37 results on '"Jannin, Vincent"'
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2. We've come a long, long way together: investigating the fascinating structures and functions of lipid excipients in drug delivery
3. Penetration and Permeation Enhancers for Oral Delivery of Peptides
4. Oral delivery of peptides
5. Lipid-based formulations; solubilizing and super-saturating systems with complex interplay with cell membranes
6. Solidification of liquid self-emulsifying lipid formulations by loading on solid mesoporous carriers
7. Solid State Structural Aspects of Solid Self-microemulsifying Drug Delivery Systems (sSMEDDS) during Digestion
8. Tabletting of solid particles obtained by adsorbing liquid or semi-solid lipid formulations onto inert carriers
9. Formulation of solid self-emulsifying lipid formulations by adsorption on solid carriers
10. Formulation of a self-emulsifying lipid formulation of Nifedipine
11. New Insights into the Stability of SR Lipid Matrix Tablets
12. Formulation of a self-emulsifying lipid formulation of curcumin
13. Establishment of a binary phase diagrams database for the development of self-emulsifying lipid-based formulations
14. SELF formulation protocol: Part II - Excipient selection, diagram design and selection of prototype
15. In vitro lipolysis study of nanoparticulate Delivery systems: Solid Lipid Nanoparticles and Nanostructured Lipid Carriers
16. Influence of intestinal biorelevant fluids on a novel co-culture cell model able to mimic variable permeabilities of the human intestine
17. SELF formulation protocol: Part I - Solubility determination in liquid and solid excipients
18. SELF formulation protocol: Part III - Impact of lipolysis on prototype formulations
19. Characterization of a new self-emulsifying excipient to expand formulation options for poorly soluble drugs: Gelucire® 48/16
20. The LFCS Consortium: 4-Solubilisation of a weak base during in vitro digestion of 8 lipid-based formulations under 3 different conditions
21. The LFCS Consortium: 1 - Effect of saturation level of a neutral drug and a weakly acidic drug on the performance of lipid-based formulations during in vitro digestion
22. Development of a novel co-culture cell model able to mimic variable permeabilities of the human intestine and tolerate biorelevant media
23. The LFCS Consortium: 2-Toward the development of a new performance-based lipid formulation classification system (LFPCS)
24. The LFCS Consortium: 3-Effect of saturation level of a highly lipophilic drug on the performance of lipid-based formulations during in vitro digestion
25. The LFCS Consortium: 1 - Effect of bile salt concentration on in vitro digestion of a range of lipid-based formulations
26. The LFCS Consortium: 4-Effect of formulation surfactants on the extent of in vitro digestion of a range of lipid-based formulations
27. The LFCS Consortium: 2 - Effect of drug saturation level on lipid-based formulation performance during in vitro digestion
28. Preparation of hot-melt extruded supersaturating solid dispersion containing glyceryl dibehenate: Effects on processability, supersaturation and rate of release
29. The LFCS Consortium: 3 - Effect of calcium and pancreatin concentration on in vitro digestion of a range of lipid-based formulations
30. Valorisation des propriétés physico-chimiques et biologiques d’excipients lipidiques destinés à l’administration orale de substances actives
31. Sustained-release lipid matrix with glyceryl behenate – Compritol® 888 ATO
32. Investigation of the surface structure of Gelucire® 44/14 at various humidity by AFM
33. Evaluation of Spray-Congealing to obtain a Solid Self-Emulsifying Drug Delivery System (SEDDS)
34. Pharmaceutical surfactants in biorelevant media: impact on lipolysis and solubility of a poorly soluble compound; Danazol
35. Solubilization of a Poorly Soluble Model Drug During In Vitro Lipolysis of Macrogol Glyceride Surfactants at Fed and Fasted State Conditions
36. Modification of the drug release of ibuprofen by hot-melt coating with mixes of Compritol® 888 ATO and non-ionic surfactants
37. Poloxamers influence the dissolution and stability of lipid matrices of Precirol ATO 5
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