Novel water-soluble carbosilane dendrimers:: Synthesis and biocompatibility

被引:64
|
作者
Ortega, P
Bermejo, JF
Chonco, L
de Jesus, E
de la Mata, FJ
Fernández, G
Flores, JC
Gómez, R
Serramía, MJ
Muñoz-Fernandez, MA
机构
[1] Univ Alcala de Henares, Dept Quim Inorgan, Alcala De Henares 28871, Spain
[2] Univ Gregorio Maranon, Lab Immunobiol Mol, Gen Hosp, Madrid, Spain
关键词
bioinorganic chemistry; dendrimers; silicon; drug delivery; toxicity;
D O I
10.1002/ejic.200500782
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A synthetic strategy has been developed for the preparation of new peripheral amine- or ammonium-terminated carbosilane dendrimers of type nG-[Si(OCH2CH2NMe2)(y)](x), or nG[Si(OCH2CH2NMe3+I-)(y)](x), respectively. It consists of the alcoholysis of well-known chlorosilane-terminated dendrimers with N,N-dimethylethanolamine and the subsequent quaternization with MeI. All these systems are susceptible to hydrolysis, although the decomposition depends on concentration and dendrimer generation. Evaluation of dendrimer toxicities by phase-contrast light microscopy and MTT assay were carried out, and evidence of dendrimer/oligonucleotide complex formation was carried out by gel electrophoresis. ((c) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006).
引用
收藏
页码:1388 / 1396
页数:9
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