Journal of Applied Polymer Science · 2007 · 81 citations · 27 references
PharmacyPharmaceuticsPharmacologyBioavailabilityDrug DeliveryPharmaceutical FormulationControlled Release MechanismsDrug EncapsulationMicroscale Drug Delivery SystemsSelf-emulsifying Drug Delivery SystemsAlginateControlled ReleaseDrug Release MechanismsEmulsificationMicrosphere DeliveryMicrosphere Delivery SystemsMicrospheresParticle-size Distribution
Abstract Semi‐interpenetrating network (IPN) of sodium alginate (NaAlg) and N ‐isopropylacrylamide (NIPAAm) microspheres were prepared by water‐in‐oil (w/o) emulsification method. The microspheres were encapsulated with 5‐fluorouracil (5‐FU) and release patterns carried in 7.4 pH at temperatures of 25 and 37°C. The semi‐IPN microspheres were characterized by Fourier transform infrared spectroscopy (FTIR). Differential scanning calorimetry (DSC) and scanning electron microscopic studies were done on the drug‐loaded microspheres to confirm the polymorphism of 5‐FU and surface morphology of microspheres. These results indicated the molecular level dispersion of 5‐FU in the semi‐IPN microspheres. Particle size and size distribution were studied by laser light diffraction technique. Microspheres exhibited release of 5‐FU up to 12 h. The swelling studies were carried in 1.2 and 7.4 pH buffer media at 25 and 37°C. Drug release from NaAlg‐NIPAAm semi‐IPN microspheres at 25 and 37°C confirmed the thermosensitive nature by in vitro dissolution. The micro domains have released in a controlled manner due the presence of NIPAAm in the matrix. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2008
27
Determination of the cation content of alginate thin films by FTi.r. spectroscopy
Céline Sartori, Dudley S. Finch, Brian Ralph et al. · Polymer · 1997 · 436 citations