about
Spontaneous association of hydrophobized dextran and poly-beta-cyclodextrin into nanoassemblies. Formation and interaction with a hydrophobic drug.Fucosyled neoglycolipids: synthesis and interaction with a phospholipid.Interest of glycolipids in drug delivery: from physicochemical properties to drug targeting.Proteins, polysaccharides, and their complexes used as stabilizers for emulsions: alternatives to synthetic surfactants in the pharmaceutical field?Artificial plasma membrane models based on lipidomic profiling.Assessment of the relevance of supported planar bilayers for modeling specific interactions between glycodendrimeric porphyrins and retinoblastoma cells.Tumor targeting in photodynamic therapy. From glycoconjugated photosensitizers to glycodendrimeric one. Concept, design and properties.Effect of cholesterol and sugar on the penetration of glycodendrimeric phenylporphyrins into biomimetic models of retinoblastoma cells membranes.The bacterial cell envelope as delimiter of anti-infective bioavailability - An in vitro permeation model of the Gram-negative bacterial inner membrane.Charge and aggregation pattern govern the interaction of plasticins with LPS monolayers mimicking the external leaflet of the outer membrane of Gram-negative bacteria.Evaluation of the specific interactions between glycodendrimeric porphyrins, free or incorporated into liposomes, and concanavalin A by fluorescence spectroscopy, surface pressure, and QCM-D measurements.Comparison of the Micellar Incorporation and the Intestinal Cell Uptake of Cholecalciferol, 25-Hydroxycholecalciferol and 1-α-Hydroxycholecalciferol.Specific interaction of lectins with liposomes and monolayers bearing neoglycolipids.The distribution and relative hydrolysis of tocopheryl acetate in the different matrices coexisting in the lumen of the small intestine during digestion could explain its low bioavailability.Structural properties of POPC monolayers under lateral compression: computer simulations analysis.Aggregation of hydrophobically modified polysaccharides in solution and at the air-water interface.Incorporation of glycoconjugated porphyrin derivatives into phospholipid monolayers: a screening method for the evaluation of their interaction with a cell membrane.Influence of a neoglycolipid and its PEO-lipid moiety on the organization of phospholipid monolayers.Effect of high pressure homogenization on the structure and the interfacial and emulsifying properties of β-lactoglobulin.Disruption of Asymmetric Lipid Bilayer Models Mimicking the Outer Membrane of Gram-Negative Bacteria by an Active Plasticin.Molecular interactions governing the incorporation of cholecalciferol and retinyl-palmitate in mixed taurocholate-lipid micelles.Study of Surface Charge Instabilities by EOF Measurements on a Chip: A Real-Time Hysteresis and Peptide Adsorption Based Methodology.Interaction of self-assembled squalenoyl gemcitabine nanoparticles with phospholipid-cholesterol monolayers mimicking a biomembrane.Impact of lipid composition and photosensitizer hydrophobicity on the efficiency of light-triggered liposomal release.Bare and sterically stabilized PLGA nanoparticles for the stabilization of Pickering emulsionsNewly synthesized lipid-porphyrin conjugates: evaluation of their self assembling properties, their miscibility with phospholipids and their photodynamic activity in vitroComportement interfacial de tétraphénylporphyrines glycoconjuguées et leur interaction avec des modèles biomimétiques de la membrane cellulaireBiomimetic liposomes and planar supported bilayers for the assessment of glycodendrimeric porphyrins interaction with an immobilized lectinNew strategy for targeting of photosensitizers. Synthesis of glycodendrimeric phenylporphyrins, incorporation into a liposome membrane and interaction with a specific lectinInfluence of the nanoprecipitation conditions on the supramolecular structure of squalenoyled nanoparticlesRetinoblastoma membrane models and their interactions with porphyrin photosensitisers: An infrared microspectroscopy studyA physicochemical study of the morphology of progesterone-loaded microspheres fabricated from poly(D,L-lactide-co-glycolide)Chemically Modified Glucose Oxidase with Enhanced Hydrophobicity: Adsorption at Polystyrene, Silica, and Silica Coated by Lipid MonolayerspH-sensitive liposomes as a carrier for oligonucleotides: a physico-chemical study of the interaction between DOPE and a 15-mer oligonucleotide in excess waterNew bicompartmental structures are observed when stearylamine is mixed with triglyceride emulsionsFactors influencing the oligonucleotides release from O-W submicron cationic emulsionsAdsorption of Hydrophobized Glucose Oxidase at Solution/Air InterfaceLigand interaction with the purified serotonin transporter in solution and at the air/water interfacePhysical aging of progesterone-loaded poly(D,L,-lactide-co-glycolide) microspheresPenetration of Glucose Oxidase and of the Hydrophobically Modified Enzyme into Phospholipid and Cholesterol Monolayers
P50
Q31080262-C432D84A-6C8F-4D3C-AD1E-87F9A381C82DQ31860538-6B7A3137-3DE3-48F7-811F-9A4DCB9D3F31Q37780546-9C164478-3AEB-4655-9D2A-647A9CEF085BQ38023639-A0759413-1553-40E0-BD4C-C340EDB96CFFQ38755874-3F2496B9-AD8E-42F1-84CE-0646F20BF9FFQ39312430-4EFD1C94-4ED1-4805-B680-A590893EE220Q39351779-141BA6F4-03AD-41B0-8B41-8F9423A44BFEQ39696235-9945D945-EACC-4DF0-A9C8-9B7A67EA45EEQ40465892-FB09840C-E710-461F-951F-063876FB4D16Q41013643-584AA320-F5B9-4797-BDDC-5720BAB5435FQ42976257-A73EC4D3-FDB1-4065-BD69-0B1E77AA28ACQ44181782-F15C75F3-72E4-4E6A-883F-FC3AE8506052Q44590006-BFE09353-0903-4FAC-8F2C-A93586E60F66Q45027227-5465274E-78E3-4135-9DE5-FFEF57A31AA7Q45145312-7B66BFFD-54BC-4B5E-AA3C-1E67F22F3F57Q45168146-79897E43-E602-4640-82D1-C2642194D4A1Q45184947-A2BFC233-7522-4D57-A968-3DC3A7398749Q46826315-D707C92E-0456-4AB2-A318-FD90BC66E064Q47292867-AF37F3AD-7AA5-4A91-821F-154DA8CC8F2BQ48053727-87B37999-7FAE-4728-9746-32BB996E6014Q50140392-FC3E196A-BA28-48C0-B5AE-95643A0EDA37Q51483953-335CD435-BD5F-4738-A259-06192636D91AQ52609151-3847B980-C126-4CEA-BD94-38DB287F4A85Q52944985-BD1F8D97-EFFB-4A84-AA38-8D7AA59FFD93Q57798485-70711A17-1BC3-4593-864A-2CCC3420E451Q58605261-C0AAB070-DC82-4477-AC4A-3930C4A547EEQ60083900-E6208273-C733-418A-BE5E-1D30BAF1EACFQ60083914-3246177F-FD17-49B2-BDAA-B82613203D14Q60083922-81850CF6-062E-4337-B5AD-24B4FDF95D78Q61921865-345BF6E9-B887-4C19-9540-48DD2BC1676BQ64044252-D51C64BB-D128-42E0-9ED3-3A3EF05D44AEQ67941229-49443A53-D72F-4BF7-8E19-059798F0150BQ72997394-6A2932DE-E41C-411E-A66D-A1F91D79F319Q73250526-EABEAC71-F234-4BAD-863E-B8F885C1A920Q73364595-6781901C-FAF6-4F95-A0AF-E7FFB6ADC01FQ73413385-93DB37F5-FEC5-423D-B9DF-D3AD0B4231EFQ73552724-A34943E2-C91D-4F33-A71F-08D7F0AF591FQ73666046-095A6096-C339-45E4-BB51-D4D252A75A6FQ74628300-041103E0-43CB-431F-BCAD-8BCB091831B1Q77784777-C8DFF823-E558-41BA-96F9-3527FEE6C58C
P50
description
researcher ORCID ID = 0000-0002-2421-9539
@en
wetenschapper
@nl
name
V Rosilio
@ast
V Rosilio
@en
V Rosilio
@nl
type
label
V Rosilio
@ast
V Rosilio
@en
V Rosilio
@nl
prefLabel
V Rosilio
@ast
V Rosilio
@en
V Rosilio
@nl
P31
P496
0000-0002-2421-9539