FORMULATION AND EVALUATION OF LIPOSOMES OF TRAMADOL HYDROCHLORIDE
Divya Kanungo*, Sunita Patidar, Deepak sen and Nutan Mimrot, Revathi A. Gupta
ABSTRACT
Controlled drug release methods such as the utilization of liposomal or
biodegradable polymer microencapsulation are technique used for
increasing the duration of action and decreasing the toxicity of drug.
Analgesic drug, Tramadol Hydrochloride was encapsulated in
liposomes for topical application. Tramadol liposomes were prepared
by Modified “Ether Injection” method was used. In the formulation
two different surfactant and two different lipids are used in different
combinations. The prepared liposomes were characterized for size,
shape, entrapment efficiency, in-vitro drug release (by franz diffusion
cell). The studies demonstrated successful preparation of Tramadol Hydrochloride liposomes
and effect of soya lecithin: cholesterol weight ratio on entrapment efficiency and on drug
release.
Keywords: Anangesic, Liposomes, Tramadol, Soya lecithin, Cholesterol.
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