Jump to main content
博士論文

癌の光熱療法を目指した脂質エンベロープ型金ナノロッドの創製

Icons representing 博士論文
The cover of this title could differ from library to library. Link to Help Page

癌の光熱療法を目指した脂質エンベロープ型金ナノロッドの創製

Persistent ID (NDL)
info:ndljp/pid/12509797
Material type
博士論文
Author
Paraiso, West Kristian D.
Publisher
Hokkaido University
Date granted
2017-09-25
Material Format
Digital
Capacity, size, etc.
-
Degree grantor and degree
北海道大学,Hokkaido University,博士(薬科学)
View Details

Notes on use at the National Diet Library

本資料は、掲載誌(URI)等のリンク先にある学位授与機関のWebサイトやCiNii ResearchLeave the NDL website. から、本文を自由に閲覧できる場合があります。

Notes on use

Note (General):

(主査) 教授 原島 秀吉, 教授 前仲 勝実, 准教授 山田 勇磨, 教授 秋田 英万 (千葉大学)生命科学院(生命科学専攻)

Detailed bibliographic record

Summary, etc.:

Photothermal therapy (PTT) is currently an auspicious approach in treating cancer. This is exemplified by the use of gold nanorods (AuNRs) that produc...

Holdings of Libraries in Japan

This page shows libraries in Japan other than the National Diet Library that hold the material.

Please contact your local library for information on how to use materials or whether it is possible to request materials from the holding libraries.

other

  • Hokkaido University Collection of Scholarly and Academic Papers

    Digital
    You can check the holdings of institutions and databases with which Institutional Repositories DataBase(IRDB)(Institutional Repository) is linked at the site of Institutional Repositories DataBase(IRDB)(Institutional Repository).

Bibliographic Record

You can check the details of this material, its authority (keywords that refer to materials on the same subject, author's name, etc.), etc.

Digital

Material Type
博士論文
Author/Editor
Paraiso, West Kristian D.
Publication, Distribution, etc.
Publication Date
2017-09-25
Publication Date (W3CDTF)
2017-09-25
Alternative Title
Development of envelope-type lipid-coated gold nanorods for anti-cancer photothermal therapy
Contributor
原島, 秀吉
前仲, 勝実
山田, 勇磨
秋田, 英万
Degree Grantor
北海道大学
Hokkaido University
Date Granted
2017-09-25
Date Granted (W3CDTF)
2017-09-25
Dissertation Number
甲第12889号
Degree Type
博士(薬科学)
Text Language Code
eng
NDC
Target Audience
一般
Note (General)
(主査) 教授 原島 秀吉, 教授 前仲 勝実, 准教授 山田 勇磨, 教授 秋田 英万 (千葉大学)
生命科学院(生命科学専攻)
Persistent ID (NDL)
info:ndljp/pid/12509797
Collection (Materials For Handicapped People:1)
Collection (particular)
国立国会図書館デジタルコレクション > デジタル化資料 > 博士論文
Acquisition Basis
博士論文(自動収集)
Date Accepted (W3CDTF)
2023-01-30T13:49:38+09:00
Format (IMT)
application/pdf
Access Restrictions
国立国会図書館内限定公開
Service for the Digitized Contents Transmission Service
図書館・個人送信対象外
Availability of remote photoduplication service
Data Provider (Database)
国立国会図書館 : 国立国会図書館デジタルコレクション

Digital

Summary, etc.
Photothermal therapy (PTT) is currently an auspicious approach in treating cancer. This is exemplified by the use of gold nanorods (AuNRs) that produce heat in response to near infrared (NIR) irradiation. AuNRs are commonly prepared by using a highly toxic surfactant, cetyltrimethylammonium bromide (CTAB). Because of this, it is necessary to remove traces of CTAB while stabilizing the AuNR surface. In this study, the encapsulation of AuNR in liposome to improve biocompatibility, is reported. To develop this AuNR-multifunctional envelope-type nano device (AuNR-MEND), an SS-cleavable and pH-activated lipid-like material was employed as a component of the lipid envelope. Several methods were attempted in the process of encapsulation. Here, AuNRs were stabilized with bovine serum albumin (AuNR-BSA), and then further encapsulated in the lipid envelope through ethanol dilution method. Change in the ζ-potential of the nanoparticles verified the modifications in coating. Encapsulation was confirmed by transmission electron microscopy (TEM) images. More importantly, the intrinsic properties of AuNRs in terms of heat production in response to NIR irradiation was retained after AuNR-MEND preparation. The in vitro photothermal cytotoxicity of the AuNR-MEND was further demonstrated in 4T1 mouse breast cancer cells. After NIR radiation (750–900 nm) at 1 W/cm2 for six minutes, the temperature of the medium was increased to approximately 60°C, and cell viability was drastically decreased to approximately 11%. However, this cytotoxic effect cannot be explained simply using temperature increase, since incubation of cells in medium that had been pre-warmed at 60°C resulted in a slight decrease in viability (to approximately 70%). Intracellular delivery of the AuNRs therefore is a key factor for the high photothermal cytotoxicity. At a low dose, the photothermal cytotoxicity of AuNR-BSA was higher than that of AuNR-MEND. In contrast, a higher dose of AuNR-MEND resulted in the complete destruction of the cells when subjected to NIR irradiation, while the cell survival rate reached a plateau at 30% in the case of AuNR-BSA. Cellular uptake of AuNR-MEND was shown to be dose-dependent and efficient. Moreover, the increase in caspase-3 production suggests that apoptosis was induced after treatment with the nanoparticles.As for the in vivo study, AuNR-MEND was shown to be long circulating, tumor-accumulating, and non-hepatotoxic in BALB/c mice. Thus, delivering AuNR by means of functionalized lipid nanoparticles represents a promising approach to induce NIR-triggered apoptosis without non-specific cytotoxicity. This doctoral work offers an innovative concept of AuNR-encapsulation into the lipid particle for applications of future tumor photothermal therapy.
Format (IMT)
application/pdf
Access Restrictions
インターネット公開
Data Provider (Database)
国立情報学研究所 : 学術機関リポジトリデータベース(IRDB)(機関リポジトリ)
Original Data Provider (Database)
北海道大学 : 北海道大学学術成果コレクション