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Magnetic resonance imaging of high intensity focused ultrasound mediated drug delivery from temperature-sensitive liposomes: An in vivo proof-of-concept study
被引:253
作者:
de Smet, Mariska
[1
]
Heijman, Edwin
[2
]
Langereis, Sander
[2
]
Hijnen, Nicole M.
[1
]
Grull, Holger
[1
,2
]
机构:
[1] Eindhoven Univ Technol, Dept Biomed NMR, NL-5600 MB Eindhoven, Netherlands
[2] Philips Res Eindhoven, Dept Biomol Engn, Eindhoven, Netherlands
关键词:
Drug delivery;
Hyperthermia;
Temperature-sensitive liposome;
Nanomedicine;
Image guidance;
Focused ultrasound;
Magnetic resonance imaging;
Contrast agents;
Oncology;
TUMOR XENOGRAFT MODEL;
MR CONTRAST AGENT;
THERMOSENSITIVE LIPOSOMES;
MILD HYPERTHERMIA;
PHYSICOCHEMICAL PROPERTIES;
PARAMAGNETIC LIPOSOMES;
RANDOMIZED-TRIAL;
RELEASE;
VITRO;
GUIDANCE;
D O I:
10.1016/j.jconrel.2010.10.036
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Temperature-sensitive liposomes (TSLs) co-encapsulating doxorubicin and 250 mM [Gd(HPDO3A)(H2O)] were evaluated for HIFU-mediated drug delivery under MR image guidance. In vitro studies showed simultaneous and quantitative release of the drug and the MRI contrast agent from the lumen of the TSLs at 42 degrees C, while no leakage was observed over 1 h at 37 degrees C. In a proof-of-concept study, local hyperthermia has been applied for 30 min in 9L rat tumors using a clinical MR-HIFU system. The local temperature-triggered release of [Gd(HPDO3A)(H2O)] was monitored with interleaved T-1 mapping of the tumor tissue. A good correlation between the Delta R-1, the uptake of doxorubicin and the gadolinium concentration in the tumor was found, implying that the in vivo release of doxorubicin from TSLs can be probed in situ with the longitudinal relaxation time of the co-released MRI contrast agent. (C) 2010 Elsevier B.V. All rights reserved.
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页码:102 / 110
页数:9
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