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2. FIP/AAPS guidelines to dissolution/in vitro release testing of novel/special dosage forms
3. A Design and Evaluation of Layered Matrix Tablet Formulations of Metoprolol Tartrate
4. Use of Placket–Burman Statistical Design to Study Effect of Formulation Variables on the Release of Drug from Hot Melt Sustained Release Extrudates
5. Negative Thermo-responsive Microspheres Based on Hydrolyzed Gelatin as Drug Delivery Device
6. Composition Optimization and Stability Testing of a Parenteral Antifungal Solution based on a Ternary Solvent System
7. Insulin-Loaded Nanoparticles Based on N-Trimethyl Chitosan: In Vitro (Caco-2 Model) and Ex Vivo (Excised Rat Jejunum, Duodenum, and Ileum) Evaluation of Penetration Enhancement Properties
8. Development of a New Method to Get a Reliable Powder Flow Characteristics Using Only 1 to 2 g of Powder
9. Encapsulation of Ketoprofen and Ketoprofen Lysinate by Prilling for Controlled Drug Release
10. Development of Satranidazole Mucoadhesive Gel for the Treatment of Periodontitis
11. Development of an Ex Vivo Method for Evaluation of Precorneal Residence of Topical Ophthalmic Formulations
12. Compressional Behavior of a Mixture of Granules Containing High Load of Phyllanthus niruri Spray-Dried Extract and Granules of Adjuvants: Comparison between Eccentric and Rotary Tablet Machines
13. Characterization and Stability of Emulsion Gels Based on Acrylamide/Sodium Acryloyldimethyl Taurate Copolymer
14. Comparison of Three Dissolution Apparatuses for Testing Calcium Phosphate Pellets used as Ibuprofen Delivery Systems
15. The Study on the Entrapment Efficiency and In Vitro Release of Puerarin Submicron Emulsion
16. Change in Criteria for USP Dissolution Performance Verification Tests
17. The Abbreviated Impactor Measurement (AIM) Concept: Part II—Influence of Evaporation of a Volatile Component—Evaluation with a “Droplet-Producing” Pressurized Metered Dose Inhaler (pMDI)-Based Formulation Containing Ethanol as Cosolvent
18. Conventional and Dense Gas Techniques for the Production of Liposomes: A Review
19. Investigation of the Variability of NIR In-line Monitoring of Roller Compaction Process by Using Fast Fourier Transform (FFT) Analysis
20. Rapid Development and Optimization of Tablet Manufacturing Using Statistical Tools
21. Comparative In Vitro Study of Six Carbamazepine Products
22. Estimating the Number of Droplets and Drug Particles Emitted from MDIs
23. Commerical reference shape standards use in the study of particle shape effect on laser diffraction particle size analysis
24. Assessment of NIR spectroscopy for nondestructive analysis of physical and chemical attributes of sulfamethazine bolus dosage forms
25. Effect of isopropyl myristic acid ester on the physical characteristics and in vitro release of etoposide from PLGA microspheres
26. The suitability of disintegrating force kinetics for studying the effect of manufacturing parameters on spironolactone tablet properties
27. Long-term release of clodronate from biodegradable microspheres
28. Influence of Drying Procedure and of Low Degree of Substitution on the Structural and Drug Release Properties of Carboxymethyl Starch
29. Stability Assessment of Injectable Castor Oil-Based Nano-sized Emulsion Containing Cationic Droplets Stabilized by Poloxamer–Chitosan Emulsifier Films
30. Optimization of the Water-Insoluble Procedures for USP General Chapter Residual Solvents <467>
31. Dissolution Enhancement of a Drug Exhibiting Thermal and Acidic Decomposition Characteristics by Fusion Processing: A Comparative Study of Hot Melt Extrusion and KinetiSol® Dispersing
32. Preparation and Characterization of Highly Porous Direct Compression Carrier Particles with Improved Drug Loading During an Interactive Mixing Process
33. Formulation of Ketotifen Fumarate Fast-Melt Granulation Sublingual Tablet
34. Gliclazide Microcrystals Prepared by Two Methods of In Situ Micronization: Pharmacokinetic Studies in Diabetic and Normal Rats
35. Preparation and Characterization of Inclusion Complexes of a Hemisuccinate Ester Prodrug of Δ9-Tetrahydrocannabinol with Modified Beta-Cyclodextrins
36. In vitro Enhancement of Lactate Esters on the Percutaneous Penetration of Drugs with Different Lipophilicity
37. Drug-Cyclodextrin-Vesicles Dual Carrier Approach for Skin Targeting of Anti-acne Agent
38. Preparation, Safety, Pharmacokinetics, and Pharmacodynamics of Liposomes Containing Brucea javanica Oil
39. Effect of Cholesterol on the Properties of Spray-Dried Lysozyme-Loaded Liposomal Powders
40. Cephalexin Microspheres for Dairy Mastitis: Effect of Preparation Method and Surfactant Type on Physicochemical Properties of the Microspheres
41. In Situ Gelling Gelrite/Alginate Formulations as Vehicles for Ophthalmic Drug Delivery
42. Solid Dispersion as an Approach for Bioavailability Enhancement of Poorly Water-Soluble Drug Ritonavir
43. Preparation and Enhanced Oral Bioavailability of Cryptotanshinone-Loaded Solid Lipid Nanoparticles
44. Comparison of Release-Controlling Efficiency of Polymeric Coating Materials Using Matrix-type Casted Films and Diffusion-Controlled Coated Tablet
45. Physical Characterization of 1,3-dipropyl-8-cyclopentylxanthine (CPX)
46. Solid State Characterization of Commercial Crystalline and Amorphous Atorvastatin Calcium Samples
47. Nano-coating of β-galactosidase onto the Surface of Lactose by Using an Ultrasound-assisted Technique
48. In vitro Permeability Enhancement in Intestinal Epithelial Cells (Caco-2) Monolayer of Water Soluble Quaternary Ammonium Chitosan Derivatives
49. Rehydrated Lyophilized Rifampicin-Loaded mPEG–DSPE Formulations for Nebulization
50. Development and Optimization of Micro/Nanoporous Osmotic Pump Tablets
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