Formulation development and optimisation of dosage form using QbD.
Nanoparticulate & microparticulate drug delivery systems.
Rapidly disintegrating dosage forms.
Dissolution enhancement of poorly soluble APIs.
Antimicrobial activities of active pharmaceutical ingredients and dosage forms.
Formulation design, development and delivery of different types of dosage forms for various APIs.
Third-party evaluation for new equipment, excipients and solving problems related to formulation development.
Testing work for rheological analysis of injectable dosage forms, diffusion study of topical dosage forms, chew-out testing of medicated chewing gum, etc..
In-vitro and in-vivo evaluation of Novel Chemical Entities (NCEs), various oral, parenteral and topical formulations, herbal drugs, nutraceuticals, dietary supplements, and polyherbal formulations.
Development of new experimental models for pharmacological evaluation of drugs.
Pharmacological safety and efficacy studies with special reference to anticancer, neuroprotective, cognition enhancement, antiepileptic, antidepressant, antistroke, antianxiety, antifungal, antiarthritic, antiulcer, antidiabetic, anti-obesity, antioxidant, Hepatoprotective and wound healing activity, etc..
Genotoxicity and mutagenicity testing studies.
Surgical models like partial abdominal aortic constriction for cardiac hypertrophy, intra cerebrovascular injury for neurodegenerative disorders, middle cerebral artery occlusion for stroke, ovariectomy model for osteoporosis, etc..
Synthesis of potentially useful Novel Chemical Entities.
Drug design using pharmacophore modeling, docking, virtual screening, QSAR (traditional and 3D), etc..
Development of eco-friendly process chemistry.
Liquid phase combinatorial synthesis of small molecules.
Asymmetric synthesis.
Total synthesis of natural products.
Development and validation of stability-indicating assay methods for APIs and formulations.
Dissolution method development and validation for different types of dosage forms.
Development and validation of bioanalytical methods for biological fluids.
Application of Quality by Design approach in analytical method development.
Solid state analysis by spectroscopic methods like FTIR Raman Spectrometer, etc..
Supercritical fluid extraction and quantification of phytoconstituents.
Standardisation of polyherbal formulation.
Isolation and identification of biomarkers from plants and herbal formulations.
Extraction, isolation, and characterisation of phytoconstituents.
Estimation of phytoconstituents in herbal drugs, extracts, and formulations.
Quality control & standardisation of herbal formulations.
Pharmacological screening of herbal drugs with special reference to anti-diabetic, hepato-protective, anti-obesity, anti-oxidant, anti-asthmatic and wound healing activity.
Development of new herbal and polyherbal formulations, new herbal cosmetics like shampoo, creams, etc., nutraceuticals and dietary supplements.
