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Changes in the Physicochemical Properties of Piperine/β-Cyclodextrin due to the Formation of Inclusion Complexes

Piperine (PP) is a pungent component in black pepper that possesses useful biological activities; however it is practically insoluble in water. The aim of the current study was to prepare a coground mixture (GM) of PP and β-cyclodextrin (βCD) (molar ratio of PP/βCD = 1/1) and subsequently evaluate t...

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Autores principales: Ezawa, Toshinari, Inoue, Yutaka, Tunvichien, Sujimon, Suzuki, Rina, Kanamoto, Ikuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4779834/
https://www.ncbi.nlm.nih.gov/pubmed/26998357
http://dx.doi.org/10.1155/2016/8723139
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author Ezawa, Toshinari
Inoue, Yutaka
Tunvichien, Sujimon
Suzuki, Rina
Kanamoto, Ikuo
author_facet Ezawa, Toshinari
Inoue, Yutaka
Tunvichien, Sujimon
Suzuki, Rina
Kanamoto, Ikuo
author_sort Ezawa, Toshinari
collection PubMed
description Piperine (PP) is a pungent component in black pepper that possesses useful biological activities; however it is practically insoluble in water. The aim of the current study was to prepare a coground mixture (GM) of PP and β-cyclodextrin (βCD) (molar ratio of PP/βCD = 1/1) and subsequently evaluate the solubility of PP and physicochemical properties of the GM. DSC thermal behavior of the GM showed the absence of melting peak of piperine. PXRD profile of the GM exhibited halo pattern and no characteristic peaks due to PP and βCD were observed. Based on Job's plot, the PP/βCD complex in solution had a stoichiometric ratio of 1/1. Raman spectrum of the GM revealed scattering peaks assigned for the benzene ring (C=C), the methylene groups (CH(2)), and ether groups (C-O-C) of PP that were broaden and shifted to lower frequencies. SEM micrographs showed that particles in the GM were agglomerated and had rough surface, unlike pure PP and pure βCD particles. At 15 min of dissolution testing, the amount dissolved of PP in the GM was dramatically increased (about 16 times) compared to that of pure PP. Moreover the interaction between PP and βCD cavity was detected by (1)H-(1)H NMR nuclear Overhauser effect spectroscopy NMR spectroscopy.
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spelling pubmed-47798342016-03-20 Changes in the Physicochemical Properties of Piperine/β-Cyclodextrin due to the Formation of Inclusion Complexes Ezawa, Toshinari Inoue, Yutaka Tunvichien, Sujimon Suzuki, Rina Kanamoto, Ikuo Int J Med Chem Research Article Piperine (PP) is a pungent component in black pepper that possesses useful biological activities; however it is practically insoluble in water. The aim of the current study was to prepare a coground mixture (GM) of PP and β-cyclodextrin (βCD) (molar ratio of PP/βCD = 1/1) and subsequently evaluate the solubility of PP and physicochemical properties of the GM. DSC thermal behavior of the GM showed the absence of melting peak of piperine. PXRD profile of the GM exhibited halo pattern and no characteristic peaks due to PP and βCD were observed. Based on Job's plot, the PP/βCD complex in solution had a stoichiometric ratio of 1/1. Raman spectrum of the GM revealed scattering peaks assigned for the benzene ring (C=C), the methylene groups (CH(2)), and ether groups (C-O-C) of PP that were broaden and shifted to lower frequencies. SEM micrographs showed that particles in the GM were agglomerated and had rough surface, unlike pure PP and pure βCD particles. At 15 min of dissolution testing, the amount dissolved of PP in the GM was dramatically increased (about 16 times) compared to that of pure PP. Moreover the interaction between PP and βCD cavity was detected by (1)H-(1)H NMR nuclear Overhauser effect spectroscopy NMR spectroscopy. Hindawi Publishing Corporation 2016 2016-02-22 /pmc/articles/PMC4779834/ /pubmed/26998357 http://dx.doi.org/10.1155/2016/8723139 Text en Copyright © 2016 Toshinari Ezawa et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Ezawa, Toshinari
Inoue, Yutaka
Tunvichien, Sujimon
Suzuki, Rina
Kanamoto, Ikuo
Changes in the Physicochemical Properties of Piperine/β-Cyclodextrin due to the Formation of Inclusion Complexes
title Changes in the Physicochemical Properties of Piperine/β-Cyclodextrin due to the Formation of Inclusion Complexes
title_full Changes in the Physicochemical Properties of Piperine/β-Cyclodextrin due to the Formation of Inclusion Complexes
title_fullStr Changes in the Physicochemical Properties of Piperine/β-Cyclodextrin due to the Formation of Inclusion Complexes
title_full_unstemmed Changes in the Physicochemical Properties of Piperine/β-Cyclodextrin due to the Formation of Inclusion Complexes
title_short Changes in the Physicochemical Properties of Piperine/β-Cyclodextrin due to the Formation of Inclusion Complexes
title_sort changes in the physicochemical properties of piperine/β-cyclodextrin due to the formation of inclusion complexes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4779834/
https://www.ncbi.nlm.nih.gov/pubmed/26998357
http://dx.doi.org/10.1155/2016/8723139
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