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Abstract

FORMULATION AND OPTIMIZATION OF KETOCONAZOLE LOADED ETHOSOMAL GEL FOR TOPICAL APPLICATION: IN VITRO & EX-VIVO CHARACTERIZATION

Dr. Ch. Saibabu*, Bhulakshmi Kambhampati, Palaparthi Lakshmi Vyshnavi, Poojala

Sravani, Animireddy Meghana, Narapusetti Varalakshmi, Kothapalli Vijaya

Lakshmi, Kommu Sowjanya, Kankanala Akash, P. L. Hari, Shaik Imran Ahmed

Abstract

The present study aimed to develop Ketoconazole -loaded ethosomal gel intended to be applied topically for treating skin infections. Ethosomes were prepared using the cold method. The formulation variables were optimize dusing[3] factorial designand Design Expert® software for analyzing the data statistically and graphically using response surfaceplots. Phospholipid (X1) and ethanol (X2) and propylene glycol (X3) were chosen as the independent variables, while the dependent variables comprised entrapment efficiency (Y1), vesicles size (Y2) and zeta potential (Y3). Ultra-centrifugation was used to assess the encapsulated medication after confirmingthe presence and size of vesicles. There was a greater increase in value (79.62%) in sonicated particles containing 30% w/w ethanol. The optimized ethosomes were subsequently incorporated into Carbopol® 940 gel and characterized for rheological behaviour, in-vitro release, ex-vivo skin permeation and deposition. Morphologically, the produced ethosome formulations were consistent when examined by SEM. All of the vesicles met or exceeded the criteria for nanotechnology in terms of size (less than 200 nm), polydispersity index (PDI), and entrapment efficiency (of the intended medication). The percentage of Ketoconazole released after 24 hours was significantlydecreased (p 0.05) when the ethosomes were included into a variety of gel bases. By contrast, ethosomal gel showed considerably greater anthralin penetration than the other tested preparations (p

Keywords: Topicalapplication; ethosomes; Ketoconazole, ex-vivopermeation, stability studies.


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