AN OVERVIEW ON LIPOSPHERES
Rajesh Akki*, Sneha Sameera Bhattiprolu, Anjaneyulu Vinukonda and Singaram Kathirvel
Abstract
Both hydrophilic and lipophilic therapeutics can be delivered
successfully into deep and peripheral tissues such as cerebrospinal
fluid and central nervous system by encapsulating them with
crystalline lipids as lipospheres. The advent of lipospheres was meant
to deliver both therapeutic moieties with enhanced efficacy and added
stability to reach out intended tissue areas. Although extensive
information is available on physicochemical, analytical and
biopharmaceutical aspects of lipospheres, there was no specific order
pertaining to critical composition and rationale of component selection
available for academic and pilot scale processing of lipospheres. The interest of compiling
key points in a typical formulation of lipid lipospheres, this article was intrigued to discuss
melt method, co-solvent, microemulsion, super critical fluid, spray drying and spray
congealing techniques that were employed to scale up lipospheres. The selection criteria for
both the drugs and lipids in liposphere formulations were demonstrated here. The quality
assessment with variables like loading capacity and entrapment efficiency was explained. A
note on preliminary screening factors to determine the liposphere formation such as
liposphere dimensions with morphological scenario was detailed in this article. This article
also includes the stability and storage issues with reference to photolysis.
Keywords: Critical composition, entrapment efficiency, lipid drug delivery system, lipospheres, solvent emulsification- diffusion technique, stability.
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