Proteins Conjugated to Poly(Butyl Cyanoacrylate) Nanoparticles as Potential Neuroprotective Agents

被引:25
|
作者
Reukov, Vladimir [1 ]
Maximov, Victor [1 ]
Vertegel, Alexey [1 ]
机构
[1] Clemson Univ, Dept Bioengn, Clemson, SC 29634 USA
基金
美国国家科学基金会;
关键词
enzymes; nanoparticle; conjugate; glutamate; superoxide dismutase; secondary spinal cord injury; neuroprotection; poly(butyl cyanoacrylate); BLOOD-BRAIN-BARRIER; SUPEROXIDE-DISMUTASE; TAT PEPTIDE; DELIVERY; AGGREGATION; NEURONS; DRUGS;
D O I
10.1002/bit.22958
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Poly(butyl cyanoacrylate) (PBCA) nanoparticles (NPs) can penetrate blood-brain barrier providing the means for drug delivery to the central nervous system. Here, we study attachment of superoxide dismutase (SOD) and anti-glutamate N-methyl D-aspartate receptor 1 (NR1) antibody to PBCA NPs with the ultimate goal to design neuroprotective therapeutics for treatment of secondary spinal cord injury. Synthesis of monodispersed, similar to 200 nm-diameter PBCA NPs was performed using polymerization at pH 2.0 with Dextran 70,000 as the stabilizer. Sulfo-HSAB spacers were used to covalently attach SOD and NR1 antibodies to the dextran-coated NPs. The prepared protein-NP conjugates possessed SOD activity and were capable of binding to rat cerebellar neurons. Thus, SOD and NR1 antibodies may be simultaneously attached to PBCA NPs while retaining at least a fraction of enzymatic activity and receptor-binding ability. The conjugates showed neuroprotective efficacy in vitro with rat cerebellar cell cultures challenged by superoxide. Biotechnol. Bioeng. 2011;108: 243-252. (C) 2010 Wiley Periodicals, Inc.
引用
收藏
页码:243 / 252
页数:10
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