All Stories

  1. Identification and quantification of glucose degradation products in heat-sterilized glucose solutions for parenteral use by thin-layer chromatography
  2. 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 drug
  3. PermeaLoop™, a novel in vitro tool for small-scale drug-dissolution/permeation studies
  4. Archaeal lipids in oral delivery of therapeutic peptides
  5. Dynamic dissolution-/permeation-testing of nano- and microparticle formulations of fenofibrate
  6. A novel microdialysis-dissolution/permeation system for testing oral dosage forms: A proof-of-concept study
  7. 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
  8. The use of asymmetrical flow field-flow fractionation with on-line detection in the study of drug retention within liposomal nanocarriers and drug transfer kinetics
  9. A new approach for a blood-brain barrier model based on phospholipid vesicles: Membrane development and siRNA-loaded nanoparticles permeability
  10. Solid Phospholipid Dispersions for Oral Delivery of Poorly Soluble Drugs: Investigation Into Celecoxib Incorporation and Solubility-In Vitro Permeability Enhancement
  11. Phospholipid-based solid drug formulations for oral bioavailability enhancement: A meta-analysis
  12. Filter-extruded liposomes revisited: a study into size distributions and morphologies in relation to lipid-composition and process parameters
  13. Liposomes containing lipids from Sulfolobus islandicus withstand intestinal bile salts: An approach for oral drug delivery?
  14. The Effects of Temperature and Growth Phase on the Lipidomes of Sulfolobus islandicus and Sulfolobus tokodaii
  15. Structural characterization of ether lipids from the archaeonSulfolobus islandicusby high-resolution shotgun lipidomics
  16. What Is the Mechanism Behind Increased Permeation Rate of a Poorly Soluble Drug from Aqueous Dispersions of an Amorphous Solid Dispersion?
  17. Multifunctional liposomes for nasal delivery of the anti-Alzheimer drug tacrine hydrochloride
  18. Asymmetrical flow field-flow fractionation with on-line detection for drug transfer studies: a feasibility study
  19. Biopharmaceutical classification of poorly soluble drugs with respect to “enabling formulations”
  20. Physicochemical characterization of liposomes after ultrasound exposure – Mechanisms of drug release
  21. Liposomal formulations of poorly soluble camptothecin: drug retention and biodistribution
  22. Brain delivery of camptothecin by means of solid lipid nanoparticles: Formulation design, in vitro and in vivo studies
  23. The amorphous solid dispersion of the poorly soluble ABT-102 forms nano/microparticulate structures in aqueous medium: impact on solubility
  24. Amorphous solid dispersion enhances permeation of poorly soluble ABT-102: True supersaturation vs. apparent solubility enhancement
  25. Impact of FaSSIF on the solubility and dissolution-/permeation rate of a poorly water-soluble compound
  26. Oral bioavailability of ketoprofen in suspension and solution formulations in rats: the influence of poloxamer 188
  27. Multivariate design for the evaluation of lipid and surfactant composition effect for optimisation of lipid nanoparticles
  28. In vitro models to evaluate the permeability of poorly soluble drug entities: Challenges and perspectives
  29. Application of simulated intestinal fluid on the phospholipid vesicle-based drug permeation assay
  30. Relative Spatial Positions of Tryptophan and Cationic Residues in Helical Membrane-active Peptides Determine Their Cytotoxicity
  31. Effect of the non-ionic surfactant Poloxamer 188 on passive permeability of poorly soluble drugs across Caco-2 cell monolayers
  32. Sonosensitive dioleoylphosphatidylethanolamine-containing liposomes with prolonged blood circulation time of doxorubicin
  33. Compressibility study of quaternary phospholipid blend monolayers
  34. In-vitro permeability of poorly water soluble drugs in the phospholipid vesicle-based permeation assay: the influence of nonionic surfactants
  35. Solubilization of ibuprofen with β-cyclodextrin derivatives: Energetic and structural studies
  36. Lipid membrane composition influences drug release from dioleoylphosphatidylethanolamine-based liposomes on exposure to ultrasound
  37. Ultrasound-mediated destabilization and drug release from liposomes comprising dioleoylphosphatidylethanolamine
  38. Liposomal solubilization of new 3-hydroxy-quinolinone derivatives with promising anticancer activity: a screening method to identify maximum incorporation capacity
  39. Physicochemical properties of lipid nanoparticles: Effect of lipid and surfactant composition
  40. In situ formation of nanoparticles upon dispersion of melt extrudate formulations in aqueous medium assessed by asymmetrical flow field-flow fractionation
  41. In-vitro permeability screening of melt extrudate formulations containing poorly water-soluble drug compounds using the phospholipid vesicle-based barrier
  42. Distearoylphosphatidylethanolamine-based liposomes for ultrasound-mediated drug delivery
  43. Formation of nano/micro-dispersions with improved dissolution properties upon dispersion of ritonavir melt extrudate in aqueous media
  44. Vesicular phospholipid gel-based depot formulations for pharmaceutical proteins: Development and in vitro evaluation
  45. Liposome fractionation and size analysis by asymmetrical flow field-flow fractionation/multi-angle light scattering: influence of ionic strength and osmotic pressure of the carrier liquid
  46. Vesicular Phospholipid Gels
  47. Asymmetric flow field-flow fractionation of liposomes: 2. Concentration detection and adsorptive loss phenomena
  48. Altered Activity and Physicochemical Properties of Short Cationic Antimicrobial Peptides by Incorporation of Arginine Analogues
  49. Asymmetric flow field-flow fractionation of liposomes: optimization of fractionation variables
  50. The Phospholipid Vesicle-Based Drug Permeability Assay: 5. Development Toward an Automated Procedure for High-Throughput Permeability Screening
  51. Drug permeability across a phospholipid vesicle-based barrier
  52. Drug permeability across a phospholipid vesicle based barrier: 3. Characterization of drug–membrane interactions and the effect of agitation on the barrier integrity and on the permeability
  53. Vesicular Phospholipid Gels: A Technology Platform
  54. Liposome Size Analysis by Dynamic/Static Light Scattering upon Size Exclusion-/Field Flow-Fractionation
  55. Drug permeability across a phospholipid vesicle-based barrier
  56. Drug permeability across a phospholipid vesicle based barrier: A novel approach for studying passive diffusion
  57. Development and in vitro evaluation of a liposome based implant formulation for the decapeptide cetrorelix
  58. Camptothecin-catalyzed phospholipid hydrolysis in liposomes
  59. Effect of hydroxypropyl-?-cyclodextrin-complexation and pH on solubility of camptothecin
  60. Cytotoxic effect of different camptothecin formulations on human colon carcinoma in vitro
  61. Development and validation of a HPLC method for routine quantification of the decapeptide Cetrorelix in liposome dispersions
  62. Adsorption of the decapeptide Cetrorelix depends both on the composition of dissolution medium and the type of solid surface
  63. 5-Fluorouracil in vesicular phospholipid gels for anticancer treatment: entrapment and release properties
  64. Pharmacokinetics and antitumor activity of vincristine entrapped in vesicular phospholipid gels
  65. Change in pharmacokinetic and pharmacodynamic behavior of gemcitabine in human tumor xenografts upon entrapment in vesicular phospholipid gels
  66. Filter extrusion of liposomes using different devices: comparison of liposome size, encapsulation efficiency, and process characteristics
  67. Steam sterilisation of vesicular phospholipid gels
  68. Liposomes as drug carriers: a technological approach
  69. Effect of nucleoside analogues and oligonucleotides on hydrolysis of liposomal phospholipids
  70. Erosion and controlled release properties of semisolid vesicular phospholipid dispersions
  71. Preparation and characterization of semi-solid phospholipid dispersions and dilutions thereof
  72. Morphology of semisolid aqueous phosphatidylcholine dispersions, a freeze fracture electron microscopy study
  73. Biodistribution and Computed tomography Blood-Pool Imaging Properties of Polyethylene Glycol-Coated Iopromide-Carrying Liposomes
  74. Liposomes with nifedipine and nifedipine-cyclodextrin complex: calorimetrical and plasma stability comparison
  75. Surface modification of continuously extruded contrast-carrying liposomes: Effect on their physical properties
  76. Generation of contrast-carrying liposomes of defined size with a new continuous high pressure extrusion method
  77. Detection of Lipopolysaccharides in Phospholipids and Liposomes Using the Limulus Test
  78. Acute toxicity and depression of phagocytosis in vivo by liposomes: Influence of lysophosphatidylcholine
  79. Entrapment of haemoglobin into liposomes by the dehydration-rehydration method: vesicle characterization and in vivo behaviour
  80. Large-Scale Production of Liposomes of Defined size by a New Continuous High Pressure Extrusion Device
  81. Preparation of liposomes using a Mini-Lab 8.30 H high-pressure homogenizer
  82. Prozeßüberwachung und Automatisierung bei Hochleistungstablettenpressen
  83. Liposome Preparation by a New High Pressure Homogenizer Gaulin Micron Lab 40
  84. Hemoglobin-Liposomes as Blood Replacement Fluid