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  1. 学内発行誌
  2. 薬学部
  3. 薬学部研究年報
  4. 29

抗酸化作用を有する徐放性キトサン錠に関する研究(発表論文抄録(2010))

https://fukuyama-u.repo.nii.ac.jp/records/8841
https://fukuyama-u.repo.nii.ac.jp/records/8841
87d6a6fc-4cd5-41dc-974a-7458d24a79b9
名前 / ファイル ライセンス アクション
抗酸化作用を有する徐放性キトサン錠に関する研究.pdf 安福平(発表論文抄録(2010)) (588.0 kB)
Item type 紀要論文 / Departmental Bulletin Paper(1)
公開日 2018-01-15
タイトル
タイトル 抗酸化作用を有する徐放性キトサン錠に関する研究(発表論文抄録(2010))
タイトル
タイトル Useful Extend-release Chitosan Tablets with High Antioxidant Activity.
言語 en
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ departmental bulletin paper
著者 Yasufuku, Taira

× Yasufuku, Taira

WEKO 46265

Yasufuku, Taira

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Anraku, Makoto

× Anraku, Makoto

WEKO 46266

Anraku, Makoto

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Kondo, Yuko

× Kondo, Yuko

WEKO 46267

Kondo, Yuko

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Hata, Toshiyuki

× Hata, Toshiyuki

WEKO 46268

Hata, Toshiyuki

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Hirose, Junzo

× Hirose, Junzo

WEKO 46269

Hirose, Junzo

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Kobayashi, Nobuyuki

× Kobayashi, Nobuyuki

WEKO 46270

Kobayashi, Nobuyuki

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Tomida, Hisao

× Tomida, Hisao

WEKO 46271

Tomida, Hisao

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著者別名
識別子Scheme WEKO
識別子 45360
識別子Scheme CiNii ID
識別子URI http://ci.nii.ac.jp/nrid/9000018184429
識別子 9000018184429
姓名 安福, 平
著者別名
識別子Scheme WEKO
識別子 46167
識別子Scheme CiNii ID
識別子URI http://ci.nii.ac.jp/nrid/9000016655415
識別子 9000016655415
姓名 近藤, 裕子
著者別名
識別子Scheme WEKO
識別子 45236
識別子Scheme CiNii ID
識別子URI http://ci.nii.ac.jp/nrid/9000014625803
識別子 9000014625803
姓名 秦, 季之
著者別名
識別子Scheme WEKO
識別子 45879
識別子Scheme CiNii ID
識別子URI http://ci.nii.ac.jp/nrid/1000070080215
識別子 1000070080215
姓名 廣瀬, 順造
著者別名
識別子Scheme WEKO
識別子 46272
識別子Scheme CiNii ID
識別子URI http://ci.nii.ac.jp/nrid/9000019192509
識別子 9000019192509
姓名 小林, 誠幸
著者別名
識別子Scheme WEKO
識別子 45166
識別子Scheme CiNii ID
識別子URI http://ci.nii.ac.jp/nrid/9000005174459
識別子 9000005174459
姓名 冨田, 久夫
抄録
内容記述タイプ Abstract
内容記述 The antioxidant properties of different low molecular weight (LMW) chitosans (CS1; 22 kDa, CS2; 38 kDa, CS3; 52 kDa, CS4; 81 kDa) were examined for possible use in extended-release tablets. The criteria used were the ability of the chitosans to reduce Cu2+, and hydroxyl and superoxide radicals and N-centered radicals derived from 1,1'-diphenyl-2-picrylhydrazyl, via the use of ESR spectrometry. CS2 showed the highest scavenging activity. CS1 and CS3, however, were much less effective and CS4 was not a viable antioxidant. The results suggest that CS2 could be useful in combating the development of oxidative stress. A series of chitosan tablets were prepared using a spray drying method and evaluated as an extended-release matrix tablet using theophylline (TPH) as a model drug. The release of TPH from the different MW chitosan tablets increased with increasing MW of the chitosan used. CS2, CS3 and CS4 showed a reasonable release activity, but CS1 showed the shortest release activity. Moreover, the CS2-TPH tablet showed the highest scavenging activity of the three chitosan tablets (CS2-CS4) using 2,2'-azinobis (3-ethylbenzothiazoline-6-sulfonic acid) radicals. These results suggest that a CS2-TPH tablet could be potentially useful in an extended-release matrix tablet with a high antioxidant activity.
内容記述
内容記述タイプ Other
内容記述 The antioxidant properties of different low molecular weight (LMW) chitosans (CS1; 22 kDa, CS2; 38 kDa, CS3; 52 kDa, CS4; 81 kDa) were examined for possible use in extended-release tablets. The criteria used were the ability of the chitosans to reduce Cu2+, and hydroxyl and superoxide radicals and N-centered radicals derived from 1,1'-diphenyl-2-picrylhydrazyl, via the use of ESR spectrometry. CS2 showed the highest scavenging activity. CS1 and CS3, however, were much less effective and CS4 was not a viable antioxidant. The results suggest that CS2 could be useful in combating the development of oxidative stress. A series of chitosan tablets were prepared using a spray drying method and evaluated as an extended-release matrix tablet using theophylline (TPH) as a model drug. The release of TPH from the different MW chitosan tablets increased with increasing MW of the chitosan used. CS2, CS3 and CS4 showed a reasonable release activity, but CS1 showed the shortest release activity. Moreover, the CS2-TPH tablet showed the highest scavenging activity of the three chitosan tablets (CS2-CS4) using 2,2'-azinobis (3-ethylbenzothiazoline-6-sulfonic acid) radicals. These results suggest that a CS2-TPH tablet could be potentially useful in an extended-release matrix tablet with a high antioxidant activity.
書誌情報 福山大学薬学部研究年報
en : Annual report of the Faculty of Pharmacy & Pharmaceutical Sciences, Fukuyama University

号 29, p. 50-50, 発行日 2011-12-25
出版者
出版者 福山大学薬学部
ISSN
収録物識別子タイプ ISSN
収録物識別子 0288-724X
書誌レコードID
収録物識別子タイプ NCID
収録物識別子 AN10064550
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