U12-S07. Evaluation of colloidal stability (Remote) OUTSTANDING
Determination of colloidal stability of emulsions, suspensions and foams. Evaluation of sedimentation, cremation, flocculation and coalescence processes.
Determination of colloidal stability of emulsions, suspensions and foams. Evaluation of sedimentation, cremation, flocculation and coalescence processes.
Determination of aggregation state of nanodispersions, identification and location of nanoentities, both in liquid and solid matrices (e.g. nanoparticles in cells)
Classic parenteral dosage forms: solutions, suspensions, emulsions, …
Parenteral dosage forms for sustained release
Topical dossage: creams, gels,…
Classic oral dosage forms: capsules, tablets, coated tablets, microgranules, . . .
Oral dossages forms for suistanable release: hidrophylic matrixes, lipid matrixes, pellets….
Design & Development of micro- & nanocapsules for conventional drugs, for peptides & proteins
Design & Development of solid lipid nanoparticules(SLN)-based non-viral vectors
Design & Development of living cells containing microparticules
Biopharmaceutical evaluation of dosage forms, quality assurance & stability studies
Setup and validation of analytical techniques for the quantification of drugs, degradation products and impurities
Pharmacokinetic pre-clinical studies of new molecules (pre-clinial pharmacokinetics)
Study of the capacity of materials for controlled adsorption and drug delivery