A REVIEW ON: TRANSETHOSOMES AS NOVEL VESICULAR CARRIERS FOR TRANSDERMAL DRUG DELIVERY
Mohammed Muzammil*, Nagaraja T. S., Yogananda R., Abubaker Siddiq, Maruthi N., Snehalatha and Rakshitha YA.
Abstract
Transdermal drug delivery is the non-invasive delivery of medications
from the surface of skin which is the largest and most accessible organ
of human body through its layers to the circulatory system.
Transdermal drug delivery offers many advantages over conventional
injection and oral methods but the skin, particularly stratum corneum
acts as a barrier to most drug absorption, so novel vesicular drug
delivery systems such as liposomes, niosomes, ethosomes,
transferosomes and transethosomes has been developed to overcome
this limitations and to improve the transport of drugs through the skin.
Transethosomes are the attempt to combine the advantages of classical
ethosomes with deformable liposomes (Transferosomes) in one formula. Transethosomes are
composed of phospholipids, ethanol, penetration enhancer or an edge activator and water.
The penetration rate of the skin is increased by ethanol and the drug is delivered into the
deeper layers of skin. These transethosomal systems are more efficient in drug delivery when
compare to other vesicular systems and these vesicles can be used for transdermal delivery of
various classes of drugs; transethosomes are simple to prepare and safe to use. The purpose of this review is to focus on various aspects of transethosomes including their mechanism of penetration, preparation, composition and characterization.
Keywords: Transethosomes, Transdermal drug delivery, vesicular drug delivery, Ethanol, Phospholipids.
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