FORMULATION AND EVALUATION OF EMULGEL PDF

Materials and Methods: Emulgel formulations of diclofenac potassium were prepared using different . subjected to various evaluation parameters such as drug. Emulgels have been extensively covered as a promising drug delivery system for the administration of lipophilic drugs. This work was. Formulation and Evaluation of Luliconazole Emulgel for. Topical Drug Delivery. Dhobale Shankar,* Shelke Gajanan, Jadhav Suresh, Gaikwad.

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Cumulative corrections were made to obtain the total amount of drug release at each time interval. In case of control, inflammation showed an increase till 4 h, followed by a slight reduction. Ex-vivo drug release of emulgel was found to be The activity produced by the formulated emulgel was at par with the most marketed emulgel formulation.

Commercially available Terbinafine hydrochloride cream was used for comparison. Group I was diseased control, group II received dose of 25 mg of aceclofenac emulgel whereas group III received marketed diclofenac emulgel. In this investigation, a microemulsion-based emulgel of aceclofenac was successfully formulated, which lead to improved solubility and drug release of aceclofenac. If you encountered difficulties to submission of new manuscripts then you feel free to submit all the manuscripts to the Editor by e-mail as “attachment” to the electronic addresses: It is usually used to treat infections with anaerobic bacteria, but can also be used to treat some protozoal diseases, such as malaria.

The oxiconazole used in treatment of various fungal infections such as cutaneous and subcutaneous diseases like acne and psoriasis.

Formulation and evaluation of evauation topical emulgel. Undesirable skin changes, i. The objective to formulate an emulgel using non-irritating and pharmaceutically acceptable ingredients was achieved. Hence, developing formulation strategies for aceclofenac is particularly imperative 12.

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Carrageenan induced paw edema model: Formulation and evaluation of microemulsion based topical hydrogel containing lornoxicam. Amd is a non-steroidal anti-inflammatory drug NSAID glycolic ester of diclofenac, used for certain joint disorders.

Carrageenan induced paw edema and croton ear edema model.

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Aceclofenac is a non-steroidal anti-inflammatory drug used for pain relief and inflammation in certain joint disorders. The swelling in the paw of each rat was measured by plethysmometer by volume displacement method at baseline and every h till the 6th h Preparation and evaluation of aceclofenac topical microemulsion. The microemulsion region obtained in 1: Stability studies indicated that the physical appearance, rheological properties, spreadability, drug release in all the prepared emulgels remained unchanged upon storage for 3 months Keywords Terbinafine fofmulation, CarbapolAntifungal activity, Film formation, Emulgel formulation.

Moreover, the effectiveness of the formulation in delivering the drug as manifested in vitro and ex vivo studies, was transposed into significantly mitigating inflammation in animal models.

Formulation and evaluation of Cyclosporin A emulgel for ocular delivery.

The emulgel was applied on the properly shaven skin of rat. The aliquots 1 mL were collected at time intervals of 1 h formilation to 8 h. In vivo studies Skin irritation test: Ethanol was chosen for further studies.

Hence, the micro emulsion was considered optimum in terms of these pharmaceutical characteristics. Additionally, a study conducted by Patel et al.

Croton oil induced ear edema: The inflammation in the ear of each rat was noted using Vernier caliper at 1st, 2nd, 3rd and 4th h of treatment.

Anti-inflammatory studies by croton oil induced ear edema: Anbhule Department Of Pharmaceutics, P. The trend in inflammation and reduction efaluation similar as observed with the first model, in the respective groups.

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The current study focused on the development and optimization of an emulgel formulation of aceclofenac and evaluation of its anti-inflammatory activity against the standard, most preferred marketed Diclofenac emulgel in experimental animals.

FORMULATION AND EVALUATION OF CLINDAMYCIN PHOSPHATE EMULGEL | Zenodo

How to cite this article: The optimized formulation was subjected to formulatiion, resulting in formulation of an emulgel. The dual novel technique viz. Similar Articles in this Journal.

Evaluation of microemulsion 4 – 7 Appearance and pH: The drug release was found to be So, All evzluation authors and contributors must check their papers before submission to making assurance of following our anti-plagiarism policies. Isopropyl myristate formulatlon best solubility amongst all the oils, polysorbate 80 showed two times better solubility than other surfactants and Ethanol showed the 5 times better solubility amongst co-surfactants.

Microemulsion of aceclofenac was formulated with various polymers and optimized. Edema was induced in rats using 0. The study yields novel insights into the formulation strategies for designing a water soluble novel drug delivery system of an anti-inflammatory, low-solubility drug aceclofenac.

To overcome this limitation, emulgel, a novel drug delivery has emerged which is a combination of gel and emulsion, where the presence of gelling agent in the water phase converts a classical emulsion into a gel. Additionally, microemulsions have improved stability 12 – Within 24 formuoation from the Submission of Papers Review Notification: The receptor chamber was filled with freshly prepared phosphate buffer pH 6.

Microemulsion formulation for enhanced absorption of poorly soluble drugs:

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