Tumor distribution and anti-tumor effect of doxorubicin following intrapulmonary administration to mice with metastatic lung tumor

被引:9
|
作者
Kanehira, Yukimune [1 ]
Togami, Kohei [1 ]
Tada, Hitoshi [1 ]
Chono, Sumio [1 ]
机构
[1] Hokkaido Pharmaceut Univ, Sch Pharm, Div Pharmaceut, 7-15-4-1 Maeda, Sapporo, Hokkaido 0068590, Japan
基金
日本学术振兴会;
关键词
Pulmonary drug delivery system; Lung cancer; B16F10; Anti-tumor agent; Tumor region distribution; EPITHELIAL LINING FLUID; ALVEOLAR MACROPHAGES; P-GLYCOPROTEIN; CANCER; CHEMOTHERAPY; CARCINOMA; CLARITHROMYCIN; RESISTANCE; MECHANISM; DELIVERY;
D O I
10.1016/j.jddst.2016.04.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The present study evaluated the distribution of doxorubicin (DOX), as a fluorescent marker and an antitumor agent, to a lung tumor region following intrapulmonary administration. Using a Liquid Micro Sprayer (R), DOX (400 mu g/kg) was administered to mice with B16F10, which are murine melanoma cells that induce metastatic lung tumor. DOX concentrations in the lung following intrapulmonary administration were markedly higher than those following intravenous administration. On the other hand, DOX concentrations in serum following intrapulmonary administration were significantly lower than those following intravenous administration. DOX fluorescence after intrapulmonary administration was widely observed in the tumor region with P-glycoprotein expression. In contrast, DOX was not observed in the tumor region following intravenous administration. DOX administered intrapulmonarily suppressed the tumor growth than case of intravenous administration. These results indicate that intrapulmonary administration can efficiently deliver anti-tumor agents for lung cancer. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:143 / 148
页数:6
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