Search results for "CARRIERS"

showing 10 items of 391 documents

Faceted phospholipid vesicles tailored for the delivery of Santolina insularis essential oil to the skin

2015

The aim of this work was to formulate Santolina insularis essential oil-loaded nanocarriers, namely Penetration Enhancer containing Vesicles (PEVs), evaluate the physico-chemical features and stability, and gain insights into their ability to deliver the oil to the skin.S. insularis essential oil was obtained by steam distillation, and was predominantly composed of terpenes, the most abundant being β-phellandrene (22.6%), myrcene (11.4%) and curcumenes (12.1%). Vesicles were prepared using phosphatidylcholine, and ethylene or propylene glycol were added to the water phase (10% (v/v)) to improve vesicle performances as delivery systems. Vesicles were deeply characterized by light scattering,…

Pig skinAsteraceaePolyvinyl alcohollaw.inventionchemistry.chemical_compoundColloid and Surface ChemistrylawPhosphatidylcholineOils VolatilePhospholipid vesiclesHumansPhysical and Theoretical ChemistryEssential oilCells CulturedPhospholipidsSkinLiposomeChromatographyTerpenesVesicleHuman keratinocytesSurfaces and InterfacesGeneral MedicinePenetration (firestop)CreamingchemistryEthylene/propylene glycolBiophysicsNanocarriersSantolina insularis essential oilBiotechnology
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Development of polymer-based nanoparticles for Zileuton delivery to the lung : PMeOx and PMeOzi surface chemistry reduces interactions with mucins

2021

In this paper, two amphiphilic graft copolymers were synthesized by grafting polylactic acid (PLA) as hydrophobic chain and poly(2-methyl-2-oxazoline) (PMeOx) or poly(2-methyl-2-oxazine) (PMeOzi) as hydrophilic chain, respectively, to a backbone of α,β-poly(N-2-hydroxyethyl)-D,L-aspartamide (PHEA). These original graft copolymers were used to prepare nanoparticles delivering Zileuton in inhalation therapy. Among various tested methods, direct nanoprecipitation proved to be the best technique to prepare nanoparticles with the smallest dimensions, the narrowest dimensional distribution and a spherical shape. To overcome the size limitations for administration by inhalation, the nano-into-micr…

Poly(2-oxazoline)sPolymers116 Chemical sciencesPharmaceutical ScienceMedicine (miscellaneous)Nanoparticle02 engineering and technology01 natural scienceschemistry.chemical_compoundDrug Delivery SystemsNanoparticlePolylactic acidCopolymerPolyaminesHydroxyureaGeneral Materials SciencePoly(2-oxazine)sDRUG-DELIVERYCells Culturedchemistry.chemical_classificationDrug CarriersCHALLENGESAIRWAY MUCUSPolymer021001 nanoscience & nanotechnologyGraftingDIFFUSIONPolyaspartamidePULMONARY DELIVERYDrug deliveryMolecular Medicine0210 nano-technologyHydrophobic and Hydrophilic Interactionsmedicine.drugLung inflammationPolyestersBiomedical EngineeringINHIBITIONBioengineeringBronchi010402 general chemistryPolylactic acidZileutonAmphiphileAdministration InhalationmedicineHumansPoly(2-oxazoline)RELEASEMucinsBronchial DiseasesEpithelial CellsZileuton0104 chemical scienceschemistryChemical engineeringSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoNanoparticlesASTHMAPoly(2-oxazine)
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Poly(HydroxyButyrate-co-HydroxyValerate) (PHBHV) Nanocarriers for Silymarin Release as Adjuvant Therapy in Colo-rectal Cancer

2017

The aim of this study was to address one of the major challenges of the actual era of nanomedicine namely, the bioavailability of poorly water soluble drugs such as Silymarin. We developed new, biodegradable, and biocompatible nanosized shuttles for Silymarin targeted delivery in colon-cancer cells. The design of these 100 nm sized carrier nanoparticles was based on natural polymers and their biological properties such as cellular uptake potential, cytotoxicity and 3D penetrability were tested using a colon cancer cell line (HT-29) as the in vitro culture model. Comparative scanning electron microscopy (SEM) and atomic force microscopy (AFM) measurements demonstrated that the Silymarin load…

Poly(HydroxyButyrate-co-HydroxyValerate) (PHBHV)02 engineering and technologyPharmacology03 medical and health sciences0302 clinical medicineAdjuvant therapycolo-rectal cancerPharmacology (medical)CytotoxicityOriginal ResearchPharmacologynanocarriersChemistrylcsh:RM1-950021001 nanoscience & nanotechnologyIn vitroBioavailabilitylcsh:Therapeutics. Pharmacology030220 oncology & carcinogenesisToxicityDrug deliverydrug deliveryNanomedicineNanocarriers0210 nano-technologySilymarinFrontiers in Pharmacology
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Polymeric nanoparticles as a new generation of anti-oxidant carriers

2016

In recent years, polymeric nanoparticles have been the object of growing scientific interest, especially as drug carriers. In this work, PEO-PPO-PEO (F127, commercial Pluronic F127®) nanoparticles has been used as carriers for naturally occurring anti-oxidant, such as quercetin (Q).

Polymeric nanoparticles anti-oxidant nanocarriers
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Protein-Based Nanoparticles for the Delivery of Enzymes with Antibacterial Activity.

2018

Proteins represent a versatile biopolymer material for the preparation of nanoparticles due to their biocompatibility, biodegradability, and low immunogenicity. This study presents a protein-based nanoparticle system consisting of high surface PEGylated lysozyme polyethylene glycol-modified lysozyme (LYZmPEG ). This protein modification leads to a solubility switch, which allows a nanoparticle preparation using a mild double emulsion method without the need of surfactants. The method allows the encapsulation of large hydrophilic payloads inside of the protein-based nanoparticle system. Native lysozyme (LYZ) was chosen as payload because of its innate activity as natural antibiotic. The mild…

Polymers and PlasticsBiocompatibilityNanoparticle02 engineering and technologyengineering.material010402 general chemistryGram-Positive Bacteria01 natural sciencesPolyethylene Glycolschemistry.chemical_compoundMaterials ChemistryHumansSolubilityDrug CarriersChemistryOrganic ChemistryProteinsBiodegradation021001 nanoscience & nanotechnology0104 chemical sciencesAnti-Bacterial AgentsChemical engineeringengineeringNanoparticlesEmulsionsMuramidaseBiopolymerLysozyme0210 nano-technologyDrug carrierAntibacterial activityHydrophobic and Hydrophilic InteractionsMacromolecular rapid communications
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Polysaccharide-Based pH-Responsive Nanocapsules Prepared with Bio-Orthogonal Chemistry and Their Use as Responsive Delivery Systems.

2020

Bio-orthogonal reactions have become an essential tool to prepare biomaterials; for example, in the synthesis of nanocarriers, bio-orthogonal chemistry allows circumventing common obstacles related to the encapsulation of delicate payloads or the occurrence of uncontrolled side reactions, which significantly limit the range of potential payloads to encapsulate. Here, we report a new approach to prepare pH-responsive nanocarriers using dynamic bio-orthogonal chemistry. The reaction between a poly(hydrazide) crosslinker and functionalized polysaccharides was used to form a pH-responsive hydrazone network. The network formation occurred at the interface of aqueous nanodroplets in miniemulsion …

Polymers and PlasticsBioengineeringNanotechnologyBiocompatible Materials02 engineering and technology010402 general chemistryHydrazidePolysaccharide01 natural sciencesNanocapsulesArticleBiomaterialschemistry.chemical_compoundNanocapsulesPolysaccharidesMaterials Chemistrychemistry.chemical_classificationAqueous solutionChemistrytechnology industry and agricultureHydrogen-Ion Concentration021001 nanoscience & nanotechnology0104 chemical sciencesMiniemulsionNanocarriers0210 nano-technologyBiomacromolecules
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Covalently Binding of Bovine Serum Albumin to Unsaturated Poly(Globalide-Co-ε-Caprolactone) Nanoparticles by Thiol-Ene Reactions.

2019

When nanoparticles (NPs) are introduced to a biological fluid, different proteins (and other biomolecules) rapidly get adsorbed onto their surface, forming a protein corona capable of giving to the NPs a new "identity" and determine their biological fate. Protein-nanoparticle conjugation can be used in order to promote specific interactions between living systems and nanocarriers. Non-covalent conjugates are less stable and more susceptible to desorption in biological media, which makes the development of engineered nanoparticle surfaces by covalent attachment an interesting topic. In this work, the surface of poly(globalide-co-e-caprolactone) (PGlCL) nanoparticles containing double bonds i…

Polymers and PlasticsNanoparticleBioengineering02 engineering and technology010402 general chemistry01 natural sciencesBiomaterialschemistry.chemical_compoundLactonesMaterials ChemistryAnimalsHumansBovine serum albuminParticle SizeCaproateschemistry.chemical_classificationbiologyThiol-ene reactionBiomoleculeSerum Albumin Bovine021001 nanoscience & nanotechnologyCombinatorial chemistry0104 chemical scienceschemistryCovalent bondbiology.proteinNanoparticlesCattleNanocarriers0210 nano-technologyCaprolactoneBiotechnologyConjugateHeLa CellsMacromolecular bioscience
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Functionalization of Liposomes with Hydrophilic Polymers Results in Macrophage Uptake Independent of the Protein Corona

2019

Liposomes are established drug carriers that are employed to transport and deliver hydrophilic drugs in the body. To minimize unspecific cellular uptake, nanocarriers are commonly modified with poly(ethylene glycol) (PEG), which is known to minimize unspecific protein adsorption. However, to date, it has not been studied whether this is an intrinsic and specific property of PEG or if it can be transferred to hyperbranched polyglycerol (hbPG) as well. Additionally, it remains unclear if the reduction of unspecific cell uptake is independent of the “basic” carrier at which a surface functionalization with polymers is usually applied. Therefore, we studied the protein corona of differently fun…

Polymers and PlasticsPolymersBioengineeringProtein Corona02 engineering and technology010402 general chemistry01 natural sciencesArticlePolyethylene GlycolsBiomaterialsMiceHydrophilic polymersMaterials ChemistryAnimalsHumansMacrophageDrug CarriersLiposomeChemistryMacrophagesBiological Transport021001 nanoscience & nanotechnology0104 chemical sciencesRAW 264.7 CellsLiposomesBiophysicsNanoparticlesSurface modificationProtein CoronaNanocarriers0210 nano-technologyDrug carrierHydrophobic and Hydrophilic InteractionsBiomacromolecules
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Biodegradable pH-Sensitive Poly(ethylene glycol) Nanocarriers for Allergen Encapsulation and Controlled Release

2015

In the last decades, the number of allergic patients has increased dramatically. Allergen-specific immunotherapy (SIT) is the only available cause-oriented therapy so far. SIT reduces the allergic symptoms, but also exhibits some disadvantages; that is, it is a long-lasting procedure and severe side effects like anaphylactic shock can occur. In this work, we introduce a method to encapsulate allergens into nanoparticles to avoid severe side effects during SIT. Degradable nanocarriers combine the advantage of providing a physical barrier between the encapsulated cargo and the biological environment as well as responding to certain local stimuli (like pH) to release their cargo. This work int…

Polymers and PlasticsProton Magnetic Resonance SpectroscopyNanoparticleBioengineeringmacromolecular substancesmedicine.disease_causePolyethylene GlycolsBiomaterialschemistry.chemical_compoundAllergenPolymer chemistryPEG ratioMaterials ChemistrymedicineHumansNanotechnologyDrug CarriersAcetalAllergensHydrogen-Ion ConcentrationEndolysosomeControlled releaseCombinatorial chemistrychemistrySpectrometry Mass Matrix-Assisted Laser Desorption-IonizationChromatography GelNanocarriersEthylene glycolBiomacromolecules
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Synthesis of Novel Folic Acid-Functionalized Biocompatible Block Copolymers by Atom Transfer Radical Polymerization for Gene Delivery and Encapsulati…

2005

Two synthetic routes to folic acid (FA)-functionalized diblock copolymers based on 2-(methacryloyloxy)- ethyl phosphorylcholine [MPC] and either 2-(dimethylamino)ethyl methacrylate [DMA] or 2-(diisopropylamino) ethyl methacrylate [DPA] were explored. The most successful route involved atom transfer radical polymerization (ATRP) of MPC followed by the tertiary amine methacrylate using a 9-fluorenylmethyl chloroformate (Fmoc)-protected ATRP initiator. Deprotection of the Fmoc groups produced terminal primary amine groups, which were conjugated with FA to produce two series of novel FA-functionalized biocompatible block copolymers. Nonfunctionalized MPC-DMA diblock copolymers have been previou…

Polymers and PlasticsTertiary aminePolymersDrug CompoundingBiocompatible MaterialsBioengineeringChloroformateConjugated systemMethacrylateBiomaterialschemistry.chemical_compoundFolic AcidPolymer chemistryMaterials ChemistryCopolymerPOLYMER SYNTHESIS ATRPDrug CarriersMolecular StructureAtom-transfer radical-polymerizationGenetic TherapyHydrogen-Ion ConcentrationEnd-groupchemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoDrug carrierHydrophobic and Hydrophilic InteractionsBiomacromolecules
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