-droplet residues. Therefore, a drop on demand dosing device based on a modified commercial ink cartridge and a dosing interface, both accessible via a self-constructed microcontroller, were developed. This dosing device enables the precise deposition of pL-droplets onto solid samples for the generation of residues with dimensions in the low μm-range. The LA-ICP-MS analysis of such residues allows calibration over at l…

Detection limitMaterials scienceThin sectionSample (material)010401 analytical chemistryAnalytical chemistry02 engineering and technologyRepeatability021001 nanoscience & nanotechnologyMass spectrometryLaser01 natural sciences0104 chemical sciencesAnalytical Chemistrylaw.inventionCartridgelawStandard addition0210 nano-technologySpectroscopyJournal of Analytical Atomic Spectrometry
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EVALUATION OF STABILITY AND ENZYMATIC ACTIVITIES OF PROTEOLYTIC ENZYMES USED IN PANCREATIC ISLET TRANSPLANTATION

2009

In pancreatic islets purification, for cell therapy applications, the major enzymes used are obtained from Clostridium hystoliticum; class I and class II collagenases (Coll-G and Coll-H). In a well defined composition Coll-G/Coll-H together enzymes working on hydrophobic amminoacid, the neutral protease (Dispase) or the thermolysin (Thermostable Neutral Protease), are used in Langerhans islets purification. By electrophoresis and gelatin zymography approaches, in combination to densitometry quantitative valuation we have compared in composition, stability and autodigestion processes C. hystoliticum collagenases, Neutral protease and Thermolysin from two different producers, Roche and Serva.…

Diabet type 1Settore BIO/10 - BiochimicaCollagenaseClostridium hystoliticumCell transplantation
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