6533b820fe1ef96bd1279bb8

RESEARCH PRODUCT

Evaluation of polyalkylcyanoacrylate nanoparticles as a potential drug carrier: preparation, morphological characterization and loading capacity.

Bianca CarlisiGaetano GiammonaA. VillariNorberto MicaliMassimo FrestaGiovanni Puglisi

subject

Materials sciencePolymersChemistry PharmaceuticalPharmaceutical ScienceNanoparticleBioengineeringDosage formchemistry.chemical_compoundColloidSurface-Active AgentsColloid and Surface ChemistryPulmonary surfactantPolymer chemistryColloidsCyanoacrylatesPhysical and Theoretical ChemistryParticle Sizechemistry.chemical_classificationDrug CarriersOrganic ChemistryPolymerEnbucrilateHydrogen-Ion ConcentrationFluoresceinsKineticsMonomerchemistryChemical engineeringEvaluation Studies as TopicFluoresceinParticle sizeDrug carrier

description

Some physicochemical behaviours were investigated of polyethyl- (PECA) and polyisobutylcyanoacrylate (PICA), which, in recent years, have been proposed as nanoparticle colloidal systems for drug carrying. We observed the influence of preparation conditions, such as pH value and surfactant concentration, on parameters such as particle size and polymer molecular weight. Lower operating pH values (0-2) resulted in smaller nanoparticles than those prepared at pH 5.5. The polymer molecular weight was also a function of pH: low molecular weight at low pH and vice-versa. The surfactant concentration positively influenced main particle size and polymer molecular weight. These trends were independent of type of monomer; in fact, both ethyl- (ECA) and isobutyl-2-cyanoacrylate (ICA) showed the same behaviour. Loading capacity, as well as release profile, of the two polymers were evaluated using fluorescein as a model drug. Whereas both polymers showed almost the same release profile, there was a difference in the amount of encapsulated probe: higher aliquots for PICA than for PECA. Storage effects on such physicochemical parameters were also tested.

10.3109/02652049309031525https://pubmed.ncbi.nlm.nih.gov/8377093