The present study aims at preparing an Emulgel formulation of Meloxicam using emulsifiers and various gelling agents along with the use of. PDF | Emulgel is one of the recent technologies in NDDS used for dual control release of emulsion and gel for topical use. The stability of. PDF | Topical therapies in cream, ointment, gel and lotion formulation, are an important component of dermatological therapeutic.

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Abstract This study was conducted to develop an emulgel formulation of chlorphenesin CHL using 2 types of gelling agents: This article has been cited by other articles in PMC.

Optimization of chlorphenesin emulgel formulation

Transdermal controlled release systems. Please review our privacy policy. They also exhibited higher drug release and antifungal activity than the CHL powder.

Formulation and stability of chloramphenicol gel and emulgel. The Theory and Practice of Industrial Pharmacy.

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The prepared emulgels were evaluated for their physical appearance, rheological behavior, drug release, antifungal activity, and stability. This study was conducted to develop an emulgel formulation of chlorphenesin CHL using 2 types of gelling agents: Marcel Dekker Inc; Encyclopedia of Pharmaceutical Technology. Received Dec 31; Accepted May As a general conclusion, it was suggested that the CHL emulgel formulation prepared with HPMC with the oil phase concentration in its low level and emulsifying agent concentration in its high level was the formula of choice since it showed the highest drug release and antifungal activity.


The Pharmaceutical Press; All the prepared emulgels showed acceptable physical properties concerning color, homogeneity, consistency, spreadability, and pH value. Bioavailability of salbutamol sulphate from different suppository formulations.

Published online Sep 1. Preparation of an emulgel for treatment of aphthous ulcer on the basis of carbomers.

Optimization of chlorphenesin emulgel formulation

Rheological studies revealed that the CHL emulgels exhibited a shear-thinning behavior with thixotropy. Author information Article notes Copyright and License information Disclaimer.

Development of a thermoreversible gel for controlled-release ocular delivery of diclofenac sodium. Lea and Febiger; National Center for Biotechnology InformationU. Swarbrick Emulegl, Boylan JC, editors.

Analysis of data on the medicament release from ointments. Stability studies showed that the physical appearance, rheological properties, drug release, and antifungal activity in all the prepared emulgels remained unchanged upon storage for 3 months.

The Complete Drug Reference. The drug release from all the emulgels was found to follow diffusion-controlled mechanism. Support Center Support Center.


Medical Applications of Controlled Release. It was found that the emulsifying agent concentration had the most pronounced effect on the drug release from the emulgels followed formulatioh the oil phase concentration and finally the type of the gelling agent.

Commercially available CHL topical powder was used for comparison. Az J Pharm Sci. Blackwell Scientific Publications; A study of shear and compression deformations on emulgeo gels of tretinoin.