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Título
Novel Water‐Soluble Carbosilane Dendrimers: Synthesis and Biocompatibility
Autor(es)
Palabras clave
Bioinorganic chemistry
Dendrimers
Silicon
Drug delivery
Toxicity
Fecha de publicación
2006
Citación
Ortega, P., Bermejo, J. F., Chonco, L., de Jesus, E., de la Mata, F. J., Fernández, G., ... & Muñoz‐Fernandez, M. A. (2006). Novel water‐soluble carbosilane dendrimers: synthesis and biocompatibility.
Resumen
[EN] 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
URI
ISSN
1434-1948
DOI
10.1002/ejic.200500782
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