UNITEFA   23945
UNIDAD DE INVESTIGACION Y DESARROLLO EN TECNOLOGIA FARMACEUTICA
Unidad Ejecutora - UE
congresos y reuniones científicas
Título:
Development of new hidrochlrotiazide:chitosan nanoparticles. 3º Reunión Internacional de Ciencias Farmacéuticas
Autor/es:
ONNAINTY R., LONGHI M., GRANERO E
Lugar:
Córdoba
Reunión:
Congreso; 3º Reunión Internacional de Ciencias Farmacéuticas. RICifa 2014; 2014
Resumen:
Nanoparticles (NPs) are frequently defined as solid, colloidal particles in the range 10 ? 1000 nm. Chitosan (CHI) is a linear polysaccharide composed of D-glucosamine and N-acetyl-D-glucosamine. Low molecular weight (LMW) CHI shows better solubility, biocompatibility, bioactivity, biodegradability and even less toxicity than other kind of CHI. Hydrochlorotiazide (HCT) is a diuretic class of thiazides. This drug is poorly soluble in water and slightly permeable through intestinal mucosa. NPs were prepared using ionic gelation method with sodium tripolyphosphate (TPP) as a cross-linking agent. This technique is based on the ionic interactions between the positive charge of CHI and the negative charge of TPP. NPs were characterized by size, zeta potential, mucoadhesive properties using ?mucin method? and loading capacity was calculated by an indirect method with the following equation: The optimized NPs exhibited a mean hydrodynamic diameter of 220 nm when are empty and 338 nm when are loaded, with a polydispersity index (PDI) of 0.2 and 0.15, respectively. The increase in the size is due the incorporation of the drug to the NPs. Zeta potential in all cases is above +30 mV, indicating that there are stables. Mucoadhesive studies revealed a reduction in the zeta potential values for CHI nanoparticles. This reduction could be attributed to the ionic interaction between negative charge of mucin and positive charge of CHI. It resulted in the mucoadhesive properties of the CHI nanoparticles. These NP were loaded with Hydrochlorotiazide (HCT) and the loading capacity was calculated of 80%. CHI NPs represent an interesting delivery system for drug due it mucoadhesive properties enable to interact with mucosa.