EMULGEL FORMULATION PDF

EMULGEL FORMULATION PDF

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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Support Center Support Center. Abstract This study was conducted to develop an emulgel formulation of chlorphenesin CHL using 2 types of gelling agents: Az J Pharm Sci. As a general conclusion, it was suggested that the CHL emulgel formulation prepared with HPMC with the oil phase concentration rmulgel 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.

Rheological studies revealed that the CHL emulgels exhibited a shear-thinning behavior with thixotropy. The Theory and Practice of Industrial Pharmacy.

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This article has been cited by other articles in PMC. They also exhibited higher drug release and antifungal activity than the CHL powder. Egypt J Pharm Sci. All the prepared emulgels showed acceptable physical properties concerning color, homogeneity, consistency, spreadability, and pH value.

Optimization of chlorphenesin emulgel formulation

A study of shear and compression deformations on hydrophilic gels of tretinoin. This study was conducted to develop an emulgel formulation of chlorphenesin CHL using 2 types of gelling agents: Blackwell Scientific Publications; The prepared emulgels were evaluated for their physical appearance, rheological behavior, drug release, antifungal activity, and stability. It was found that the emulsifying agent concentration had the most pronounced effect on the drug release from the emulgels followed by the oil phase concentration and finally the type of the gelling agent.

Transdermal controlled release systems. Development of a thermoreversible gel for controlled-release ocular delivery of diclofenac sodium.

Bioavailability of salbutamol sulphate from different suppository formulations.

Marcel Dekker Inc; Received Dec 31; Accepted May The Pharmaceutical Press; Formulation and stability of chloramphenicol gel and emulgel. Encyclopedia of Pharmaceutical Formulatino. Author information Article notes Copyright and License information Disclaimer.

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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.

Lea and Febiger; Swarbrick J, Boylan JC, editors. The Complete Drug Reference.

Preparation of an emulgel for treatment of aphthous ulcer on the basis of carbomers. The drug release from all the emulgels was found to follow diffusion-controlled mechanism. Published online Sep 1. National Center for Biotechnology InformationU. Formulation and evaluation of topical preparations containing phenol and local vesicants.

Optimization of chlorphenesin emulgel formulation

Analysis of data on the medicament release from ointments. Medical Applications of Controlled Release. Please review our privacy policy.