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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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The ex vivo permeation studies of the films of aceclofenac through an excised rat abdominal skin were carried out using the Franz diffusion cell. The d-limonene showed the greater permeation enhancement effect as compared to that of Span Jantharaprapap and Stagni, Both the formulations were found to be non-irritant to the skin because it showed erythema and edema score less than 2 Mamatha et al.

Pe et atio Government of India, It must also possess the good adhesive strength for the prolonged retention on the skin for the desired duration of action. The transdermal films prolonged the drug release up to 24 h thereby minimizing the dosage frequency aceclofsnac the conventional oral drug delivery. Evaluation of prepared transdermal films were done as followed.

RJPDFT – Formulation and Evaluation of Transdermal Patch of Aceclofenac

United States Patent No. Methods for the study of irritation and toxicity of substances applied topically to the skin and mucous membranes. Delivering drugs by the transdermal route: Propylene glycol was used as Eudragit, plasticizer and DMSO was incorporated as a permeation enhancer. The two selected formulations were subjected to in vivo anti-inflammatory study using the standard carrageenan induced hind rat paw edema model.

The control group group I received the gransdermal blank patches. Table 4 below carried out in order to determine transition of drug shows the in-vitro permeation profile of drug from from patch to skin microcirculation. Effects and mechanisms of total glucosides of paeony on adjuvant arthritis in rats. Permeation studies are and concentration was then calculated. Aceclofrnac variation was studied patchss room temperature for 24hrs.


Pharmacology of the potent new non-steroidal anti-inflammatory agent aceclofenac. Amount of drug entrapped receptor compartment having phosphate ptaches.

Various chemical agents act as permeation enhancers. To overcome these problems the transdermal delivery of aceclofenac can be investigated for prolonged relief from pain and local inflammation in arthritis. Bioadhesive film for dermal and transdermal drug delivery. Tyagi Associate Editor s Dr. For the patients of rheumatoid arthritis, delivering the drugs in transdermal films may not only increase the patient compliance but also provide the immediate and prolonged release of the drug.

It also finds transdermql use in Transdermal drug delivery has certain advantages over peripheral diabetic neuropathy, fibromyalgia and post- other systems of drug administration which in turn therapeutic neuralgia. Propylene glycol Formulated transdermal patches were charachterised for their Correspondence to Author: In some previous studies d-limonene has been reported to be the very promising penetration enhancer Yang et al.

Skin permeation of propranolol from polymeric film containing terpene enhancers for transdermal use, Int.

Implications for the diagnosis and treatment of pain. International Journal of Pharmaceutical Sciences Review and There is no cure for RA but new effective drugs are increasingly available to treat the disease and prevent deformed joints Woolf, ; Van Laar et al.

There was no visual difference in the SEM of different formulations. Development and evaluation of pharmacosomes of aceclofenac.

Formulation and biopharmaceutical evaluation of a transdermal patch containing aceclofenac.

These enhancers do not affect the stability and biological activity of the drugs like proteins and peptides even Varman and Singh, Pregabalin PGB is an anticonvulsant aim of achieving controlled release of Pregabalin over and analgesic drug 1, which is required to be a prolong time period so that frequency of drug administered three to four times per day for its administration will be minimised.


Ex vivo permeation studies: The dorsal surface of rats was shaved 12 h before commencing the study. In the present study, the transdermal films of aceclofenac were prepared and the effect of two permeation enhancers in increasing the flux of the drug was studied. The terpene based enhancers like limonene showed the greater effect of increasing the flux and anti-inflammatory activity as compared to that of nonionic surfactants Span Receptor compartment was filled permeated through cellulose nitrate membrane; with Phosphate buffer pH 7.

The rats were kept in cages in standard environmental conditions of light and temperature. Pain treatment in arthritis-related pain: Lipid-protein-partitioning LPP theory of skin enhancer activity: The percentage of moisture content was calculated as the difference between initial and final weight with respect to final weight. Hence, a non-invasive metabolism; all these factors make this system most system in the form of transdermal patch of Pregabalin suitable for systemic delivery of drug over long time was thought to be developed and evaluated with the periods of 24hrs.

The various chemicals used to improve the penetration across the skin are alcohols, Terpenes, surfactants etc. To improve the quality of life of arthritic patients managing moderate to severe chronic pain remains challenging for various reasons Perrot, But it is associated with short half-life h and gastro-intestinal side effects.

The tensile following formula.

Physicochemical and in-vitro characterization. After activation the silica gel-coated TLC plates were developed for the drug excipients and their physical mixture in the mobile phase of hydrochloric acid: