All Stories

  1. Influence of Polymer Molecular Weight on Drug–polymer Solubility: A Comparison between Experimentally Determined Solubility in PVP and Prediction Derived from Solubility in Monomer
  2. Investigation of enzyme-sensitive lipid nanoparticles for delivery of siRNA to blood–brain barrier and glioma cells
  3. Evaluation of pharmacokinetic properties and anaesthetic effects of propofol in a new perfluorohexyloctane (F6H8) emulsion in rats – A comparative study
  4. Kolliphor Surfactants Affect Solubilization and Bioavailability of Fenofibrate. Studies of in Vitro Digestion and Absorption in Rats
  5. Evaluation of Drug–Polymer Solubility Curves Through Formal Statistical Analysis: Comparison of Preparation Techniques
  6. Evaluation of the Use of Göttingen Minipigs to Predict Food Effects on the Oral Absorption of Drugs in Humans
  7. Lipophilic prodrugs of apomorphine I: Preparation, characterisation, and in vitro enzymatic hydrolysis in biorelevant media
  8. Combining in vitro and in silico methods for better prediction of surfactant effects on the absorption of poorly water soluble drugs—a fenofibrate case example
  9. The anti-epileptic drug substance vigabatrin inhibits taurine transport in intestinal and renal cell culture models
  10. Computational Investigation of Enthalpy–Entropy Compensation in Complexation of Glycoconjugated Bile Salts with β-Cyclodextrin and Analogs
  11. In vivo and In vitro Evaluations of Intestinal Gabapentin Absorption: Effect of Dose and Inhibitors on Carrier-Mediated Transport
  12. Complexation Thermodynamics of Modified Cyclodextrins: Extended Cavities and Distorted Structures
  13. The solid-state continuum: a perspective on the interrelationships between different solid-state forms in drug substance and drug product
  14. Pharmacokinetic aspects of the anti-epileptic drug substance vigabatrin: focus on transporter interactions
  15. Ex Vivo Correlation of the Permeability of Metoprolol Across Human and Porcine Buccal Mucosa
  16. Determination of the aggregation number for micelles by isothermal titration calorimetry
  17. Fed and fasted state gastro-intestinal in vitro lipolysis: In vitro in vivo relations of a conventional tablet, a SNEDDS and a solidified SNEDDS
  18. Cinnarizine food-effects in beagle dogs can be avoided by administration in a Self Nano Emulsifying Drug Delivery System (SNEDDS)
  19. In vitro models for the prediction of in vivo performance of oral dosage forms
  20. Early pharmaceutical profiling to predict oral drug absorption: Current status and unmet needs
  21. In vivo methods for drug absorption – Comparative physiologies, model selection, correlations with in vitro methods (IVIVC), and applications for formulation/API/excipient characterization including food effects
  22. Intestinal absorption of the antiepileptic drug substance vigabatrin in Göttingen mini-pigs is unaffected by co-administration of amino acids
  23. In Vitro Lipolysis Data Does Not Adequately Predict the In Vivo Performance of Lipid-Based Drug Delivery Systems Containing Fenofibrate
  24. Azone® Decreases the Buccal Mucosal Permeation of Diazepam in a Concentration-Dependent Manner via a Reservoir Effect
  25. Intestinal absorption of the antiepileptic drug substance vigabatrin is altered by infant formula in vitro and in vivo.
  26. Conscious and anaesthetised Göttingen mini-pigs as anin-vivomodel for buccal absorption – pH-dependent absorption of metoprolol from bioadhesive tablets
  27. A study of salt effects on the complexation between β-cyclodextrins and bile salts based on the Hofmeister series
  28. Investigating the correlation between in vivo absorption and in vitro release of fenofibrate from lipid matrix particles in biorelevant medium
  29. The absorptive flux of the anti-epileptic drug substance vigabatrin is carrier-mediated across Caco-2 cell monolayers
  30. Biological conversion of aripiprazole lauroxil − An N-acyloxymethyl aripiprazole prodrug
  31. Buccal absorption of propofol when dosed in 1-perfluorobutylpentane to anaesthetised and conscious Wistar rats and Göttingen mini-pigs
  32. Preparation of an amorphous sodium furosemide salt improves solubility and dissolution rate and leads to a faster Tmax after oral dosing to rats
  33. Bile salts and their importance for drug absorption
  34. Aqueous solubility: Simple predictive methods (in silico, in vitro and bio-relevant approaches)
  35. Use of pharmaceutical salts and cocrystals to address the issue of poor solubility
  36. Lipid-based formulations for oral administration of poorly water-soluble drugs
  37. In vitro, ex vivo and in vivo examination of buccal absorption of metoprolol with varying pH in TR146 cell culture, porcine buccal mucosa and Göttingen minipigs
  38. Extending the hydrophobic cavity of β-cyclodextrin results in more negative heat capacity changes but reduced binding affinities
  39. Determination of stability constants of tauro- and glyco-conjugated bile salts with the negatively charged sulfobutylether-β-cyclodextrin: comparison of affinity capillary electrophoresis and isothermal titration calorimetry and thermodynamic analysis ...
  40. Supersaturated Self-Nanoemulsifying Drug Delivery Systems (Super-SNEDDS) Enhance the Bioavailability of the Poorly Water-Soluble Drug Simvastatin in Dogs
  41. In vitro investigations of α-amylase mediated hydrolysis of cyclodextrins in the presence of ibuprofen, flurbiprofen, or benzo[a]pyrene
  42. Affinity capillary electrophoresis method for investigation of bile salts complexation with sulfobutyl ether-β-cyclodextrin
  43. Characterising Lipid Lipolysis and Its Implication in Lipid-Based Formulation Development
  44. Intestinal Drug Transport via the Proton-Coupled Amino Acid Transporter PAT1 (SLC36A1) Is Inhibited by Gly-X aa Dipeptides
  45. Using resin to generate a non-invasive intestinal bile-depleted rat model was unsuccessful
  46. Thermodynamics of the interaction of γ-cyclodextrin and tauro- and glyco-conjugated bile salts
  47. Influence of bile on the absorption of halofantrine from lipid-based formulations
  48. Higher Order Inclusion Complexes and Secondary Interactions Studied by Global Analysis of Calorimetric Titrations
  49. Rectal Absorption of Vigabatrin, a Substrate of the Proton Coupled Amino Acid Transporter (PAT1, Slc36a1), in Rats
  50. Complexation of tauro- and glyco-conjugated bile salts with α-cyclodextrin and hydroxypropyl-α-cyclodextrin studied by affinity capillary electrophoresis and molecular modelling
  51. Solid state compatibility studies with tablet excipients using non thermal methods
  52. Effect of bile on the oral absorption of halofantrine in polyethylene glycol 400 and polysorbate 80 formulations dosed to bile duct cannulated rats
  53. Oral bioavailability of a poorly aqueous drug from three different SBE7-β-cyclodextrin based formulations in beagle dogs
  54. A novel excipient, 1-perfluorohexyloctane shows limited utility for the oral delivery of poorly water-soluble drugs
  55. Thermodynamics of complexation of tauro- and glyco-conjugated bile salts with two modified β-cyclodextrins
  56. 5-Hydroxy-l-tryptophan alters gaboxadol pharmacokinetics in rats: Involvement of PAT1 and rOat1 in gaboxadol absorption and elimination
  57. Effects of polysorbate 80 on the in-vitro precipitation and oral bioavailability of halofantrine from polyethylene glycol 400 formulations in rats
  58. Use of correction factors in mobility shift affinity capillary electrophoresis for weak analyte - ligand interactions
  59. Thermodynamics and structure of inclusion compounds of tauro- and glyco-conjugated bile salts and β-cyclodextrin
  60. Intestinal lymphatic transport of halofantrine in rats assessed using a chylomicron flow blocking approach: The influence of polysorbate 60 and 80
  61. Effects of acute and chronic aripiprazole treatment on choice between cocaine self-administration and food under a concurrent schedule of reinforcement in rats
  62. Lipid-based Formulations for Danazol Containing a Digestible Surfactant, Labrafil M2125CS: In Vivo Bioavailability and Dynamic In Vitro Lipolysis
  63. Characterization of the complexation of tauro- and glyco-conjugated bile salts with γ-cyclodextrin and 2-hydroxypropyl-γ-cyclodextrin using affinity capillary electrophoresis
  64. Characterization and Physical Stability of Spray Dried Solid Dispersions of Probucol and PVP-K30
  65. Development of simulated intestinal fluids containing nutrients as transport media in the Caco-2 cell culture model: Assessment of cell viability, monolayer integrity and transport of a poorly aqueous soluble drug and a substrate of efflux mechanisms
  66. Complexation of tauro- and glyco-conjugated bile salts with three neutral β-CDs studied by ACE
  67. Food matrices affect the bioavailability of (n−3) polyunsaturated fatty acids in a single meal study in humans
  68. Lymphatic fatty acids in canines dosed with pharmaceutical formulations containing structured triacylglycerols
  69. Effect of different surfactants in biorelevant medium on the secretion of a lipophilic compound in lipoproteins using Caco-2 cell culture
  70. Influence of the Type of Surfactant and the Degree of Dispersion on the Lymphatic Transport of Halofantrine in Conscious Rats
  71. Successful in silico predicting of intestinal lymphatic transfer
  72. Comparison of total oral bioavailability and the lymphatic transport of halofantrine from three different unsaturated triglycerides in lymph-cannulated conscious rats