The critical micelle concentration was 6mM (surface tension), wit

The critical micelle concentration was 6mM (surface tension), with a hydrodynamic radius of 30Å (light scattering) and 25.4Å (SANS), area per molecule of about 57.6Å, and aggregation number of 84. Solubilization of drugs in ASC-8 micellar dispersions was reported by Palma et al. [16]. Solubilization of drugs was performed above the CMC and Krafft temperature Inhibitors,research,lifescience,medical determined by surface tension and conductivity measurements. The solubility of hydrophobic drugs, such as phenacetin, Oligomycin A danthron, selleck Pazopanib anthralin, and retinoic acid, was greatly enhanced by the solubilization. Furthermore, the antioxidant activity exhibited by the ascorbate rings

that form the hydrophilic external shells in ASC-8 micellar dispersions can protect degradable materials that have been solubilized in the internal hydrophobic micellar core from radical-initiated oxidation. 1.4. Encapsulation of Ascorbyl Palmitate (ASC-P) in Carriers ASC-P has been used as a model drug for nanosized lipid carriers. Inhibitors,research,lifescience,medical As an antioxidant, ASC-P has been also used

in the cosmetics, food, and pharmaceutical industries. Teeranachaideekul et al. reported the physicochemical characterization and in vitro release studies of ASC-P-loaded nanostructured lipid carriers (NLC gels) [17, 18]. NLC gels were prepared Inhibitors,research,lifescience,medical by a high-pressure homogenization technique using oil Labrafil M1944 and solid lipids such as cetyl alcohol (CA), Imwitor 900 (GMS), and nonionic hydrophilic white beeswax (BW). Nanosized particles <250nm with low polydispersity indices were prepared although microscopic observation indicated that the nanoparticles were nonspherical. The encapsulation efficiency of ASC-P was almost 100%, and its zeta potential was less than −30mV. Differential Inhibitors,research,lifescience,medical scanning calorimetry (DSC) and powder X-ray diffraction (PXRD) measurements indicated that the lipid in each formulation was recrystallized in the solid state, possessing a less-ordered structure compared to that of the bulk material. The release study of ASC-P from each formulation

using Franz diffusion cells revealed that the lipid matrix type affects both the rate and the release pattern. Inhibitors,research,lifescience,medical The release rate was in the order of ASC-P-loaded BW > ASC-P-loaded GMS > ASC-P-loaded CA. In viscoelastic analysis, all formulations showed that the storage modulus (G′) was higher than the loss modulus (G′′) and that the phase angle was <45°, indicating that they possess more elastic than viscous properties. Drug_discovery Thus, NLC gel can be used as a colloidal carrier for topical application. Wittayasuporn et al. reported encapsulation of ASC-P into methyl ether-terminated poly(ethylene oxide)-4-methoxycinnamolyphthaloylchitosan (PCPLC) nanoparticles [19]. PCPLC is a UV-screening amphiphilic chitosan derivative and is able to self-assemble into nanoparticles. Encapsulation of ASC-P into PCPLC resulted in 689nm particles with encapsulation efficiency of 84% at a 56% drug-loading rate.

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