Search results for "DELIVERY"

showing 10 items of 1271 documents

Interventions for Family Members and Carers of Patients with Borderline Personality Disorder: A Systematic Review.

2020

Carers of patients with borderline personality disorder (BPD) experience high levels of distress. Several studies have been carried out on interventions designed to decrease their burden. However, the evidence from these studies has not been summarized. The objective of this work is to explore the clinical utility of interventions developed for family members of patients with BPD. A systematic review was conducted following the PRISMA guidelines (registration number CRD42018107318), including psychological interventions focused on relatives of patients with BPD. The following databases were used: PsycINFO, PubMed, EBSCOhost, and Web of Science. Two independent researchers reviewed the studi…

Social PsychologyWeb of scienceCarersPsychological interventionPsycINFORelativePsychological treatment to relativesEmpirical researchFamily membersBorderline Personality DisorderMedicineHumans0501 psychology and cognitive sciencesFamilyMethodological qualityBorderline personality disorderbusiness.industry05 social sciencesmedicine.diseaseClinical PsychologyDistressCaregivers050902 family studiesBorderline personality disorderDialectical behaviour therapy0509 other social sciencesPsychoeducationbusinessInclusion (education)Delivery of Health CareSocial Sciences (miscellaneous)050104 developmental & child psychologyClinical psychologyFamily processReferences
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Cancer Patients and Medical Practice. Some Historical and Cultural Considerations

1997

Social adjustmentAttitude of Health PersonnelCultureMEDLINEGuidelines as TopicTruth DisclosureGeneral Biochemistry Genetics and Molecular BiologySociologyHistory and Philosophy of ScienceNeoplasmsmedicineHumansPhysician-Patient RelationsMedical educationTruth DisclosureCommunicationGeneral NeuroscienceCancerMedical practicemedicine.diseaseHealthPsychologyAttitude to HealthDelivery of Health CareSocial AdjustmentHospital-Patient RelationsAnnals of the New York Academy of Sciences
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Doing gendered and (dis)embodied work. Care work in the context of medico-managerial welfare state

2013

Whether and how technology-driven managerial reforms affect the field of human service work is a timely question for social sciences. In an increasingly technology-assisted working-life, material conditions such as one’s age and gender may be losing their significance as signifiers of professional identity. Welfare service work is traditionally understood as feminine work that comprises of embodied, situational and social practices of care work. Over the past few decades, public management reforms have called for reassessment of welfare service workers’ occupational skills through practices of medico-managerial service management and occupational accountability. As a result, workers technic…

Social workbusiness.industryService delivery frameworkEmotion workWelfare stateta5142Public relationsAccountabilityCare workSociologybusinessSocial psychologyCompetence (human resources)Human servicesNordic Social Work Research
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Ion-exchange fibers and drugs: an equilibrium study

2001

The purpose of this study was to investigate the mechanisms of drug binding into and drug release from cation-exchange fibers in vitro under equilibrium conditions. Ion-exchange groups of the fibers were weakly drug binding carboxylic acid groups (-COOH), strongly drug binding sulphonic acid groups (-SO(3)H), or combinations thereof. Parameters determining the drug absorption and drug release properties of the fibers were: (i) the lipophilicity of the drug (tacrine and propranolol are lipophilic compounds, nadolol is a relatively hydrophilic molecule), (ii) the ion-exchange capacity of the fibers, which was increased by activating the cation-exchange groups with NaOH, (iii) the ionic streng…

SodiumCarboxylic acidPharmaceutical Sciencechemistry.chemical_element02 engineering and technology030226 pharmacology & pharmacyDivalent03 medical and health sciencesDrug Delivery Systems0302 clinical medicineFiberchemistry.chemical_classificationChromatographyOsmolar Concentration021001 nanoscience & nanotechnologyPropranololIon ExchangeNadololSolubilitychemistryIonic strengthLipophilicityTacrineCalcium0210 nano-technologyDrug carrierDrug metabolismNuclear chemistry
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Physical Methods for Enhancing Oral Mucosal Delivery: Sonophoresis, Iontophoresis and Electroporation

2015

The need for more rapid onset of action and improved absorption of medications has resulted in great development of drug delivery technologies. Transmucosal drug delivery offers a convenient route of administration for a variety of clinical indications. Unfortunately, the wide variability in structure of the oral mucosal tissues could constitute a key factor in drug penetration and absorption. To circumvent this obstacle and to increase the drug flux through the mucosal membranes, different approaches to permeation enhancement are used. This chapter describes the most significant aspects of the physical techniques widely used such as sonophoresis, iontophoresis, and electroporation. These p…

Sonophoresis iontophoresis electromigration electroosmosis electroporation physical permeation enhancement oral mucosal deliveryIontophoresisSettore CHIM/09 - Farmaceutico Tecnologico Applicativobusiness.industryElectroporationRapid onsetDrug deliveryMedicineAbsorption (skin)PharmacologybusinessSonophoresis
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Transdermal and Skin-Targeted Drug Delivery

1997

Background: The application of therapeutic agents to the skin addresses three general objectives: (a) the treatment of a variety of dermatologic diseases; (b) the “targeted” delivery of drugs to deeper subcutaneous tissues, with a concomitant reduction in systemic exposure; and (c) socalled transdermal administration to elicit a systemic pharmacologic effect. Objective: Recently, significant progress towards all three goals has been recorded and the level of research and development activity remains high. We aim to discuss these advances from mechanistic and clinical standpoints. Results: For the topical treatment of skin disease, novel vehicles (e.g., stabilized, supersaturated systems and…

SonophoresisDermatologyPharmacology030226 pharmacology & pharmacy03 medical and health sciences0302 clinical medicineSmall peptideTransdermal drug deliveryMedicineChemical penetration enhancersTransdermalddc:615LiposomeIontophoresisbusiness.industryIontophoresisControlled releasePatch technologyBioavailabilityElectroporationTargeted drug delivery030220 oncology & carcinogenesisLiposomesDrug deliverySurgerybusinessJournal of Cutaneous Medicine and Surgery
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Rethinking Cysteine Protective Groups:S-Alkylsulfonyl-l-Cysteines for Chemoselective Disulfide Formation

2016

The ability to reversibly cross-link proteins and peptides grants the amino acid cysteine its unique role in nature as well as in peptide chemistry. We report a novel class of S-alkylsulfonyl-l-cysteines and N-carboxy anhydrides (NCA) thereof for peptide synthesis. The S-alkylsulfonyl group is stable against amines and thus enables its use under Fmoc chemistry conditions and the controlled polymerization of the corresponding NCAs yielding well-defined homo- as well as block co-polymers. Yet, thiols react immediately with the S-alkylsulfonyl group forming asymmetric disulfides. Therefore, we introduce the first reactive cysteine derivative for efficient and chemoselective disulfide formation…

Stereochemistry010402 general chemistryCleavage (embryo)01 natural sciencesRing-opening polymerizationCatalysisAnhydridesPolymerizationchemistry.chemical_compoundPeptide synthesisCysteineDisulfidesSulfhydryl CompoundsAmineschemistry.chemical_classification010405 organic chemistryOrganic ChemistryGeneral Chemistry0104 chemical sciencesAmino acidchemistryPolymerizationDrug deliveryPeptidesDerivative (chemistry)CysteineChemistry - A European Journal
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N-Heterocyclic choline analogues based on 1,2,3,4-tetrahydro(iso)quinoline scaffold with anticancer and anti-infective dual action

2016

Pharmacological effects of biologically active “small molecules” can be improved by their targeted modification, which affects drug delivery and interaction with tumor cells and microorganisms. We aimed to evaluate anticancer and antimicrobial activity of lipid-like choline derivatives modified via simultaneous introduction of tetrahydro(iso)quinoline based pharmacophore system at nitrogen atom and long chain alkyl substituent at oxygen atom. Target compounds were synthesized under phase-transfer catalysis conditions followed by quaternization, and evaluated for cytotoxicity and NO-generation ability on HT-1080 and MG-22A tumor cell lines and NIH 3T3 normal mouse fibroblasts, and screened f…

StereochemistryAntineoplastic AgentsMicrobial Sensitivity TestsGram-Positive Bacteriamedicine.disease_cause01 natural sciencesDNA gyraseCholineInhibitory Concentration 50Mice03 medical and health scienceschemistry.chemical_compoundDrug Delivery Systems0302 clinical medicineAnti-Infective AgentsCell Line TumorNeoplasmsGram-Negative BacteriamedicineAnimalsHumansCytotoxicityEscherichia coliPharmacologybiology010405 organic chemistryQuinolineFungiBiological activityGeneral MedicineAntimicrobialbiology.organism_classificationProteus mirabilis0104 chemical scienceschemistry030220 oncology & carcinogenesisNIH 3T3 CellsQuinolinesAntibacterial activityPharmacological Reports
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Dry adsorbed emulsion: 2. Dissolution behaviour of an intricate formulation

2002

The behaviour of a pharmaceutical form, called dry adsorbed emulsion (DAE), containing a sparingly soluble drug (i.e. theophylline) was studied for dissolution drug release kinetic, in relation with DAE structure characterisation. In vitro dissolution testings were performed under different experimental conditions (medium at pH 1.2 and 7.4, medium with or without surfactant addition, different particle sizes, discrete or densified particles). Discrete DAE particles showed an extended release, in comparison with the native drug powder, depending on both drug solubility in the medium and particle size. The relevance of dissolution data was not improved by surfactant addition (0.1% sodium laur…

StereochemistryChemistryChemistry PharmaceuticalPharmaceutical ScienceDosage formBronchodilator AgentsSolubilityTheophyllineChemical engineeringPulmonary surfactantDelayed-Action PreparationsDrug deliveryEmulsionMicroscopy Electron ScanningParticleEmulsionsAdsorptionParticle sizeParticle SizePowdersSolubilityDissolutionInternational Journal of Pharmaceutics
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Polysaccharide/polyaminoacid composite scaffolds for modified DNA release.

2009

Abstract In this work composite polymeric films or sponges, based on hyaluronic acid (HA) covalently crosslinked with α,β-poly(N-2-hydroxyethyl)(2-aminoethylcarbamate)- d , l -aspartamide (PE), have been prepared and characterized as local gene delivery systems. In particular, HA/PE scaffolds have been loaded with PE/DNA interpolyelectrolyte complexes, employing PE as a macromolecular crosslinker for HA and as a non-viral vector for DNA. In vitro studies showed that HA/PE films and sponges have high compatibility with human dermal fibroblasts and they give a sustained DNA release, whose trend can be easily tailored by varying the crosslinking ratio between HA and PE. Electrophoresis analysi…

StereochemistryMelanoma ExperimentalPharmaceutical ScienceHyaluronoglucosaminidaseElectrophoretic Mobility Shift Assaymacromolecular substancesBiologyGene deliveryTransfectionchemistry.chemical_compoundMiceTissue engineeringHyaluronic acidPolyaminesCOMPOSITE SCAFFOLD SCAFFOLD AMINOACID DNA RELEASE.AnimalsHumansHyaluronic AcidAspartameCells CulturedMolecular StructureGenetic transfertechnology industry and agricultureBiological TransportTransfectionDNAFibroblastsIn vitroKineticsCross-Linking ReagentschemistrySolubilitySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoNucleic Acid ConformationDNAMacromoleculeNuclear chemistryInternational journal of pharmaceutics
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