CD44 targeted delivery of hyaluronic acid-Doxorubicin/NIR dye conjugates as nanocarrier for the photothermal/chemotherapy

碩士 === 國立臺灣大學 === 醫學工程學研究所 === 105 === In this study, a photothermal drug, IR-780, and a chemotherapy drug, doxorubicin, were conjugated to hyaluronic acid respectively to form two kinds of amphiphilic polymers, HA-IR and HA-DOX. Based on the amphiphilic property, the HA-IR and HA-DOX mixture can s...

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Main Authors: Wan-Yun Lien, 連婉蘊
Other Authors: Ming-Jium Shieh
Format: Others
Language:en_US
Published: 2017
Online Access:http://ndltd.ncl.edu.tw/handle/9ftgv8
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spelling ndltd-TW-105NTU055300442019-05-15T23:39:40Z http://ndltd.ncl.edu.tw/handle/9ftgv8 CD44 targeted delivery of hyaluronic acid-Doxorubicin/NIR dye conjugates as nanocarrier for the photothermal/chemotherapy 玻尿酸接枝阿黴素及近紅外光染料作為CD44標靶之奈米載體以結合光熱與化學治療 Wan-Yun Lien 連婉蘊 碩士 國立臺灣大學 醫學工程學研究所 105 In this study, a photothermal drug, IR-780, and a chemotherapy drug, doxorubicin, were conjugated to hyaluronic acid respectively to form two kinds of amphiphilic polymers, HA-IR and HA-DOX. Based on the amphiphilic property, the HA-IR and HA-DOX mixture can self-assembly to nanoparticles, HA-IR/DOX NP. With different HA-IR/HA-DOX ratios, HA-IR/DOX NPs exhibited particle size from 120 to 170 nm with relatively narrow size distribution. The stability test showed that the HA-IR/DOX NP were stable in 4°C storage condition. From in vitro test, HA-IR/DOX NP targeted to CD44-overexpression cancer cell line, MDA-MB-231. The HA-IR/DOX NP showed photothermal effect and phototoxicity both in vitro and in vivo. On the other hand, the fluorescent property of IR-780 provide a function of in vivo imaging, which shows that the HA-IR/DOX NP accumulated to the tumor via EPR effect and CD44-targeting ligand. The antitumor effect showed that the HA-IR/DOX NP combined the chemo-therapy and the photo-thermal therapy. Ming-Jium Shieh 謝銘鈞 2017 學位論文 ; thesis 41 en_US
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language en_US
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sources NDLTD
description 碩士 === 國立臺灣大學 === 醫學工程學研究所 === 105 === In this study, a photothermal drug, IR-780, and a chemotherapy drug, doxorubicin, were conjugated to hyaluronic acid respectively to form two kinds of amphiphilic polymers, HA-IR and HA-DOX. Based on the amphiphilic property, the HA-IR and HA-DOX mixture can self-assembly to nanoparticles, HA-IR/DOX NP. With different HA-IR/HA-DOX ratios, HA-IR/DOX NPs exhibited particle size from 120 to 170 nm with relatively narrow size distribution. The stability test showed that the HA-IR/DOX NP were stable in 4°C storage condition. From in vitro test, HA-IR/DOX NP targeted to CD44-overexpression cancer cell line, MDA-MB-231. The HA-IR/DOX NP showed photothermal effect and phototoxicity both in vitro and in vivo. On the other hand, the fluorescent property of IR-780 provide a function of in vivo imaging, which shows that the HA-IR/DOX NP accumulated to the tumor via EPR effect and CD44-targeting ligand. The antitumor effect showed that the HA-IR/DOX NP combined the chemo-therapy and the photo-thermal therapy.
author2 Ming-Jium Shieh
author_facet Ming-Jium Shieh
Wan-Yun Lien
連婉蘊
author Wan-Yun Lien
連婉蘊
spellingShingle Wan-Yun Lien
連婉蘊
CD44 targeted delivery of hyaluronic acid-Doxorubicin/NIR dye conjugates as nanocarrier for the photothermal/chemotherapy
author_sort Wan-Yun Lien
title CD44 targeted delivery of hyaluronic acid-Doxorubicin/NIR dye conjugates as nanocarrier for the photothermal/chemotherapy
title_short CD44 targeted delivery of hyaluronic acid-Doxorubicin/NIR dye conjugates as nanocarrier for the photothermal/chemotherapy
title_full CD44 targeted delivery of hyaluronic acid-Doxorubicin/NIR dye conjugates as nanocarrier for the photothermal/chemotherapy
title_fullStr CD44 targeted delivery of hyaluronic acid-Doxorubicin/NIR dye conjugates as nanocarrier for the photothermal/chemotherapy
title_full_unstemmed CD44 targeted delivery of hyaluronic acid-Doxorubicin/NIR dye conjugates as nanocarrier for the photothermal/chemotherapy
title_sort cd44 targeted delivery of hyaluronic acid-doxorubicin/nir dye conjugates as nanocarrier for the photothermal/chemotherapy
publishDate 2017
url http://ndltd.ncl.edu.tw/handle/9ftgv8
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