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@article{204871,
author = {Sulugoori Swetha and A.Aparna and Y.Shravan Kumar and Ch.Ramya},
title = {ENHANCING ORAL BIOAVAILABILITY OF FELODIPINE USING SOLID SELF-MICRO EMULSIFYING DRUG DELIVERY SYSTEMS},
journal = {International Journal of Innovative Research in Technology},
year = {2026},
volume = {13},
number = {1},
pages = {4770-4777},
issn = {2349-6002},
url = {https://ijirt.org/article?manuscript=204871},
abstract = {Developing a drug product with improved solubility and bioavailability is a challenge for poorly water-soluble drugs such as Felodipine. The aim of the present work was to develop a solid self-micro emulsifying drug delivery system (SMEDDS) of Felodipine to improve its solubility and dissolution rate. Solubility of Felodipine was determined in various oils, surfactants, and co-surfactants, and the micro emulsion region was identified by constructing a pseudo ternary phase diagram using the water titration method. Stable SMEDDS was prepared using a combination of Tween 20 and PEG 600 (2:1) with clove oil (7.5% v/v), and liquid SMEDDS was subsequently converted into solid SMEDDS (S-SMEDDS) by adsorption onto Aerosil 200 as a solid carrier. The S-SMEDDS was evaluated for micromeritic properties and in-vitro drug release, with results showing a cumulative drug release of 99% within 90 minutes, a particle size of 78.3 nm, a zeta potential of -17.4 mV, and a polydispersibility index of 0.27. These findings conclude that S-SMEDDS is a promising solid dosage form that significantly improves the solubility, dissolution rate, and oral bioavailability of Felodipine.},
keywords = {S-SMEDDS, Pseudo ternary phase diagram, bioavailability, dissolution rate.},
month = {June},
}
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