SELF-EMULSIFYING DRUG DELIVERY SYSTEM: A REVIEW
Suresh Chandra Pandey*, Rajveer Kaur, Gangadharapp H.V., Sachin J.
ABSTRACT
Purpose: The oral delivery of poorly water soluble drug can be prepared by SEDDS. The major advantages of this approach overcome the primary rate limiting step of drug dissolution in GIT. Sometime the drug may precipitate out of solution when the formulation dispersion in the GIT, mainly when hydrophilic solvent in used. This problem can be overcome by dissolving the drug in the liqid vehicle there is less potential for precipitation on dilution in the GIT.[18] Mehtods: Solid SEDDS were developed mainly by
Spray drying,
Spray cooling,
Solid carriers,
Melt extrusion,
Dry emulsion,
Melt Granulation
Supercritical Fluid Based Method
Solid Lipid Nanoparticles andNanostructured Lipid Carriers
Capsule Filling With Liquid and Semisolids Self Emulsifying Formulations
Solid dispersion etc.
Conclusions: By using SEDDS we can Improvement in solubility & Bioavailability and we can use SEDDS for Herbal Drugs and Traditional Medicine.
Results:
Improvement in solubility & Bioavailability
Protection against Biodegradation
SEDDS for Herbal Drugs and Traditional Medicine.
Keywords: Self-emulsifying drug delivery systems, lipophilic drugs and oral delivery.
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