Gold nanoparticles are suitable cores for building tunable iminosugar multivalency

被引:20
作者
Matassini, C. [1 ,2 ]
Marradi, M. [2 ,3 ]
Cardona, F. [1 ]
Parmeggiani, C. [1 ,4 ,5 ]
Robina, I. [6 ]
Moreno-Vargas, A. J. [6 ]
Penades, S. [2 ,3 ]
Goti, A. [1 ]
机构
[1] Univ Firenze, Dipartimento Chim Ugo Schiff, I-50019 Sesto Fiorentino, FI, Italy
[2] CIC BiomaGUNE, Biofunct Nanomat Unit, Lab GlycoNanoTechnol, San Sebastian, Spain
[3] CIBER BBN, San Sebastian 20009, Spain
[4] CNR INO, I-50019 Sesto Fiorentino, FI, Italy
[5] LENS, I-50019 Sesto Fiorentino, FI, Italy
[6] Univ Seville, Fac Quim, Dept Quim Organ, E-41012 Seville, Spain
来源
RSC ADVANCES | 2015年 / 5卷 / 116期
关键词
SELF-ASSEMBLED MONOLAYERS; CARBOHYDRATE-PROCESSING ENZYMES; GLYCOSIDASE INHIBITION; CLICK CLUSTERS; PHARMACOLOGICAL CHAPERONES; GAUCHER-DISEASE; GLYCONANOPARTICLES; LIGANDS; BINDING; PYRROLIZIDINE;
D O I
10.1039/c5ra22152h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The first example of iminosugars multimerization based on gold nanoparticle cores was achieved by a straightforward synthetic strategy based on the use of simple glycosides of alpha-D-mannose or beta-Dglucose to modulate the density of biologically active pyrrolizidine and piperidine iminosugars at the gold surface. Exceptionally small and water dispersible gold colloids were obtained by self assembly of thiol ending sugar and novel iminosugar conjugates on the surface of in situ forming gold nanoparticles. The resulting nanostructures were characterized by different techniques. Preliminary screenings demonstrated that the novel nanosized architectures retain their bioactivity and make possible its modulation.
引用
收藏
页码:95817 / 95822
页数:6
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