Search results for "Vivo"

showing 10 items of 1905 documents

Long-term biodistribution study of HPMA- ran -LMA copolymers in vivo by means of 131 I-labeling

2018

Abstract Background For the evaluation of macromolecular drug delivery systems suitable pre-clinical monitoring of potential nanocarrier systems is needed. In this regard, both short-term as well as long-term in vivo tracking is crucial to understand structure-property relationships of polymer carrier systems and their resulting pharmacokinetic profile. Based on former studies revealing favorable in vivo characteristics for 18 F–labeled random (ran) copolymers consisting of N-(2-hydroxypropyl)methacrylamide (HPMA) and lauryl methacrylate (LMA) – including prolonged plasma half-life as well as enhanced tumor accumulation – the presented work focuses on their long-term investigation in the li…

chemistry.chemical_classificationCancer ResearchBiodistribution02 engineering and technologyPolymer010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical scienceschemistry.chemical_compoundchemistryIn vivoCritical micelle concentrationBiophysicsMolecular MedicineDistribution (pharmacology)MethacrylamideRadiology Nuclear Medicine and imagingNanocarriers0210 nano-technologyEx vivoNuclear Medicine and Biology
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Synthetic single and double aza-scorpiand macrocycles acting as inhibitors of the antioxidant enzymes iron superoxide dismutase and trypanothione red…

2014

The anti-chagasic activity of a series of eleven derivatives of aza-scorpiand-like macrocycles, some of them newly synthesised, was assayed. The four compounds with the best selectivity indices in vitro were subjected to in vivo assays. Tests in a murine model of the acute phase of Chagas disease showed a two-fold reduction in parasitaemia compared to that with benznidazole. Furthermore, compounds 7 and 11, with 4-pyridine and phenanthroline substituents in the lateral chain, caused a remarkable decrease in parasitaemia reactivation during the chronic phase after inducing immunosuppression in mice. These activity studies were complemented by measuring their inhibitory effect towards the ant…

chemistry.chemical_classificationChagas diseaseAntioxidantbiologyChemistryStereochemistryGeneral Chemical EngineeringPhenanthrolinemedicine.medical_treatmentGeneral Chemistrybiology.organism_classificationmedicine.diseaseIn vitrochemistry.chemical_compoundEnzymeBiochemistryBenznidazoleIn vivomedicineTrypanosoma cruzimedicine.drugRSC Adv.
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2-Aryl-substituted 4H-3,1-benzoxazin-4-ones as novel active substances for the cardiovascular system

1991

4H-3,1-Benzoxazin-4-ones of the structural types 3 and 4 are accessible by cyclization reactions. The introduction of the phosphonate group was achieved by way of Wohl-Ziegler bromination and subsequent Michaelis-Arbuzow reaction with a trialkyl phosphite. Pharmacological investigations on isolated left atria, ileum specimens, and Langendorff hearts as well as in vivo circulatory studies on anesthetized rats revealed that the phosphonates 4 exert calcium antagonistic effects. Whereas 2-(arylvinyl)benzoxazinones gave rise to pronounced negative inotropic effects, compound 3e exhibited relaxing effects on smooth musculature in particular and markedly increased the coronary flow through Langen…

chemistry.chemical_classificationChemistryBenzoxazinonesArylOrganic Chemistrychemistry.chemical_elementBiological activityCalciumMedicinal chemistryPhosphonatechemistry.chemical_compoundIn vivoCirculatory systemLactoneJournal of Heterocyclic Chemistry
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ChemInform Abstract: Synthesis and Pharmacological Evaluation of 1-Methyl-5- [substituted-4(3H)-oxo-1,2,3-benzotriazin-3-yl]-1H-pyrazole-4-acetic Aci…

2010

Abstract Several new 1-methyl-5-[substituted-4-oxo-1,2,3-benzotriazin-3-yl]-1H-pyrazole-4-acetic acids and their ethyl ester derivatives were prepared. The compounds were tested for analgesic and antiinflammatory activities, acute toxicity, ulcerogenic effect, and as in vitro inhibitors of 3α-hydroxysteroid dehydrogenase (3α-HSD), since it is claimed that the inhibition of such an enzyme predicts in vivo antiinflammatory activity. Some compounds were more active than phenylbutazone in the phenylbenzoquinone and acetic acid peritonitis tests, and equiactive to the same drug in the carrageenin paw edema test. All the compounds inhibited the 3α-HSD, but no correlation was observed with the paw…

chemistry.chemical_classificationChemistryDehydrogenaseGeneral MedicinePyrazoleMedicinal chemistryAcute toxicityIn vitroAcetic acidchemistry.chemical_compoundEnzymeIn vivoPhenylbutazonemedicinemedicine.drugChemInform
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Radiosynthesis of (±)-(2-((4-(2-[18F]fluoro-ethoxy)phenyl)bis(4-methoxy-phenyl)methoxy)ethylpiperidine-3-carboxylic acid: a potential GAT-3 PET ligan…

2001

A dysfunction of GABAergic neurotransmission is related to diseases such as epilepsy, Huntington-disease and Parkinson-syndrome. A new 18F-fluorine labelled GABA transporter ligand for the GABA-transporter subtype GAT-3 was developed which may allow the in vivo visualisation of GABAergic neurotransmission. The precursors ethyl (2-(4-hydroxyphenyl)bis(4-methoxyphenyl)-methoxy)ethyl)-piperidine-3-carboxylate and ethyl(2-((4-(2-tosylethoxy)phenyl)-bis(4-methoxyphenyl)-methoxy) ethyl)-piperidine3-carboxylate were synthesised and labelled by the use of 2-[18F]fluoroethyltosylate or [18F]fluoride. Subsequent cleavage of the ester moiety gave the final product (±)-(2-((4-(2-[18F]fluoroethoxy)pheny…

chemistry.chemical_classificationChemistryStereochemistryCarboxylic acidOrganic ChemistryRadiosynthesisLigand (biochemistry)BiochemistryChemical synthesisAnalytical ChemistryIn vivoDrug DiscoveryAlkoxy groupMoietyRadiology Nuclear Medicine and imagingSpectroscopyEx vivoJournal of Labelled Compounds and Radiopharmaceuticals
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Synthesis of C1-[18F]fluoroethylamnino asparagine for imaging cancer

2001

C1-[18F]fluoroethylamino asparagine was synthesised from N1-t-boc C1-p-nitrophenol asparagine and the radiolabelled precursor [18F]flouroethylamine in a one-pot-synthesis. The yield of this synthesis was 22% referring to [18F]fluoride, including the removal of the protection groups. The in vivo tests are in progress.

chemistry.chemical_classificationChemistryStereochemistryOrganic ChemistryCancermedicine.diseaseBiochemistryIn vivo testsAnalytical ChemistryAmino acidchemistry.chemical_compoundYield (chemistry)Drug DiscoverymedicineOrganic chemistryRadiology Nuclear Medicine and imagingAsparagineFluorideSpectroscopyJournal of Labelled Compounds and Radiopharmaceuticals
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Interaction of pHPMA–pLMA Copolymers with Human Blood Serum and Its Components

2013

Immediately after administration, polymer therapeutics are exposed to complex biological media like blood which may influence and alter their physicochemical properties due to interactions with proteins or serum components. Among such interactions those leading to larger sized aggregates can be sensitively detected by dynamic light scattering (DLS) as a pre in vivo screening method. Random copolymers from N-(2-hydroxypropyl)methacrylamide and lauryl methacrylate p(HPMA-co-LMA) and copolymers loaded with the model drug domperidone were characterized by DLS in isotonic salt solution and in blood serum. The bare amphiphilic copolymer micelles (Rh=30 nm in isotonic salt solution) formed large a…

chemistry.chemical_classificationChromatographyPolymersPharmaceutical SciencePolymerLipoproteins VLDLMicelleDomperidoneLipoproteins LDLchemistry.chemical_compoundBlood serumchemistryDynamic light scatteringIn vivoDrug DiscoveryBiophysicsmedicineCopolymerHumansMolecular MedicineMethacrylamideMicellesmedicine.drugMolecular Pharmaceutics
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Novel, potent calmodulin antagonists derived from an all-dhexapeptide combinatorial library that inhibitin vivocell proliferation: activity and struc…

2000

: Calmodulin is known to bind to various amphipathic helical peptide sequences, and the calmodulin–peptide binding surface has been shown to be remarkably tolerant sterically. d-Amino acid peptides, therefore, represent potential non-hydrolysable intracellular antagonists of calmodulin. In the present study, synthetic combinatorial libraries have been used to develop novel d-amino acid hexapeptide antagonists to calmodulin-regulated phosphodiesterase activity. Five hexapeptides were identified from a library containing over 52 million sequences. These peptides inhibited cell proliferation both in cell culture using normal rat kidney cells and by injection via the femoral vein following part…

chemistry.chemical_classificationCircular dichroismCalmodulinbiologyCell growthChemistryPeptideNuclear magnetic resonance spectroscopyBiochemistryEndocrinologyBiochemistryIn vivoAmphiphilebiology.proteinIntracellularThe Journal of Peptide Research
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New Tools for Streamlined In Vivo Homing Peptide Identification

2021

In vivo peptide-phage display is an unbiased technique for mapping of the vascular diversity and identification of homing peptides. This chapter is intended to serve as a structured practical guide to execute in vivo T7 phage biopanning and data analysis experiments. We discuss experimental designs and protocols with emphasis on application of high-throughput sequencing-based technologies for streamlined in vivo biopanning and validation of homing peptides.

chemistry.chemical_classificationComputingMethodologies_PATTERNRECOGNITIONT7 bacteriophagechemistryIn vivoComputer sciencePeptideIdentification (biology)BiopanningComputational biologyHoming (hematopoietic)
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Physiological, morphological and metabolic changes in Tetrahymena pyriformis for the in vivo cytotoxicity assessment of metallic pollution: Impact on…

2007

Abstract The individual cytotoxicity of cadmium chloride, iron sulphate and chromium nitrate has been investigated by using the freshwater ciliate Tetrahymena pyriformis. The metabolic enzymes and antioxidant defense biomarkers were assessed. The results obtained reveal that their metal salts have perturbed the physiology and morphology of T. pyriformis. Also, the biomarkers assessed were sensitive to the presence of metal salts and this sensitivity was metal salt and dose dependant. To estimate the impact of their metal salts on mitochondria, we studied their effects in vivo and in vitro on the d -β-hydroxybutyrate dehydrogenase (BDH) (EC 1.1.1.30) inner mitochondrial membrane enzyme. The …

chemistry.chemical_classificationEcologyGeneral Decision SciencesDehydrogenaseMitochondrionCadmium chlorideBiologychemistry.chemical_compoundEnzymechemistryBiochemistryIn vivoTetrahymena pyriformisInner mitochondrial membraneCytotoxicityEcology Evolution Behavior and SystematicsEcological Indicators
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