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Changes in the Physicochemical Properties of Piperine/β-Cyclodextrin due to the Formation of Inclusion Complexes
Author(s) -
Toshinari Ezawa,
Yutaka Inoue,
Sujimon Tunvichien,
Rina Suzuki,
Ikuo Kanamoto
Publication year - 2016
Publication title -
international journal of medicinal chemistry
Language(s) - English
Resource type - Journals
eISSN - 2090-2069
pISSN - 2090-2077
DOI - 10.1155/2016/8723139
Subject(s) - chemistry , solubility , piperine , dissolution , cyclodextrin , raman spectroscopy , glass transition , spectroscopy , nuclear chemistry , nuclear overhauser effect , crystallography , nuclear magnetic resonance spectroscopy , analytical chemistry (journal) , stereochemistry , organic chemistry , physics , optics , polymer , quantum mechanics
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 ( β CD) (molar ratio of PP/ β CD = 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 β CD were observed. Based on Job's plot, the PP/ β CD 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 β CD 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 β CD cavity was detected by 1 H- 1 H NMR nuclear Overhauser effect spectroscopy NMR spectroscopy.

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