Magnetic targeting of thermosensitive magnetoliposomes to mouse livers in an in situ on-line perfusion system

被引:59
作者
Viroonchatapan, E
Sato, H
Ueno, M
Adachi, I
Tazawa, K
Horikoshi, I
机构
[1] TOYAMA MED & PHARMACEUT UNIV, DEPT HOSP PHARM, TOYAMA 93001, JAPAN
[2] TOYAMA MED & PHARMACEUT UNIV, FAC PHARMACEUT SCI, TOYAMA 93001, JAPAN
[3] TOYAMA MED & PHARMACEUT UNIV, FAC MED, DEPT SURG 2, TOYAMA 93001, JAPAN
关键词
thermosensitive magnetoliposomes; dextran magnetite; magnetic targeting; in situ liver perfusion; on-line flow system; factorial design;
D O I
10.1016/0024-3205(96)00220-2
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
We recently reported the preparation and in vitro targeting of dextran magnetite (DM)-incorporated thermosensitive liposomes, namely thermosensitive magneto-liposomes (TMs) [Viroonchatapan et al., Pharm. Res. 12 1176-1183 (1995)]. The current study was designed to determine whether these novel liposomes can be targeted to the mouse liver with the aid of an extracorporeal magnet. An on-line liver perfusion system consisting primarily of a sample injector, permanent magnets, and a fluorescence detector was established for a real-time measurement of targeting efficiency of TMs containing calcein as a fluorescent marker. Normal and reticuloendothelial system (RES)-blocked livers from mice were used for the perfusion experiments. In the RES-blocked livers, percentage holdings of TMs were 73-80% and 26-45% in the presence and absence of magnetic field, respectively, indicating an efficient targeting of TMs with a targeting advantage index (TAI) of 1.6-3.1. On the other hand, TAI in the normal livers was found to be 1.1-1.4 and less than that in the RES-blocked livers, suggesting a role of RES uptake of TMs. The effects of DM concentrations in TM suspensions on the percentage holding of TMs were shown to be minor. Liposome concentration dependence was observed for hepatic uptake of TMs, possibly because of the saturation of phagocytosis by Kupffer cells. The present results suggest that TMs would be useful in future cancer treatment by magnetic targeting combined with drug release in response to hyperthermia.
引用
收藏
页码:2251 / 2261
页数:11
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