Mechanochemical Effect on Controlled Drug Release of Konjac Glucomannan Matrix Tablets during Dry Grinding

To design a controlled drug release preparation based on a safe natural material, a Konjac glucomannan (KGM) mixture containing 16.0 <i>w/w</i>% calcium hydroxide (Ca(OH)<sub>2</sub>) was ground in a planetary ball mill for 0–120 min. The mechanochemical effect on the physico...

Full description

Bibliographic Details
Main Authors: Fuminori Okazaki, Yusuke Hattori, Tetsuo Sasaki, Makoto Otsuka
Format: Article
Language:English
Published: MDPI AG 2022-03-01
Series:Gels
Subjects:
Online Access:https://www.mdpi.com/2310-2861/8/3/181
_version_ 1827648896508100608
author Fuminori Okazaki
Yusuke Hattori
Tetsuo Sasaki
Makoto Otsuka
author_facet Fuminori Okazaki
Yusuke Hattori
Tetsuo Sasaki
Makoto Otsuka
author_sort Fuminori Okazaki
collection DOAJ
description To design a controlled drug release preparation based on a safe natural material, a Konjac glucomannan (KGM) mixture containing 16.0 <i>w/w</i>% calcium hydroxide (Ca(OH)<sub>2</sub>) was ground in a planetary ball mill for 0–120 min. The mechanochemical effect on the physicochemical properties of the KGM ground product was investigated by Fourier-transform infrared spectroscopy (FT-IR), powder X-ray spectroscopy, scanning electron microscopy with energy-dispersive X-ray spectroscopy, and drug release testing. The FT-IR spectra of the ground KGM indicated that the deacetylation reaction of KGM was accelerated in the Ca(OH)<sub>2</sub>-containing sols by mechanochemical energy, and the degree of deacetylation of KGM was dependent on the grinding time. The time required for tablet disintegration of the KGM matrix tablets containing theophylline increased as the grinding time increased; therefore, drug release was sustained. The Higuchi plots of the matrix tablets obtained from KGM ground for 60–120 min exhibited good linearity because they maintained their gel matrix tablet shape during the release test. However, KGM tablets ground for 0–30 min exhibited nonlinear curves, which were caused by tablet disintegration. This suggests that drug release from the KGM matrix tablet can be freely controlled by the degree of mechanochemical treatment.
first_indexed 2024-03-09T19:48:24Z
format Article
id doaj.art-80a7ce7e49db4b308478aa9f4de19c8f
institution Directory Open Access Journal
issn 2310-2861
language English
last_indexed 2024-03-09T19:48:24Z
publishDate 2022-03-01
publisher MDPI AG
record_format Article
series Gels
spelling doaj.art-80a7ce7e49db4b308478aa9f4de19c8f2023-11-24T01:16:53ZengMDPI AGGels2310-28612022-03-018318110.3390/gels8030181Mechanochemical Effect on Controlled Drug Release of Konjac Glucomannan Matrix Tablets during Dry GrindingFuminori Okazaki0Yusuke Hattori1Tetsuo Sasaki2Makoto Otsuka3Faculty of Pharmacy, Musashino University, 1-1-20 Shinmachi, Nishi-Tokyo 202-8585, Tokyo, JapanFaculty of Pharmacy, Musashino University, 1-1-20 Shinmachi, Nishi-Tokyo 202-8585, Tokyo, JapanGraduate School of Medical Photonics, Shizuoka University, 3-5-1 Johoku, Naka-ku, Hamamatsu 432-8011, Shizuoka, JapanFaculty of Pharmacy, Musashino University, 1-1-20 Shinmachi, Nishi-Tokyo 202-8585, Tokyo, JapanTo design a controlled drug release preparation based on a safe natural material, a Konjac glucomannan (KGM) mixture containing 16.0 <i>w/w</i>% calcium hydroxide (Ca(OH)<sub>2</sub>) was ground in a planetary ball mill for 0–120 min. The mechanochemical effect on the physicochemical properties of the KGM ground product was investigated by Fourier-transform infrared spectroscopy (FT-IR), powder X-ray spectroscopy, scanning electron microscopy with energy-dispersive X-ray spectroscopy, and drug release testing. The FT-IR spectra of the ground KGM indicated that the deacetylation reaction of KGM was accelerated in the Ca(OH)<sub>2</sub>-containing sols by mechanochemical energy, and the degree of deacetylation of KGM was dependent on the grinding time. The time required for tablet disintegration of the KGM matrix tablets containing theophylline increased as the grinding time increased; therefore, drug release was sustained. The Higuchi plots of the matrix tablets obtained from KGM ground for 60–120 min exhibited good linearity because they maintained their gel matrix tablet shape during the release test. However, KGM tablets ground for 0–30 min exhibited nonlinear curves, which were caused by tablet disintegration. This suggests that drug release from the KGM matrix tablet can be freely controlled by the degree of mechanochemical treatment.https://www.mdpi.com/2310-2861/8/3/181konjac glucomannansolid-state mechanochemical reactionswelling and disintegration propertyFourier-transform infrared spectral changepolymer matrix tabletssustained drug release kinetics
spellingShingle Fuminori Okazaki
Yusuke Hattori
Tetsuo Sasaki
Makoto Otsuka
Mechanochemical Effect on Controlled Drug Release of Konjac Glucomannan Matrix Tablets during Dry Grinding
Gels
konjac glucomannan
solid-state mechanochemical reaction
swelling and disintegration property
Fourier-transform infrared spectral change
polymer matrix tablets
sustained drug release kinetics
title Mechanochemical Effect on Controlled Drug Release of Konjac Glucomannan Matrix Tablets during Dry Grinding
title_full Mechanochemical Effect on Controlled Drug Release of Konjac Glucomannan Matrix Tablets during Dry Grinding
title_fullStr Mechanochemical Effect on Controlled Drug Release of Konjac Glucomannan Matrix Tablets during Dry Grinding
title_full_unstemmed Mechanochemical Effect on Controlled Drug Release of Konjac Glucomannan Matrix Tablets during Dry Grinding
title_short Mechanochemical Effect on Controlled Drug Release of Konjac Glucomannan Matrix Tablets during Dry Grinding
title_sort mechanochemical effect on controlled drug release of konjac glucomannan matrix tablets during dry grinding
topic konjac glucomannan
solid-state mechanochemical reaction
swelling and disintegration property
Fourier-transform infrared spectral change
polymer matrix tablets
sustained drug release kinetics
url https://www.mdpi.com/2310-2861/8/3/181
work_keys_str_mv AT fuminoriokazaki mechanochemicaleffectoncontrolleddrugreleaseofkonjacglucomannanmatrixtabletsduringdrygrinding
AT yusukehattori mechanochemicaleffectoncontrolleddrugreleaseofkonjacglucomannanmatrixtabletsduringdrygrinding
AT tetsuosasaki mechanochemicaleffectoncontrolleddrugreleaseofkonjacglucomannanmatrixtabletsduringdrygrinding
AT makotootsuka mechanochemicaleffectoncontrolleddrugreleaseofkonjacglucomannanmatrixtabletsduringdrygrinding