Rajiv Academy for Pharmacy, National Highway #2 P.O. Chhattikara, Mathura Uttar Pradesh 281001, India; Faculty of Pharmacy, Rhodes University, Grahamstown 6140, South Africa
Sharma, R., Rajiv Academy for Pharmacy, National Highway #2 P.O. Chhattikara, Mathura Uttar Pradesh 281001, India; Walker, R.B., Faculty of Pharmacy, Rhodes University, Grahamstown 6140, South Africa; Pathak, K., Rajiv Academy for Pharmacy, National Highway #2 P.O. Chhattikara, Mathura Uttar Pradesh 281001, India
The objective of this study was to investigate the mechanism of release of econazole nitrate (EN) nanosponges loaded hydrogel and to compare it with EN hydrogel so as to develop an extended release topical drug delivery system of EN. Nanosponges of EN were prepared using ethyl cellulose and PVA by emulsion solvent evaporation method. On the basis of pharmacotechnical evaluation nanosponges with least particle size of 230.1 nm and good rheological properties were formulated as hydrogel (F1 - F7). In vitro drug release data of EN nanosponges loaded hydrogels in phosphate buffer pH 6.8 and 7.4 when analysed by GraphPad Prism software version 4.0 San Diego, USA best fitted the Makoid-2 Banakar model (R value greater than 0.98). The Korsmeyer-Peppas release exponent (n) ranged between 0.331 - 0.418, which confirmed diffusion as the principle mechanism of drug release. The release mechanism was further confirmed by calculating the ratio of exponents A/B ratio derived from the Kopcha model.
carbopol 934; econazole; ethyl cellulose; nanomaterial; nanosphere; nanosponge; unclassified drug; article; controlled study; drug administration route; drug delivery system; drug formulation; emulsion; flow kinetics; hydrogel; in vitro study; nanoanalysis; nanofabrication; nanopharmaceutics; particle size; patient attitude; pH measurement; scanning electron microscopy; surface property; sustained drug release