Search results for "chemical science"

showing 10 items of 9771 documents

The Influence of Nanoparticle Shape on Protein Corona Formation

2020

Nanoparticles have become an important utility in many areas of medical treatment such as targeted drug and treatment delivery as well as imaging and diagnostics. These advances require a complete understanding of nanoparticles' fate once placed in the body. Upon exposure to blood, proteins adsorb onto the nanoparticles surface and form a protein corona, which determines the particles' biological fate. This study reports on the protein corona formation from blood serum and plasma on spherical and rod‐shaped nanoparticles. These two types of mesoporous silica nanoparticles have identical chemistry, porosity, surface potential, and size in the y ‐dimension, one being a sphere and the other a …

rod shapeSurface Propertiesnanoparticle shapeNanoparticleProtein Corona02 engineering and technology010402 general chemistry01 natural sciencesBiomaterialsCorona (optical phenomenon)protein coronaAdsorptionBlood serumDrug Delivery SystemsGeneral Materials ScienceChemistryAlbuminsphere shapeGeneral ChemistryMesoporous silica021001 nanoscience & nanotechnologySilicon Dioxideprotein adsorption0104 chemical sciences3. Good healthBiophysicsbio-nanoparticle interactionsNanoparticlesProtein Corona0210 nano-technologymesoporous nanoparticlesBiotechnologyProtein adsorption
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Photoluminescent Detection of Human T-Lymphoblastic Cells by ZnO Nanorods.

2020

The precise detection of cancer cells currently remains a global challenge. One-dimensional (1D) semiconductor nanostructures (e.g., ZnO nanorods) have attracted attention due to their potential use in cancer biosensors. In the current study, it was demonstrated that the possibility of a photoluminescent detection of human leukemic T-cells by using a zinc oxide nanorods (ZnO NRs) platform. Monoclonal antibodies (MABs) anti-CD5 against a cluster of differentiation (CD) proteins on the pathologic cell surface have been used as a bioselective layer on the ZnO surface. The optimal concentration of the protein anti-CD5 to form an effective bioselective layer on the ZnO NRs surface was selected. …

room temperature photoluminescenceT-LymphocytesPharmaceutical Science02 engineering and technologyBiosensing TechniquesT-lymphoblasts detection01 natural sciencesAnalytical Chemistryhemic and lymphatic diseasesDrug Discoveryeducation.field_of_studyNanotubesmedicine.diagnostic_testAntibodies MonoclonalPrecursor Cell Lymphoblastic Leukemia-Lymphoma021001 nanoscience & nanotechnologyFlow CytometryChemistry (miscellaneous)Molecular MedicineNanorodZinc Oxide0210 nano-technologymonoclonal antibody anti-CD5PhotoluminescenceMaterials sciencePopulationchemistry.chemical_elementNanotechnologyZincCD5 AntigensArticleFlow cytometrylcsh:QD241-441Adsorptionlcsh:Organic chemistryCell Line TumormedicineHumansPhysical and Theoretical ChemistryeducationMOLT-4 cell linecluster of differentiation proteins010401 analytical chemistryOrganic Chemistry0104 chemical sciencesNanostructureschemistryCancer cellLuminescent MeasurementsGlassBiosensorzinc oxide nanorodsMolecules (Basel, Switzerland)
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Defying Stereotypes with Nanodiamonds: Stable Primary Diamondoid Phosphines

2016

International audience; Direct unequal C-H bond difunctionalization of phosphorylated diamantane was achieved in high yield from the corresponding phosphonates. Reduction of the functionalized phosphonates provides access to novel primary and secondary alkyl/aryl diamantane phosphines. The prepared primary diamantyl phosphines are quite air stable compared to their adamantyl and especially alkyl or aryl analogues. This finding is corroborated by comparing the singly occupied molecular orbital energy levels of the corresponding phosphine radical cations obtained by density functional theory computations.

room-temperaturemolecular tripoddeactivated aryl chlorideshomogeneous catalysts010402 general chemistryDiamondoidselective preparationchemistry01 natural sciencesMedicinal chemistryChemical reaction[ CHIM ] Chemical Scienceschemistry.chemical_compoundOrganic chemistry[CHIM]Chemical SciencesarylationAlkylNanodiamonds ; Diamondoid Phosphines ; diamantane ; adamantane ; adamantylphosphinechemistry.chemical_classification010405 organic chemistryChemistryligandsArylOrganic Chemistrypalladiumphosphorylated adamantanes3. Good health0104 chemical sciencesChemical bondDensity functional theoryDiamantanePhosphine
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3,4,5-Trimethoxy-4'-methylbiphenyl

2013

In the title compound, C16H18O3, the dihedral angle between the benzene rings is 33.4 (2)°. In the crystal, mol­ecules are packed in a zigzag arrangement along the b-axis and are inter­connected via weak C—H⋯O hydrogen bonds, and C—H⋯π inter­actions involving the meth­oxy groups and the benzene rings of neighbouring molecules.

röntgendiffraktiocrystal structure010405 organic chemistryHydrogen bonddendrimeeri prekursoriGeneral ChemistrykiderakenneDihedral angle010402 general chemistryCondensed Matter Physics01 natural sciencesOrganic Papers3. Good health0104 chemical sciencesX-ray diffractionCrystalchemistry.chemical_compoundCrystallographychemistryZigzagdendrimer precursorMoleculeGeneral Materials ScienceBenzeneta116Acta Crystallographica Section E-Structure Reports Online
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3,5-Dimethoxy-4'-methylbiphenyl

2013

The title compound, C15H16O2, crystallizes with three independent mol­ecules in the asymmetric unit. The intra­molecular torsion angle between the aromatic rings of each mol­ecule are −36.4 (3), 41.3 (3) and −37.8 (3)°. In the crystal, the complicated packing of the mol­ecules forms wave-like layers along the b and c axes. The mol­ecules are connected via extensive meth­oxy–phenyl C—H…π inter­actions. A weak C—H…O hydrogen-bonding network also exists between meth­oxy O atoms and aromatic or meth­oxy H atoms.

röntgendiffraktiocrystal structuredendrimeeri prekursori010405 organic chemistryChemistryX-ray DiffractionAromaticitykiderakenneGeneral ChemistryDihedral angle010402 general chemistryCondensed Matter PhysicsBioinformaticsOrganic Papers01 natural sciences0104 chemical sciences3. Good healthCrystalCrystallographydendrimer precursorGeneral Materials Scienceta116
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3,4-Dimethoxy-4'-methylbiphenyl

2013

In the title compound, C15H16O2, the dihedral angle between the planes of the aromatic rings is 30.5 (2). In the crystal, molecules are linked via C—HO hydrogen bonds and C— H interactions, forming a two-dimensional network lying parallel to (100). peerReviewed

röntgendiffraktiocrystal structuredendrimeeri prekursori010405 organic chemistryHydrogen bondChemistryAromaticitykiderakenneGeneral ChemistryDihedral angle010402 general chemistryCondensed Matter Physics01 natural sciencesOrganic PapersX-ray diffraction0104 chemical sciences3. Good healthCrystalCrystallographydendrimer precursorGeneral Materials Scienceta116Acta Crystallographica Section E-Structure Reports Online
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Methyl 3',5'-dimethoxybiphenyl-4-carboxylate

2013

In the title compound, C16H16O4, the dihedral angle between the benzene rings is 28.9 (2)°. In the crystal, mol­ecules are packed in layers parallel to the b axis in which they are connected via weak inter­molecular C-H...O contacts. Face-to-face π-π inter­actions also exist between the benzene rings of adjacent mol­ecules, with centroid-centroid and plane-to-plane shift distances of 3.8597 (14) and 1.843 (2) Å, respectively.

röntgendiffraktiocrystal structuredendrimeeri prekursorikiderakenneDihedral angle010402 general chemistryBioinformatics01 natural sciencesOrganic PapersCrystalchemistry.chemical_compoundGeneral Materials ScienceBenzeneta116Biphenyl010405 organic chemistryHydrogen bondGeneral ChemistryMeth-Condensed Matter PhysicsX-ray diffraction0104 chemical sciences3. Good healthCrystallographychemistrydendrimer precursorLayer (electronics)
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Methyl 3',4',5'-trimethoxybiphenyl-4-carboxylate

2013

In the title compound, C17H18O5, the dihedral angle between the benzene rings is 31.23 (16)°. In the crystal, the mol­ecules are packed in an anti­parallel fashion in layers along the a axis. In each layer, very weak C-H...O hydrogen bonds occur between the meth­oxy and methyl ester groups. Weak C-H...[pi] inter­actions between the 4'- and 5'-meth­oxy groups and neighbouring benzene rings [meth­oxy-C-ring centroid distances = 4.075 and 3.486 Å, respectively] connect the layers.

röntgendiffraktiocrystal structuredendrimeeriprekursorikiderakenneDihedral angle010402 general chemistry010403 inorganic & nuclear chemistryAntiparallel (biochemistry)01 natural sciencesOrganic PapersCrystalchemistry.chemical_compoundMoleculeGeneral Materials ScienceCarboxylateBenzeneta116ChemistryHydrogen bondGeneral ChemistryCondensed Matter Physics3. Good health0104 chemical sciencesX-ray diffractionCrystallographydendrimer precursorSingle crystal
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Polyphenols and Pharmacological Screening of a Monarda fistulosa L. dry Extract Based on a Hydrodistilled Residue By-Product

2021

This study aimed to determine the composition and content of polyphenols in the dry extract obtained from the hydrodistilled residue by-product of the wild bergamot (Monarda fistulosa L., Lamiaceae Martinov family) herb (MFDE) and to evaluate its safety and pharmacological properties. The total phenolic content (TPC) in the MFDE was 120.64 mg GAE/g. The high-performance liquid chromatography (HPLC) analysis showed the presence of a plethora of phenolic compounds, including hydroxycinnamic acids and flavone derivatives in the MFDE, with rosmarinic acid and luteolin-7-O-glucoside being the main components. With an IC50 value of 0.285 mg/mL, it was found to be a strong DPPH radical scavenger. …

safetyDPPHRM1-950phenolic compoundsMonarda fistulosa01 natural sciencesHigh-performance liquid chromatographywild bergamot03 medical and health scienceschemistry.chemical_compound0302 clinical medicineantiradical activityPharmacology (medical)anti-inflammatory activityanalgesic activityOriginal ResearchPharmacologyResidue (complex analysis)biologyTraditional medicine010405 organic chemistryRosmarinic acidbiology.organism_classificationAcute toxicity0104 chemical scienceschemistryherbPolyphenol030220 oncology & carcinogenesispostdistillation wasteLamiaceaeTherapeutics. PharmacologyFrontiers in Pharmacology
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Saliva: A key driver of flavour release and perception in human

2013

WOS:000323851300235; International audience

saliva[SDV.AEN] Life Sciences [q-bio]/Food and Nutritionfood oral processingaroma[CHIM.OTHE] Chemical Sciences/Other[ SDV.AEN ] Life Sciences [q-bio]/Food and Nutrition[SDV.IDA]Life Sciences [q-bio]/Food engineering[ SDV.IDA ] Life Sciences [q-bio]/Food engineering[SDV.IDA] Life Sciences [q-bio]/Food engineering[CHIM.OTHE]Chemical Sciences/Other[SDV.AEN]Life Sciences [q-bio]/Food and NutritionComputingMilieux_MISCELLANEOUS
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