FORMULATION AND EVALUATION OF NANOPARTICULATE DRUG DELIVERY SYSTEM OF ACYCLOVIR FOR TOPICAL DRUG DELIVERY
Divya Bhanu Parchuri, GS Shantha Kumar*, Divakar Goli1, Roopa Karki
ABSTRACT
The purpose of this research was to prepare Acyclovir nanoparticles
using Eudragit RS 100 by nanoprecipitation method with different
drugs to polymer (1:1, 1:2 and 1:3) and stabilizer (Pluronic F-68) ratio
(0.5%, 0.75% and 1%). Acyclovir nanoparticles potential was
evaluated in the topical drug delivery to reduce the dosing frequency.
The particle size and Zeta potential of all the formulations were found
found in the range of 48.3 to 356.1nm and 0.341 to 35.39 mV. From
SEM studies it was revealed that nanoparticles showed rough and
irregular in shape and no agglomeration. From the in vitro drug release
study, it was revealed that sustained release of same formulation last
up to 12 hours. Acyclovir loaded nanoparticles based topical gels were
formulated using nanoparticles and characterized for pH,
spreadability, drug content, viscosity, in vitro drug diffusion and
release kinetics comparatively compared with the commercial product.
The pH of all formulations was found near to the skin pH value. The in
vitro diffusion study of Acyclovir gel (G2) showed 64.92% and was 1.54 times more than the
commercial product. The release rate of G2 was compared to the marketed cream for 12 h
and was found to have no similarity and there is difference between the products. The results
suggest that DMSO (Dimethyl Sulfoxide) may be useful for enhancing the skin permeability
of Acyclovir from Acyclovir gel containing carbopol 934P gel as reservoir. The prepared
nanoparticles proved to be a potential candidate as a nanoparticulate controlled drug delivery
system and it is more potential for the topical drug delivery.
Keywords: Nanoparticles, Acyclovir, Eudragit RS 100, Pluronic F-68, Carbopol 934P.
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