Formulation and Evaluation of Microemulsion

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Authors: Devika Thengal, Amruta Wable*, Anuja Wayase, Priyanka Yadave
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Abstract

Due to their unit optical properties, micro-emulsions macroscopically isotropic blends of at least of an associated hydrophilic, hydrophobic, and an amphiphilic half. These are more stable than other units. Clear emulsion forms, typically combined with a co the diameter of the surfactant falls within the range of 10-140 µm. The micro-emulsion is now Formulations are universally recognized as Transmit the hydrophilic, but due to the lipophilic Drugs as drug transporters, so they require Numerous other fantastic drug-solving Capacity, extended duration, improved bioavailability, the Ease of preparation and extremely low surface tension and vast amounts of surface area. Micro- emulsions are one of the most agreeable candidates for the new medication Delivery mechanism because of their extended shelf life, sophisticated drug solubilization without any issues Administration and preparation. Micro- emulsions are Water and oil solutions that are thermodynamically stable As well as amphiphile. They have become new. Vehicles for the transportation of drugs that permit Sustained or regulated release for the eyes, Parenteral, transdermal, topical, and percutaneous Medication administration. Micro-emulsions Is readily discernible from common emulsions. Due to their transparency, low viscosity, and more precisely their stability in thermodynamics.

Fields of Study & Subjects

Surfactants and Colloidal Systems Advanced Drug Delivery Systems Drug Solubulity and Delivery Systems

Publication details

Journal / source
Zenodo (CERN European Organization for Nuclear Research)
Publication date
31 January 2026