WEKO3
アイテム
{"_buckets": {"deposit": "4157df7c-733d-478d-a27f-7d8dbe698bdd"}, "_deposit": {"created_by": 2, "id": "1508", "owners": [2], "pid": {"revision_id": 0, "type": "depid", "value": "1508"}, "status": "published"}, "_oai": {"id": "oai:nagasaki-u.repo.nii.ac.jp:00001508", "sets": ["74"]}, "author_link": ["7213", "7215", "7211", "7214", "7212", "7210"], "item_2_biblio_info_6": {"attribute_name": "書誌情報", "attribute_value_mlt": [{"bibliographicIssueDates": {"bibliographicIssueDate": "2018-12-17", "bibliographicIssueDateType": "Issued"}, "bibliographicIssueNumber": "1", "bibliographicPageStart": "5", "bibliographicVolumeNumber": "20", "bibliographic_titles": [{"bibliographic_title": "AAPS PharmSciTech"}]}]}, "item_2_description_4": {"attribute_name": "抄録", "attribute_value_mlt": [{"subitem_description": "Vancomycin (VCM) is an important antibiotic for treating methicillin-resistant Staphylococcus aureus (MRSA) infections. To treat bacterial meningitis caused by MRSA, it is necessary to deliver VCM into the meninges, but the rate of VCM\ntranslocation through the blood-brain barrier is poor. Additionally, high doses of intravascularly (i.v.) administered VCM may cause renal impairments. Thus, VCM is sometimes administered intracerebroventricularly (i.c.v.) for clinical treatment. However, information on the VCM pharmacokinetics in cerebrospinal fluid (CSF) after\ni.c.v. administration is lacking. In the present study, we evaluated the VCM pharmacokinetics in the CSF and systemic circulation after i.c.v. compared to that after i.v. administration, using the brain microdialysis method in mice. VCM administered\nvia i.c.v. showed a highly selective distribution in the CSF, without migration to systemic circulation. Moreover, to assess renal impairments after i.c.v. administration of VCM, we histologically evaluated damage to the mouse kidney by hematoxylin and eosin staining. No significant morphological change in the kidney was observed in the i.c.v. administration group compared to that in the i.v. administration group. Our results \ndemonstrate that i.c.v. administration of VCM can be partially prevented from entering the systemic circulation to prevent renal impairments caused by VCM.", "subitem_description_type": "Abstract"}]}, "item_2_description_63": {"attribute_name": "引用", "attribute_value_mlt": [{"subitem_description": "AAPS PharmSciTech, 20(1), art.no.5; 2019", "subitem_description_type": "Other"}]}, "item_2_publisher_33": {"attribute_name": "出版者", "attribute_value_mlt": [{"subitem_publisher": "Springer International Publishing"}]}, "item_2_relation_12": {"attribute_name": "DOI", "attribute_value_mlt": [{"subitem_relation_type": "isVersionOf", "subitem_relation_type_id": {"subitem_relation_type_id_text": "10.1208/s12249-018-1232-8", "subitem_relation_type_select": "DOI"}}]}, "item_2_rights_13": {"attribute_name": "権利", "attribute_value_mlt": [{"subitem_rights": "c 2018, American Association of Pharmaceutical Scientists."}, {"subitem_rights": "The original publication is available at www.springerlink.com."}]}, "item_2_source_id_8": {"attribute_name": "EISSN", "attribute_value_mlt": [{"subitem_source_identifier": "15309932", "subitem_source_identifier_type": "ISSN"}]}, "item_2_version_type_16": {"attribute_name": "著者版フラグ", "attribute_value_mlt": [{"subitem_version_resource": "http://purl.org/coar/version/c_ab4af688f83e57aa", "subitem_version_type": "AM"}]}, "item_creator": {"attribute_name": "著者", "attribute_type": "creator", "attribute_value_mlt": [{"creatorNames": [{"creatorName": "Miura, Yusuke"}], "nameIdentifiers": [{"nameIdentifier": "7210", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Fuchigami, Yuki"}], "nameIdentifiers": [{"nameIdentifier": "7211", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Nomura, Sakiko"}], "nameIdentifiers": [{"nameIdentifier": "7212", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Nishimura, Koyo"}], "nameIdentifiers": [{"nameIdentifier": "7213", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Hagimori, Masayori"}], "nameIdentifiers": [{"nameIdentifier": "7214", "nameIdentifierScheme": "WEKO"}]}, {"creatorNames": [{"creatorName": "Kawakami, Shigeru"}], "nameIdentifiers": [{"nameIdentifier": "7215", "nameIdentifierScheme": "WEKO"}]}]}, "item_files": {"attribute_name": "ファイル情報", "attribute_type": "file", "attribute_value_mlt": [{"accessrole": "open_date", "date": [{"dateType": "Available", "dateValue": "2020-12-18"}], "displaytype": "detail", "download_preview_message": "", "file_order": 0, "filename": "AAPS-PST20_5.pdf", "filesize": [{"value": "445.0 kB"}], "format": "application/pdf", "future_date_message": "", "is_thumbnail": false, "licensetype": "license_free", "mimetype": "application/pdf", "size": 445000.0, "url": {"label": "AAPS-PST20_5.pdf", "url": "https://nagasaki-u.repo.nii.ac.jp/record/1508/files/AAPS-PST20_5.pdf"}, "version_id": "006b4f7e-1129-4713-8fd9-5153390cfaf9"}]}, "item_keyword": {"attribute_name": "キーワード", "attribute_value_mlt": [{"subitem_subject": "intracerebroventricular administration", "subitem_subject_scheme": "Other"}, {"subitem_subject": "vancomycin", "subitem_subject_scheme": "Other"}, {"subitem_subject": "microdialysis", "subitem_subject_scheme": "Other"}, {"subitem_subject": "pharmacokinetics", "subitem_subject_scheme": "Other"}]}, "item_language": {"attribute_name": "言語", "attribute_value_mlt": [{"subitem_language": "eng"}]}, "item_resource_type": {"attribute_name": "資源タイプ", "attribute_value_mlt": [{"resourcetype": "journal article", "resourceuri": "http://purl.org/coar/resource_type/c_6501"}]}, "item_title": "Brain Microdialysis Study of Vancomycin in the Cerebrospinal Fluid After Intracerebroventricular Administration in Mice", "item_titles": {"attribute_name": "タイトル", "attribute_value_mlt": [{"subitem_title": "Brain Microdialysis Study of Vancomycin in the Cerebrospinal Fluid After Intracerebroventricular Administration in Mice"}]}, "item_type_id": "2", "owner": "2", "path": ["74"], "permalink_uri": "http://hdl.handle.net/10069/38774", "pubdate": {"attribute_name": "公開日", "attribute_value": "2019-12-17"}, "publish_date": "2019-12-17", "publish_status": "0", "recid": "1508", "relation": {}, "relation_version_is_last": true, "title": ["Brain Microdialysis Study of Vancomycin in the Cerebrospinal Fluid After Intracerebroventricular Administration in Mice"], "weko_shared_id": -1}
Brain Microdialysis Study of Vancomycin in the Cerebrospinal Fluid After Intracerebroventricular Administration in Mice
http://hdl.handle.net/10069/38774
http://hdl.handle.net/10069/387743a92e446-17ef-45cf-b837-2d5e85309e65
名前 / ファイル | ライセンス | アクション |
---|---|---|
AAPS-PST20_5.pdf (445.0 kB)
|
|
Item type | 学術雑誌論文 / Journal Article(1) | |||||
---|---|---|---|---|---|---|
公開日 | 2019-12-17 | |||||
タイトル | ||||||
タイトル | Brain Microdialysis Study of Vancomycin in the Cerebrospinal Fluid After Intracerebroventricular Administration in Mice | |||||
言語 | ||||||
言語 | eng | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | intracerebroventricular administration | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | vancomycin | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | microdialysis | |||||
キーワード | ||||||
主題Scheme | Other | |||||
主題 | pharmacokinetics | |||||
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 | journal article | |||||
著者 |
Miura, Yusuke
× Miura, Yusuke× Fuchigami, Yuki× Nomura, Sakiko× Nishimura, Koyo× Hagimori, Masayori× Kawakami, Shigeru |
|||||
抄録 | ||||||
内容記述タイプ | Abstract | |||||
内容記述 | Vancomycin (VCM) is an important antibiotic for treating methicillin-resistant Staphylococcus aureus (MRSA) infections. To treat bacterial meningitis caused by MRSA, it is necessary to deliver VCM into the meninges, but the rate of VCM translocation through the blood-brain barrier is poor. Additionally, high doses of intravascularly (i.v.) administered VCM may cause renal impairments. Thus, VCM is sometimes administered intracerebroventricularly (i.c.v.) for clinical treatment. However, information on the VCM pharmacokinetics in cerebrospinal fluid (CSF) after i.c.v. administration is lacking. In the present study, we evaluated the VCM pharmacokinetics in the CSF and systemic circulation after i.c.v. compared to that after i.v. administration, using the brain microdialysis method in mice. VCM administered via i.c.v. showed a highly selective distribution in the CSF, without migration to systemic circulation. Moreover, to assess renal impairments after i.c.v. administration of VCM, we histologically evaluated damage to the mouse kidney by hematoxylin and eosin staining. No significant morphological change in the kidney was observed in the i.c.v. administration group compared to that in the i.v. administration group. Our results demonstrate that i.c.v. administration of VCM can be partially prevented from entering the systemic circulation to prevent renal impairments caused by VCM. |
|||||
書誌情報 |
AAPS PharmSciTech 巻 20, 号 1, p. 5, 発行日 2018-12-17 |
|||||
出版者 | ||||||
出版者 | Springer International Publishing | |||||
EISSN | ||||||
収録物識別子タイプ | ISSN | |||||
収録物識別子 | 15309932 | |||||
DOI | ||||||
関連タイプ | isVersionOf | |||||
識別子タイプ | DOI | |||||
関連識別子 | 10.1208/s12249-018-1232-8 | |||||
権利 | ||||||
権利情報 | c 2018, American Association of Pharmaceutical Scientists. | |||||
権利 | ||||||
権利情報 | The original publication is available at www.springerlink.com. | |||||
著者版フラグ | ||||||
出版タイプ | AM | |||||
出版タイプResource | http://purl.org/coar/version/c_ab4af688f83e57aa | |||||
引用 | ||||||
内容記述タイプ | Other | |||||
内容記述 | AAPS PharmSciTech, 20(1), art.no.5; 2019 |