All Stories

  1. Engineering High-Performance Inhalable Monoclonal Antibody Powders via Spray Freeze Drying
  2. Towards a Scalable Production of Staphylococcus epidermidis Extracellular Vesicles: Integration of Stirred-Tank Bioreactor and Ultrafiltration-Based Recovery
  3. Stabilizing Probiotics by Drying: A Review on Processes, Protective Strategies, and Viability Assessment
  4. Modular Design of Vacuum Systems for Lyophilization
  5. Analysis of the Shear Stresses in a Filling Line of Parenteral Products: The Role of Peristaltic Pumping
  6. Molecular Drivers of Self-Assembly in RNA-Loaded lipid nanoparticles Revealed by Coarse-Grained simulations
  7. Continuous lyophilization of suspended vials with per-vial inline analytics
  8. Controlling Mannitol Polymorphism for Enhanced Dispersibility in Spray Freeze-Dried Inhalable Microparticles
  9. Vacuum compatible spring wire system for mass measurement of vials during lyophilization
  10. Mathematical modelling of thermal interactions during freezing: Effects on product morphology and drying behaviour
  11. Turning Down the Inhibition Effect of Silica Gels in Protein Crystallization
  12. The impact of process parameters on the lyophilized porous micro-structure: A case study of dextran
  13. Enhancing Mass Transfer Coefficient Prediction from Field Emission Scanning Electron Microscope Images Through Convolutional Neural Networks and Data Augmentation Techniques
  14. The impact of the stopper position and geometry on the freeze-drying cycle of pharmaceutical products
  15. Analysis of the shear stresses in a filling line of parenteral products: The role of sterilizing filters
  16. Understanding Glucagon Aggregation: In Silico Insights and Experimental Validation
  17. Insights into Thermal Interactions in Frozen Pharmaceutical Vials: Effects on Ice Nucleation Times and Inhibition
  18. A review on micro and nanoengineering in Powder-Based pulmonary drug delivery
  19. Chondroitin sulfate and caseinophosphopeptides doped polyurethane-based highly porous 3D scaffolds for tendon-to-bone regeneration
  20. Shear stress as a driver of degradation for protein-based therapeutics: More accomplice than culprit
  21. Advances in Ascorbic Acid (Vitamin C) Manufacturing: Green Extraction Techniques from Natural Sources
  22. The Freeze-Drying of Pharmaceuticals in Vials Nested in a Rack System—Part II: Primary Drying Behaviour
  23. Tailoring Dry Microparticles for Pulmonary Drug Delivery: Ultrasonic Spray Freeze-Drying with Mannitol and Salbutamol Sulphate
  24. Comparative Studies of Different Preservation Methods and Relative Freeze-Drying Formulations for Extracellular Vesicle Pharmaceutical Applications
  25. New Trends in Freeze-Drying of Pharmaceutical Products
  26. Thermodynamic Modeling and Experimental Data Reveal That Sugars Stabilize Proteins According to an Excluded Volume Mechanism
  27. Mechanistic Investigation of tert-Butanol’s Impact on Biopharmaceutical Formulations: When Experiments Meet Molecular Dynamics
  28. A diffused-interface model for the lyophilization of a packed bed of spray-frozen particles
  29. Analysis of the Shear Stresses in a Filling Line of Parenteral Products: The Role of Fittings
  30. Self-Assembled Monolayers As a Tool to Investigate the Effect of Surface Chemistry on Protein Nucleation
  31. Analysis of the Shear Stresses in a Filling Line of Parenteral Products: The Role of Tubing
  32. On the Use of Temperature Measurements as a Process Analytical Technology (PAT) for the Monitoring of a Pharmaceutical Freeze-Drying Process
  33. Freeze-Drying of Pharmaceuticals in Vials Nested in a Rack System—Part I: Freezing Behaviour
  34. Modernizing Manufacturing of Parenteral Products
  35. Cytotoxicity and Thermal Characterization Assessment of Excipients for the Development of Innovative Lyophilized Formulations for Oncological Applications
  36. A New Transfer Free Energy Based Implicit Solvation Model for the Description of Disordered and Folded Proteins
  37. An Experimental and Modeling Combined Approach in Preparative Hydrophobic Interaction Chromatography
  38. Combining Mathematical Modeling and Thermal Infrared Data in the Freezing of Pharmaceutical Liquid Formulations
  39. Ultrasonic spray freeze-drying of sucrose and mannitol-based formulations: Impact of the atomization conditions on the particle morphology and drying performance
  40. Lipid-Based Nanovesicular Drug Delivery Systems
  41. Use of Microfluidic Capillary Electrophoresis for the Determination of Multi-Component Protein Adsorption Isotherms: Application to High-Throughput Analysis for Hydrophobic Interaction Chromatography
  42. Surface Treatment of Glass Vials for Lyophilization: Implications for Vacuum-Induced Surface Freezing
  43. Investigation of the Freezing Phenomenon in Vials Using an Infrared Camera
  44. Alginate Nanohydrogels as a Biocompatible Platform for the Controlled Release of a Hydrophilic Herbicide
  45. Effect of Polymerization Time on the Binding Properties of Ciprofloxacin-Imprinted nanoMIPs Prepared by Solid-Phase Synthesis
  46. Force Field Parameterization for the Description of the Interactions between Hydroxypropyl-β-Cyclodextrin and Proteins
  47. In-Line Monitoring of the Freeze-Drying Process by Means of Heat Flux Sensors
  48. The Role of Cyclodextrins against Interface-Induced Denaturation in Pharmaceutical Formulations: A Molecular Dynamics Approach
  49. Tuning Transport Phenomena in Agarose Gels for the Control of Protein Nucleation Density and Crystal Form
  50. Role of Self-Assembled Surface Functionalization on Nucleation Kinetics and Oriented Crystallization of a Small-Molecule Drug: Batch and Thin-Film Growth of Aspirin as a Case Study
  51. Enhancing the preservation of liposomes: The role of cryoprotectants, lipid formulations and freezing approaches
  52. Economic Analysis of a Freeze-Drying Cycle
  53. ADD Force Field for Sugars and Polyols: Predicting the Additivity of Protein–Osmolyte Interaction
  54. Agarose Gel as a Medium for Growing and Tailoring Protein Crystals
  55. General and adaptive synthesis protocol for high-quality organosilane self-assembled monolayers as tunable surface chemistry platforms for biochemical applications
  56. Spray Freeze-Drying as a Solution to Continuous Manufacturing of Pharmaceutical Products in Bulk
  57. Automatic control of a freeze-drying process: Detection of the end point of primary drying
  58. A model-based approach for the rational design of the freeze-thawing of a protein-based formulation
  59. Heightened Cold-Denaturation of Proteins at the Ice–Water Interface
  60. Impact of Controlled Vacuum Induced Surface Freezing on the Freeze Drying of Human Plasma
  61. Synthesis of high payload nanohydrogels for the ecapsulation of hydrophilic molecules via inverse miniemulsion polymerization: caffeine as a case study
  62. From Batch to Continuous: Freeze-Drying of Suspended Vials for Pharmaceuticals in Unit-Doses
  63. Tuning, measurement and prediction of the impact of freezing on product morphology: A step toward improved design of freeze-drying cycles
  64. Supporting data and methods for the multi-scale modelling of freeze-drying of microparticles in packed-beds
  65. A multi-scale computational framework for modeling the freeze-drying of microparticles in packed-beds
  66. Process intensification and process control in freeze-drying
  67. Effect of Surfactants on Surface-Induced Denaturation of Proteins: Evidence of an Orientation-Dependent Mechanism
  68. Looking inside the ‘black box’: Freezing engineering to ensure the quality of freeze-dried biopharmaceuticals
  69. Surface-induced crystallization of pharmaceuticals and biopharmaceuticals: A review
  70. Surfactants as stabilizers for biopharmaceuticals: An insight into the molecular mechanisms for inhibition of protein aggregation
  71. Vacuum Induced Surface Freezing as an effective method for improved inter- and intra-vial product homogeneity
  72. The Preservation of Lyophilized Human Growth Hormone Activity: how Do Buffers and Sugars Interact?
  73. Process analytical technology for monitoring pharmaceuticals freeze-drying – A comprehensive review
  74. Measuring and predicting pore size distribution of freeze-dried solutions
  75. Water entrapment and structure ordering as protection mechanisms for protein structural preservation
  76. Clarifying the role of cryo- and lyo-protectants in the biopreservation of proteins
  77. Inclusion complexes dispersed in polystyrene-based labels for fruit ripening on demand
  78. Stability of Proteins in Carbohydrates and Other Additives during Freezing: The Human Growth Hormone as a Case Study
  79. Prediction of product morphology of lyophilized drugs in the case of Vacuum Induced Surface Freezing
  80. Prediction of Ice Crystal Size Distribution after Freezing of Pharmaceutical Solutions
  81. Impact of vacuum-induced surface freezing on inter- and intra-vial heterogeneity
  82. Non-Invasive Temperature Monitoring in Freeze Drying: Control of Freezing as a Case Study
  83. Computer-Aided Framework for the Design of Freeze-Drying Cycles: Optimization of the Operating Conditions of the Primary Drying Stage
  84. Wavelet image decomposition for characterization of freeze-dried pharmaceutical product structures
  85. Effect of Electron Beam Irradiation on Remaining Activity of Lyophilized Acid Phosphatase with Water-Binding and Non-Water–Binding Additives
  86. Vacuum-Induced Nucleation as a Method for Freeze-Drying Cycle Optimization
  87. Tailoring of Bone Scaffold Properties Using Silicate/Phosphate Glass Mixtures
  88. A New Method Based on the Regression of Step Response Data for Monitoring a Freeze-Drying Cycle
  89. Characterization of freeze-dried pharmaceutical product structures by an FFT-imaging approach
  90. Real-time temperature monitoring in pharmaceutical freeze-drying
  91. Sputtered thermocouple array for vial temperature mapping
  92. Applying quality-by-design to develop a coffee freeze-drying process
  93. Intensification of Freeze‐Drying for the Pharmaceutical and Food Industries
  94. Freeze-drying of enzymes in case of water-binding and non-water-binding substrates
  95. Quality by Design: Scale-Up of Freeze-Drying Cycles in Pharmaceutical Industry
  96. In-Line and Off-Line Optimization of Freeze-Drying Cycles for Pharmaceutical Products
  97. Quality by design: optimization of a freeze-drying cycle via design space in case of heterogeneous drying behavior and influence of the freezing protocol
  98. Model-Based Framework for the Analysis of Failure Consequences in a Freeze-Drying Process
  99. Quality by Design in the Secondary Drying Step of a Freeze-Drying Process
  100. A Model-Based Framework to Optimize Pharmaceuticals Freeze Drying
  101. Innovation in Monitoring Food Freeze Drying
  102. Advanced approach to build the design space for the primary drying of a pharmaceutical freeze‐drying process
  103. Heat Transfer in Freeze-Drying Apparatus
  104. Freeze-Drying Cycle Optimization Using Model Predictive Control Techniques
  105. Monitoring of the Secondary Drying in Freeze-Drying of Pharmaceuticals
  106. On the Methods Based on the Pressure Rise Test for Monitoring a Freeze-Drying Process
  107. In-Line Optimization and Control of an Industrial Freeze-Drying Process for Pharmaceuticals
  108. Model-Based Monitoring and Control of Industrial Freeze-Drying Processes: Effect of Batch Nonuniformity
  109. In-line control of the lyophilization process. A gentle PAT approach using software sensors
  110. Freeze Drying of Pharmaceutical Excipients Close to Collapse Temperature: Influence of the Process Conditions on Process Time and Product Quality
  111. On the Design of an In-Line Control System for a Vial Freeze-Drying Process: The Role of Chamber Pressure
  112. Monitoring of the primary drying of a lyophilization process in vials
  113. Observer design for the Selective Catalytic Reduction of NO in a loop reactor