172 results on '"Khan, Mansoor A."'
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2. Development and Validation Of A Discriminatory Dissolution Method for Portioned Moist Snuff and Snus
3. Development of Methamphetamine Abuse–Deterrent Formulations Using Sucrose Acetate Isobutyrate
4. Univariate and Multivariate Models for Determination of Prasugrel Base in the Formulation of Prasugrel Hydrochloride Using XRPD Method
5. Development and Validation of a Discriminatory Dissolution Method for Rifaximin Products
6. Quality and In-Use Stability Comparison of Brand and Generics of Extended-Release Phenytoin Sodium Capsules
7. Chemometric Models for Quantification of Carbamazepine Anhydrous and Dihydrate Forms in the Formulation
8. Evaluation of the In Vitro Efficacy of Sevelamer Hydrochloride and Sevelamer Carbonate
9. Spectroscopic-Based Chemometric Models for Quantifying Low Levels of Solid-State Transitions in Extended Release Theophylline Formulations
10. Evaluation of In-Use Stability of Anticoagulant Drug Products: Warfarin Sodium
11. Chemometric Model Development and Comparison of Raman and 13C Solid-State Nuclear Magnetic Resonance–Chemometric Methods for Quantification of Crystalline/Amorphous Warfarin Sodium Fraction in the Formulations
12. Comparison of X-ray Powder Diffraction and Solid-State Nuclear Magnetic Resonance in Estimating Crystalline Fraction of Tacrolimus in Sustained-Release Amorphous Solid Dispersion and Development of Discriminating Dissolution Method
13. Chemometric Methods for the Quantification of Crystalline Tacrolimus in Solid Dispersion by Powder X‐Ray Diffractrometry
14. Near-Infrared and Fourier Transform Infrared Chemometric Methods for the Quantification of Crystalline Tacrolimus from Sustained-Release Amorphous Solid Dispersion
15. An Integrated Process Analytical Technology (PAT) Approach to Monitoring the Effect of Supercooling on Lyophilization Product and Process Parameters of Model Monoclonal Antibody Formulations
16. Stereomicroscopic Imaging Technique for the Quantification of Cold Flow in Drug-in-Adhesive Type of Transdermal Drug Delivery Systems
17. Analytical Methods for the Evaluation of Melamine Contamination
18. Characterization of a Nonribosomal Peptide Antibiotic Solid Dispersion Formulation by Process Analytical Technologies Sensors
19. Development and Evaluation of Paclitaxel Nanoparticles Using a Quality-by-Design Approach
20. Oseltamivir Phosphate–Amberlite™ IRP 64 Ionic Complex for Taste Masking: Preparation and Chemometric Evaluation
21. Process Analytical Technology to Understand the Disintegration Behavior of Alendronate Sodium Tablets
22. Comparative Evaluation of the In Vitro Efficacy of Lanthanum Carbonate Chewable Tablets
23. Spontaneous Carbonate Formation in an Amorphous, Amine-Rich, Polymeric Drug Substance: Sevelamer HCl Product Quality
24. Chemometric Evaluation of Brompheniramine–Tannate Complexes
25. Quality-by-Design: An Integrated Process Analytical Technology Approach to Determine the Nucleation and Growth Mechanisms During a Dynamic Pharmaceutical Coprecipitation Process
26. Development and Validation Of A Discriminatory Dissolution Method for Portioned Moist Snuff and Snus
27. Thermodynamic stability assessment of a colloidal iron drug product: Sodium ferric gluconate
28. United States Food and Drug Administration and Department of Defense Shelf-Life Extension Program of Pharmaceutical Products: Progress and Promise
29. Chemometric Evaluation of Near Infrared, Fourier Transform Infrared, and Raman Spectroscopic Models for the Prediction of Nimodipine Polymorphs
30. Spectral and Spatial Characterization of Protein Loaded PLGA Nanoparticles
31. Quality‐by‐Design (QbD): An Integrated Process Analytical Technology (PAT) Approach for Real‐Time Monitoring and Mapping the State of a Pharmaceutical Coprecipitation Process
32. Quality-By-Design (QbD): An Integrated Approach for Evaluation of Powder Blending Process Kinetics and Determination of Powder Blending End-point
33. Robust Calibration Design in the Pharmaceutical Quantitative Measurements with Near-Infrared (NIR) Spectroscopy: Avoiding the Chemometric Pitfalls
34. Functionality of magnesium stearate derived from bovine and vegetable sources: Dry granulated tablets
35. Quality-by-Design (QbD): Effects of Testing Parameters and Formulation Variables on the Segregation Tendency of Pharmaceutical Powder Measured by the ASTM D 6940-04 Segregation Tester
36. Process Analytical Technology: Nondestructive Evaluation of Cyclosporine A and Phospholipid Solid Dispersions by Near Infrared Spectroscopy and Imaging
37. Process Analytical Technology (PAT): Quantification Approaches in Terahertz Spectroscopy for Pharmaceutical Application
38. Drug product characterization by Macropixel Analysis of chemical images
39. Quality by Design: Understanding The Product Variability of a Self-Nanoemulsified Drug Delivery System of Cyclosporine A
40. Process Analytical Technology: Chemometric Analysis of Raman and Near Infra-Red Spectroscopic Data for Predicting Physical Properties of Extended Release Matrix Tablets
41. Cytotoxicity evaluation of enzyme inhibitors and absorption enhancers in Caco-2 cells for oral delivery of salmon calcitonin
42. Chain Length-Dependent Effects of Alkylmaltosides on Nasal Absorption of Enoxaparin
43. Protection of salmon calcitonin breakdown with serine proteases by various ovomucoid species for oral drug delivery
44. Preparation and characterization of a customized cellulose acetate butyrate dispersion for controlled drug delivery
45. Design, in vitro stability, and ocular hypotensive activity of t-butalone chemical delivery systems
46. Permeability characteristics of novel mydriatic agents using an in vitro cell culture model that utilizes sirc rabbit corneal cells
47. Racemate and Enantiomers of Ketoprofen: Phase Diagram, Thermodynamic Studies, Skin Permeability, and Use of Chiral Permeation Enhancers
48. Morpholinoalkyl Ester Prodrugs of Diclofenac: Synthesis,In VitroandIn VivoEvaluation
49. Quality-by-Design (QbD): An integrated process analytical technology (PAT) approach for real-time monitoring and mapping the state of a pharmaceutical coprecipitation process.
50. Quality-by-design (QbD): An integrated approach for evaluation of powder blending process kinetics and determination of powder blending end-point.
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