259 results on '"Khan, Mansoor A."'
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2. In-use stability assessment of FDA approved metformin immediate release and extended release products for N-Nitrosodimethylamine and dissolution quality attributes
3. Assessing impact of formulation and process variables on in-vitro performance of directly compressed abuse deterrent formulations
4. Risk based in vitro performance assessment of extended release abuse deterrent formulations
5. Impact of formulation and process variables on solid-state stability of theophylline in controlled release formulations
6. Influence of drug loading and type of ointment base on the in vitro performance of acyclovir ophthalmic ointment
7. Understanding effect of formulation and manufacturing variables on the critical quality attributes of warfarin sodium product
8. Kinetics of drug release from ointments: Role of transient-boundary layer
9. Formulation and process factors influencing product quality and in vitro performance of ophthalmic ointments
10. Development and validation of X-ray diffraction method for quantitative determination of crystallinity in warfarin sodium products
11. Product and process understanding to relate the effect of freezing method on glycation and aggregation of lyophilized monoclonal antibody formulations
12. Stability characterization and appearance of particulates in a lyophilized formulation of a model peptide hormone-human secretin
13. Long-term stability study of Prussian blue – A quality assessment of water content and thallium binding
14. Cold flow of estradiol transdermal systems: Influence of drug loss on the in vitro flux and drug transfer across human epidermis
15. Determination of tacrolimus crystalline fraction in the commercial immediate release amorphous solid dispersion products by a standardized X-ray powder diffraction method with chemometrics
16. Development of performance matrix for generic product equivalence of acyclovir topical creams
17. Root cause evaluation of particulates in the lyophilized indomethacin sodium trihydrate plug for parenteral administration
18. Pharmaceutical characterization and thermodynamic stability assessment of a colloidal iron drug product: Iron sucrose
19. Quantitative estimation of phenytoin sodium disproportionation in the formulations using vibration spectroscopies and multivariate methodologies
20. Hunter screening design to understand the product variability of solid dispersion formulation of a peptide antibiotic
21. Assessing the impact of nimodipine devitrification in the ternary cosolvent system through quality by design approach
22. Effects of excipients and curing process on the abuse deterrent properties of directly compressed tablets
23. Ultra-long acting prodrug of dolutegravir and delivery system – Physicochemical, pharmacokinetic and formulation characterizations
24. Development of stable amorphous solid dispersion and quantification of crystalline fraction of lopinavir by spectroscopic-chemometric methods
25. Quantitative determination of thallium binding to ferric hexacyanoferrate: Prussian blue
26. 3D-printing of lopinavir printlets by selective laser sintering and quantification of crystalline fraction by XRPD-chemometric models
27. Challenges of pediatric formulations: A FDA science perspective☆
28. Focused beam reflectance measurement to monitor nimodipine precipitation process
29. Process analytical technology (PAT): Effects of instrumental and compositional variables on terahertz spectral data quality to characterize pharmaceutical materials and tablets
30. Quality by design: Understanding the formulation variables of a cyclosporine A self-nanoemulsified drug delivery systems by Box–Behnken design and desirability function
31. Studying effect of glyceryl palmitostearate amount, manufacturing method and stability on polymorphic transformation and dissolution of rifaximin tablets
32. Impact of controlled ice nucleation on process performance and quality attributes of a lyophilized monoclonal antibody☆
33. Quality by design: Impact of formulation variables and their interactions on quality attributes of a lyophilized monoclonal antibody
34. Cholorpheniramine tannate complexes: Physicochemical, chemometric, and taste masking evaluation
35. FDA: Contribution to developing pediatric formulations and transatlantic collaboration
36. Controlled release of a self-emulsifying formulation from a tablet dosage form: Stability assessment and optimization of some processing parameters
37. Application of quality by design to formulation and processing of protein liposomes
38. A two-stage reverse dialysis in vitro dissolution testing method for passive targeted liposomes
39. A quality by design (QbD) case study on liposomes containing hydrophilic API: II. Screening of critical variables, and establishment of design space at laboratory scale
40. Predicting hydrophilic drug encapsulation inside unilamellar liposomes
41. Crystallinity evaluation of tacrolimus solid dispersions by chemometric analysis
42. Tannate complexes of antihistaminic drug: Sustained release and taste masking approaches
43. A quality by design (QbD) case study on liposomes containing hydrophilic API: I. Formulation, processing design and risk assessment
44. Quality-by-Design (QbD): An integrated process analytical technology (PAT) approach for a dynamic pharmaceutical co-precipitation process characterization and process design space development
45. Combination of Paclitaxel and R-flurbiprofen loaded PLGA nanoparticles suppresses glioblastoma growth on systemic administration
46. Tablet splitting: Product quality assessment of metoprolol succinate extended release tablets
47. Risperidone solid dispersion for orally disintegrating tablet: Its formulation design and non-destructive methods of evaluation
48. Quantitative evaluation of the thallium binding of soluble and insoluble Prussian blue hexacyanoferrate analogs: A scientific comparison based on their critical quality attributes
49. Understanding the effects of formulation and process variables on the printlets quality manufactured by selective laser sintering 3D printing
50. Understanding the quality of protein loaded PLGA nanoparticles variability by Plackett–Burman design
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