Dissolution Enhancemnet of Curcumin by Hydroxypropy-β-Cyclodextrin Complexation
The purpose of this study describes the formation of inclusion complex by coevaporation of curcumin using hydroxypropyl-β- cyclodextrin as carriers, to improve the solubility and dissolution of drug. Methods: The preparation of inclusion complex was carried out by using solvent method. The drug a...
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2013
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id-langga.565302017-05-08T21:21:15Z http://repository.unair.ac.id/56530/ Dissolution Enhancemnet of Curcumin by Hydroxypropy-β-Cyclodextrin Complexation ACHMAD, FUAD HAFID ACHMAD, RADJARAM DWI, SETYAWAN R Medicine RS Pharmacy and materia medica RS1-441 Pharmacy and materia medica The purpose of this study describes the formation of inclusion complex by coevaporation of curcumin using hydroxypropyl-β- cyclodextrin as carriers, to improve the solubility and dissolution of drug. Methods: The preparation of inclusion complex was carried out by using solvent method. The drug and carrier were dissolved in alcohol and subjected to solvent evaporation by a rotary evaporator. The residual powder preparation was allowed to dry overnight in vacuum desiccator, pulverized and sieved through # 60 mesh. The invitro dissolution testing was performed media in HCl 0.1 N aqueous solution. Characterization of inclusion complex and physical mixture was further evaluation using differential thermal analysis (DTA), powder X-ray diffraction (PXRD), FTIR spectrophotometry and a scanning electron microscope (SEM). The results: Evaluation of the phase solubility studies revealed a AL type diagram with complexation of equimolar ratio and solubility constant of 30.09 mM -1 . In-vitro dissolution studies showed that the curcumin entrapped in coevaporated complexes dissolved much faster than the incomplexed dissolved drug and physical mixtures. X-ray diffraction indicated loss a crystalline nature of the drug, FTIR, DTA studies revealed no interaction between curcumin and HPβCD. Conclusions: Inclusion complex of curcumin with HPβCD appears to have the advantage of dissolution enhancement and that may lead to improved bioavailability. Innovare Academic Sciences 2013-06-22 Article PeerReviewed text en http://repository.unair.ac.id/56530/1/7346.pdf text id http://repository.unair.ac.id/56530/2/2%20Penilaian%20Reviwear.pdf ACHMAD, FUAD HAFID and ACHMAD, RADJARAM and DWI, SETYAWAN (2013) Dissolution Enhancemnet of Curcumin by Hydroxypropy-β-Cyclodextrin Complexation. International journal of Pharmacy Pharmaceutical Sciences, 5 (3). pp. 401-405. ISSN 0975 - 1491 https://www.ijppsjournal.com/Vol5Suppl3.htm |
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R Medicine RS Pharmacy and materia medica RS1-441 Pharmacy and materia medica ACHMAD, FUAD HAFID ACHMAD, RADJARAM DWI, SETYAWAN Dissolution Enhancemnet of Curcumin by Hydroxypropy-β-Cyclodextrin Complexation |
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The purpose of this study describes the formation of inclusion complex by coevaporation of curcumin using hydroxypropyl-β-
cyclodextrin as carriers, to improve the solubility and dissolution of drug.
Methods: The preparation of inclusion complex was carried out by using solvent method. The drug and carrier were dissolved in alcohol and
subjected to solvent evaporation by a rotary evaporator. The residual powder preparation was allowed to dry overnight in vacuum desiccator,
pulverized and sieved through # 60 mesh. The invitro dissolution testing was performed media in HCl 0.1 N aqueous solution. Characterization of
inclusion complex and physical mixture was further evaluation using differential thermal analysis (DTA), powder X-ray diffraction (PXRD), FTIR
spectrophotometry and a scanning electron microscope (SEM).
The results: Evaluation of the phase solubility studies revealed a AL type diagram with complexation of equimolar ratio and solubility constant of
30.09 mM
-1
. In-vitro dissolution studies showed that the curcumin entrapped in coevaporated complexes dissolved much faster than the
incomplexed dissolved drug and physical mixtures. X-ray diffraction indicated loss a crystalline nature of the drug, FTIR, DTA studies revealed no
interaction between curcumin and HPβCD.
Conclusions: Inclusion complex of curcumin with HPβCD appears to have the advantage of dissolution enhancement and that may lead to improved
bioavailability. |
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Article PeerReviewed |
author |
ACHMAD, FUAD HAFID ACHMAD, RADJARAM DWI, SETYAWAN |
author_facet |
ACHMAD, FUAD HAFID ACHMAD, RADJARAM DWI, SETYAWAN |
author_sort |
ACHMAD, FUAD HAFID |
title |
Dissolution Enhancemnet of Curcumin by Hydroxypropy-β-Cyclodextrin Complexation |
title_short |
Dissolution Enhancemnet of Curcumin by Hydroxypropy-β-Cyclodextrin Complexation |
title_full |
Dissolution Enhancemnet of Curcumin by Hydroxypropy-β-Cyclodextrin Complexation |
title_fullStr |
Dissolution Enhancemnet of Curcumin by Hydroxypropy-β-Cyclodextrin Complexation |
title_full_unstemmed |
Dissolution Enhancemnet of Curcumin by Hydroxypropy-β-Cyclodextrin Complexation |
title_sort |
dissolution enhancemnet of curcumin by hydroxypropy-β-cyclodextrin complexation |
publisher |
Innovare Academic Sciences |
publishDate |
2013 |
url |
http://repository.unair.ac.id/56530/1/7346.pdf http://repository.unair.ac.id/56530/2/2%20Penilaian%20Reviwear.pdf http://repository.unair.ac.id/56530/ https://www.ijppsjournal.com/Vol5Suppl3.htm |
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