FORMULATION DEVELOPMENT AND EVALUATION OF EMULGEL DRUG DELIVERY SYSTEM FOR THE TREATMENT OF PSORIASIS
Monesh Patil*, Rahul Sharma, Dr. Jagdish Chandra Rathi
ABSTRACT
Mometasone furoate (MF) is a topical glucocorticoid having antiinflammatory,
anti-pruritic, anti-hyper proliferative activity. Owing to
these properties it is recommended in chronic inflammation and
psoriasis. In market, MF cream and lotion (0.1%) are available, which
show slight skin irritation, burning and common side-effects due to
steroids. To overcome the shortcomings of conventional formulations,
there is a need to develop a novel formulation that can reduce these
side-effects and show maximum desired effects. Thus, Emulgel can be
prepared which would help in increasing skin deposition as well as
provide sustained release. Developed formulations of Mometasone
furoate were evaluated for the physiochemical parameters such as drug content, viscosity,
spreadability, in vitro diffusion. Viscosity studies of various formulations revealed that
formulation F4 is better compare to others. Release of drug from Mometasone furoate
emulgel was significantly slower, which confirmed that slight prolonged drug release rate.
Incorporation of carbomer affected the release rate of the drug. By increasing the amount of
carbomer, the release rate of the drug decreased, which could be related to the increased
rigidity of the formulation, followed by its decreased permeability for the drug. In vitro drug
release from the semisolid preparation of Mometasone furoate emulgel optimized formulation
F4 shows significantly improved in drug release rate as compare to marketed preparation.
Keywords: Psoriasis, Formulation development, Carbopol 940, Mometasone furoate, Emulgel, In vitro drug release.
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