HEAT-INDUCED DRUG RELEASE RATE AND MAXIMAL TARGETING INDEX OF THERMOSENSITIVE LIPOSOME IN TUMOR-BEARING MICE

被引:20
作者
IGA, K
OGAWA, Y
TOGUCHI, H
机构
[1] Pharmaceutics Research Laboratories, Research and Development Division, Takeda Chemical Industries, Ltd., Yodogawa-Ku, Osaka, 532, 17-85
关键词
THERMOSENSITIVE LIPOSOME; CISPLATIN; HYPERTHERMIA; BLOOD-DRUG LEVEL; TUMOR-DRUG LEVEL; TARGETING INDEX; DRUG RELEASE;
D O I
10.1023/A:1015858228394
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
To evaluate the rate of drug release at the tumor and maximal drug targeting after administration of thermosensitive liposomes with hyperthermia, a theoretical and experimental method was derived assessing the fraction of drug released from liposomes in a single pass through the heated tumor, F, and the drug targeting index when drug release occurs completely in response to heat (F = 1), DTI(max). The F and DTI(max) were evaluated for four types of liposomes (LUV-1 and LUV-2, thermosensitive large unilamellar liposomes; LUV-3, a nonthermosensitive large unilamellar liposome; and SUV-1, a thermosensitive small unilamellar liposome) using reported data on blood liposome levels and tumor drug levels after the liposomes were administered to tumor bearing mice. DTI(max) values for LUV-1 and SUV-1 were approximately 6, while the value for LUV-2 with a relatively large systemic clearance was only 2.3. The F values for LUV-1, LUV-2, and SUV-1 with hyperthermia were 0.71, 1.17, and 0.34, respectively, whereas the values for these liposomes without hyperthermia and for LUV-3 with or without hyperthermia were nearly zero. These results confirm earlier findings that LUV-1 and LUV-2 release CDDP almost completely at the heated tumor and that the large DTI value obtained in LUV-1 (DTI = 4.6) was due to its high heat sensitivity and its small systemic clearance.
引用
收藏
页码:658 / 662
页数:5
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