DEVELOPMENT OF CURCUMIN NANOCRYSTALS AND EVALUATION OF GI ABSORPTION EFFICIENCY IN COPMPARISON WITH CURCUMIN AND TURMERIC POWDER
Jeevana Jyothi B.* and Sravani R.
ABSTRACT
The aim of the present research work was to prepare curcumin
nanocrystals and to assess GI absorption in comparison with pure
curcumin and turmeric powder, an INDIAN food ingredient. Eight
formulations of nanocrystals of curcumin were prepared in two steps
involving homogenization and lyophillization each containing 500 mg
of curcumin. polyvinylpyrrolidone, poloxomer 407, PEG 15000,
pluronics f-68 stabilizers were used as stabilizers. The prepared
nanocrystals were evaluated for uniformity of drug content, solubility
studies, in-vitro drug release studies. The drug content values ranging
in between 93.25 to 99.23% were acceptable. Solubility of curcumin
was reasonably enhanced from all nanocrystals and free solubility of
211.61 μg/ml was evidenced from formulation F5.In-vitro drug release
of 92.24%. in 120 min was highest from formulation, F5. Ex-vivo
absorption studies using intestinal membrane of goat revealed highest
release 72.83% from promising formulation, F5 than pure curcumin and turmeric powder
release data of 44.6% and 41.3% after 24 hr. Hence it is concluded from these studies that
domestic Indian food ingredient, turmeric do not aid reasonable absorption and dissolution of
curcumin through GI membrane and hence cannot expect beneficial pharmacological effects
of its principle ingredient curcumin when it is used in foods. But the solubility and absorption
of curcumin nanocrystals were enhanced to appreciably extent to elicit its clinical
applications.
Keywords: Curcumin, Turmeric, curcumin nanosrystals, solubility, enhanced absorption, in-vitro dissolution.
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