A REVIEW ON: LIPOSOMAL DRUG DELIVERY
*Lalita K. Lende, N. D. Grampurohit,D.D. Gaikwad, M. V. Gadhave, Jadhav S.L.
VJSM’s Vishal Institutes Of Pharmaceutical Education And Research, Ale, (412411) Pune, Maharashtra,India.
ABSTRACT
The discovery of liposome or lipid vesicle emerged from self-forming
enclosed lipid bi-layer upon hydration; liposome drug delivery
systems have played a significant role in formulation of potent drug to
improve therapeutics. Recently the liposome formulations are targeted
to reduce toxicity and increase accumulation at the target site. There
are several new methods of liposome preparation based on lipid drug
interaction and liposome disposition mechanism including the
inhibition of rapid clearance of liposome by controlling particlesize,
charge and surface hydration. Most clinical applications of liposomal
drug delivery are targeting to tissue with or without expression of
target recognition molecules on lipid membrane. The liposomes are
characterized with respect to physical, chemical and biological
parameters. This mode of drug delivery lends more safety and
efficacy to administration of several classes of drugs like antiviral,
antifungal, antimicrobial, vaccines, anti-tubercular drugs and gene therapeutics. Present
applications of the liposomes are in the immunology, dermatology, vaccine adjuvant, eye
disorders, brain targeting, infective disease and in tumour therapy. The new developments in
this field are the specific binding properties of a drug-carrying liposome to a target cell such
as a tumor cell and specific molecules in the body (antibodies, proteins, peptides etc.); stealth
liposomes which are especially being used as carriers for hydrophilic (water soluble)
anticancer drugs like doxorubicin and bisphosphonate- liposome mediated depletion of
macrophages. This review would be a help to the researchers working in the area of
liposomal drug delivery.
Keywords: Liposomes, ULV, SLV, Applications.
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