Search results for "Drug Compounding"

showing 10 items of 90 documents

Comparison of two artificial tear formulations for dry eye through high‐resolution optical coherence tomography

2011

Purpose:  The aim was to determine the efficacy of two artificial eye-drop formulations by analysing the lower tear film meniscus volume through a commercial high-resolution spectral-domain optical coherence tomographer. Methods:  Twenty dry eye patients (12 men, eight women, aged 57.5 ± 8.4 years) with refractive errors from -2.50 to +0.75 D (mean -1.34 ± 1.02 D) and cylinders lower than 1.00 D were examined. Tear meniscus volume was measured before, immediately after and 10, 30 and 60 minutes after instillation using the Copernicus high-resolution spectral-domain optical coherence tomographer (Optopol Tech SA, Zawiercie, Poland). Volume was calculated from the local area obtained from tom…

Malemedicine.medical_specialtyDrug Compoundingmedicine.medical_treatmentDry Eye SyndromesHigh resolutionMeniscus (anatomy)Young AdultOptical coherence tomographyReference ValuesOphthalmologymedicineHumansSurface Tensionmedicine.diagnostic_testbusiness.industryImage Enhancementeye diseasesSurgeryOphthalmologyArtificial tearsmedicine.anatomical_structureVolume (thermodynamics)TearsTearsDry Eye SyndromesFemalesense organsEyelidOphthalmic SolutionsbusinessTomography Optical CoherenceFollow-Up StudiesOptometryClinical and Experimental Optometry
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Nanostructured Lipid Carriers-Containing Anticancer Compounds: Preparation, Characterization, and Cytotoxicity Studies

2007

This article describes the development of nanostructured lipid carriers (NLC) as colloidal carriers for two antitumor compounds that possess a remarkable antineoplastic activity. But their limited stability and low solubility in water could give a very low parenteral bioavailability. Results revealed an enhancement of the cytotoxicity effect of drug-loaded NLC on human prostate cancer (PC-3) and human hepatocellular carcinoma (HuH-6, HuH-7) cell lines with respect to that of both free drugs. Results of characterization studies strongly support the potential application of these drugs-loaded NLC as prolonged delivery systems for lipophilic drugs by several administration routes, in particula…

Materials scienceCell SurvivalDrug CompoundingPharmaceutical ScienceNanoparticleAntineoplastic AgentsPharmacologynanostructured lipid carrierHuman prostatehuman prostate carcinoma cellPlasmaCell Line TumorElectrochemistryHumansParticle SizeSolubilityCytotoxicityChromatography High Pressure LiquidDrug CarriersGeneral Medicineantitumor drugLipidsControlled releaseBioavailabilitySolubilityPlasma chemistryNanoparticleshuman hepatocellular carcinoma cellcontrolled releaseDrug metabolism
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Impact of excipient choice on the aerodynamic performance of inhalable spray-freeze-dried powders

2020

Abstract Spray-freeze-drying (SFD) is a process in which a solution is dispersed into a freezing medium and dried by sublimation, resulting in lyophilized powders with spherical particles. This study aims at screening and evaluating the impact of the excipient choice and spray solution characteristics in SFD on the physico-chemical characteristics of lyospheres and rate their suitability for producing pulmonary applicable powders using a novel SFD method. A monodisperse droplet-stream was injected into a vortex of cold gas for the production of inhalable, uniform spherical lyophilisates with a narrow particle size distribution. Model solutions containing graded contents (0.3%, 1.0%, and 3.0…

Materials scienceChemistry PharmaceuticalDrug CompoundingDispersityPharmaceutical ScienceExcipient02 engineering and technology030226 pharmacology & pharmacyExcipients03 medical and health scienceschemistry.chemical_compound0302 clinical medicineDrug StabilityPolysaccharidesAdministration InhalationmedicineTechnology PharmaceuticalMannitolParticle SizePorosity021001 nanoscience & nanotechnologyMaltodextrinOhnesorge numberFreeze DryingChemical engineeringchemistryParticle-size distributionParticle sizeMannitolPowders0210 nano-technologyPorositymedicine.drugInternational Journal of Pharmaceutics
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Development and evaluation of occlusive systems employing polyvinyl alcohol for transdermal delivery of sumatriptan succinate

2010

The aim of the present study was to develop a sumatriptan succinate transdermal system for applying migraine treatments efficiently and easily. For this system polyvinyl alcohol was employed as a matrix and Azone((R)) was added as a permeability enhancer. The physical characteristics, mechanical properties, and in vivo bioadhesion of the systems were evaluated, as was in vitro permeation across porcine skin. A uniform distribution of the drug in the matrix was observed, and moisture uptake values were constant. With regard to mechanical parameters, occlusive layer inclusion made the system more resistant, and no significant differences were detected with respect to other systems. Although A…

Materials scienceChemistry PharmaceuticalDrug CompoundingMigraine DisordersSkin AbsorptionPharmaceutical SciencePharmacologyAdministration CutaneousPolyvinyl alcoholPermeabilitychemistry.chemical_compoundDrug Delivery SystemsDrug StabilityIn vivoSumatriptan SuccinatemedicineTechnology PharmaceuticalVasoconstrictor AgentsDrug InteractionsAntihypertensive AgentsTransdermalDrug CarriersSumatriptanAzepinesGeneral MedicineHydrogen-Ion ConcentrationPermeationSerotonin Receptor AgonistsSumatriptanSolubilitychemistryPermeability (electromagnetism)Polyvinyl AlcoholPolyvinylsAzoneBiomedical engineeringmedicine.drugDrug Delivery
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Performance of Multilayered Particles: Influence of a Thin Cushioning Layer

2005

Nowadays, oral dosage forms with controlled release kinetics have known an increasing interest. The polymer coating of drug-loaded particles is one of the most common methods used for controlling drug delivery. Such multilayered particles could be either filled into capsules or compressed into tablets for their oral administration. However, many studies have noticed that coating films are damaged during the compression process, leading to significant changes in drug release profiles. The aims of this study were to investigate the effects of a thin cushioning layer [made of HydroxyPropylMethyl Cellulose (HPMC)] applied on coated theophylline particles upon particle characteristics, tablet pr…

Materials scienceChemistry PharmaceuticalDrug CompoundingPharmaceutical ScienceExcipientMethylcelluloseengineering.materialDosage formExcipientsHypromellose DerivativesTheophyllineCoatingDrug DiscoverymedicineComposite materialCellulosePharmacologyOrganic ChemistryCushioningControlled releaseSolubilityDrug deliveryengineeringParticleTablets Enteric-CoatedLayer (electronics)medicine.drugDrug Development and Industrial Pharmacy
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Comparative study of the lubricant performance of Compritol 888 ATO either used by blending or by hot melt coating.

2003

Compritol 888 ATO is used as a lubricant in oral solid dosage formulations. It can also be used as a hot melt coating agent sprayed onto a powder. In this study, we compare the lubricant performance of Compritol 888 ATO either used by classical blending or by hot melt coating onto Lactopress by compression tests. In physical mix, the Compritol concentration does not affect the compressibility. The same compressibility is obtained with lactose coated by 0.5 or 1% of Compritol, but a higher compressibility can be observed with 2 and 3%. Cohesiveness of lactose depends on the process: hot melt coating induces a decrease of tablet tensile strength. In terms of forces transmission during compres…

Materials scienceCompressive StrengthChemistry PharmaceuticalDrug CompoundingFatty AcidsMixing (process engineering)Pharmaceutical ScienceAdministration OralLactoseengineering.materialExcipientsHeatingCompressive strengthCoatingUltimate tensile strengthLubricationLubricationCompressibilityengineeringHot melt coatingLubricantComposite materialPowdersTabletsInternational journal of pharmaceutics
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Jet-vortex spray freeze drying for the production of inhalable lyophilisate powders

2016

Abstract Spray-freeze-dried powders were suggested for nasal, epidermal (needle-free injection) or pulmonary application of proteins, peptides or nucleic acids. In spray-freeze-drying processes an aqueous solution is atomized into a refrigerant medium and subsequently dried by sublimation. Droplet-stream generators produce a fast stream of monodisperse droplets, where droplets are subject to collisions and therefore the initial monodispersity is lost and droplets increase in diameter, which reduces their suitability for pulmonary application. In jet-vortex-freezing, a droplet-stream is injected into a vortex of cold process gas to prevent droplet collisions. Both the injection position of t…

Materials scienceDrug CompoundingNozzlePharmaceutical Science02 engineering and technology030226 pharmacology & pharmacyExcipientsRefrigerant03 medical and health scienceschemistry.chemical_compoundFreeze-drying0302 clinical medicinePolysaccharidesAdministration InhalationMannitolParticle SizeChromatographyAqueous solution021001 nanoscience & nanotechnologyMaltodextrinBulk densityVortexFreeze DryingChemical engineeringchemistryFluoresceinSublimation (phase transition)Powders0210 nano-technologyEuropean Journal of Pharmaceutical Sciences
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Role of continuous moisture profile monitoring by inline NIR spectroscopy during fluid bed granulation of an Enalapril formulation

2010

Granulation and tableting are closely related process steps in the supply chain of pharmaceutical products. Even today, these steps are still optimized independently by trial and error. On the framework of a process analytical technology approach, these processes were evaluated in an integrated approach. Enalapril maleate is a low-dose drug substance with poor granulating and tableting behavior. In order to verify how granulation influences tableting properties, different granulation experiments were performed.Granulation experiments with fast spraying rate and fast drying as well as fast spraying rate and slow drying, and also combinations of both were run. The obtained granules were then …

Materials scienceDrug CompoundingProcess analytical technologyPharmaceutical ScienceAngiotensin-Converting Enzyme InhibitorsIndentation hardnessQuality by DesignPlacebosGranulationTabletingEnalaprilHardnessDrug DiscoveryDesiccationParticle SizeProcess engineeringFluid Bed GranulationPharmacologySpectroscopy Near-InfraredMoisturebusiness.industryOrganic ChemistryNear-infrared spectroscopyWaterbusinessTabletsDrug Development and Industrial Pharmacy
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Spray-Drying, Solvent-Casting and Freeze-Drying Techniques: a Comparative Study on their Suitability for the Enhancement of Drug Dissolution Rates.

2019

Purpose Solid dispersions (SDs) represent the most common formulation technique used to increase the dissolution rate of a drug. In this work, the three most common methods used to prepare SDs, namely spray-drying, solvent-casting and freezedrying, have been compared in order to investigate their effect on increasing drug dissolution rate. Methods Three formulation strategies were used to prepare a polymer mixture of polyvinyl-alcohol (PVA) and maltodextrin (MDX) as SDs loaded with the following three model drugs, all of which possess a poor solubility: Olanzapine, Dexamethasone, and Triamcinolone acetonide. The SDs obtained were analysed and compared in terms of drug particle size, drug-lo…

Materials scienceDrug Compoundingdissolution rate . freeze-drying . solid dispersion . solvent-casting method . spray-dryingPharmaceutical Science02 engineering and technology030226 pharmacology & pharmacyTriamcinolone AcetonideDexamethasoneExcipients03 medical and health sciencesFreeze-dryingchemistry.chemical_compound0302 clinical medicinePolysaccharidesPharmacology (medical)Dissolution testingSolubilityDesiccationDissolutionPharmacologyOrganic Chemistry021001 nanoscience & nanotechnologyMaltodextrinSolventDrug LiberationFreeze DryingChemical engineeringchemistryPharmaceutical PreparationsSolubilityOlanzapineSpray dryingPolyvinyl AlcoholSolventsMolecular MedicineParticle size0210 nano-technologyBiotechnologyPharmaceutical research
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A one-pot method to enhance dissolution rate of low solubility drug molecules using dispersion polymerization in supercritical carbon dioxide

2009

The surfactant assisted polymerization of 1-vinyl-2-pyrrolidone in supercritical carbon dioxide in the presence of Piroxicam, selected as a model of a low aqueous solubility drug, was studied in order to prepare in a single step a polymeric composite to enhance the rate of dissolution of the pharmaceutical compound. Reactive entrapping was carried out at 65 degrees C in the P range 21-38MPa. Under proper operative conditions we obtained the composite under the form of sub-micron spherical particles with relatively narrow particle size distribution. Drug loadings higher than 12% (w/w) were obtained and XRD and Raman spectroscopy suggest that the anti-inflammatory agent is dispersed in the ma…

Materials sciencePolymersDrug CompoundingComposite numberPharmaceutical ScienceSpectrum Analysis RamanPiroxicamOrganic chemistryTechnology PharmaceuticalSolubilityParticle SizeDissolutionchemistry.chemical_classificationDispersion polymerizationDrug CarriersSupercritical carbon dioxideTemperatureChromatography Supercritical FluidPolymerCarbon DioxideSettore ING-IND/27 - Chimica Industriale E TecnologicaSupercritical fluidPyrrolidinonesPolymerizationChemical engineeringchemistrySolubilitySupercritical fluid Drug release kineticsSolid dispersion Dissolution enhancement Polymer microspheres
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