about
A novel method for the investigation of liquid/liquid distribution coefficients and interface permeabilities applied to the water-octanol-drug system.Quality by design (QbD) approaches for the compression step of tableting.Phospholipid-based solid drug formulations for oral bioavailability enhancement: A meta-analysis.Oral bioavailability enhancement through supersaturation: an update and meta-analysis.Direct compression behavior of low- and high-methoxylated pectins.New biomimetic barrier Permeapad™ for efficient investigation of passive permeability of drugs.Influence of position and size of substituents on the mechanism of partitioning: a thermodynamic study on acetaminophens, hydroxybenzoic acids, and parabensOn the drug-loading capacity of pectin powder for direct compression.Multivariate analysis of relationships between material properties, process parameters and tablet tensile strength for alpha-lactose monohydrates.The methanol hemisolvate of amiloride hydrochloride.Thermodynamics of solutions. II. Flurbiprofen and diflunisal as models for studying solvation of drug substances.Driving forces and the influence of the buffer composition on the complexation reaction between ibuprofen and HPCD.Thermodynamics of solutions IV: Solvation of ketoprofen in comparison with other NSAIDs.Thermodynamics of sublimation, crystal lattice energies, and crystal structures of racemates and enantiomers: (+)- and (+/-)-ibuprofen.Thermodynamics of solutions III: comparison of the solvation of (+)-naproxen with other NSAIDs.Effect of hydroxypropyl-beta-cyclodextrin-complexation and pH on solubility of camptothecin.Thermodynamics of solubility, sublimation and solvation processes of parabens.On the physical interpretation of the initial bending of a Shapiro-Konopicky-Heckel compression profile.Single step bottom-up process to generate solid phospholipid nano-particles.The difference between partitioning and distribution from a thermodynamic point of view: NSAIDs as an example.Extent and mechanism of solvation and partitioning of isomers of substituted benzoic acids: a thermodynamic study in the solid state and in solution.Thermodynamic study of sublimation, solubility, solvation, and distribution processes of atenolol and pindolol.Effect of degree of methoxylation and particle size on compression properties and compactibility of pectin powders.Simultaneous lipolysis/permeation in vitro model, for the estimation of bioavailability of lipid based drug delivery systems.Evaluation of a dynamic dissolution/permeation model: Mutual influence of dissolution and barrier-flux under non-steady state conditions.Dynamic dissolution-/permeation-testing of nano- and microparticle formulations of fenofibrate.Permeapad™ for investigation of passive drug permeability: The effect of surfactants, co-solvents and simulated intestinal fluids (FaSSIF and FeSSIF).Surfactants enhance recovery of poorly soluble drugs during microdialysis sampling: Implications for in vitro dissolution-/permeation-studies.Mechanism and kinetics of the loss of poorly soluble drugs from liposomal carriers studied by a novel flow field-flow fractionation-based drug release-/transfer-assay.A novel microdialysis-dissolution/permeation system for testing oral dosage forms: A proof-of-concept study.Application of multivariate methods to compression behavior evaluation of directly compressible materials.Influence of tableting forces and lubricant concentration on the adhesion strength in complex layer tablets.pH-independent drug release of an extremely poorly soluble weakly acidic drug from multiparticulate extended release formulations.Co-existing colloidal phases in artificial intestinal fluids assessed by AF4/MALLS and DLS: A systematic study into cholate & (lyso-) phospholipid blends, incorporating celecoxib as a model drugPermeaLoop™, a novel in vitro tool for small-scale drug-dissolution/permeation studiesβ-Cyclodextrin-dextran polymers for the solubilization of poorly soluble drugsA dynamic in vitro permeation study on solid mono- and diacyl-phospholipid dispersions of celecoxibDrug permeability profiling using cell-free permeation tools: Overview and applicationsComparative evaluation of the powder and compression properties of various grades and brands of microcrystalline cellulose by multivariate methodsEvaluation of a rapid approximation method for the elastic recovery of tablets
P50
Q33872366-102E3F34-87CF-4233-B225-E0C3D83D3B8CQ37957958-7B16CD17-F910-4EB3-A81D-6013E53A0587Q38571316-ED38C0B0-8B8B-45A7-8EAC-887B2DE98841Q38917369-DDED1FFF-1987-4A0A-BDF8-15AE88EDC598Q39923942-42E3DFF0-6F74-46FF-B5F2-7ADFEF6E1C57Q41118157-E8D4CBC4-46F0-4058-9748-294BC5EE5FB6Q41818831-1F1AC5E5-BFB0-405D-891B-D88464B817C6Q42181891-0A6645F6-355F-47E2-82CD-DE19B0C54465Q43288013-91445991-FD56-45FD-A649-FF747522ABB2Q43766765-12051985-7202-48E1-A717-16F875248F93Q44542112-60DC8BDE-B7F3-4ADF-8085-24F417F3939FQ44612810-E254330F-7E02-458E-9716-7F416FD12B6FQ44645942-5FA050FD-A170-452F-BBBA-983F8652707BQ44755764-6B2C5278-31F1-4618-AD37-0443A8F2BB7BQ44798381-45E73BED-94C8-442C-BB16-581CDF64A9A7Q45083165-272368C9-5363-4648-8EE0-322545AA13BFQ45207248-2D36D03A-A9AA-422A-BC0C-9009414FCF6BQ46305742-3304EE18-FEAA-45B3-AA0C-3EB137C4C416Q46724408-7420FD8A-3974-4B53-9CF6-DAC11AEC7BDCQ46777567-5A61F76F-A2A8-4BBF-B703-073C87E856F8Q46804507-0F0934D7-E962-4DDF-9523-1CCC2CF3310FQ46957794-575CC994-F920-406D-BDBB-132FD2778E93Q47401701-F63350CB-9B3E-4A75-AEF8-2284FD79F554Q47830388-328A3C29-00D0-4B19-AE2A-FE14DC01E9AFQ47838127-1B8C61FA-0104-49BE-A0A6-AE5FF7EFBB48Q47853923-3D24D466-1761-4C60-8DE5-ABCED8D67AFBQ47919511-D9AE27B7-0A06-465C-A8D3-864F4AF2E00BQ47939137-393231DE-F563-42D2-B1AE-C6F53EE7256BQ50243093-9CC2A4C7-51FD-48C5-B2C5-8010B7A1B6C5Q51748946-22C9C76A-B065-4394-B0EA-59995CE64D1EQ51860009-153D6573-1868-4B0B-80EE-D6B95CC26971Q52112154-03794C2A-F2EE-4C4A-9D1C-CE084B4580FDQ52931055-2E4024A9-0786-4B66-8598-DAF0B1CB9A15Q57113851-28A3D868-45FD-4879-89E4-B351795F9C21Q57621622-CB9F9EDB-BA7C-4926-9318-05FDAA33AB01Q58602394-DCEC33F9-7353-4AFC-8813-12176DE5BA9FQ58610165-C09FD2F9-D015-4338-A3A8-8F9D3EAF2DB9Q59285252-E9DF8832-A7FA-4299-ABF9-0DC1774A9BAAQ59405456-F5FEF131-9498-422F-8636-0272B97B2454Q59405519-8F6990D7-7B6C-43AC-B95A-3F4259E4C4CC
P50
description
hulumtuese
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Annette Bauer-Brandl
@ast
Annette Bauer-Brandl
@en
Annette Bauer-Brandl
@es
Annette Bauer-Brandl
@nl
type
label
Annette Bauer-Brandl
@ast
Annette Bauer-Brandl
@en
Annette Bauer-Brandl
@es
Annette Bauer-Brandl
@nl
prefLabel
Annette Bauer-Brandl
@ast
Annette Bauer-Brandl
@en
Annette Bauer-Brandl
@es
Annette Bauer-Brandl
@nl
P1053
G-8116-2016
P106
P1153
56112594600
P21
P31
P3829
P496
0000-0002-8238-6984