All Stories

  1. N-Nitrosation in the absence of nitrosating agents in pharmaceuticals?
  2. Nitrites as precursors of N-nitrosation in pharmaceutical samples – A trace level analysis
  3. The determination of two analogues of 4-(azidomethyl)-1,1'-biphenyl as potential genotoxic impurities in the active pharmaceutical ingredient of several sartans containing a tetrazole group
  4. Analytical quality by design in the development of a solvent-modified micellar electrokinetic chromatography method for the determination of sitagliptin and its related compounds
  5. Separation of pharmaceutically active compounds by multimodal chromatography with ultraviolet detection
  6. Insight into the formation of N-nitrosodimethylamine in metformin products
  7. HILIC-MS determination of dimethylamine in the active pharmaceutical ingredients and in the dosage forms of metformin
  8. Development of HPLC Method for the Purity Test by Design of Experiments and Determination of Activation Energy of Hydrolytic Degradation Reactions of Sofosbuvir
  9. Detection and structure elucidation of the new degradation impurities in the pharmaceutical formulations of ruxolitinib hydrobromide
  10. Supercritical fluid chromatography in chiral separations: Evaluation of equivalency of polysaccharide stationary phases
  11. Quality by Design as a risk-based strategy in pharmaceutical analysis: Development of a liquid chromatography-tandem mass spectrometry method for the determination of nintedanib and its impurities
  12. Enantioseparation of N-acetyl-dl-cysteine as o-phtaldialdehyde derivatives obtained with various primary aliphatic amine additives on polysaccharide-based chiral stationary phases
  13. Chiral separation of aliphatic primary amino alcohols as o -phthaldialdehyde/mercaptoethanol derivatives on polysaccharide-based chiral stationary phases
  14. HPLC/UV/MS method application for the separation of obeticholic acid and its related compounds in development process and quality control
  15. 1H-Tetrazole-5-amine Immobilized on Substituted Polymer Gel/Silica as a New Stationary Phase for Hydrophilic Interaction Chromatography
  16. Separation of structurally related primary aliphatic amines using hydrophilic interaction chromatography with fluorescence detection after postcolumn derivatization with o -phthaldialdehyde/mercaptoethanol
  17. Esterification of Ibuprofen in Soft Gelatin Capsules Formulations—Identification, Synthesis and Liquid Chromatography Separation of the Degradation Products
  18. Enantiomeric Separation of (R,S)-Aclidinium Bromide with Negatively Charged Gamma-Cyclodextrin by CE
  19. General screening and optimization strategy for fast chiral separations in modern supercritical fluid chromatography
  20. A novel approach for HPLC determination of 2-cynaoacetamide using derivatization procedure with 2-hydroxyacetophenone as a new useful derivatization reagent
  21. Optimization ofo-phtaldialdehyde/2-mercaptoethanol postcolumn reaction for the hydrophilic interaction liquid chromatography determination of memantine utilizing a silica hydride stationary phase
  22. Quality by Design-Guided Development of a Capillary Electrophoresis Method for the Chiral Purity Determination of Ambrisentan
  23. Utilization of Photochemically Induced Fluorescence Detection for HPLC Determination of Genotoxic Impurities in the Vortioxetine Manufacturing Process
  24. Development, validation and comparison of UHPSFC and UHPLC methods for the determination of agomelatine and its impurities
  25. Effect of Chromatographic Conditions on Enantioseparation of Bedaquiline Using Polysaccharide-based Chiral Stationary Phases in RP-HPLC
  26. Quantification of structurally related aliphatic amino alcohols inl-valinol by hydrophilic interaction liquid chromatography separation combined with postcolumn derivatization and fluorescence detection
  27. Enantiomeric purity control of R-cinacalcet in pharmaceutical product by capillary electrophoresis
  28. New approach of validation using internal normalization technique for quantification of related substances in raw material, intermediates and pharmaceutical substances by HPLC
  29. HILIC–MS Determination of Genotoxic Impurity of 2-Chloro-N-(2-Chloroethyl)Ethanamine in the Vortioxetine Manufacturing Process
  30. Enantiomeric separation of tapentadol by capillary electrophoresis—Study of chiral selectivity manipulation by various types of cyclodextrins
  31. Direct analysis in real time – High resolution mass spectrometry as a valuable tool for the pharmaceutical drug development
  32. Identification, characterization, synthesis and HPLC quantification of new process-related impurities and degradation products in retigabine
  33. Retention behavior of a homologous series and positional isomers of aliphatic amino acids in hydrophilic interaction chromatography
  34. Underivatized amylose and cellulose as new stationary phases for hydrophilic interaction chromatography
  35. Enantiomeric separation ofR,S-tolterodine andR,S-methoxytolterodine with negatively charged cyclodextrins by capillary electrophoresis
  36. Fundamental study of enantioselective HPLC separation of tapentadol enantiomers using cellulose-based chiral stationary phase in normal phase mode
  37. Chiral Chromatography Studies of Chemical Behavior of Cinacalcet on Polysaccharide Chiral Reversed-Phase HPLC Stationary Phases
  38. Rapid HILIC method with fluorescence detection using derivatization reaction utilizing o-phthaldialdehyde for determination of degradation product of aliskiren
  39. The Formation of Furfural Compounds in Selected Saccharide- and Polysaccharide-based Pharmaceutical Excipients
  40. Rapid determination of ambrisentan enantiomers by enantioselective liquid chromatography using cellulose-based chiral stationary phase in reverse phase mode
  41. Rapid determination of ambrisentan enantiomers by enantioselective liquid chromatography using cellulose-based chiral stationary phase in reverse phase mode
  42. Identification, preparation and UHPLC determination of process-related impurity in zolmitriptan
  43. Drug-excipient compatibility testing—Identification and characterization of degradation products of phenylephrine in several pharmaceutical formulations against the common cold
  44. Liquid chromatographic method for enantiopurity control of alaptide using polysaccharide stationary phases
  45. Rapid hydrophilic interaction chromatography determination of lysine in pharmaceutical preparations with fluorescence detection after postcolumn derivatization with o-phtaldialdehyde
  46. Liquid chromatographic separation of pregabalin and its possible impurities with fluorescence detection after postcolumn derivatization with o-phtaldialdehyde
  47. HPLC determination of lincomycin in premixes and feedstuffs with solid-phase extraction on HLB OASIS and LC–MS/MS confirmation
  48. Rapid determination of amoxicillin in premixes by HPLC