All Stories

  1. Early assessment of bulk powder processability as a part of solid form screening
  2. The use of molecular descriptors in the development of co-amorphous formulations
  3. Ribbon density and milling parameters that determine fines fraction in a dry granulation
  4. Additive manufacturing of prototype elements with process interfaces for continuously operating manufacturing lines
  5. Quantification of microwave-induced amorphization of celecoxib in PVP tablets using transmission Raman spectroscopy
  6. Role of Solvent Selection on Crystal Habit of 5-Aminosalicylic Acid—Combined Experimental and Computational Approach
  7. Transforming nanomedicine manufacturing toward Quality by Design and microfluidics
  8. Characterisation of pore structures of pharmaceutical tablets: A review
  9. Ciprofloxacin-loaded sodium alginate/poly (lactic-co-glycolic acid) electrospun fibrous mats for wound healing
  10. Toward quality assessment of 3D printed oral dosage forms
  11. Multivariate Analysis Supporting Pharmaceutical Research
  12. QR encoded smart oral dosage forms by inkjet printing
  13. The effect of HPMC and MC as pore formers on the rheology of the implant microenvironment and the drug release in vitro
  14. Anti-tuberculosis drug combination for controlled oral delivery using 3D printed compartmental dosage forms: From drug product design to in vivo testing
  15. Investigation of factors affecting the stability of lysozyme spray dried from ethanol-water solutions
  16. Using 3D Printing for Rapid Prototyping of Characterization Tools for Investigating Powder Blend Behavior
  17. An experimental evaluation of powder flow predictions in small-scale process equipment based on Jenike's hopper design methodology
  18. Melt Extrusion of High-Dose Co-Amorphous Drug-Drug Combinations
  19. Continuous Manufacturing of Pharmaceuticals
  20. Tracking Dehydration Mechanisms in Crystalline Hydrates with Molecular Dynamics Simulations
  21. Cardiac vagal tone, a non-invasive measure of parasympathetic tone, is a clinically relevant tool in Type 1 diabetes mellitus
  22. The flow properties and presence of crystals in drug-polymer mixtures: Rheological investigation combined with light microscopy
  23. The effect of poly (lactic-co-glycolic) acid composition on the mechanical properties of electrospun fibrous mats
  24. Drivers for a Change - Manufacturing of Future Medicines for Personalized Drug Therapies
  25. Dehydration of Nitrofurantoin Monohydrate during Melt Extrusion
  26. Investigation of nanocarriers and excipients for preparation of nanoembedded microparticles
  27. Correlation between calculated molecular descriptors of excipient amino acids and experimentally observed thermal stability of lysozyme
  28. Printing medicine: New technique and its impact on society
  29. Downstream Processability of Crystal Habit-Modified Active Pharmaceutical Ingredient
  30. High-Throughput Fabrication of Nanocomplexes Using 3D-Printed Micromixers
  31. Visualization and Non-Destructive Quantification of Inkjet-Printed Pharmaceuticals on Different Substrates Using Raman Spectroscopy and Raman Chemical Imaging
  32. The evaluation of physical properties of injection molded systems based on poly(ethylene oxide) (PEO)
  33. Unveiling multiple solid-state transitions in pharmaceutical solid dosage forms using multi-series hyperspectral imaging and different curve resolution approaches
  34. Electrospinnability of Poly Lactic-co-glycolic Acid (PLGA): the Role of Solvent Type and Solvent Composition
  35. Professor Peter York—A Distinguished Career in Powders, Processing, and Particle Design
  36. Computational Dehydration of Crystalline Hydrates Using Molecular Dynamics Simulations
  37. Chitosan-Based Nano-Embedded Microparticles: Impact of Nanogel Composition on Physicochemical Properties
  38. Analysis of 3D Prints by X-ray Computed Microtomography and Terahertz Pulsed Imaging
  39. Social aspects in additive manufacturing of pharmaceutical products
  40. Near-infrared chemical imaging (NIR-CI) of 3D printed pharmaceuticals
  41. Effect of ethanol as a co-solvent on the aerosol performance and stability of spray-dried lysozyme
  42. Colorimetry as Quality Control Tool for Individual Inkjet-Printed Pediatric Formulations
  43. Process optimization of dry granulation based tableting line: Extracting physical material characteristics from granules, ribbons and tablets using near-IR (NIR) spectroscopic measurement
  44. Analytical method development for powder characterization: Visualization of the critical drug loading affecting the processability of a formulation for direct compression
  45. Modifying release characteristics from 3D printed drug-eluting products
  46. Multispectral UV imaging for fast and non-destructive quality control of chemical and physical tablet attributes
  47. Strategic framework for education and training in Quality by Design (QbD) and process analytical technology (PAT)
  48. Preface of EuPAT 7 Special Issue - Inventing Tomorrow’s Development and Manufacturing
  49. Properties of the Sodium Naproxen-Lactose-Tetrahydrate Co-Crystal upon Processing and Storage
  50. In silico product design of pharmaceuticals
  51. Anhydrate to hydrate solid-state transformations of carbamazepine and nitrofurantoin in biorelevant media studied in situ using time-resolved synchrotron X-ray diffraction
  52. Oscillatory Shear Rheology in Examining the Drug-Polymer Interactions Relevant in Hot Melt Extrusion
  53. The Future of Pharmaceutical Manufacturing Sciences
  54. Rapid Assessment of Tablet Film Coating Quality by Multispectral UV Imaging
  55. Rheology as a tool for evaluation of melt processability of innovative dosage forms
  56. Image Analytical Approach for Needle-Shaped Crystal Counting and Length Estimation
  57. Detecting Blending End-Point Using Mean Squares Successive Difference Test and Near-Infrared Spectroscopy
  58. Raman spectroscopy in pharmaceutical product design
  59. Near-infrared chemical imaging (NIR-CI) as a process monitoring solution for a production line of roll compaction and tableting
  60. Monitoring of multiple solid-state transformations at tablet surfaces using multi-series near-infrared hyperspectral imaging and multivariate curve resolution
  61. Visualization and prediction of porosity in roller compacted ribbons with near-infrared chemical imaging (NIR-CI)
  62. Three-Dimensional Printing of Drug-Eluting Implants: Preparation of an Antimicrobial Polylactide Feedstock Material
  63. Raman Mapping of Mannitol/Lysozyme Particles Produced Via Spray Drying and Single Droplet Drying
  64. Chemical imaging and solid state analysis at compact surfaces using UV imaging
  65. Processing-induced salt formation of two oxicams in solid dosage forms affects dissolution behavior and chemical degradation
  66. Evaluation of ring shear testing as a characterization method for powder flow in small-scale powder processing equipment
  67. Near‐Infrared Imaging for High‐Throughput Screening of Moisture Induced Changes in Freeze‐Dried Formulations
  68. Structural basis for the transformation pathways of the sodium naproxen anhydrate–hydrate system
  69. In situ monitoring of hydration and dehydration in pharmaceutical solids
  70. Industrial Crystallization
  71. Crystallization of Piroxicam Solid Forms and the Effects of Additives
  72. Designing Printable Medicinal Products: Solvent System and Carrier-Substrate Screening
  73. Influence of raw material properties upon critical quality attributes of continuously produced granules and tablets
  74. Modulating Protein Release Profiles by Incorporating Hyaluronic Acid into PLGA Microparticles Via a Spray Dryer Equipped with a 3-Fluid Nozzle
  75. Simultaneous UV Imaging and Raman Spectroscopy for the Measurement of Solvent-Mediated Phase Transformations During Dissolution Testing
  76. Miniaturized Approach for Excipient Selection During the Development of Oral Solid Dosage Form
  77. One-Step Production of Protein-Loaded PLGA Microparticles via Spray Drying Using 3-Fluid Nozzle
  78. Current Advances and Future Trends in Characterizing Poorly Water-soluble Drugs Using Spectroscopic, Imaging and Data Analytical Techniques
  79. Application of Spray-drying and Electrospraying/Electospinning for Poorly Watersoluble Drugs: A Particle Engineering Approach
  80. Well-plate freeze-drying: a high throughput platform for screening of physical properties of freeze-dried formulations
  81. Fuzzy Logic-Based Expert System for Evaluating Cake Quality of Freeze-Dried Formulations
  82. Intestinal mucosa permeability following oral insulin delivery using core shell corona nanolipoparticles
  83. Investigation of the phase separation of PNIPAM using infrared spectroscopy together with multivariate data analysis
  84. Evaluating the effect of coating equipment on tablet film quality using terahertz pulsed imaging
  85. Dissolution study of nanocrystal powders of a poorly soluble drug by UV imaging and channel flow methods
  86. High-shear granulation as a manufacturing method for cocrystal granules
  87. Tailored beads made of dissolved cellulose—Investigation of their drug release properties
  88. Characterization of spray dried bioadhesive metformin microparticles for oromucosal administration
  89. Structures of cefradine dihydrate and cefaclor dihydrate from DFT-D calculations
  90. A Step Toward Development of Printable Dosage Forms for Poorly Soluble Drugs
  91. Impact of PLGA molecular behavior in the feed solution on the drug release kinetics of spray dried microparticles
  92. Detecting phase separation of freeze-dried binary amorphous systems using pair-wise distribution function and multivariate data analysis
  93. Real-time in vitro dissolution of 5-aminosalicylic acid from single ethyl cellulose coated extrudates studied by UV imaging
  94. A high throughput platform for understanding the influence of excipients on physical and chemical stability
  95. Process development for spray drying of sticky pharmaceuticals; case study of bioadhesive nicotine microparticles for compressed medicated chewing gum
  96. Interpreting the Disordered Crystal Structure of Sodium Naproxen Tetrahydrate
  97. Engineering of an Inhalable DDA/TDB Liposomal Adjuvant: A Quality-by-Design Approach Towards Optimization of the Spray Drying Process
  98. Foreign matter identification from solid dosage forms
  99. Towards Better Process Understanding: Chemometrics and Multivariate Measurements in Manufacturing of Solid Dosage Forms
  100. Designing CAF-adjuvanted dry powder vaccines: Spray drying preserves the adjuvant activity of CAF01
  101. Excipients-Induced Salt-to-Free Base Phase Transformation
  102. The influence of lysozyme on mannitol polymorphism in freeze-dried and spray-dried formulations depends on the selection of the drying process
  103. Fast-track to A Solid Dispersion Formulation Using Multi-way Analysis of Complex Interactions
  104. Dissolution testing of amorphous solid dispersions
  105. A New Approach to Dissolution Testing by UV Imaging and Finite Element Simulations
  106. A case study of real-time monitoring of solid-state phase transformations in acoustically levitated particles using near infrared and Raman spectroscopy
  107. Critical Solvent Properties Affecting the Particle Formation Process and Characteristics of Celecoxib-Loaded PLGA Microparticles via Spray-Drying
  108. Evaluation of droplet size distributions using univariate and multivariate approaches
  109. Rapid Insight into Heating-Induced Phase Transformations in the Solid State of the Calcium Salt of Atorvastatin Using Multivariate Data Analysis
  110. Real-time dissolution behavior of furosemide in biorelevant media as determined by UV imaging
  111. Complementing High-Throughput X-ray Powder Diffraction Data With Quantum–Chemical Calculations: Application to Piroxicam Form III
  112. Disproportionation of the calcium salt of atorvastatin in the presence of acidic excipients
  113. Exploring the Solid-Form Landscape of Pharmaceutical Hydrates: Transformation Pathways of the Sodium Naproxen Anhydrate-Hydrate System
  114. Strategic funding priorities in the pharmaceutical sciences allied to Quality by Design (QbD) and Process Analytical Technology (PAT)
  115. Structural Elucidation of Rapid Solution-Mediated Phase Transitions in Pharmaceutical Solids Using in Situ Synchrotron SAXS/WAXS
  116. A novel image analysis methodology for online monitoring of nucleation and crystal growth during solid state phase transformations
  117. Solvent-mediated amorphous-to-crystalline transformation of nitrendipine in amorphous particle suspensions containing polymers
  118. Insight into the solubility and dissolution behavior of piroxicam anhydrate and monohydrate forms
  119. Process-induced phase transformations in a pharmaceutically relevant salt-free form system
  120. Polymorphic form of piroxicam influences the performance of amorphous material prepared by ball-milling
  121. Crystal Morphology Modification by the Addition of Tailor-Made Stereocontrolled Poly(N-isopropyl acrylamide)
  122. Behaviour of HPMC compacts investigated using UV-imaging
  123. Role of Excipients on Solid-State Properties of Piroxicam During Processing
  124. Atomic Pairwise Distribution Function Analysis of the Amorphous Phase Prepared by Different Manufacturing Routes
  125. Design space approach in the optimization of the spray-drying process
  126. Influence of solvent evaporation rate and formulation factors on solid dispersion physical stability
  127. Investigations on the effect of different cooling rates on the stability of amorphous indomethacin
  128. Assessment of crystalline disorder in cryo-milled samples of indomethacin using atomic pair-wise distribution functions
  129. Particle size dependence of polymorphism in spray-dried mannitol
  130. 4th BBBB International Conference on Pharmaceutical Sciences
  131. Monitoring lidocaine single‐crystal dissolution by ultraviolet imaging
  132. Polymer-Mediated Anti-solvent Crystallization of Nitrendipine: Monodispersed Spherical Crystals and Growth Mechanism
  133. Investigation of Solid Phase Composition on Tablet Surfaces by Grazing Incidence X-ray Diffraction
  134. Rapid Solid-State Analysis of Freeze-Dried Protein Formulations Using NIR and Raman Spectroscopies
  135. X-ray powder diffractometry in combination with principal component analysis – A tool for monitoring solid state changes
  136. Phase Transformations of Amlodipine Besylate Solid Forms
  137. Insights into the Early Dissolution Events of Amlodipine Using UV Imaging and Raman Spectroscopy
  138. Perspective on Water of Crystallization Affecting the Functionality of Pharmaceuticals
  139. Behaviour of stereoblock poly(N-isopropyl acrylamide) in acetone–water mixtures
  140. Stabilization of liposomes during drying
  141. Quality by design approach in the optimization of the spray-drying process
  142. Building the quality into pellet manufacturing environment – Feasibility study and validation of an in-line quantitative near infrared (NIR) method
  143. Solid Forms of Amlodipine Besylate: Physicochemical, Structural, and Thermodynamic Characterization
  144. The influence of thermal history on the physical behavior of poly(ethylene glycol) (PEG)
  145. Factors affecting crystallization of hydrates
  146. Influence of Temperature on Solvent-Mediated Anhydrate-to-Hydrate Transformation Kinetics
  147. Towards Effective Solid Form Screening
  148. Integrated Approach to Study the Dehydration Kinetics of Nitrofurantoin Monohydrate
  149. Towards a robust water content determination of freeze-dried samples by near-infrared spectroscopy
  150. A Novel Hybrid Chromatography−Crystallization Process for the Isolation and Purification of a Natural Pharmaceutical Ingredient from a Medicinal Herb
  151. Chromatography-Crystallization Hybrid Process for Artemisinin Purification from Artemisia annua
  152. Insight into Crystallization Mechanisms of Polymorphic Hydrate Systems
  153. Classification of lyophilised mixtures using multivariate analysis of NIR spectra
  154. Crystallization of a polymorphic hydrate system
  155. Building quality into a coating process
  156. An insight into water of crystallization during processing using vibrational spectroscopy
  157. Structural Characterisation and Dehydration Behaviour of Siramesine Hydrochloride
  158. Building quality into a coating process
  159. Enhanced dissolution rate and synchronized release of drugs in binary systems through formulation: Amorphous naproxen–cimetidine mixtures prepared by mechanical activation
  160. Role of excipients in the quantification of water in lyophilised mixtures using NIR spectroscopy
  161. Increasing Process Understanding by Analyzing Complex Interactions in Experimental Data
  162. Mechanistic insight into the evaporative crystallization of two polymorphs of nitrofurantoin monohydrate
  163. Solvent-Mediated Solid Phase Transformations of cArbamazepine: Effects of Simulated Intestinal Fluid and Fasted State Simulated Intestinal Fluid
  164. Effects of Polymer Additives on the Crystallization of Hydrates: A Molecular-Level Modulation
  165. Crystal Morphology Engineering of Pharmaceutical Solids: Tabletting Performance Enhancement
  166. Solid form screening – A review
  167. Influence of the Solid Form of Siramesine Hydrochloride on its Behavior in Aqueous Environments
  168. NIR transmission spectroscopy for rapid determination of lipid and lyoprotector content in liposomal vaccine adjuvant system CAF01
  169. Simultaneous measurement of liquid-phase and solid-phase transformation kinetics in rotating disc and channel flow cell dissolution devices
  170. Editorial
  171. Establishing quantitative in-line analysis of multiple solid-state transformations during dehydration
  172. Erratum: Solvent subset selection for polymorph screening
  173. Hydroxypropyl Methylcellulose-Controlled Crystallization of Erythromycin A Dihydrate Crystals with Modified Morphology
  174. Near-Infrared Spectroscopy for Cocrystal Screening. A Comparative Study with Raman Spectroscopy
  175. Phase Transformation of Erythromycin A Dihydrate During Fluid Bed Drying
  176. Toward an Understanding of the Factors Influencing Anhydrate-to-Hydrate Transformation Kinetics in Aqueous Environments
  177. Solvent Diversity in Polymorph Screening
  178. Building the quality into manufacturing of macromolecular systems
  179. Identifying sources of batch to batch variation in processability
  180. Solvent subset selection for polymorph screening
  181. Investigating Dehydration from Compacts Using Terahertz Pulsed, Raman, and Near-Infrared Spectroscopy
  182. Implementation of a Process Analytical Technology System in a Freeze-Drying Process Using Raman Spectroscopy for In-Line Process Monitoring
  183. Solid‐state properties and relationship between anhydrate and monohydrate of baclofen
  184. Comparison of vibrational spectroscopy techniques to investigate the dehydration behaviour of piroxicam monohydrate from compacts
  185. HPMC-controlled crystallization of erythromycin A dihydrate with improved compaction properties
  186. Insight into the metastable form of theophylline monohydrate using vibrational spectroscopy, computational chemistry and multivariate analysis
  187. Solid-state transformation of erythromycin A dihydrate during drying monitored by near infrared spectroscopy
  188. Phase transformations of erythromycin A dihydrate during pelletisation and drying
  189. Qualitative in situ analysis of multiple solid‐state forms using spectroscopy and partial least squares discriminant modeling
  190. Hyphenated spectroscopy as a polymorph screening tool
  191. Drug hydrate systems and dehydration processes studied by terahertz pulsed spectroscopy
  192. Influence of Polymorphic Form, Morphology, and Excipient Interactions on the Dissolution of Carbamazepine Compacts
  193. Characterisation of blends of paracetamol and citric acid
  194. Process analytical applications of Raman spectroscopy
  195. Determination of amorphous content in the pharmaceutical process environment
  196. Raman spectroscopy for quantitative analysis of pharmaceutical solids
  197. In-line monitoring of solid-state transitions during fluidisation
  198. In Situ Measurement of Solvent-Mediated Phase Transformations During Dissolution Testing
  199. Dynamic PCA-based MSPC charts for nucleation prediction in batch cooling crystallization processes
  200. Crystallization of glycine with ultrasound
  201. Solvent-Mediated Phase Transformation Kinetics of an Anhydrate/Hydrate System
  202. Understanding processing-induced phase transformations in erythromycin–PEG 6000 solid dispersions
  203. Monitoring tablet surface roughness during the film coating process
  204. Multivariate data analysis as a fast tool in evaluation of solid state phenomena
  205. Insight into Thermally Induced Phase Transformations of Erythromycin A Dihydrate
  206. Role of Water in the Physical Stability of Solid Dosage Formulations
  207. Physical changes of β-sitosterol crystals in oily suspensions during heating
  208. Characterization of polymorphic solid-state changes using variable temperature X-ray powder diffraction
  209. Improved Understanding of Factors Contributing to Quantification of Anhydrate/Hydrate Powder Mixtures
  210. DRIFT-IR for quantitative characterization of polymorphic composition of sulfathiazole
  211. Excipient selection can significantly affect solid-state phase transformation in formulation during wet granulation
  212. IR spectroscopy together with multivariate data analysis as a process analytical tool for in-line monitoring of crystallization process and solid-state analysis of crystalline product
  213. Pellet manufacturing by extrusion-spheronization using process analytical technology
  214. Batch cooling crystallization and pressure filtration of sulphathiazole: the influence of solvent composition
  215. Use of roughness maps in visualisation of surfaces
  216. Use of In-Line Near-Infrared Spectroscopy in Combination with Chemometrics for Improved Understanding of Pharmaceutical Processes
  217. Static electrification of powders during spray drying
  218. Comparison of torque measurements and near-infrared spectroscopy in characterization of a wet granulation process
  219. Role of excipients in hydrate formation kinetics of theophylline in wet masses studied by near-infrared spectroscopy
  220. Visualization of a Pharmaceutical Unit Operation:  Wet Granulation
  221. Physical stability and moisture sorption of aqueous chitosan–amylose starch films plasticized with polyols
  222. Comparison of the effects of two drying methods on polymorphism of theophylline
  223. The Characterization of Fluidization Behavior Using a Novel Multichamber Microscale Fluid Bed
  224. New Perspectives for Visual Characterization of Pharmaceutical Solids
  225. Dehydration Studies Using a Novel Multichamber Microscale Fluid Bed Dryer with In‐Line Near‐Infrared Measurement
  226. Polymorph Screening Using Near-Infrared Spectroscopy
  227. Optimizing the crystal size and habit of β-sitosterol in suspension
  228. Development and characterization of aqueous amylose-rich maize starch dispersion for film formation
  229. Physical stability of a microcrystalline β-sitosterol suspension in oil
  230. Tablet surface characterisation by various imaging techniques
  231. Effects of Excipients on Hydrate Formation in Wet Masses Containing Theophylline
  232. Electrostatic measurements on a miniaturized fluidized bed
  233. Development of an automation system for a tablet coater
  234. Visualization of particle size and shape distributions using self-organizing maps
  235. A novel method of producing a microcrystalline β-sitosterol suspension in oil
  236. Process analysis of fluidized bed granulation
  237. In-line moisture measurement during granulation with a four-wavelength near-infrared sensor: an evaluation of process-related variables and a development of non-linear calibration model
  238. Novel Identification of Pseudopolymorphic Changes of Theophylline During Wet Granulation Using Near Infrared Spectroscopy
  239. Visualization of fluid-bed granulation with self-organizing maps
  240. Characterization of Wet Massing Behavior of Silicified Microcrystalline Cellulose and α-Lactose Monohydrate Using Near-Infrared Spectroscopy
  241. Near infrared reflectance spectroscopy for the fast identification of PVC-based films
  242. Prediction of aqueous solubility for a diverse set of organic compounds based on atom-type electrotopological state indices
  243. In-line moisture measurement during granulation with a four-wavelength near infrared sensor: an evaluation of particle size and binder effects
  244. Next generation fluidized bed granulator automation
  245. Next generation fluidized bed granulator automation
  246. Use of the Near-Infrared Reflectance Method for Measurement of Moisture Content During Granulation
  247. On-line monitoring of moisture content in an instrumented fluidized bed granulator with a multi-channel NIR moisture sensor