Synthesis of magnetic and upconversion nanocapsules as multifunctional drug delivery system

被引:12
|
作者
Huang, Shanshan [1 ]
Chen, Yinyin [1 ]
Liu, Bei [1 ]
He, Fei [1 ]
Ma, Ping'an [1 ]
Deng, Xiaoran [1 ]
Cheng, Ziyong [1 ]
Lin, Jun [1 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Rare Earth Resource Utilizat, Changchun 130022, Peoples R China
基金
中国国家自然科学基金;
关键词
Multifunctional nanocapsules; Upconversion luminescence; Magnetic resonance imaging; Drug targeting delivery; CORE; LUMINESCENT; NANOSTRUCTURE; NANOCRYSTALS; NANOSPHERES; RESONANCE;
D O I
10.1016/j.jssc.2015.06.024
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Multifunctional hollow nanocapsules with magnetic and upconversion luminescence properties were synthesized. Hollow Fe3O4@SiO2 was firstly prepared by using rodlike beta-FeOOH as the template followed by silica coating, calcinations and reduction. Then Fe3O4@SiO2@alpha-NaYF4:Yb3+,Er3+ nanocapsules (FeS-iUCHP) were synthesized by the hydrothermal transformation of the Y(Yb3+, Er3+)(OH)CO3 (YOC) deposited onto the surface of nanocapsules through a urea-assisted homogeneous precipitation method. The hollow nanocapsules with porous structure provide space and entrance for the drug molecules. Due to the outside shell of alpha-NaYF4:Yb3+, Er3+, the nanomaterial shows upconverting red emission upon 980 nm NIR-light excitation. Moreover, the nanocomposites with hollow magnetite core exhibit a high relaxivity with r(2) value of 183 mM(-1) s(-1), which reveal the potential as T-2-weighted contrast agents for magnetic resonance imaging (MRI). The as-prepared nanocapsules can be performed as anti-cancer drug carriers for investigation of drug loading/release properties, which demonstrated a sustained drug release pattern and a comparable cytotoxicity with free doxorubicin (DOX). The multifunctional nanocapsules incorporated upconverting luminescence, T-2-weighted MRI imaging and drug targeting delivery modalities have great potential for theranostic applications in cancer treatment. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:322 / 329
页数:8
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