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Synthesis of fluorescent BAPAD dendrimeric structrures for biomedical applications

机译:用于生物医学应用的荧光BapaD树枝状结构的合成

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摘要

In this work, we present the synthesis and characterization of BAPAD1 fluorescent Dendrimeric-Antigens (DeAn), to study the dendritic cell maturation as a test to detect drug allergy reactions.Recently our research group developed a new kind of dendrimer, called BAPAD1, that we have used in this work to obtain the dendrimeric moiety of the target molecule. To this avail we synthesized a generation two BAPAD dendrimer using cystamine as core. Then, the free amine groups on the surface of the dendrimer were functionalized with an amoxiciloyl group (AXO), the allergenic determinant to the beta-lactam antibiotic amoxicillin. By the reduction of the disulfur bond we obtained two dendrons with a thiol group in the focal point, useful to attach a fluorescent probe.We synthesize as fluorescent moiety a naphthalimide derivative with a maleimide group upon which the thiol group of the dendron is added by a click reaction.2 In this way we obtained the target molecule to be used in the basophil activation test. The fluorescent DeAn (F-DeAn) has been fully characterized by NMR and MS techniques, and their fluorescent properties well established in aqueous biological media. The fluorescent dendron without the haptenic moieties at the periphery has been also obtained and fully characterized as a control assay. Both molecules have been also characterized using molecular dynamics simulation calculations.We show also here how these dendrimeric structures interact with dendritic cells and are internalized by them.
机译:在这项工作中,我们介绍了BAPAD1荧光树状抗原(DeAn)的合成和表征,以研究树突状细胞的成熟作为检测药物过敏反应的测试方法。我们已经在这项工作中使用以获得目标分子的树枝状部分。为此,我们以胱胺为核心合成了第二代BAPAD树状聚合物。然后,将树状聚合物表面上的游离胺基团与阿莫西林酰基(AXO)(β-内酰胺类抗生素阿莫西林的致敏性决定因素)官能化。通过还原二硫键,我们得到了两个在焦点处带有硫醇基的树枝状分子,可用于连接荧光探针。我们合成了带有马来酰亚胺基团的萘二甲酰亚胺衍生物作为荧光部分,并在其上添加了树枝状的巯基。 2这样,我们获得了用于嗜碱性粒细胞活化测试的目标分子。荧光DeAn(F-DeAn)已通过NMR和MS技术进行了充分表征,其荧光性质在水性生物介质中得到了很好的确立。还获得了在外围没有半抗原部分的荧光树突,并将其完全表征为对照测定。这两个分子也已经使用分子动力学模拟计算进行了表征。在这里,我们还展示了这些树状结构如何与树突状细胞相互作用并被它们内在化。

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