Search results for "targeted drug delivery"

showing 10 items of 56 documents

Chemical modification of halloysite nanotubes for controlled loading and release.

2020

Clay minerals have been used for medical purposes from ancient times. Among them, the halloysite nanotube, an aluminosilicate of the kaolin group, is an emerging nanomaterial which possesses peculiar chemical characteristics. By means of suitable modifications, such as supramolecular functionalization or covalent modifications, it is possible to obtain novel nanomaterials with tunable properties for several applications. In this context the covalent grafting of suitable organic moieties on the external surface or in the halloysite lumen has been exploited to improve the loading and release of several biologically active molecules. The resulting hybrid nanomaterials have been applied as drug…

NanotubeMaterials scienceTunable properties Controlled drug deliveryHalloysite nanotubeBiomedical EngineeringSupramolecular chemistryNanotechnology02 engineering and technologyengineering.materialChemical characteristic010402 general chemistryYarn Biologically active molecule01 natural sciencesHalloysiteNanomaterialsAluminosilicateKaoliniteGeneral Materials ScienceFunctionalizationGene transferSettore CHIM/02 - Chimica FisicaTargeted drug deliveryCovalent modificationMoleculeGeneral ChemistryGeneral MedicineSettore CHIM/06 - Chimica Organica021001 nanoscience & nanotechnology0104 chemical sciencesNanostructured materialNanotubeSelf-healing hydrogelsengineeringTissue regenerationSurface modificationClay0210 nano-technologyDrug carrierHybrid nanomaterialChemical modificationCovalent graftingJournal of materials chemistry. B
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Optimizing taxane use in MBC in the emerging era of targeted chemotherapy.

2013

The first-generation taxanes, conventional paclitaxel and docetaxel, are established treatment options for adjuvant and metastatic breast cancer (MBC). However, these agents have limitations, including primary/secondary resistance and harsh toxicities. The introduction of paclitaxel albumin represents a significant advance in taxane therapy as the first of a new generation of taxanes. This agent utilizes albumin pathways to achieve enhanced and targeted drug delivery to the tumour. The lack of solvent also means that it is well tolerated, despite the lack of premedications. Paclitaxel albumin is licensed in the United States and Europe as ≥2nd-line therapy in MBC (260mg/m(2) once every thre…

OncologyBridged-Ring Compoundsmedicine.medical_specialtymedicine.medical_treatmentAntineoplastic AgentsBreast NeoplasmsPharmacologychemistry.chemical_compoundBreast cancerInternal medicineAntineoplastic Combined Chemotherapy ProtocolsMedicineHumansMolecular Targeted TherapyNeoplasm MetastasisChemotherapyClinical Trials as TopicTaxanebusiness.industryHematologymedicine.diseaseMetastatic breast cancerTreatment OutcomeOncologyPaclitaxelchemistryTargeted drug deliveryDocetaxelFemaleTaxoidsbusinessAdjuvantmedicine.drugCritical reviews in oncology/hematology
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Future Trends, Challenges, and Opportunities with Polymer‐Based Combination Therapy in Cancer

2011

Oncologymedicine.medical_specialtyCombination therapyTargeted drug deliverybusiness.industryInternal medicinemedicineCancerNanomedicinePharmacologymedicine.diseasebusinessDrug Delivery in Oncology
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Molecular insights and novel approaches for targeting tumor metastasis

2020

In recent years, due to the effective drug delivery and preciseness of tumor sites or microenvironment, the targeted drug delivery approaches have gained ample attention for tumor metastasis therapy. The conventional treatment approaches for metastasis therapy have reported with immense adverse effects because they exhibited maximum probability of killing the carcinogenic cells along with healthy cells. The tumor vasculature, comprising of vasculogenic impressions and angiogenesis, greatly depends upon the growth and metastasis in the tumors. Therefore, various nanocarriers-based delivery approaches for targeting to tumor vasculature have been attempted as efficient and potential approaches…

PolymersAngiogenesisMetal NanoparticlesPharmaceutical ScienceAntineoplastic Agents02 engineering and technologyTumor vasculature030226 pharmacology & pharmacyMetastasis03 medical and health sciencesDrug Delivery Systems0302 clinical medicineNeoplasmsTumor MicroenvironmentHumansMedicineNeoplasm MetastasisAdverse effectDrug CarriersNeovascularization Pathologicbusiness.industryConventional treatmentPhototherapy021001 nanoscience & nanotechnologymedicine.diseaseLipidsTargeted drug deliveryDrug deliveryCancer researchNanoparticlesRNANanocarriersPeptides0210 nano-technologybusinessInternational Journal of Pharmaceutics
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Polysorbate-80 coating enhances uptake of polybutylcyanoacrylate (PBCA)-nanoparticles by human and bovine primary brain capillary endothelial cells

2000

Certain drugs such as dalargin, loperamide or tubocurarine are not transported across the blood-brain barrier (BBB) and therefore exhibit no effects on the central nervous system. However, effects on the central nervous system can be observed when these drugs are loaded onto polybutylcyanoacrylate (PBCA)-nanoparticles and coated with polysorbate 80. The mechanism by which these complexed nanoparticles cross the BBB and exhibit their effects has not been elucidated. Cultured microvessel brain endothelial cells of human and bovine origin were used as an in vitro model for the BBB to gain further insight into the mechanism of uptake of nanoparticles. With cells from these species we were able …

PolysorbateEndotheliumGeneral NeuroscienceConfocalDrug delivery to the brainBiologyBlood–brain barrierchemistry.chemical_compoundmedicine.anatomical_structurechemistryTargeted drug deliveryNanoparticles for drug delivery to the brainImmunologyBiophysicsmedicineMicrovesselEuropean Journal of Neuroscience
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Surface Modification of Nanoparticles and Nanovesicles via Click-Chemistry

2019

Surface modification of nanocarriers offers the possibility of targeted drug delivery, which is of major interest in modern pharmaceutical science. Click-chemistry affords an easy and fast way to modify the surface with targeting structures under mild reaction conditions. Here we describe our current method for the post-preparational surface modification of multifunctional sterically stabilized (stealth) liposomes via copper-catalyzed azide-alkyne cycloaddition (CuAAC) and inverse electron demand Diels-Alder norbornene-tetrazine cycloaddition (IEDDA). We emphasize the use of these in a one-pot orthogonal reaction for deep investigation on stability and targeting of nanocarriers. As the prod…

Reaction conditionsLiposomeChemistryNanoparticleNanotechnology02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesCycloaddition0104 chemical sciencesTargeted drug deliveryClick chemistrySurface modificationNanocarriers0210 nano-technology
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2014

In the pathogenesis of Alzheimer’s disease (AD) the homeostasis of amyloid precursor protein (APP) processing in the brain is impaired. The expression of the competing proteases ADAM10 (a disintegrin and metalloproteinase 10) and BACE-1 (beta site APP cleaving enzyme 1) is shifted in favor of the A-beta generating enzyme BACE-1. Acitretin–a synthetic retinoid–e.g., has been shown to increase ADAM10 gene expression, resulting in a decreased level of A-beta peptides within the brain of AD model mice and thus is of possible value for AD therapy. A striking challenge in evaluating novel therapeutically applicable drugs is the analysis of their potential to overcome the blood-brain barrier (BBB)…

Reporter geneMultidisciplinarybiologyADAM10TransfectionPharmacologyBlood–brain barriermedicine.anatomical_structureBeta-secretase 1Targeted drug deliverymedicinebiology.proteinAmyloid precursor proteinAmyloid precursor protein secretasePLOS ONE
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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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THERAPEUTIC-LOADED LIPID NANOSTRUCTURES AND BRAIN DISEASES.

2012

Central Nervous System (CNS) diseases represent the largest and fastest growing area of unmet medical need since an alarming increase in brain disease incidence is going on. Despite major advances in neuroscience, many potential therapeutic agents are denied access to the CNS because of the existence of a physiological low permeable barrier, the Blood-Brain Barrier (BBB). To obtain an improvement of drug CNS performance, sophisticated approaches such as nanoparticulate systems are rapidly developing. In particular, in this chapter, the most recent data demonstrating the potential of lipid nanostructures, such as Solid Lipid Nanoparticles (SLN) and Nanostructured Lipid Carriers (NLC), to tra…

Targeted drug delivery systemsSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoSolid lipid nanoparticleNanostructured lipid carrierBlood-brain barrier
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SYNTHESIS, CHARACTERIZATION AND IN VITRO CYTOTOXICITY STUDIES OF A MACROMOLECULAR CONJUGATE OF PACLITAXEL BEARING OXYTOCIN AS TARGETING MOIETY.

2007

The present study describes the experimental synthetic procedure and the characterization of a new polyaspartamide macromolecular prodrug of paclitaxel, bearing oxytocin residues as targeting moieties. In vitro stability studies of bioconjugate, performed in media mimicking biological fluids (buffer solutions at pH 7.4 and 5.5) and in human plasma, evidenced the high stability of the targeting portion (oxytocin)-polymer linkage and the ability of this conjugate to release linked paclitaxel in a prolonged way in plasma. Moreover, preliminary in vitro antiproliferative studies, carried out on MCF-7 cells, that are oxytocin receptor positive cells, showed that the polymeric conjugate has the s…

Time FactorsChemistry PharmaceuticalDrug CompoundingpolyaspartamidePharmaceutical ScienceBreast NeoplasmsPolyethylene Glycolschemistry.chemical_compoundpaclitaxelDrug StabilityCell Line TumoroxytocinHumansMoietyProdrugsbioconjugateCytotoxicityCell ProliferationDrug CarriersDose-Response Relationship DrugMolecular StructureHydrolysisdrug targetingGeneral MedicineHydrogen-Ion ConcentrationAntineoplastic Agents PhytogenicOxytocin receptorIn vitroSolubilityPaclitaxelchemistryBiochemistryTargeted drug deliveryReceptors OxytocinDelayed-Action PreparationsFemalePeptidesDrug carrierBiotechnologyConjugate
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