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Engineering large gelatin nanospheres coated with quantum dots for targeted delivery of human osteosarcoma with enhanced cellular internalization

机译:工程大明胶纳米球,涂有量子点,用于靶向递送人骨瘤,具有增强的细胞内化

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Due to the special structures of cell membrane, good internalization is one of major concerns on using large nanospheres as carriers for labeling and treatment of cancer. We herein report fluorescent gelatin nanosphers (GNs) coated with CdSe/ZnS quantum dots (QDs) to form a viable vehicle for theranostic applications. Anti-human immunoglobulin G Fab formation, anti-IgG Fab, is bioconjugated on to the hybrid fluorescent GNs for targeted delivery (QDs-GNs-anti-IgG Fab). Human osteosarcoma cell line is used in studying the interaction between hybrid fluorescent GNs with and without anti-IgG Fab. The average particle size of the fluorescent GNs bioconjugated with antibodies is estimated at 480±50 nm. The emission (λem) of the fluorescent GNs is around 652 nm. The quantitative analysis on the surface modification and bioconjugation of GNs has been discussed in this paper. The three-dimensional z-stacking fluorescent images reveal that the hybrid GNs with anti-IgG Fab has ~1.5 times increase in internalization with human osteosarcoma cells than GNs without the antibody fragment. The improved cellular interaction of the QDs-GN-anti IgG Fab is attributed to the bioconjugation of antibodies which can provide specificity for targeted drug delivery. Relative cell viability (%) is larger than 80% for each type of functionalized GNs up to 40 μg/mL. We expect that the functionalized gelatin sphere can offer an effective theranostic tool for targeted drug delivery and direct imaging confirmation simultaneously.
机译:由于细胞膜的特殊结构,良好的内化是使用大纳米球作为用于标记和治疗癌症的载体的主要问题之一。本文在此报告涂有CDSE / ZnS量子点(QDS)的荧光明胶纳米鏻(GNS),以形成用于治疗方法的活力。抗人免疫球蛋白G Fab形成,抗IgG Fab,用于靶向递送的杂化荧光GNS(QDS-GNS-抗IgG Fab)。人骨肉瘤细胞系用于研究杂种荧光GNS与抗IgG Fab之间的相互作用。用抗体生物缀合的荧光GNS的平均粒径估计为480±50nm。荧光GNS的发射(λem)约为652nm。本文讨论了对GNS的表面改性和生物缀合的定量分析。三维Z堆叠荧光图像表明,具有抗IgG Fab的杂化GNS在没有抗体片段的情况下与L人骨肉瘤细胞内化增加〜1.5倍。 QDS-GN-抗IgG Fab的改善的细胞相互作用归因于抗体的生物缀合物,其可以为靶向药物递送提供特异性。对于每种类型的官能化GNS,相对细胞活力(%)大于80μg/ mL的官能化GNS。我们预计官能化的明胶球可以为有效的药物递送和同时直接成像确认提供有效的治疗工具。

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