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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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 Cyclosporin A emulgel for ocular delivery.

Search in Google Scholar. Based on the results of solubility studies, Isopropyl myristate, Polysorbate 80 and Ethanol were chosen as oil, surfactant and co-surfactant, respectively.

The microemulsion when diluted in 1: Hence, F3 with 1. The particle size of the microemulsion was found to be The study was initiated in December, and completed in May, The drug release was found to be higher for optimized formulation as compared to the marketed Terbinafine hydrochloride cream.

Formulation and Evaluation of Tioconazole Emulgel for Topical Drug Delivery System

November 12, DOI: Both of these models differ in terms of underlying pathways of the inflammatory cascade. The anti-inflammatory activity was numerically more in voltaren emulgel as compared to aceclofenac emulgel.


You can cite all versions by using the DOI Eric Randy Reyes Politud. Moreover, the reduction in inflammation was comparable to that of the most consumer preferred anti-inflammatory emulgel brand of diclofenac.

The objective to formulate an emulgel using non-irritating and pharmaceutically acceptable ingredients was achieved. The aceclofenac evaluatioh was transparent yellow colored solution with a pH of 5. The micro emulsion formulation developed in this maneuver was found to be satisfactory in terms of physical characteristics like clarity, particle size as well and in vitro drug diffusion Fig. Absorbance was measured after suitable dilution at nm using UV-Vis spectrophotometer.

All other chemicals and solvents were of analytical reagent grade. The test substance was diluted in 1: The dialysis membrane eemulgel attached between the donor and the receptor chamber of diffusion cell.

Formulation and evaluation of oxiconazole emulgel for topical drug delivery

Jatinder Pal Singh Chawla. It has a better tolerability profile as well as a better analgesic activity in comparison with diclofenac. Thus, the formulated emulgel was considered optimum, based on the firmulation characteristics and further subjected to animal testing for anti-inflammatory activity using two animal models viz. November 12, Journal article Open Access. Ethics committee approval number: So, All of authors and contributors must check their papers before submission to making assurance of following our anti-plagiarism policies.


Emulgel is one of the emerging topical drug delivery system for the delivery of hydrophobic drugs which overcome various disadvantages of ointments and creams such as greasiness and phase inversion. Formulation and evaluation of aceclofenac topical emulgel.

Evaluation of microemulsion Appearance and Ph: The activity produced by the formulated emulgel was at par with the most marketed emulgel formulation. These are applied as wide spectrum of preparations in case of both cosmetic and dermatological, to the healthy or diseased skin.

The anti-inflammatory activity of aceclofenac emulgel was evaluated using carrageenan induced paw edema in rats by a method described by Gerald et al. However, the implications of this phenomenon, when the drugs are administered topically remain evaluarion question to be addressed in future studies. Pseudo ternary phase diagram was constructed by varying Polysorbate 80 and ethanol in 1: Formulation and evaluation of mefenamic acid emulgel for topical delivery.