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RESEARCH PRODUCT

Influence of Polyvinyl Alcohol (PVA) on PVA-Poly-N-hydroxyethyl-aspartamide (PVA-PHEA) Microcrystalline Solid Dispersion Films

Laura Modica De MohacMariano LicciardiZahra Al-sahafBahijja Tolulope Raimi-abraham

subject

Materials sciencePolymersbuccal filmPharmaceutical ScienceIbuprofen02 engineering and technologyAquatic Science030226 pharmacology & pharmacyPolyvinyl alcohol03 medical and health scienceschemistry.chemical_compound0302 clinical medicineDifferential scanning calorimetrySpectroscopy Fourier Transform InfraredDrug Discoveryibuprofen sodiumcrystallineSolubilityFourier transform infrared spectroscopyDissolutionPolyhydroxyethyl MethacrylateEcology Evolution Behavior and SystematicsAspartic AcidCalorimetry Differential ScanningEcologyGeneral MedicinePHEA021001 nanoscience & nanotechnologyAmidesSolventDrug LiberationMicrocrystallineSolubilitychemistryPolyvinyl AlcoholAttenuated total reflectionPVAMicroscopy Electron ScanningCrystallization0210 nano-technologyAgronomy and Crop ScienceResearch ArticleNuclear chemistry

description

AbstractThis study was conducted to formulate buccal films consisting of polyvinyl alcohol (PVA) and poly-N-hydroxyethyl-aspartamide (PHEA), to improve the dissolution of the drug through the oral mucosa. Ibuprofen sodium salt was used as a model drug, and the buccal film was expected to enhance its dissolution rate. Two different concentrations of PVA (5% w/v and 7.5% w/v) were used. Solvent casting was used to prepare films, where a solution consisting of drug and polymer was cast and allowed to dry. Attenuated total reflection Fourier transform infrared spectroscopy (ATR-FTIR), differential scanning calorimetry (DSC), and scanning electron microscopy (SEM) were used to investigate the properties of films. In vitro dissolution studies were also conducted to investigate drug release. SEM studies showed that films containing a higher concentration of PVA had larger particles in microrange. FTIR studies confirmed the presence of the drug in films and indicated that ibuprofen sodium did not react with polymers. DSC studies confirmed the crystalline form of ibuprofen sodium when incorporated within films. In vitro dissolution studies found that the dissolution percentage of ibuprofen sodium alone was increased when incorporated within the film from 59 to 74%. This study led to the development of solid microcrystalline dispersion as a buccal film with a faster dissolution rate than the drug alone overcoming problem of poor solubility.

10.1208/s12249-020-01811-zhttp://hdl.handle.net/10447/434573