32 results on '"Khan, Mansoor A."'
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2. Patient In-Use Stability Testing of FDA-Approved Metformin Combination Products for N-Nitrosamine Impurity.
3. Preparation and Characterization of 3D-Printed Dose-Flexible Printlets of Tenofovir Disoproxil Fumarate
4. Nitroso Impurities in Drug Products: An Overview of Risk Assessment, Regulatory Milieu, and Control Strategy
5. Preparation and Characterization of Stable Amorphous Glassy Solution of BCS II and IV Drugs
6. Coating characterization by hyperspectroscopy and predictive dissolution models of tablets coated with blends of cellulose acetate and cellulose acetate phthalate
7. Influence of Formulation and Processing Factors on Stability of Levothyroxine Sodium Pentahydrate
8. Difference in the Lubrication Efficiency of Bovine and Vegetable-Derived Magnesium Stearate During Tabletting
9. Disintegration of Highly Soluble Immediate Release Tablets: A Surrogate for Dissolution
10. Comparative Evaluation of Flow for Pharmaceutical Powders and Granules
11. Salt Engineering of Aripiprazole with Polycarboxylic Acids to Improve Physicochemical Properties
12. Potential Application of USP Paddle and Basket Dissolution Methods in Discriminating for Portioned Moist Snuff and Snus Smokeless Tobacco Products
13. Response surface methodology for optimization and characterization of limonene-based coenzyme Q10 self-nanoemulsified capsule dosage form
14. Response surface methodology for the optimization of ubiquinone self-nanoemulsified drug delivery system
15. Preparation and Characterization of Stable Amorphous Glassy Solution of BCS II and IV Drugs.
16. A QbD Case Study: Bayesian Prediction of Lyophilization Cycle Parameters
17. NIR Spectroscopy Applications in the Development of a Compacted Multiparticulate System for Modified Release
18. Formulation Optimization of Selective Laser Sintering 3D-Printed Tablets of Clindamycin Palmitate Hydrochloride by Response Surface Methodology
19. Effects of Diluents on Physical and Chemical Stability of Phenytoin and Phenytoin Sodium
20. Development of Abuse-Deterrent Formulations Using Sucrose Acetate Isobutyrate
21. Tablet Splitting of a Narrow Therapeutic Index Drug: A Case with Levothyroxine Sodium
22. Evaluation of Abuse-Deterrent Characteristics of Tablets Prepared via Hot-Melt Extrusion
23. In Vitro Drug Transfer Due to Drug Retention in Human Epidermis Pretreated with Application of Marketed Estradiol Transdermal Systems
24. Comparison of Univariate and Multivariate Models of 13C SSNMR and XRPD Techniques for Quantification of Nimodipine Polymorphs
25. In Vitro Drug Transfer Due to Drug Retention in Human Epidermis Pretreated with Application of Marketed Estradiol Transdermal Systems.
26. Considerations for a Pediatric Biopharmaceutics Classification System (BCS): Application to Five Drugs
27. Development and Validation of a HPLC Method for Dissolution and Stability Assay of Liquid-Filled Cyclosporine Capsule Drug Products
28. Comparison of Univariate and Multivariate Models of C SSNMR and XRPD Techniques for Quantification of Nimodipine Polymorphs.
29. Improvement of Physicochemical Properties of an Antiepileptic Drug by Salt Engineering
30. Physico-mechanical and Stability Evaluation of Carbamazepine Cocrystal with Nicotinamide
31. Comparison of Univariate and Multivariate Models of ¹³C SSNMR and XRPD Techniques for Quantification of Nimodipine Polymorphs.
32. Formulation of anastrozole microparticles as biodegradable anticancer drug carriers.
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