All Stories

  1. Future-proofing RP-HPLC method for quantification of beta-sitosterol in Pygeum extract and cholecalciferol: Promising approaches for prostate health and dietary supplementation
  2. State-of-the-art mean centering of ratio spectra and HPLC methodologies for comprehensive analysis of some dry eyes drugs: investigation of white and green practices
  3. Micellar HPLC and UV Methods with Time Programming for Synchronically Quantifying Gatifloxacin and Its Preservative in Eye Drops: Appraisal of Ecological Impact
  4. Quantitative analysis of quaternary mixtures in topical creams using cutting-edge HPLC technique: environmental impact and sigma methodology
  5. Impressive stability-indicating RP-HPLC method for concurrent quantification of salbutamol, guaifenesin, and sodium benzoate in cough syrup: Application of six sigma and green metrics
  6. Comparative analysis using UPLC and UV methods for concurrent quantification of therapeutic drugs for overactive bladder: Effective approach in green and white chemistry
  7. Evaluating the greenness, blueness, and whiteness of spectroscopic and UPLC techniques for the simultaneous measurement of anti-glaucoma drugs and the preservation agent
  8. Green HPLC method for determination of paracetamol and ibuprofen in human plasma: applications to pharmacokinetics
  9. Innovative UPLC technique for concurrent quantification of etofenamate and benzyl nicotinate in the presence of methylparaben and benzyl alcohol in their topical cream: Greens, white, and Six Sigma methodologies
  10. Assessment of activated carbon/alginate for the concurrent removal efficiency of paracetamol and caffeine from wastewater in their binary solutions
  11. Cutting‐edge HPLC and MCR techniques for synchronically quantifying anticholinergic drugs in the presence of C12 and C14 homologs: Robust application to green and white chemistry
  12. Adsorption separation of oxytetracycline hydrochloride using natural and nanostructured clay mineral of silica in synthetic solution: Integration to white and green chemistry metrics
  13. Eco-Friendly HPLC Method for Quantification of Metformin and Dapagliflozin in Tablets Dosage Form and Spiked Human Plasma Utilizing Solid Phase Extraction
  14. Green voltammetric method for determination of diclofenac sodium in environmental and biological samples using aluminium tungstate nanoparticles modified carbon paste electrode
  15. Cellulose-based Co Fe LDH composite as a nano-adsorbent for sulfamethoxazole and cefixime residues: Evaluation of performance, green metrics and cytotoxicity
  16. Greens appraisal of validated stability indicating RP-HPLC method and forced degradation study for quantification of Ebastine in wastewater and dosage form
  17. Novel RP‐HPLC method for estimation of a newly developed combination of tizanidine and etoricoxib in rat plasma: Eight criteria for greens evaluation
  18. Eco-friendly chromatographic techniques for appraisal of Amlodipine, Hydrochlorothiazide, Telmisartan, and their related substances in dosage form: Application to six sigma and content uniformity approaches
  19. Removal of arsenic(V) using pure zeolite (PZ) and activated dithizone zeolite (ADZ) from aqueous liquids: application to green analytical chemistry
  20. Greens assessment of RP-UPLC method for estimating Triamcinolone Acetonide and its degraded products compared to Box-Behnken and Six Sigma designs
  21. Eco-friendly RP-HPLC approach for simultaneously estimating the promising combination of pentoxifylline and simvastatin in therapeutic potential for breast cancer: Appraisal of greenness, whiteness, and Box–Behnken design
  22. Sustainable HPLC technique for measurement of antidiabetic drugs: Appraisal of green and white metrics, content uniformity, andin vitrodissolution
  23. A novel Six Sigma approach and eco-friendly RP-HPLC technique for determination of pimavanserin and its degraded products: Application of Box–Behnken design
  24. Analytical assessment of a novel RP-HPLC method for the concurrent quantification of selected pharmaceutical drugs levodopa and carbidopa using eight greenness metrics comparing to the lean six sigma approach
  25. Stability indicating high‐performance liquid chromatography method for determining doxycycline hyclate and related substances in their various dosage forms: Utilizing Six Sigma tools, uniformity testing, and in‐vitro dissolution approaches
  26. Five greenness assessments of novel RP-UPLC and MCR methods for concurrent determination of selected pharmaceutical drugs in comparison with the lean Six Sigma approach
  27. Green UPLC method for estimation of ciprofloxacin, diclofenac sodium, and ibuprofen with application to pharmacokinetic study of human samples
  28. Facile synthesis and eco-friendly analytical methods for concurrent estimation of selected pharmaceutical drugs in their solutions: application to quality by design, lean six sigma, and stability studies
  29. Condition optimization of eco-friendly RP-HPLC and MCR methods via Box–Behnken design and six sigma approach for detecting antibiotic residues
  30. Validated stability indicating Eco-friendly RP-HPLC method for the concurrent quantification of Gabapentin and Diclofenac K in wastewater and pharmaceutical formulations
  31. Chromatographic Techniques for Assessment of Bisoprolol Fumarate and Perindopril Arginine in Solid Formulations under Various Stress Conditions and Application to Six Sigma, Content Uniformity, and Comparative Dissolution Approaches
  32. Ecofriendly Spectrophotometric and Chromatographic Methods for Simultaneous Analysis of a Quaternary Mixture of Cephalexin, Sodium Benzoate, Methylparaben and Propylparaben with Application of the Holding Time Study in Bulk and Pharmaceutical Dosage Forms
  33. Validated stability indicating chromatographic method for determination of baricitinib and its degradation products in their tablet dosage form: Implementation to content uniformity and in vitro dissolution studies
  34. Stability-indicating RP-UPLC method for determination of antihypertensive drugs and their degradation products in tablets: application to content uniformity and dissolution studies
  35. Stability Indicating RP-HPLC and Spectrophotometric Methods for Simultaneous Estimation of Sodium Benzoate and Cefdinir in the Presence of its Degradation Products-Application to Blank Subtraction Method
  36. An Effective Chromatographic Method for Simultaneous Quantification of Antidiabetic Drugs Alogliptin Benzoate and Pioglitazone HCl in Their Tablet Dosage Form: Implementation toIn vitroDissolution Studies and Uniformity of Dosage Unit
  37. Optimization and Modelling of Novel RP-UPLC Method for Simultaneous Determination of Cefradine, Cefalexin, Sodium Benzoate and Methylparaben in Some Biological Fluids. Application to Experimental Design.
  38. Stability-Indicating New RP-UPLC Method for Simultaneous Determination of a Quaternary Mixture of Paracetamol, Pseudoephedrine, Chlorpheniramine, and Sodium Benzoate in (Cold–Flu) Syrup Dosage Form
  39. Simultaneous Quantification of Cephalexin and Sodium Benzoate in their Dosage forms by high analytical technique. Application of Lean Six Sigma and In-Vitro Dissolution studies
  40. Modeling and optimization of a novel RP-UPLC and MCR spectrophotometric methods for simultaneous determination of five cephalosporins in spiked human plasma: Application to lean six sigma thinking hats and antimicrobial activity
  41. Simultaneous Determination of Amlodipine Besylate, Valsartan, and Its Related Substances in Their Film-Coated Tablets Dosage form by RP-HPLC Method
  42. Efficient HPLC method for determination of cephalosporin residues on spiked stainless-steel plates and human plasma: application of a worst-case product for Cosa®CIP
  43. Application of Lean Six Sigma Methodologies and In-VitroDissolution Studies for Simultaneous Determination of Cefdinir and Sodium Benzoate by RP-HPLC and UPLC Methods in their Dosage Forms
  44. Novel RP-HPLC-DAD and RP-UPLC Methods for Simultaneous Determination of Cefaclor and Methylparaben in their Dosage form and in its Impurity Cefaclor -Delta-3- Isomer
  45. Efficient UPLC and spectrophotometric MC methods for simultaneous determination of cefixime and sodium benzoate in their dosage form and in its degradation product of cefixime-E Isomer. Application of lean six sigma and in-vitro dissolution studies
  46. Development and validation of RP-HPLC method for determination of amoxicillin residues and application to NICOMAC coating machine
  47. Stability Indicating New-UPLC Method for Determination of Dimethyl Fumarate in their Pure and Capsule Dosage Form
  48. Comparative In-Vitro Dissolution Studies for Determination of Cefixime in an Innovator Product of Suprax Powder for Oral Suspension Dosage form Using Rp-Hplc Method
  49. Novel and facile spectrophotometric techniques for the determination of sofosbuvir and ledipasvir in their tablet dosage form
  50. Specific, accurate, simple, selective and stability-indicating RP-HPLC method
  51. Stability Indicating Rp-HPLC Method for Simultaneous Estimation of Ceftazidime Pentahydrate and its Impurity Product Pyridine in Powder Used for Making Solution in Vial for 1M & IV Injections
  52. Validation and Comparative In-vitro Dissolution Studies of Cefaclor in Their Powder for Oral Suspension Dosage Forms
  53. Specific, accurate, simple, selective and stability-indicating RP-HPLC method
  54. Specific, accurate, simple, selective and stability-indicating RP-HPLC method
  55. Simultaneous Determination of Azelastine hydrochloride and Benzalkonium chloride by RP-HPLC Method in their Ophthalmic Solution
  56. Specific, accurate, simple, selective and stability-indicating RP-HPLC method