Dermal drug delivery system that is required to localizes methotrexate (MTX) in the synovial joint is needed to treat inflammation in rheumatoid arthritis (RA). The present investigation aims at exploring the potential of fatty acid vesicles for the topical delivery of methotrexate. Vesicles were prepared by film hydration method using oleic acid as a fatty acid principal component. Developed vesicles were characterized for size, size distribution, shape, in vitro release, pH dependent, and storage stability. Interaction between MTX and oleic acid was investigated using differential scanning calorimetry. The MTX amount permeated through rat skin was three- to fourfold higher using oleic acid compared to those from plain drug solution or carbopol gel. At the end of the skin permeation assay using ufasomes, up to 50% of the administered dose was found in the skin. These results suggest that methotrexate encapsulated in oleic acid vesicles may be of value for the topical administration of MTX in the treatment of psoriasis.
The purpose of study is to formulate and evaluate ufasomal gel of dexamethasone. Ufasomal suspension was made by sonication method using different concentrations of Span 80, Span 20 and cholesterol along with 25 mg of drug. Ufasomal gel was formulated by hydration method using carbopol 940. Ufasomal vesicles appeared as spherical and multilamellar under Transmission Electron Microscope. Ufasomal formulation prepared with drug to oleic acid molar ratio 8:2 (UF-2) produced greater number of vesicles and greater entrapment efficiency. UF-2 was optimized for further evaluation. The transdermal permeation and skin partitioning of from optimized formulation was significantly higher (P < 0.05) as compared to plain drug and plain gel formulation which is due to presence of surfactant acting as permeation enhancer. Permeation of optimized formulation was found to be about 4.7 times higher than plain drug gel. Anti-inflammatory activity evaluated by inhibition Carrageenan induced rat paw edema model. Significant reduction of edema (P < 0.10) was observed in comparison to the commercial product. Hence oleic acid based vesicles can be used as alternate carrier for topical delivery.
We have studied correlational properties of quasi-one-dimensional electron gas at finite temperature T by incorporating the dynamics of electron correlations within the quantum version of the self-consistent mean-field approach of Singwi, Tosi, Land, and Sjölander. Static structure factor, pair-correlation function, static density susceptibility, excess kinetic energy, and free correlation energy are calculated covering a wide range of temperature and electron number density. As at absolute zero temperature, the inclusion of dynamics of correlations results in stronger spatial electron correlations, with a pronounced peak in the static structure factor at wave vector q ∼ 3.5k F , which grows further with decreasing electron density. Below a critical density, the static density susceptibility seems to diverge at this value of q, signaling a transition from liquid to the Wigner crystal state-a prediction in qualitative agreement with recent simulations and experiment. However, thermal effects tend to impede crystallization with the consequence that the critical density decreases significantly with rising T. On the other hand, the pair-correlation function at short range exhibits a non-monotonic dependence on T, initially becoming somewhat stronger with rising T and then weakening continuously above a sufficiently high T. The calculated free correlation energy shows a noticeable dependence on T, with its magnitude increasing with increase in T. Further, we have looked into the effect of temperature on the frequency-dependence of dynamic local-field correction factor and the plasmon dispersion. It is found that with rising T the dynamics of correlations weakens, and the plasmon frequency exhibits a blue shift. Wherever interesting, we have compared our results with the lower-order approximate calculations and zero-T quantum Monte Carlo simulations.
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