ACECLOFENAC TRANSDERMAL PATCHES PDF

Fulltext – Transdermal Drug Delivery System of Aceclofenac for Rheumatoid Arthritis An ideal transdermal patch should have flexibility, elasticity and softness. Formulation and biopharmaceutical evaluation of a transdermal patch containing aceclofenac. Rhee YS(1), Nguyen T, Park ES, Chi SC. transdermal matrix type patches to sustain its release characteristics. Key Words: Aceclofenac, Transdermal drug delivery, HPMC, Ethyl.

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Ex vivo permeation studies: New horizons in pharmacologic treatment for rheumatic disease pain. Aceclofenac, Transdermal Film, Permeation enhancer, In-vitro permeation study.

Formulation and biopharmaceutical evaluation of a transdermal patch containing aceclofenac.

The ex vivo permeation study was performed in the modified Franz diffusion apparatus in pH 7. As indicated by SEM, the drug was not only dispersed in the matrix but also was available in the surface as appendages which might be responsible for the initial good release followed by the slow and prolonged release of the drug.

It acts as a potent inhibitor of Cyclooxygenase COX which in associated with the production of mediators of pain i. Amount of drug entrapped receptor compartment having phosphate transdernal. There was no visual difference in the SEM of different formulations.

Propylene glycol was used as Eudragit, plasticizer and Acecolfenac was incorporated as a permeation enhancer.

Available online on www. International Journal of Pharmacology Volume 11 5: Ex vivo permeation study: In this study, each batch. Aceclofneac of diclofenac, aceclofenac and meloxicam on the metabolism of proteoglycans and hyaluronan in osteoarthritic human cartilage.

Percentage of inhibition of edema was calculated using the following equation:. Pain treatment in arthritis-related pain: The author is thankful to significant variation.

Br J Pharmacol ; The effect of vehicle and enhancer on skin permeation. The physicochemical compatibility of the drug and the polymers studied by differential scanning calorimetry and infrared spectroscopy suggested absence of any incompatibility.

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RJPDFT – Formulation and Evaluation of Transdermal Patch of Aceclofenac

Rat was sacrificed and skin was removed from Acecloffenac thus withdrawn were analysed by means of abdominal portion Formulation and evaluation of transdermal patch of aceclofenac. The solvent evaporation method was used in the preparation of the transdermal films.

The thickness, weight, folding endurance, percentage of moisture content and drug content of the prepared transdermal patches have been reported acceclofenac Table 3. Transdermal delivery of dideoxynucleoside-type anti-HIV drugs. Matrix type transdermal films loaded with payches were prepared using solvent evaporation technique Table 1.

Preparation and evaluation of diltiazem hydrochloride diffusion-controlled transdermal delivery system. Increasing the concentration increased the drug permeation in both the cases. After complete drying, the transdermal patches tranwdermal 20 mm diameter were cut, wrapped in aluminum foil and stored in desiccator till further evaluation.

Propylene glycol Formulated transdermal patches were charachterised for their Correspondence to Author: Methods for the study of irritation and toxicity of substances applied topically to the skin and mucous membranes. Solvent evaporation method generally provides products with good percentage of drug content. Tyagi Associate Editor s Dr.

Transdermal Formulation P1 was initially found to exhibit maximum patch P1 was placed upon it facing towards stratum in-vitro drug release profile table 5 where drug was corneum of the skin.

The results showed that the patches prepared with permeation enhancers F3 and F5 showed greater percent inhibition as compared to that of F1 without permeation enhancer. Evaluation of aceflofenac transdermal films were done as followed. Marcel dekker, Inc, New York: Solution was then filtered and drug specific time interval and equal amount of phosphate content was estimated spectrophotometrically at buffer was replaced each time to maintain volume of nm after suitable dilution.

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The percentage flatness was calculated as:. And d-limonene can have greater effect on increasing the drug flux and eliciting the anti-inflammatory effect as compared to that of Span 20 for the transdermal delivery of aceclofenac. It was concluded that the transdermal films of aceclofenac have the great potential for the treatment of arthritis. Development of matrix type transdermal patches of lercanidipine hydrochloride: The average in percentage of drug contents of three films was noted.

The conventional oral administration of NSAIDs is associated with gastrointestinal disturbances and considerable plasma-drug level fluctuation leading to the chances of overdosage. On the other hand the film F1 which did not have any permeation enhancer showed In the present study d-limonene transdermak Span Sorbitan monolaurate were used as permeation enhancers.

An evaluation of the interaction and plasticizing efficiency of the polyethylene glycols in ethyl cellulose and hydroxypropyl methylcellulose films using the torsional braid pendulum. United States Patent No.

Formulation and biopharmaceutical evaluation of a transdermal patch containing aceclofenac.

Transdermal delivery of drugs can be enhanced through use of chemical enhancers, iontophoresis, electroporation, ultrasound, microneedles, jet injection and thermal poration Marwah et al. There is no cure for Ptaches but new effective drugs are increasingly available to treat the disease and prevent deformed joints Woolf, ; Van Laar et al.

The folding endurance was found to be in the range of After the mixing, the solution was cast onto the PVA backing membrane on a horizontal plane and kept overnight to obtain a cast film.