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Thermosensitive liposomal drug delivery systems: state of the art review
被引:285
作者:
Kneidl, Barbara
[1
,2
]
Peller, Michael
[3
]
Winter, Gerhard
[2
]
Lindner, Lars H.
[1
]
Hossann, Martin
[1
]
机构:
[1] Univ Hosp Munich, Dept Internal Med 3, Munich, Germany
[2] Univ Munich, Univ Hosp Munich, Dept Pharm Pharmaceut Technol & Biopharmaceut, Munich, Germany
[3] Univ Munich, Univ Hosp Munich, Inst Clin Radiol, Munich, Germany
关键词:
thermosensitive liposomes;
phosphatidyloligoglycerol;
hyperthermia;
high intensity focused ultrasound;
drug delivery;
drug targeting;
TEMPERATURE-SENSITIVE LIPOSOMES;
INTENSITY FOCUSED ULTRASOUND;
STERICALLY STABILIZED LIPOSOMES;
IN-VITRO CHARACTERIZATION;
MRI CONTRAST AGENTS;
MILD HYPERTHERMIA;
PARAMAGNETIC LIPOSOMES;
DOXORUBICIN RELEASE;
TRIGGERED RELEASE;
BILAYER-MEMBRANES;
D O I:
10.2147/IJN.S49297
中图分类号:
TB3 [工程材料学];
学科分类号:
0805 ;
080502 ;
摘要:
Thermosensitive liposomes are a promising tool for external targeting of drugs to solid tumors when used in combination with local hyperthermia or high intensity focused ultrasound. In vivo results have demonstrated strong evidence that external targeting is superior over passive targeting achieved by highly stable long-circulating drug formulations like PEGylated liposomal doxorubicin. Up to March 2014, the Web of Science listed 371 original papers in this field, with 45 in 2013 alone. Several formulations have been developed since 1978, with lysolipid-containing, low temperature-sensitive liposomes currently under clinical investigation. This review summarizes the historical development and effects of particular phospholipids and surfactants on the biophysical properties and in vivo efficacy of thermosensitive liposome formulations. Further, treatment strategies for solid tumors are discussed. Here we focus on temperature-triggered intravascular and interstitial drug release. Drug delivery guided by magnetic resonance imaging further adds the possibility of performing online monitoring of a heating focus to calculate locally released drug concentrations and to externally control drug release by steering the heating volume and power. The combination of external targeting with thermosensitive liposomes and magnetic resonance-guided drug delivery will be the unique characteristic of this nanotechnology approach in medicine.
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页码:4387 / 4398
页数:12
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