Visualization of exogenous delivery of nanoformulated butyrylcholinesterase to the central nervous system

被引:38
作者
Gaydess, Andrea [2 ,3 ]
Duysen, Ellen [1 ]
Li, Yuan [2 ,3 ]
Gilman, Vladimir [4 ]
Kabanov, Alexander [2 ,3 ]
Lockridge, Oksana [1 ]
Bronich, Tatiana [2 ,3 ]
机构
[1] Univ Nebraska Med Ctr, Eppley Inst, Omaha, NE 68198 USA
[2] Univ Nebraska Med Ctr, Coll Pharm, Omaha, NE 68198 USA
[3] Univ Nebraska Med Ctr, Ctr Drug Delivery & Nanomed, Omaha, NE 68198 USA
[4] InfoSciTex Corp, Waltham, MA 02451 USA
关键词
Butyrylcholinesterase; Nanotechnology; CNS drug delivery; Block ionomer complexes; KNOCKOUT MOUSE; BRAIN; RAT;
D O I
10.1016/j.cbi.2010.01.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Butyrylcholinesterase (BChE) is an efficient bioscavenger of highly toxic organophosphorus poisons and nerve agents. However, BChE administered into the periphery does not provide significant protection of the central nervous system (CNS) due to rejection by the blood-brain barrier. In this study, we evaluated the feasibility of delivering BChE to the CNS by packing it into a block ionomer complex of nanoscale size with a cationic poly(L-lysine)-graft-poly(ethylene oxide) (PLL-g-PEO) copolymer. The multimolecular structure of BChE/PLL-g-PEO complexes was further reinforced by formation of cross-links between the polymer chains. The resulting cross-linked complexes were stable against dilution without significant loss of BChE enzymatic activity. In some cases the BChE was labeled with fluorescent IRDye 800CW before it was incorporated into nanoparticles.BChE/PLL-g-PEO complexes were injected into mice intramuscularly and intravenously. In vivo imaging showed incorporation of the fluorescently labeled BChE in brain. Activity assays showed that BChE remained active in the brain at 72-h post-injection. It was concluded that nanocomplexes can deliver the 340 kDa BChE tetramer to the brain. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:295 / 298
页数:4
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