Search results for "biodistribution"

showing 10 items of 94 documents

Highly Loaded Semipermeable Nanocapsules for Magnetic Resonance Imaging.

2017

Magnetic resonance imaging has become an essential tool in medicine for the investigation of physiological processes. The key issues related to contrast agents, i.e., substances that are injected in the body for imaging, are the efficient enhancement of contrast, their low toxicity, and their defined biodistribution. Polyurea nanocapsules containing the gadolinium complex Gadobutrol as a contrast agent in high local concentration and high relaxivity up to 40 s-1 mmol-1 L are described. A high concentration of the contrast agent inside the nanocapsules can be ensured by increasing the crystallinity in the shell of the nanocapsules. Nanocapsules from aliphatic polyurea are found to display hi…

BiodistributionPolymers and PlasticsPolymersGadoliniumMRI contrast agentchemistry.chemical_elementContrast MediaBioengineeringGadolinium02 engineering and technology010402 general chemistry01 natural sciencesNanocapsulesGadobutrolBiomaterialschemistry.chemical_compoundCrystallinityMiceNanocapsulesMaterials ChemistrymedicineOrganometallic CompoundsAnimalsHumansTissue DistributionPolyureaMesenchymal Stem CellsDendrites021001 nanoscience & nanotechnologyMagnetic Resonance Imaging0104 chemical scienceschemistryLiverNanocarriers0210 nano-technologySpleenBiotechnologyBiomedical engineeringmedicine.drugMacromolecular bioscience
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Neodymium-140 DOTA-LM3: Evaluation of an In Vivo Generator for PET with a Non-Internalizing Vector

2017

140Nd (t1/2 = 3.4 days), owing to its short-lived positron emitting daughter 140Pr (t1/2 = 3.4 min), has promise as an in vivo generator for positron emission tomography (PET). However, the electron capture decay of 140Nd is chemically disruptive to macrocycle-based radiolabeling, meaning that an in vivo redistribution of the daughter 140Pr is expected before positron emission. The purpose of this study was to determine how the delayed positron from the de-labeled 140Pr affects preclinical imaging with 140Nd. To explore the effect, 140Nd was produced at CERN-ISOLDE, reacted with the somatostatin analogue, DOTA-LM3 (1,4,7,10- tetraazacyclododecane, 1,4,7- tri acetic acid, 10- acetamide N - p…

BiodistributionPositron emission tomographypositron emission tomographyElectron captureDOTA-LM3030218 nuclear medicine & medical imaging03 medical and health scienceschemistry.chemical_compound0302 clinical medicinePositronin vivo generatorIn vivomedicineDOTAPositron emissionOriginal Research140Prlcsh:R5-920medicine.diagnostic_test140Ndbusiness.industryChemistryGeneral MedicineinternalizationPositron emission tomography030220 oncology & carcinogenesisBiophysicsMedicineNuclear medicinebusinesslcsh:Medicine (General)Preclinical imagingInternalizationFrontiers in Medicine
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Unraveling the In Vivo Protein Corona

2021

Understanding the behavior of nanoparticles upon contact with a physiological environment is of urgent need in order to improve their properties for a successful therapeutic application. Most commonly, the interaction of nanoparticles with plasma proteins are studied under in vitro conditions. However, this has been shown to not reflect the complex situation after in vivo administration. Therefore, here we focused on the investigation of magnetic nanoparticles with blood proteins under in vivo conditions. Importantly, we observed a radically different proteome in vivo in comparison to the in vitro situation underlining the significance of in vivo protein corona studies. Next to this, we fou…

BiodistributionProtein CoronaCell Communication02 engineering and technology010402 general chemistry01 natural sciencesArticleMiceprotein coronaIn vivoAnimalsTissue DistributionMagnetite Nanoparticleslcsh:QH301-705.5biodistributionplasmaWhole bloodChemistrynanoparticleGeneral Medicine021001 nanoscience & nanotechnologyBlood proteinsIn vitro0104 chemical sciencesMice Inbred C57BLin vivoRAW 264.7 Cellslcsh:Biology (General)ProteomeBiophysics0210 nano-technologyserumEx vivoCells
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PET: Theoretical Background and Practical Aspects

2012

Positron emission tomography (PET) is a nuclear medicine imaging tool utilized for investigation of physiological processes in vivo. PET uses the decay characteristics of positron-emitting radionuclides which are produced in a cyclotron and then used to label compounds involved in physiological processes. Usually, the labeled compound—the tracer—is administered intravenously and distributed in the tissue. The radionuclide decays and the emitted photons are detected by the PET scanner. PET then offers the possibility to compute three-dimensional images of the biodistribution and kinetics of the regional radioactivity concentration. There are several options to analyze reconstructed PET image…

BiodistributionRadioactive tracermedicine.diagnostic_testComputer sciencePharmacokinetic modelingCerebral metabolic rateContext (language use)law.inventionlawPositron emission tomographyPet scannerNuclear medicine imagingmedicineBiomedical engineering
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Synthesis of [11C]SSR149415 and preliminary imaging studies using positron emission tomography.

2010

Abstract SSR149415 was the first non-peptide vasopressin-(V1b) receptor antagonist reported. It has been used to probe the role of V1b receptors in animal models of depression, aggression, and stress-anxiety, and was progressed to clinical trials for the treatment of depression. Due to the interest in V1b receptors as a therapeutic target and the growing use of SSR149415 in preclinical research, we developed a method to label SSR145419 with carbon-11 and have studied its pharmacokinetics in non-human primates using positron emission tomography.

BiodistributionReceptors VasopressinIndolesPyrrolidinesmedicine.drug_classClinical BiochemistryPharmaceutical ScienceAnxietyBiochemistryPreclinical researchAnimal models of depressionDrug DiscoverymedicineAnimalsCarbon RadioisotopesReceptorMolecular Biologymedicine.diagnostic_testbusiness.industryChemistryDepressionOrganic ChemistryAntagonistReceptor antagonistClinical trialBiochemistryAnti-Anxiety AgentsPositron emission tomographyPositron-Emission TomographyMolecular MedicineNuclear medicinebusinessAntidiuretic Hormone Receptor AntagonistsPapioBioorganicmedicinal chemistry letters
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Continuously manufactured magnetic polymersomes--a versatile tool (not only) for targeted cancer therapy.

2013

Micromixer technology was used to prepare polymeric vesicles (Pluronic® L-121) dual loaded with the anti-cancer drug camptothecin and magnetic nanoparticles. Successful incorporation of the magnetic nanoparticles was confirmed by transmission electron microscopy. Dynamic light scattering measurements showed a relatively narrow size distribution of the hybrid polymersomes. Camptothecin polymersomes reduced the cell viability of prostate cancer cells (PC-3) measured after 72 h significantly, while drug-free polymersomes showed no cytotoxic effects. Covalent attachment of a cancer targeting peptide (bombesin) as well as a fluorescent label (Alexa Fluor® 647) to the hybrid polymersomes was perf…

BiodistributionRelaxometryMaterials scienceCell SurvivalMicromixerNanotechnologyAntineoplastic AgentsPoloxamerlaw.inventionPolyethylene GlycolsConfocal microscopylawCell Line TumorNeoplasmsmedicineHumansGeneral Materials SciencePrecision MedicineMagnetite NanoparticlesDrug CarriersCarbocyaninesPropylene GlycolsDrug deliveryPolymersomeMagnetic nanoparticlesBombesinCamptothecinCamptothecinmedicine.drugNanoscale
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Novel heterobimetallic radiotheranostic: preparation, activity, and biodistribution.

2014

A novel Ru(II) (arene) theranostic complex is presented. It is based on a 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid macrocycle bearing a triarylphosphine and can be tracked in vivo by using the γ emission of (153) Sm atoms. Notably, the heteroditopic ligand can be selectively metalated with ruthenium at the phosphorus atom despite the presence of other functionalities that are prone to metal coordination. Subsequent labeling with radionuclides such as (153) Sm can then be performed easily. The resulting heterobimetallic complex exhibits favorable solubility and stability properties in biologically relevant media. It also shows in vitro cytotoxicity in line with that expected …

BiodistributionStereochemistryCell SurvivalPhosphinesIn vitro cytotoxicitychemistry.chemical_elementBiochemistryRutheniumMetalHeterocyclic Compounds 1-RingMiceIn vivoCoordination ComplexesCell Line TumorDrug DiscoveryAnimalsHumansTissue DistributionGeneral Pharmacology Toxicology and PharmaceuticsSolubilityPharmacologyChemistryLigandOrganic ChemistryWaterRutheniumvisual_artPhosphorus atomIsotope Labelingvisual_art.visual_art_mediumMolecular MedicineRadiopharmaceuticalsChemMedChem
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Biocompatibility and biodistribution of functionalized carbon nano-onions (f-CNOs) in a vertebrate model

2016

AbstractFunctionalized carbon nano-onions (f-CNOs) are of great interest as platforms for imaging, diagnostic and therapeutic applications due to their high cellular uptake and low cytotoxicity. To date, the toxicological effects of f-CNOs on vertebrates have not been reported. In this study, the possible biological impact of f-CNOs on zebrafish during development is investigated, evaluating different toxicity end-points such as the survival rate, hatching rate, and heart beat rate. Furthermore, a bio-distribution study of boron dipyrromethene (BODIPY) functionalized CNOs in zebrafish larvae is performed by utilizing inverted selective plane illumination microscopy (iSPIM), due to its intri…

Biodistributionanimal structuresMultidisciplinarybiologyBiocompatibilityChemistryfungi02 engineering and technologyAnatomy010402 general chemistry021001 nanoscience & nanotechnologybiology.organism_classification01 natural sciencesArticle0104 chemical scienceschemistry.chemical_compoundIn vivoNano-ToxicityBiophysicsBODIPY0210 nano-technologyCytotoxicityZebrafish
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Density of conjugated antibody determines the extent of Fc receptor dependent capture of nanoparticles by liver sinusoidal endothelial cells

2021

Despite considerable progress in the design of multifunctionalized nanoparticles (NPs) that selectively target specific cell types, their systemic application often results in unwanted liver accumulation. The exact mechanisms for this general observation are still unclear. Here we asked whether the number of cell-targeting antibodies per NP determines the extent of NP liver accumulation and also addressed the mechanisms by which antibody-coated NPs are retained in the liver. We used polysarcosine-based peptobrushes (PBs), which in an unmodified form remain in the circulation for >24 h due to the absence of a protein corona formation and low unspecific cell binding, and conjugated them with …

Biodistributionbiologymedicine.diagnostic_testChemistryCellGeneral EngineeringFc receptorGeneral Physics and AstronomyEndothelial CellsDendritic cellReceptors FcFlow cytometryCell biologymedicine.anatomical_structureLiverbiology.proteinmedicineSystemic administrationNanoparticlesGeneral Materials ScienceTissue DistributionAntibodyReceptor
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CMR 2005: 12.06: Ultra-small iron oxide nanoparticle (USPIO)-labeled baculoviruses as novel MRI agents for imaging viral vector biodistributionin vivo

2006

Biodistributionchemistry.chemical_compoundChemistryIn vivoBiophysicsIron oxideNanoparticleRadiology Nuclear Medicine and imagingVirologyViral vectorContrast Media & Molecular Imaging
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