Gold and silver nanoparticles conjugated with heparin derivative possess anti-angiogenesis properties

被引:128
作者
Kemp, Melissa M. [1 ]
Kumar, Ashavani [2 ]
Mousa, Shaymaa [3 ]
Dyskin, Evgeny [3 ]
Yalcin, Murat [3 ]
Ajayan, Pulickel [2 ]
Linhardt, Robert J. [1 ,4 ,5 ]
Mousa, Shaker A. [3 ]
机构
[1] Rensselaer Polytech Inst, Dept Biol, Troy, NY 12180 USA
[2] Rice Univ, Dept Mech Engn & Mat Sci, Houston, TX 77005 USA
[3] Albany Coll Pharm & Hlth Sci, Pharmaceut Res Inst, Albany, NY 12208 USA
[4] Rensselaer Polytech Inst, Dept Chem & Biol Chem, Troy, NY 12180 USA
[5] Rensselaer Polytech Inst, Dept Biol & Chem Engn, Troy, NY 12180 USA
关键词
MOLECULAR-WEIGHT HEPARIN; FIBROBLAST-GROWTH-FACTOR; THYROID-HORMONE; PROANGIOGENIC ACTION; METAL NANOPARTICLES; ANTICANCER EFFICACY; CELL-SURFACE; INTEGRIN; ACID; INHIBITION;
D O I
10.1088/0957-4484/20/45/455104
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Silver and gold nanoparticles display unique physical and biological properties that have been extensively studied for biological and medical applications. Typically, gold and silver nanoparticles are prepared by chemical reductants that utilize excess toxic reactants, which need to be removed for biological purposes. We utilized a clean method involving a single synthetic step to prepare metal nanoparticles for evaluating potential effects on angiogenesis modulation. These nanoparticles were prepared by reducing silver nitrate and gold chloride with diaminopyridinyl (DAP)-derivatized heparin (HP) polysaccharides. Both gold and silver nanoparticles reduced with DAPHP exhibited effective inhibition of basic fibroblast growth factor (FGF-2)-induced angiogenesis, with an enhanced anti-angiogenesis efficacy with the conjugation to DAPHP (P < 0.01) as compared to glucose conjugation. These results suggest that DAPHP-reduced silver nanoparticles and gold nanoparticles have potential in pathological angiogenesis accelerated disorders such as cancer and inflammatory diseases.
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页数:7
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