All Stories

  1. Preservatives in Pharmaceuticals: Are They Really Safe?
  2. Stability Indicating Analytical Method, Characterization of Degradation Impurity by UPLC-Q-TOF-MS/MS, and Establishment of Degradation Mechanism of Evodiamine
  3. Recent Reviews on Dendrimers as an Immunotherapy-based Nanosystem for the Effective Treatment of Cancer
  4. Nanomaterial-based delivery of vaccine through nasal route: Opportunities, challenges, advantages, and limitations
  5. A Recent Review On 3D-Printing: Scope and Challenges with Special Focus on Pharmaceutical Field
  6. An Updated Account on Formulations and Strategies for the Treatment of Burn Infection – A Review
  7. Recent Applications of Derivatization Techniques for Pharmaceutical and Bioanalytical Analysis through High-performance Liquid Chromatography
  8. Sustained release matrix tablet of 100 mg losartan potassium: Formulation development and in vitro characterization
  9. In-vitro Dissolution Study of Pharmaceutical Products with USP Apparatus- IV
  10. Review on Disease, Dose, Destination and Delivery Aspects of Simvastatin
  11. Nanoparticles as budding trends in colon drug delivery for the management of ulcerative colitis
  12. Reactive metabolites: Generation and estimation with electrochemistry based analytical strategy as an emerging screening tool
  13. Effects of Different Formulation Methods on Drug Crystallinity, Drug-Carrier Interaction, and Ex Vivo Permeation of a Ternary Solid Dispersion Containing Nisoldipine
  14. Quantitation of Pregabalin by HPLC-UV Method using Ninhydrin derivatization: Development and Validation
  15. Pharmacological properties of Centella asiatica hydrogel in accelerating wound healing in rabbits
  16. Advancements in the Analytical Quantification of Nitroxidative Stress Biomarker 3-Nitrotyrosine in Biological Matrices
  17. Targeted drug delivery to the brain via intranasal nanoemulsion: Available proof of concept and existing challenges
  18. Current Standing and Technical Guidance on Intracellular Drug Quantification: A New Site Specific Bioavailability Prediction Approach
  19. Current direction and advances in analytical sample extraction techniques for drugs with special emphasis on bioanalysis
  20. Liquid Chromatography Based Methods for Analysis of Disease-Modifying Antirheumatic Drugs (DMARDs) in Biological Matrices
  21. Development and Validation of a UV Spectrophotometric method of Mycophenolate mofetil useful at Preformulation stage of Microemulsion Formulation
  22. Drug development and bioanalytical method validation for a novel anticancer molecule, 4-(dimethylamino)-2-(p-tolylamino) thiazole-5-carbonitrile
  23. Transdermal delivery of raloxifene HCl via ethosomal system: Formulation, advanced characterizations and pharmacokinetic evaluation
  24. Functionalized Carbon Nano-scale Drug Delivery Systems From Biowaste Sago Bark For Cancer Cell Imaging
  25. Development and validation of a high throughput LC–MS/MS method for simultaneous quantitation of pioglitazone and telmisartan in rat plasma and its application to a pharmacokinetic study
  26. Highly efficient and visible light driven Ni0.5Zn0.5Fe2O4@PANI modified BiOCl heterocomposite catalyst for water remediation
  27. Pharmacokinetic and Pharmacodynamic Features of Nanoemulsion Following Oral, Intravenous, Topical and Nasal Route
  28. PVA-PEG physically cross-linked hydrogel film as a wound dressing: experimental design and optimization
  29. Glidant effect of hydrophobic and hydrophilic nanosilica on a cohesive powder: Comparison of different flow characterization techniques
  30. Fast and simple gas chromatographic method for simultaneous estimation of camphor, menthol and methyl salicylate in analgesic ointment: application in stability study
  31. Advanced characterizations of nanoparticles for drug delivery: investigating their properties through the techniques used in their evaluations
  32. Mucoadhesive Polymers and Their Mode of Action: A Recent Update
  33. Safety profiling of pioglitazone and telmisartan combination by sub-chronic toxicity study in rat
  34. Gastro-retentive drug delivery systems and their in vivo success: A recent update
  35. Self emulsifying drug delivery system
  36. Synthesis and liquid crystalline behaviour of substituted (E)-phenyl-4-(phenyldiazenyl) benzoate derivatives and their photo switching ability
  37. Photoisomerization behavior of photochromic amide-based azobenzene dyes exhibiting H-bonding effect: Synthesis and characterization
  38. Differential scanning calorimetric characterization of pharmaceutical powder blend uniformity in a laboratory-scale V-blender
  39. Binary carrier for solid dispersion
  40. Synthesis, characterization and magnetic properties of monodisperse Ni, Zn-ferrite nanocrystals
  41. Experimental design and optimization of raloxifene hydrochloride loaded nanotransfersomes for transdermal application
  42. Chitosan and Alginate Nanoparticles as Oral Insulin Carrier
  43. Bioequivalence Study of a Sustained Release Fixed Dose Combination Capsule Containing Esomeprazole and Domperidone in Healthy Subjects
  44. Evaluation of the Bioequivalence of Two Faropenem Formulations in Healthy Indian Subjects
  45. Bioequivalence Study of Two Capsule Formulations Containing Diacerein 50 mg in Healthy Human Subjects
  46. Bioequivalence Study of Two Formulations Containing 400 mg Dexibuprofen in Healthy Indian Subjects
  47. Synthesis of 1-dimensional polyaniline nanofibers by reverse microemulsion
  48. Determination of Drospirenone in Human Plasma by LC–Tandem-MS
  49. Simultaneous determination of metoprolol succinate and amlodipine besylate in human plasma by liquid chromatography–tandem mass spectrometry method and its application in bioequivalence study
  50. Determination of Pregabalin in Human Plasma Using LC-MS-MS
  51. Extended Release Dosage Form of Glipizide: Development and Validation of a Level A in Vitro–in Vivo Correlation
  52. Optimization of Metformin HCl 500 mg Sustained Release Matrix Tablets Using Artificial Neural Network (ANN) Based on Multilayer Perceptrons (MLP) Model
  53. Formulation and In Vitro Studies of a Fixed-Dose Combination of a Bilayer Matrix Tablet Containing Metformin HCl as Sustained Release and Glipizide as Immediate Release
  54. Liquid chromatography tandem mass spectrometry method for simultaneous determination of metoprolol tartrate and ramipril in human plasma
  55. Simultaneous determination of fixed dose combination of nebivolol and valsartan in human plasma by liquid chromatographic-tandem mass spectrometry and its application to pharmacokinetic study
  56. Determination of duloxetine in human plasma by liquid chromatography with atmospheric pressure ionization–tandem mass spectrometry and its application to pharmacokinetic study
  57. Analysis of Pyridostigmine Bromide in Human Plasma and its Application in Bioequivalence Studies
  58. In-vitro and in-vivo correlation for two gliclazide extended-release tablets
  59. Formulation and Optimization of Sustained Release Matrix Tablet of Metformin HCl 500 mg Using Response Surface Methodology
  60. Evaluation of Bioequivalence of Two Formulations Containing 100 Milligrams of Aceclofenac
  61. Development and validation of an HPLC method for analysis of etoricoxib in human plasma
  62. Development of RP-HPLC for analysis of human insulin
  63. How far did India drift during the Late Cretaceous?—Placenticeras kaffrarium Etheridge, 1904 (Ammonoidea) used as a measuring tape