Fluorescein labelled cationic carbosilane dendritic systems for biological studies

Cationic carbosilane dendrimers and dendrons labelled with one fluorescein unit have been synthesized. For dendrimers (generations 1–3), a random procedure was followed by successive addition of two types of thiol compounds to vinyl terminated derivatives, first one with –NH3Cl and second one with –...

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Bibliographic Details
Authors: Fuentes Paniagua, María Elena, Serramía Lobera, María Jesús, Sánchez-Nieves Fernández, Javier|||0000-0003-0410-2285, Álvarez, Susana, Muñoz Fernández, María Ángeles, Gómez Ramírez, Rafael|||0000-0001-6448-2414, Mata de la Mata, Francisco Javier de la|||0000-0003-0418-3935
Format: article
Publication Date:2015
Country:España
Institution:Universidad de Alcalá (UAH)
Repository:e_Buah Biblioteca Digital Universidad de Alcalá
Language:English
OAI Identifier:oai:ebuah.uah.es:10017/34022
Online Access:http://hdl.handle.net/10017/34022
https://dx.doi.org/10.1016/j.eurpolymj.2015.07.043
Access Level:Open access
Keyword:Labelled dendrimers and dendrons
Carbosilane
Gene therapy
HIV
Biodistribution
Química
Chemistry
Description
Summary:Cationic carbosilane dendrimers and dendrons labelled with one fluorescein unit have been synthesized. For dendrimers (generations 1–3), a random procedure was followed by successive addition of two types of thiol compounds to vinyl terminated derivatives, first one with –NH3Cl and second one with –NMe2HCl functions, subsequent reaction with FITC and finally quaternization with MeI. For dendrons, the use of compounds with a –NH2 group at the focal point and –NMe2 functions at the periphery allowed us to obtain the corresponding fluoresceinated cationic derivatives. The toxicity of these dendritic molecules was studied by MTT and their interaction with siRNA Nef by electrophoresis. Finally, second generation dendrimer and their dendriplexes with siRNA Nef were chosen as a model to analyse their in vivo biodistribution in a BALB/c mouse model. The highest levels for dendriplexes were found in spleen and liver, followed in lymph nodes, while lower levels were found in kidneys. This distribution is in accordance with long circulation times.