Targeted Mesoporous Iron Oxide Nanoparticles-Encapsulated Perfluorohexane and a Hydrophobic Drug for Deep Tumor Penetration and Therapy

被引:75
作者
Su, Yu-Lin [1 ]
Fang, Jen-Hung [1 ]
Liao, Chia-Ying [1 ]
Lin, Chein-Ting [1 ]
Li, Yun-Ting [1 ]
Hu, Shang-Hsiu [1 ]
机构
[1] Natl Tsing Hua Univ, Dept Biomed Engn & Environm Sci, Hsinchu 30013, Taiwan
关键词
Mesoporous particles; drug delivery; combinatorial therapy; magneto-responsive; 3D tumor model; PHASE-III TRIAL; GOLD NANOPARTICLES; 1ST-LINE TREATMENT; DELIVERY-SYSTEM; STEM-CELLS; CANCER; NANOCAPSULES; DOXORUBICIN; RELEASE; NANOSPHERES;
D O I
10.7150/thno.12843
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
A magneto-responsive energy/drug carrier that enhances deep tumor penetration with a porous nano-composite is constructed by using a tumor-targeted lactoferrin (Lf) bio-gate as a cap on mesoporous iron oxide nanoparticles (MIONs). With a large payload of a gas-generated molecule, perfluorohexane (PFH), and a hydrophobic anti-cancer drug, paclitaxel (PTX), Lf-MIONs can simultaneously perform bursting gas generation and on-demand drug release upon high-frequency magnetic field (MF) exposure. Biocompatible PFH was chosen and encapsulated in MIONs due to its favorable phase transition temperature (56 degrees C) and its hydrophobicity. After a short-duration MF treatment induces heat generation, the local pressure increase via the gasifying of the PFH embedded in MION can substantially rupture the three-dimensional tumor spheroids in vitro as well as enhance drug and carrier penetration. As the MF treatment duration increases, Lf-MIONs entering the tumor spheroids provide an intense heat and burst-like drug release, leading to superior drug delivery and deep tumor thermo-chemo-therapy. With their high efficiency for targeting tumors, Lf-MIONs/PTX-PFH suppressed subcutaneous tumors in 16 days after a single MF exposure. This work presents the first study of using MF-induced PFH gasification as a deep tumor-penetrating agent for drug delivery.
引用
收藏
页码:1233 / 1248
页数:16
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