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Mechanistic Insight into Cell Growth, Internalization, and Cytotoxicity of PAMAM Dendrimers

机译:机械了解PAMAM树状大分子的细胞生长,内在化和细胞毒性

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We report on the role of PAMAM dendrimer concentration and generation (G2, G4, G6) on cell growth and cytotoxicity in HEK293T and HeLa cell lines and make comparisons with dendrimer-induced leakage from liposomes to probe the mechanisms in action. Specifically, we observed a striking transition from cell growth enhancement to a reduction in cell viability at a critical PAMAM dendrimer concentration, that is, ~500 nM. Confocal microscopy studies show evidence of a transition from cell membrane adhesion to cell internalization and cell nucleus interaction at equivalent dendrimer concentrations. A dendrimer concentration window of 500—700 nM was identified for effective cell internalization without significant cytotoxicity. Though liposome leakage correlated with cytotoxicity, no quantitative agreement was observed, that is, cells are 100 times (based on surface coverage) more resistant to dendrimers than liposomes. These findings have significant implications in the design of effective drug/gene delivery vehicles based on dendrimers.
机译:我们报告在HEK293T和HeLa细胞系中PAMAM树状聚合物浓度和生成(G2,G4,G6)对细胞生长和细胞毒性的作用,并与树状聚合物诱导的脂质体渗漏进行比较,以探究其作用机理。具体来说,我们观察到在临界PAMAM树枝状大分子浓度(约500 nM)下,从细胞生长增强到细胞活力降低的惊人过渡。共聚焦显微镜研究表明,在等效的树状聚合物浓度下,从细胞膜粘附到细胞内在化和细胞核相互作用的过渡证据。可以确定500-700 nM的树状聚合物浓度窗口可有效地进行细胞内在化,而没有明显的细胞毒性。尽管脂质体泄漏与细胞毒性有关,但未观察到定量一致性,也就是说,细胞对树状聚合物的抗性(基于表面覆盖率)是脂质体的100倍。这些发现对基于树状聚合物的有效药物/基因递送载体的设计具有重要意义。

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