Remotely triggered release of small molecules from LaB6@SiO2-loaded polycaprolactone microneedles

被引:71
作者
Chen, Mei-Chin [1 ]
Wang, Kuan-Wen [1 ]
Chen, Dong-Hwang [1 ]
Ling, Ming-Hung [1 ]
Liu, Chih-Ying [1 ]
机构
[1] Natl Cheng Kung Univ, Dept Chem Engn, Tainan, Taiwan
关键词
Controlled release; Near-infrared light; On-demand; Stimuli-responsive; Transdermal drug delivery; DRUG-DELIVERY SYSTEMS; TRANSDERMAL DELIVERY; LAB6; NANOPARTICLES; CANCER-CELLS; IN-VIVO; HYPERTHERMIA; THERAPY; ABLATION; CARRIERS; TISSUE;
D O I
10.1016/j.actbio.2014.11.040
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
We established near-infrared (NIR)-light-triggered transdermal delivery systems by encapsulating NIR absorbers, silica-coated lanthanum hexaboride (LaB6@SiO2) nanostructures and the cargo molecule to be released in biodegradable polycaprolactone (PCL) microneedles. Acting as a local heat source when exposed to an NIR laser, these nanostructures cause a phase transition of the microneedles, thereby increasing the mobility of the polymer chains and triggering drug release from the microneedles. On IR thermal images, the light-triggered melting behavior of the LaB6@SiO2-loaded microneedles was observed. By adjusting the irradiation time and the laser on/off cycles, the amount of molecules released was controlled accurately. Drug release was switched on and off for at least three cycles, and a consistent dose was delivered in each cycle with high reproducibility. The designed microneedles were remotely triggered by laser irradiation for the controlled release of a chemotherapeutic drug, doxorubicin hydrochloride, in vivo. This system would enable dosages to be adjusted accurately to achieve a desired effect, feature a low off-state drug leakage to minimize basal effects and can increase the flexibility of pharmacotherapy performed to treat various medical conditions. (C) 2014 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:344 / 353
页数:10
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