6533b860fe1ef96bd12c31d6

RESEARCH PRODUCT

Entrapment of Phenytoin into Microspheres of Oleaginous Materials: Process Development and in Vitro Evaluation of Drug Release

Libero Italo GiannolaV. De Caro

subject

PharmacologyChromatographyOrganic ChemistryPharmaceutical Sciencechemistry.chemical_compoundEntrapmentchemistryDrug DiscoveryDrug deliveryEmulsionGlycerolParticleParticle sizeDispersion (chemistry)Stearyl alcohol

description

AbstractA novel multiparticulate preparation of the antiepileptic agent phenytoin (1) was developed and evaluated in vitro. The preparation consists of gastroresistant microparticulate drug delivery system formulated with oleaginous material (lipospheres) to minimize unwanted effects of l on gastric apparatus. The drug was dispersed in a spherical micromatrix consisting of a mixture of stearyl alcohol and glycerol esters of various fatty acids. The best mixture to obtain discrete, reproducible, free-flowing lipospheres consisted of glyceryl monostearate dilaurate and stearyl alcohol (ratio 3: 17). The lipospheres were obtained by a technique involving melting and dispersion of drug-containing oleaginous material in aqueous medium. The oily droplets of the resulting emulsion after cooling under rapid stirring were transformed into solid. About 99% of the lipospheres were of particle size range 100–800 pm. The lipospheres were analyzed to determine the drug content in various particle sizes and to character...

https://doi.org/10.3109/03639049709146151