Development and Thermophysical Profile of Cetyl Alcohol-in-Water Nanoemulsions for Thermal Management

This study focuses on the preparation, thermophysical and rheological characterization of phase change material nanoemulsions as latent functionally thermal fluids. Aqueous dispersions with fine droplets of cetyl alcohol (with a melting temperature at ~321 K) were prepared by means of a solvent-assisted method, combining ultrasonication with non-ionic and anionic emulsifiers. Eicosyl alcohol (melting at ~337 K) and hydrophobic silica nanoparticles were tested as nucleating agents. Droplet size studies through time and after freeze–thaw cycles confirmed the good stability of formulated nanoemulsions. Phase change analyses proved the effectiveness of eicosyl alcohol to reduce subcooling to a few Kelvin. Although phase change material emulsions exhibited thermal conductivities much larger than bulk cetyl alcohol (at least 60% higher when droplets are solid), reductions in this property reached 15% when compared to water. Samples mainly showed desirable Newtonian behavior (or slight shear thinning viscosities) and modifications in density around melting transition were lower than 1.2%. In the case of phase change material nanoemulsions with 8 wt.% content of dispersed phase, enhancements in the energy storage capacity overcome 20% (considering an operational temperature interval of 10 K around solid–liquid phase change). Formulated dispersions also showed good thermal reliability throughout 200 solidification–melting cycles.

DoE-Based Design of a Simple but Efficient Preparation Method for a Non-Effervescent Gastro-Retentive Floating Tablet Containing Metformin HCl

A sustained-release non-effervescent floating matrix tablet was prepared using a simple and efficient direct compression of spray-dried granules containing metformin hydrochloride and cetyl alcohol with hydroxypropyl methylcellulose K15M (HPMC K15M). The design of experiments was employed to explore the optimal composition of the tablet. The similarity factor was employed to evaluate the equivalence in dissolution profiles between the test tablets and Glucophage XR as a reference. Bootstrap analysis was used to eliminate the formulations for which the dissolution profile was potentially inequivalent to that of the reference. The optimized tablet consisting of 150 mg of cetyl alcohol and 17% HPMC K15M showed a dissolution profile comparable with that of the reference with a similarity factor of 52.41, exhibited a floating lag time of less than 3 s in buffer media, remained floating for 24 h, and reduced the tablet weight by about 20% compared to that of the reference. The current study sheds light on the potential use of non-effervescent gastro-retentive extended-release tablets for high-dose drugs using a simple and efficient direct compression method, and as a potential alternative treatment for Glucophage XR. This study also highlights the importance of a systematic approach to formulation optimization and the evaluation of the dissolution profile.

UJI STABILITAS DAN IRITASI FORMULA KRIM ANTI NYERI EKSTRAK ETANOL DAUN KELOR (Moringa oleifera)

Moringa oleifera leaf contains quercetin act as an analgesic by inhibiting cyclooxygenase and lipooxygenase. These enzymes interfere synthesis of prostaglandins by arachidonic acid and lead to reduce pain. This study aimed to obtain a physically stable M/A cream formula from the lyophilized ethanol extract of Moringa leaf and to determine the irritation effect. The cream prepared with variations of cetyl alcohol concentration F1 (2%), F2 (4%,) and F3 (6%). The cream stability was determined with organoleptic, homogeneity, type of emulsion, pH, viscosity, and spreadability parameters after accelerated condition. The Irritancy test was determined to the Albino Oryctolagus cuniculus. The results showed that F1 has the best stability than F2 and F3 and showed irritation index 0,5 classified as moderate irritation.