Search results for "pharmaceutical"

showing 10 items of 3243 documents

Synthesis and preliminary in vivo evaluation of well-dispersed biomimetic nanocrystalline apatites labeled with positron emission tomographic imaging…

2015

In recent years, biomimetic synthetic apatite nanoparticles (AP-NPs), having chemical similarity with the mineral phase of bone, have attracted a great interest in nanomedicine as potential drug carriers. To evaluate the therapeutic perspectives of AP-NPs through the mechanisms of action and organs they interact with, the noninvasive monitoring of their in vivo behavior is of paramount importance. To this aim, here the feasibility to radiolabel AP-NPs ("naked" and surface-modified with citrate to reduce their aggregation) with two positron emission tomographic (PET) imaging agents ([F-18]NaF and Ga-68-NO(2)AP(BP)) was investigated. [F-18]NaF was used for the direct incorporation of the radi…

inorganic chemicalsMalepositron emission tomographyMaterials scienceNanoparticleNanotechnologyPilot ProjectsDiffusionNanocapsulesIn vivoBiomimetic MaterialsApatitesMaterials TestingmedicineAnimalsGeneral Materials ScienceChelationWhole Body ImagingColloidsParticle SizeRats Wistarmedicine.diagnostic_testtechnology industry and agriculturenanomedicinecalcium phosphatesPositron emission tomographyIsotope LabelingPositron-Emission Tomographydrug deliveryDrug deliverySurface modificationNanomedicineFeasibility StudiesNanoparticlesRadiopharmaceuticalsDrug carrierCrystallizationACS applied materialsinterfaces
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One pot light assisted green synthesis, storage and antimicrobial activity of dextran stabilized silver nanoparticles.

2014

Background Green synthesis of nanomaterials finds the edge over chemical methods due to its environmental compatibility. Herein, we report green synthesis of silver nanoparticles (Ag NPs) mediated with dextran. Dextran was used as a stabilizer and capping agent to synthesize Ag NPs using silver nitrate (AgNO3) under diffused sunlight conditions. Results UV–vis spectra of as synthesized Ag nanoparticles showed characteristic surface plasmon band in the range from ~405-452 nm. Scanning electron microscopy (SEM) and atomic force microscopy (AFM) studies showed spherical Ag NPs in the size regime of ~50-70 nm. Face centered cubic lattice of Ag NPs was confirmed by powder X-ray diffraction (PXRD…

inorganic chemicalsMaterials scienceSilverReducing agentScanning electron microscopeeducationBiomedical EngineeringDrug Evaluation PreclinicalMedicine (miscellaneous)Pharmaceutical ScienceMetal NanoparticlesNanotechnologyBioengineeringMicrobial Sensitivity TestsAntimicrobial activityMicroscopy Atomic ForceApplied Microbiology and BiotechnologySilver nanoparticleNanomaterialsStorage of nanoparticleschemistry.chemical_compoundAnti-Infective AgentsX-Ray DiffractionDiffused sun lightSpectroscopy Fourier Transform InfraredThin filmhealth care economics and organizationsAg nanoparticlesResearchtechnology industry and agricultureDextransGreen Chemistry TechnologySilver nitrateDextranchemistryMicroscopy Electron ScanningMolecular MedicineSilver NitrateSpectrophotometry UltravioletPowder diffractionNuclear chemistryJournal of nanobiotechnology
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closo-borane conjugated regulatory peptides retain high biological affinity: synthesis of closo-borane conjugated Tyr(3)-octreotate derivatives for B…

2008

Despite the improvements in cancer therapy during the past years, high-grade gliomas and many other types of cancer are still extremely resistant to current forms of therapy. Boron neutron capture therapy (BNCT) provides a promising way to destroy cancer cells without damaging healthy tissue. However, BNCT in practice is still limited due to the lack of boron-containing compounds that selectively deliver boron to cancer cells. Since many neuroendocrine tumors show an overexpression of the somatostatin receptor, it was our aim to synthesize compounds that contain a large number of boron atoms and still show high affinity toward this transmembrane receptor. The synthetic peptide Tyr (3)-octre…

inorganic chemicalsStereochemistryBiomedical EngineeringPharmaceutical ScienceBioengineeringPeptideBoron Neutron Capture TherapyCHO CellsConjugated systemBoranePeptides CyclicCell Linechemistry.chemical_compoundCricetulusCricetinaeNeoplasmsMoietyAnimalsHumansBinding siteBoranesPharmacologychemistry.chemical_classificationOctreotateBinding SitesSomatostatin receptorOrganic ChemistryCell MembranechemistryCancer cellBiotechnologyBioconjugate chemistry
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Synthese und pharmakologische Wirkung von carbocyclischen Muskarinanalogen

1974

Als carbocyclische Muskarinanaloga wurden das (3-Hydroxycyclopentylmethyl)trimethyl-ammonium-jodid und dessen Acetat dargestellt und am isolierten Ileum des Meerschweinchens untersucht. Synthesis and Pharmacological Activity of Carbocyclic Analogs of Muscarine As carbocyclic analogs of muscarine (3-hydroxycyclopentylmethyl)trimethylammonium iodide and (3-acetoxycyclopentylmethyl)trimethylammonium iodide were synthesized and tested on the isolated guinea pig ileum.

inorganic chemicalschemistry.chemical_classificationMuscarineChemistryStereochemistryIodidetechnology industry and agriculturePharmaceutical ScienceBiological activityIleumchemistry.chemical_compoundmedicine.anatomical_structureDrug Discoverymedicinelipids (amino acids peptides and proteins)Guinea pig ileumArchiv der Pharmazie
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Effects of magnesium chloride on the contractile response of uterus to several agonists in Ca-free solution

1987

Abstract The effects of MgCl2 on the oestrogen-dominated rat uterus have been examined. Tissues were preincubated in a Ca2+- and Mg2+-free medium containing 3 mM EDTA. Most experiments were subsequently performed in a similar medium containing either no EDTA or EDTA (1 mM). When MgCl2 was added cumulatively (1–32 mM) no contractile responses were obtained in Ca,Mg-free medium or in Ca,Mg-free high K+ solution. When 2 mM CaCl2 as added, a sustained contraction was obtained. Subsequent addition of cumulative concentrations of MgCl2 caused concentration-dependent relaxation. Oxytocin, 2 μM, produced a small and sustained contraction in a Ca,Mg-free medium. Addition of MgCl2, 2 mM, increased th…

inorganic chemicalsmedicine.medical_specialtyContraction (grammar)PotassiumMagnesium ChloridePharmaceutical Sciencechemistry.chemical_elementIn Vitro TechniquesCalciumOxytocinPotassium ChlorideUterine contractionUterine ContractionInternal medicinemedicineAnimalsMagnesiumVanadateEdetic AcidPharmacologyMagnesiumRats Inbred StrainsVanadiumRatsEndocrinologychemistryOxytocinCalciumFemaleVanadatesmedicine.symptommedicine.drugMuscle contractionJournal of Pharmacy and Pharmacology
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Increased carrier peptide stability through ph adjustment improves insulin and pth(1-34) delivery in vitro and in vivo rather than by enforced carrie…

2020

Oral delivery of therapeutic peptides is hampered by their large molecular size and labile nature, thus limiting their permeation across the intestinal epithelium. Promising approaches to overcome the latter include co-administration with carrier peptides. In this study, the cell-penetrating peptide penetratin was employed to investigate effects of co-administration with insulin and the pharmacologically active part of parathyroid hormone (PTH(1-34)) at pH 5, 6.5, and 7.4 with respect to complexation, enzymatic stability, and transepithelial permeation of the therapeutic peptide in vitro and in vivo. Complex formation between insulin or PTH(1-34) and penetratin was pH-dependent. Micron-size…

insulinmedicine.medical_treatmentlcsh:RS1-441Pharmaceutical ScienceParathyroid hormonePeptide02 engineering and technologyArticlelcsh:Pharmacy and materia medica03 medical and health sciencespenetratinIn vivoCarrier peptide Cell-penetrating peptide Insulin Intestinal peptide delivery Penetratin PTH(1-34)Membrane activitymedicine030304 developmental biologychemistry.chemical_classification0303 health sciencesLiposomecarrier peptideChemistryInsulinPermeationintestinal peptide delivery021001 nanoscience & nanotechnologyBiophysicsCell-penetrating peptide0210 nano-technologyPTH(1-34)cell-penetrating peptide
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In Vitro and In Vivo Regulation of SRD5A mRNA Expression of Supercritical Carbon Dioxide Extract from Asparagus racemosus Willd. Root as Anti-Sebum a…

2022

Oily skin from overactive sebaceous glands affects self-confidence and personality. There is report of an association between steroid 5-alpha reductase gene (SRD5A) expression and facial sebum production. There is no study of the effect of Asparagus racemosus Willd. root extract on the regulation of SRD5A mRNA expression and anti-sebum efficacy. This study extracted A. racemosus using the supercritical carbon dioxide fluid technique with ethanol and investigated its biological compounds and activities. The A. racemosus root extract had a high content of polyphenolic compounds, including quercetin, naringenin, and p-coumaric acid, and DPPH scavenging activity comparable to that of the standa…

integumentary systemChemistry (miscellaneous)Organic ChemistryDrug DiscoveryMolecular MedicinePharmaceutical SciencePellPhysical and Theoretical Chemistryanti-sebum efficacy; <i>Asparagus racemosus</i>; facial-pore-minimizing efficacy; facial sebum production; 5-alpha reductase enzymes; human volunteer; oily skin; polyphenols; <i>SRD5A</i>; supercritical carbon dioxide fluid extractionPlantes medicinalsAndrògensAnalytical ChemistryMolecules
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A discourse on human hair fibers and reflections on the conservation of drug molecules

1996

A gross discourse on human hair fibers and their formation is presented stressing the various interdisciplinary aspects, such as the morphological, biological, structural and biochemical data considered to be important in the field of hair analysis. An attempt is made to explain the incorporation of drug molecules during hair fiber formation by using the classical concepts of drug absorption based on lipoid theory and the pH-partition hypothesis as well as a modern biological approach on the permeability of cell membranes. In addition to the physiochemical considerations of the transport properties of a particular drug molecule such as a) the lipophilicity, which determines permeability thr…

integumentary systemStereochemistryChemistryHair analysisBiological TransportPlasma protein bindingPathology and Forensic MedicineCell membraneMembranemedicine.anatomical_structurePharmaceutical PreparationsPermeability (electromagnetism)ExtracellularBiophysicsmedicineHumansPharmacokineticsFiberDrug MonitoringIntracellularHairInternational Journal Of Legal Medicine
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Pharmacokinetics of Intravitreal Anti-VEGF Drugs in Age-Related Macular Degeneration

2019

Intravitreal administration of anti-vascular endothelial growth factor (VEGF) antibodies has become the standard treatment for Age-Related Macular Degeneration; however, the knowledge of their pharmacokinetics is limited. A comprehensive review of the preclinical and clinical pharmacokinetic data that were obtained in different studies with intravitreal bevacizumab, ranibizumab, and aflibercept has been conducted. Moreover, the factors that can influence the vitreous pharmacokinetics of these drugs, as well as the methods that were used in the studies for analytical determination, have been exposed. These anti-VEGF drugs present different charge and molecular weights, which play an importan…

intravitrealgenetic structuresBevacizumabmedicine.medical_treatmentlcsh:RS1-441Pharmaceutical ScienceVitrectomyReviewvascular endothelial growth factor/antagonists &ampbevacizumabPharmacologylcsh:Pharmacy and materia medica03 medical and health sciences0302 clinical medicinePharmacokineticsRanibizumabinhibitorsVascular endothelial growth factor/antagonists & inhibitorsMedicineDistribution (pharmacology)Pharmacokineticsranibizumab030304 developmental biologyAflibercept0303 health sciencesbusiness.industryafliberceptvascular endothelial growth factor/antagonists & inhibitorsIntravitreal administrationMacular degenerationmedicine.diseaseBevacizumabAge-Related Macular Degeneration030221 ophthalmology & optometryRanibizumabbusinessAfliberceptIntravitrealpharmacokineticsmedicine.drug
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Spaghetti Enriched with Inulin: Effect of Polymerization Degree on Quality Traits and α-Amylase Inhibition.

2022

Inulin is considered a dietary fiber and represents a noteworthy ingredient for food biofortification due to its health effects and its neutral taste. The aim of the work was the evaluation of the quality of pasta produced using whole-meal flours of two ancient Sicilian landraces (Senatore Cappelli-CAP and Timilia&mdash;TIM) fortified with two types of inulin (long-chain topinambur inulin IT and low-chain chicory inulin IC), at two different levels of substitution (2 and 4%) to evaluate its possible effect on &alpha;-amylase inhibition. The color indices L* and a* were mainly influenced by cultivars, while IT improved the sensory attributes, mainly the elasticity sensation, and influenced l…

inulin; durum wheat; Sicilian landraces; spaghetti; quality; aminoacids; glycemic index; α amylase? amylaseSettore CHIM/10 - Chimica Degli AlimentiSicilian landracesOrganic ChemistryFlourInulinPharmaceutical Sciencedurum wheataminoacidsAnalytical ChemistryPolymerizationα amylaseChemistry (miscellaneous)qualityDrug DiscoveryMolecular Medicineglycemic indexCookingPhysical and Theoretical ChemistrySicilian landracealpha-AmylasesaminoacidspaghettiTriticumMolecules (Basel, Switzerland)
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