Search results for "YB"

showing 10 items of 4411 documents

CCDC 962106: Experimental Crystal Structure Determination

2017

Related Article: B. Elsler, D. Schollmeyer, S. R. Waldvogel|2014|Faraday Discuss.|172|413|doi:10.1039/C4FD00049H

33'-di-t-butyl-55'-dimethoxybiphenyl-22'-diolSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 2077766: Experimental Crystal Structure Determination

2022

Related Article: Aija Trimdale, Anatoly Mishnev, Agris Bērziņš|2021|Pharmaceutics|13|734|doi:10.3390/pharmaceutics13050734

35-dihydroxybenzoic acid tetrahydrofuran solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Glycerosomes: Use of hydrogenated soy phosphatidylcholine mixture and its effect on vesicle features and diclofenac skin penetration.

2016

In this work, diclofenac was encapsulated, as sodium salt, in glycerosomes containing 10, 20 or 30% of glycerol in the water phase with the aim to ameliorate its topical efficacy. Taking into account previous findings, glycerosome formulation was modified, in terms of economic suitability, using a cheap and commercially available mixture of hydrogenated soy phosphatidylcholine (P90H). P90H glycerosomes were spherical and multilamellar; photon correlation spectroscopy showed that obtained vesicles were ∼131nm, slightly larger and more polydispersed than those made with dipalmitoylphosphatidylcholine (DPPC) but, surprisingly, they were able to ameliorate the local delivery of diclofenac, whic…

3003GlycerolKeratinocytesDiclofenacSwineSkin Absorptionpig skinPharmaceutical Science02 engineering and technology030226 pharmacology & pharmacyDSC03 medical and health scienceschemistry.chemical_compound0302 clinical medicineDiclofenacDrug Delivery SystemsOrgan Culture TechniquesDynamic light scatteringPhosphatidylcholinemedicineGlycerolAnimalsHumansCells CulturedChromatographyhydrogenated phospholipid vesiclesChemistryVesicle(trans)dermal drug delivery; DSC; hydrogenated phospholipid vesicles; keratinocytes; pig skin; rheology; 3003021001 nanoscience & nanotechnology(trans)dermal drug deliveryDipalmitoylphosphatidylcholineSkin penetrationDrug deliveryPhosphatidylcholinesrheologyHydrogenationSoybeans0210 nano-technologymedicine.drugInternational journal of pharmaceutics
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π-Stacked polymers in drug delivery applications

2016

Abstract Polybenzofulvenes are π-stacked polymers, which can be synthesized by spontaneous polymerization of the corresponding monomers without the use of catalysts or initiators. Therefore, they can be obtained completely free from byproducts, impurities, or harmful substances. The absence of any relevant toxic effects and cell viability impairments allows PEGylated polybenzofulvene brushes to be potentially functional in a wide range of biological, biomedical, and biotechnological applications. Moreover, the properties of these polymers, in terms of interaction with pharmacological active agents and the ability to self-assemble into nanoaggregates or a quite compact physical gel useful as…

3003Materials sciencePharmaceutical ScienceNanotechnology02 engineering and technology010402 general chemistry01 natural scienceschemistry.chemical_compoundSide chainOrganic chemistrychemistry.chemical_classificationPolymer brusheClick chemistryPolymerPegylation021001 nanoscience & nanotechnologySmall molecule0104 chemical sciencesMonomerchemistryPolymerizationDrug deliveryDrug deliveryClick chemistryPEGylationPolybenzofulvene0210 nano-technology
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Enhanced adhesion and in situ photothermal ablation of cancer cells in surface-functionalized electrospun microfiber scaffold with graphene oxide

2017

The physicochemical characteristics of a biomaterial surface highly affect the interaction with living cells. Recently, much attention has been focused on the adhesion properties of functional biomaterials toward cancer cells, since is expected to control metastatic spread of a tumor, which is related to good probability containing the progression of disease burden. Here, we designed an implantable poly(caprolactone)-based electrospun microfiber scaffold, henceforth PCLMF-GO, to simultaneously capture and kill cancer cells by tuning physicochemical features of the hybrid surface through nitrogen plasma activation and hetero-phase graphene oxide (GO) covalent functionalization. The surface i…

3003business.product_categoryCancer therapyPharmaceutical ScienceNanotechnologyBiocompatible Materials02 engineering and technologyCell capture010402 general chemistry01 natural scienceslaw.inventionPlasmalawNeoplasmsMicrofiberCell AdhesionHumansCell adhesionGraphene oxideHybrid materialChemistryGrapheneBiomaterialOxidesAdhesionPhotothermal therapyPhototherapy021001 nanoscience & nanotechnology0104 chemical sciencesPolycaprolactoneCancer cellMCF-7 CellsSurface modificationGraphite0210 nano-technologybusiness
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Integrated CGH/WES Analyses Advance Understanding of Aggressive Neuroblastoma Evolution: A Case Study

2021

Neuroblastoma (NB) is the most common extra-cranial malignancy in preschool children. To portray the genetic landscape of an overly aggressive NB leading to a rapid clinical progression of the disease, tumor DNA collected pre- and post-treatment has been analyzed. Array comparative genomic hybridization (aCGH), whole-exome sequencing (WES), and pharmacogenetics approaches, respectively, have identified relevant copy number alterations (CNAs), single nucleotide variants (SNVs), and polymorphisms (SNPs) that were then combined into an integrated analysis. Spontaneously formed 3D tumoroids obtained from the recurrent mass have also been characterized. The results prove the power of combining C…

3D tumoroids; Array CGH; Clonal evolution; Neuroblastoma; Pharmacogenetics; Recurrent tumor; Single nucleotide variants; Whole exome sequencing; Child Preschool; Disease Progression; Drug Resistance Neoplasm; Fatal Outcome; Humans; Immunophenotyping; Neuroblastoma; Polymorphism Single Nucleotide; Comparative Genomic Hybridization; Whole Exome SequencingQH301-705.5Drug Resistanceclonal evolutionCase Report3D tumoroidsSingle-nucleotide polymorphismDiseaseComputational biologyBiologyMalignancyPolymorphism Single NucleotideSomatic evolution in cancerImmunophenotypingwhole exome sequencingNeuroblastomaFatal OutcomeNeuroblastomaExome SequencingmedicineHumansarray CGHrecurrent tumorPolymorphismBiology (General)ChildPreschoolExome sequencingTumorsComparative Genomic HybridizationSingle NucleotideGeneral Medicinemedicine.diseaseSingle nucleotide variantsDrug Resistance NeoplasmPharmacogeneticsChild PreschoolDisease ProgressionFarmacogenèticaNeoplasmPharmacogeneticsComparative genomic hybridization
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CCDC 634267: Experimental Crystal Structure Determination

2007

Related Article: S.Dobis, D.Schollmeyer, Chunmei Gao, Derong Cao, H.Meier|2007|Eur.J.Org.Chem.|2007|2964|doi:10.1002/ejoc.200700140

511-bis(((3-Methoxybenzyl)oxy)methyl)-561112-tetrahydro-512(1'2'):611(1''2'')dibenzenodibenzo(ae)cycloocteneSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Variations of selective separability II: Discrete sets and the influence of convergence and maximality

2012

A space $X$ is called selectively separable(R-separable) if for every sequence of dense subspaces $(D_n : n\in\omega)$ one can pick finite (respectively, one-point) subsets $F_n\subset D_n$ such that $\bigcup_{n\in\omega}F_n$ is dense in $X$. These properties are much stronger than separability, but are equivalent to it in the presence of certain convergence properties. For example, we show that every Hausdorff separable radial space is R-separable and note that neither separable sequential nor separable Whyburn spaces have to be selectively separable. A space is called \emph{d-separable} if it has a dense $\sigma$-discrete subspace. We call a space $X$ D-separable if for every sequence of …

54D65 54A25 54D55 54A20H-separable spaceSubmaximalD+-separable spaceSequential spaceFUNCTION-SPACESSeparable spaceSpace (mathematics)INVARIANTSSeparable spaceCombinatoricsGN-separable spaceStrong fan tightnessM-separable spaceMaximal spaceConvergence (routing)Radial spaceFOS: MathematicsFréchet spaceCountable setStratifiable spaceWhyburn propertyTOPOLOGIESDH+-separable spaceTightnessMathematics - General TopologyMathematicsDH-separable spaceD-separable spaceSequenceExtra-resolvable spaceGeneral Topology (math.GN)Hausdorff spaceResolvableR-separable spaceLinear subspaceResolvable spaceSequentialDiscretely generated spaceSubmaximal spaceGeometry and TopologyTOPOLOGIES; FUNCTION-SPACES; INVARIANTSSS+ spaceFan tightnessCrowded spaceSubspace topologyTopology and its Applications
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CCDC 1968536: Experimental Crystal Structure Determination

2021

Related Article: Ni Putu Ariantari, Marian Frank, Ying Gao, Fabian Stuhldreier, Anna-Lene Kiffe-Delf, Rudolf Hartmann, Simon-Patrick Höfert, Christoph Janiak, Sebastian Wesselborg, Werner E.G. Müller, Rainer Kalscheuer, Zhen Liu, Peter Proksch|2021|Tetrahedron|85|132065|doi:10.1016/j.tet.2021.132065

6-(3-hydroxybutan-2-yl)-5-(hydroxymethyl)-4-methoxy-2H-pyran-2-oneSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1402129: Experimental Crystal Structure Determination

2016

Related Article: Carla Queirós, Andreia Leite, Maria G. M. Couto, mLuís Cunha-Silva, Giampaolo Barone, Baltazar de Castro, Maria Rangel, André M. N. Silva, Ana M. G. Silva|2015|Chem.-Eur.J.|21|15692|doi:10.1002/chem.201502093

6-(Diethylamino)-9-(4-((23-dihydroxybenzyl)carbamoyl)phenyl)-NN-diethyl-3H-xanthen-3-iminium chloride chloroform solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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