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Multi-functionalized hyaluronic acid nanogels crosslinked with carbon dots as dual receptor-mediated targeting tumor theranostics
被引:74
作者:

Jia, Xu
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机构: Lanzhou Univ, Coll Chem & Chem Engn, State Key Lab Appl Organ Chem, Lanzhou 730000, Peoples R China

Han, Yu
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机构: Lanzhou Univ, Coll Chem & Chem Engn, State Key Lab Appl Organ Chem, Lanzhou 730000, Peoples R China

Pei, Mingliang
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h-index: 0
机构: Lanzhou Univ, Coll Chem & Chem Engn, State Key Lab Appl Organ Chem, Lanzhou 730000, Peoples R China

Zhao, Xubo
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h-index: 0
机构: Lanzhou Univ, Coll Chem & Chem Engn, State Key Lab Appl Organ Chem, Lanzhou 730000, Peoples R China

Tian, Kun
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机构: Lanzhou Univ, Coll Chem & Chem Engn, State Key Lab Appl Organ Chem, Lanzhou 730000, Peoples R China

Zhou, Tingting
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h-index: 0
机构: Lanzhou Univ, Coll Chem & Chem Engn, State Key Lab Appl Organ Chem, Lanzhou 730000, Peoples R China

Liu, Peng
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h-index: 0
机构:
Lanzhou Univ, Coll Chem & Chem Engn, State Key Lab Appl Organ Chem, Lanzhou 730000, Peoples R China Lanzhou Univ, Coll Chem & Chem Engn, State Key Lab Appl Organ Chem, Lanzhou 730000, Peoples R China
机构:
[1] Lanzhou Univ, Coll Chem & Chem Engn, State Key Lab Appl Organ Chem, Lanzhou 730000, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Tumor theranostics;
Hyaluronic acid;
Carbon dots;
Dual receptor-mediated targeting;
Tumor microenvironment-responsive controlled release;
DRUG-DELIVERY PLATFORM;
ANTICANCER DRUG;
COPOLYMER MICELLES;
CANCER-THERAPY;
RELEASE;
DOXORUBICIN;
DERIVATIVES;
D O I:
10.1016/j.carbpol.2016.06.109
中图分类号:
O69 [应用化学];
学科分类号:
081704 ;
摘要:
Hyaluronic acid (HA)-based theranostic nanogels were designed for the tumor diagnosis and chemotherapy, by crosslinking the folate-terminated poly(ethylene glycol) modified hyaluronic acid (FA-PEG-HA) with carbon dots (CDs) for the first time. Due to the extraordinary fluorescence property of the integrated CDs, the theranostic nanogels could be used for the real-time and noninvasive location tracking to cancer cells. HA could load Doxorubicin (DOX) via electrostatic interaction with a drug-loading capacity (DLC) of 32.5%. The nanogels possessed an ideal release of DOX in the weak acid environment, while it was restrained in the neutral media, demonstrating the pH-responsive controlled release behavior. The cytotoxicity and cellular uptake results clearly illustrated that most DOX was released and accumulated in the cell nuclei and killed the cancer cells efficaciously, due to their dual receptor-mediated targeting characteristics. (C) 2016 Elsevier Ltd. All rights reserved.
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页码:391 / 397
页数:7
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Duke Univ, Dept Biomed Engn, Durham, NC 27708 USA Duke Univ, Dept Biomed Engn, Durham, NC 27708 USA

Leong, Kam W.
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Duke Univ, Dept Biomed Engn, Durham, NC 27708 USA Duke Univ, Dept Biomed Engn, Durham, NC 27708 USA