FORMULATION AND EVALUATION OF COMPRESSION COATING FLOATING TABLETS OF CARVEDILOL PHOSPHATE ONCE DAILY DOSE

Objective: The rationale for the study was to develop a once-daily dose of immediate as well as a gastro-retentive form of carvedilol phosphate by compression coating floating technique.Methods: In the presented study the core tablet was containing half the quantity of the drug formulated as floating drug delivery using different controlled release polymers blend in various proportions like ethyl cellulose, carbopol, hydroxypropyl methylcellulose (HPMC) K4, K15, and K100 by direct compression method. Outer coat layer was formulated with rest of the drug with the blend of different super disintegrants in various proportions like crospovidone, croscarmellose sodium (CCS), sodium starch glycolate (SSG) for the immediate release of the drug. Both the immediate and controlled formulation was separately formulated from sf1 to sf9 and f1 to f9 respectively. Based on the evaluation parameters finally, formulation F1 to F9 were formulated by applying compression coating floating method. These formulations were characterized for their tablet density, disintegration time, floating lag time, in vitro drug release, drug-excipients interaction and accelerated stability studies etc.Results: The result revealed formulation sf9 containing SSG of 15% was able to 97.2% of drug release within 15 min towards the achievement of immediate release. Similarly, the formulation f9 containing 0.5:0.5:4.5 ratios of ethyl cellulose, carbopol and HPMC K15 was able to 95.3% of drug release within 16h. From compressed coat tablets batches of F1 to F9, based on the dissolution data F9 was considered as an optimized formulation which was able to release 48.6% of drug release within 15 min and cumulatively controlled the release up to 96.4% for 16 h, followed zero-order kinetics and Higuchi pattern.Conclusion: The results obtained in this research work clearly indicated that the compression coating floating tablet of carvedilol phosphate was the best dosage form for the treatment of hypertension. Results of the evaluation of prepared batches indicate that the batch F9 is a promising formulation for both a quick onset of action as well as gastro-retentive dosage form to maintain the constant drug action which would improve the maximum therapeutic efficacy and patient compliance

Design and evaluation of Moringa oleifera loaded transferosome vesicles: In vitro characterization

Moringa oleifera  herb is widely found in western ghat. The anticancer potential especially against breast cancer is proved by many scientific investigators. However poor skin permeability of active constituents limits the therapeutic use of this herbal active. Transfersomes are modified liposomes with improve skin permeation ability. Thus, extract loaded transfersomes were formulated to improve skin permeation of extract. The transfersomes are phospholipid based vesicles with edge activators. The edge activators increase skin permeation of transfersomes. The extract loaded transfersomes were fabricated using thin film hydration and assessed for vesicle size, microscopic imaging and thermal behavior. The transfersomes showed acceptable vesicle size and zeta potential. Thus, formulated transfersomes could be promising alternative for skin permeation enhancement of herbal active

Formulation and Evaluation of Tacrolimus Transdermal Gel

The present investigation is concerned with formulation and evaluation of Transdermal gels of Tacrolimus, anti-psoriasis drug, to circumvent the first pass effect and to improve its bioavailability with reduction in dosing frequency and dose related side effects. Twelve formulations were developed with varying concentrations of polymers like Carbopol 934P, HPMCK4M and Sodium CMC. The gels were tested for clarity, Homogeneity, Spreadability, Extrudability, Viscosity, surface pH, drug Content uniformity, in-vitro drug diffusion study and ex-vivo permeation study using rat abdominal skin. FTIR studies showed no evidence on interactions between drug, polymers and excipients. The best in-vitro drug release profile was achieved with the formulation F4 containing 0.5 mg of exhibited 6 hr drug release i.e. 98.68 % with desired therapeutic concentration which contains the drug and Carbopol 934p in the ratio of 1:2. The surface pH, drug content and viscosity of the formulation F4 was found to be 6.27, 101.3% and 3, 10,000cps respectively. The drug permeation from formulation F4 was slow and steady and 0.89gm of tacrolimus could permeate through the rat abdominal skin membrane with a flux of 0.071 gm hr-1 cm-2. The in-vitro release kinetics studies reveal that all formulations fit well with zero order kinetics followed by non-Fickian diffusion mechanism. Keywords: Transdermal gel, Viscosity, In-vitro drug release, In-vitro drug release kinetics study, Ex-vivo permeation stud

THERM_VENATION: Active Thermal Façade Venation: Fabricating a concrete twin-wall façade panel optimised for integrated heat exchange system

Passive measures to tackle increasing energy demands of modern buildings are aimed to generate energy from the roof or the ground beneath and by improving insulation to isolate indoors and outdoors. The author targets the opaque facade sections of a building to develop an active panel to exchange solar thermal energy with his project THERM_VENATION- Active Thermal Façade Venation. It is a project dealing with designing and fabrication of a twin-wall concrete façade panel with heat exchange tubular network embedded within it inspired by the leaf venation, which by actively exchanging fluid between the two panels conditions the indoor temperature, in the extreme composite climate of Delhi, India. This project follows a design through research methodology with computation tools, boundary conditions, material properties and the method of fabrication guiding the design and its result.Architecture, Urbanism and Building Sciences | Building Technolog