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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Main Authors: ACHMAD, FUAD HAFID, ACHMAD, RADJARAM, DWI, SETYAWAN
Format: Article PeerReviewed
Language:English
Indonesian
Published: Innovare Academic Sciences 2013
Subjects:
Online Access: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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Institution: Universitas Airlangga
Language: English
Indonesian
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spelling 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
institution Universitas Airlangga
building Universitas Airlangga Library
country Indonesia
collection UNAIR Repository
language English
Indonesian
topic R Medicine
RS Pharmacy and materia medica
RS1-441 Pharmacy and materia medica
spellingShingle 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
description 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.
format 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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