Targeting atherosclerosis by using modular, multifunctional micelles

被引:215
作者
Peters, David [1 ,2 ]
Kastantin, Mark [3 ]
Kotamraju, Venkata Ramana [1 ]
Karmali, Priya P. [4 ]
Gujraty, Kunal [1 ]
Tirrell, Matthew [3 ]
Ruoslahti, Erkki [1 ,4 ]
机构
[1] Univ Calif Santa Barbara, Burnham Inst Med Res, Vasc Mapping Ctr, Santa Barbara, CA 93106 USA
[2] Univ Calif San Diego, Biomed Sci Grad Grp, La Jolla, CA 92037 USA
[3] Univ Calif Santa Barbara, Dept Chem Engn, Santa Barbara, CA 93106 USA
[4] Canc Res Ctr, Burnham Inst Med Res, La Jolla, CA 92037 USA
基金
美国国家科学基金会;
关键词
cysteine-arginine-glutamic acid-lysine-alanine; hirulog; plaque; imaging; nanoparicles; DEFICIENT MICE; DISPLAY; LESIONS;
D O I
10.1073/pnas.0903369106
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Subtle clotting that occurs on the luminal surface of atherosclerotic plaques presents a novel target for nanoparticle-based diagnostics and therapeutics. We have developed modular multifunctional micelles that contain a targeting element, a fluorophore, and, when desired, a drug component in the same particle. Targeting atherosclerotic plaques in ApoE-null mice fed a high-fat diet was accomplished with the pentapeptide cysteine-arginine-glutamic acid-lysine-alanine, which binds to clotted plasma proteins. The fluorescent micelles bind to the entire surface of the plaque, and notably, concentrate at the shoulders of the plaque, a location that is prone to rupture. We also show that the targeted micelles deliver an increased concentration of the anticoagulant drug hirulog to the plaque compared with untargeted micelles.
引用
收藏
页码:9815 / 9819
页数:5
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