Thermoactivatable polymer-grafted liposomes for low-invasive image-guided chemotherapy

被引:10
作者
Aoki, Ichio
Yoneyama, Misao
Hirose, Jun
Minemoto, Yuzuru
Koyama, Takayoshi
Kokuryo, Daisuke
Bakalova, Rumiana
Murayama, Shuhei
Saga, Tsuneo
Aoshima, Sadahito
Ishizaka, Yukihito
Kono, Kenji
机构
[1] Natl Inst Radiol Sci, Mol Imaging Ctr, Chiba 2638555, Japan
[2] Osaka Prefecture Univ, Grad Sch Engn, Dept Appl Chem, Sakai, Osaka 591, Japan
[3] Natl Ctr Global Hlth & Med, Dept Intractable Dis, Tokyo, Japan
[4] Osaka Univ, Grad Sch Sci, Dept Macromol Sci, Toyonaka, Osaka 560, Japan
关键词
TEMPERATURE-SENSITIVE LIPOSOMES; LIVING CATIONIC-POLYMERIZATION; POSITRON-EMISSION-TOMOGRAPHY; TUMOR-SPECIFIC CHEMOTHERAPY; TRIGGERED DRUG-RELEASE; MAGNETIC-RESONANCE; THERMOSENSITIVE LIPOSOMES; MANGANESE NEUROTOXICITY; LOCAL HYPERTHERMIA; XENOGRAFT MODEL;
D O I
10.1016/j.trsl.2015.07.009
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
The objective of this study was to develop a thermotriggered, polymer-based liposomal drug carrier with an activatable magnetic resonance imaging (MRI) contrast property for monitoring the release of substances and for localized tumor therapy. The multimodal thermoactivatable polymer-grafted liposomes (MTPLs) were tested to investigate whether the accumulation of MTPLs in colon-26 grafted tumors could be visualized in vivo using MRI and optical imaging, whether MTPLs induce signal enhancement, reflecting the release of their contents, after triggering by short-term heating (42.5 degrees C for 10 minutes) 9 hours after MTPL administration (late-phase triggering), and whether MTPLs can provide a sufficient antitumor effect. The imaging and therapeutic properties of MTPLs were tested both in vitro and in vivo (BALB/c nude mice: heated group with MTPLs (n = 5), nonheated group with MTPLs (n = 5), heated group with doxorubicin-free MTPLs (n = 5), nonheated group with manganese-free MTPLs (n = 5), and kinetics observation group (n = 3); N = 23). Through in vivo MRI and fluorescent imaging, the MTPLs were shown to have significantly accumulated in the grafted colon-26 tumors 8 hours after administration. Delayed thermotriggering (9 hours after administration) caused MR signal enhancement, reflecting the release of their contents, after a short exposure to tolerable heat. In addition, significant antitumor effects were observed after treatment. The proposed polymer-based activatable MTPLs with a "delayed thermotrigger" provide a promising technology for cancer theranostics that allows minimal adverse effects and rapid interactive therapy.
引用
收藏
页码:660 / 673
页数:14
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