Temperature-sensitive liposomes for doxorubicin delivery under MRI guidance

被引:195
|
作者
de Smet, Mariska [1 ]
Langereis, Sander [2 ]
van den Bosch, Sandra [2 ]
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; Liposome; Image guidance; Focused ultrasound; Magnetic resonance imaging; THERMOSENSITIVE LIPOSOMES; CONTRAST AGENT; CONVENTIONAL DOXORUBICIN; PARAMAGNETIC LIPOSOMES; POLYETHYLENE-GLYCOL; TUMOR-LOCALIZATION; MILD HYPERTHERMIA; DRUG-RELEASE; IN-VITRO; PHARMACOKINETICS;
D O I
10.1016/j.jconrel.2009.12.002
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Local drug delivery of doxorubicin holds promise to improve the therapeutic efficacy and to reduce toxicity profiles. Here, we investigated the release of doxorubicin and [Gd(HPDO3A)(H2O)] from different temperature-sensitive liposomes for applications in temperature-induced drug delivery under magnetic resonance image guidance. In particular, two temperature-sensitive systems composed of DPPC:MPPC:DPPE-PEG2000 (low temperature-sensitive liposomes, LTSL) and DPPC:HSPC:cholesterol:DPPE-PEG2000 (traditional temperature-sensitive liposomes, TTSL) were investigated. The co-encapsulation of Gd (HPDO3A)(H2O)], a clinically approved MRI contrast agent, did not influence the encapsulation and release of doxorubicin. The LTSL system showed a higher leakage of doxorubicin at 37 degrees C, but a faster release of doxorubicin at 42 degrees C compared to the TTSL system. Furthermore, the rapid release of both doxorubicin and the MRI contrast agent from the liposomes occurred near the melting phase transition temperature, making it possible to image the release of doxorubicin using MRI. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:120 / 127
页数:8
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