1. Dissolution enhancement by cyclodextrin complexation.
2. Improvement of dissolution characteristics of slightly soluble drugs by some methods (Co-solvent approach).
3. Comparison of dissolution studies of two different marketed products of same drug.
4. Influence of polymorphism on solubility and dissolution of a drug.
5. Determination drug protein binding.
6. Absorption studies in animal everted intestine.
7. Diffusion study using Franz diffusion cell.
8. Oral bioavailability of Paracetamol in Wistar rats by plasma analysis.
9. Case study for calculation of Pharmacokinetic parameters from plasma data.
10. Case study for calculation of Absorption Rate Constant (Ka) from plasma data.
11. Bioequivalence of paracetamol tablets.
12. In vitro-in vivo correlation for paracetamol sustained release tablet.
13. To establish the bioequivalence between two aspirin products by urine analysis.
14. To calculate the elimination rate constant, half life and renal clearance from the given urinary excretion data.