首页> 外文会议>IEEE International Conference on Nanotechnology >Engineering large gelatin nanospheres coated with quantum dots for targeted delivery of human osteosarcoma with enhanced cellular internalization
【24h】

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

机译:工程化涂有量子点的大型明胶纳米球,可靶向递送人类骨肉瘤并增强细胞内在化

获取原文

摘要

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,良好的内在化是使用大型纳米球作为癌症标记和治疗载体的主要问题之一。我们在本文中报道了涂有CdSe / ZnS量子点(QDs)的荧光明胶纳米球(GNs),以形成用于治疗学应用的可行载体。将抗人免疫球蛋白G Fab(抗IgG Fab)生物偶联到杂交荧光GNs上以进行靶向递送(QDs-GNs-抗IgG Fab)。人类骨肉瘤细胞系用于研究具有和不具有抗IgG Fab的杂交荧光GN之间的相互作用。与抗体生物缀合的荧光GNs的平均粒径估计为480±50 nm。荧光GN的发射(λem)约为652 nm。本文讨论了对GNs的表面修饰和生物结合的定量分析。三维z堆叠荧光图像显示,具有抗IgG Fab的杂交GNs在人骨肉瘤细胞中的内在化程度是没有抗体片段的GN的约1.5倍。 QDs-GN-抗IgG Fab改善的细胞相互作用归因于抗体的生物缀合,可以为靶向药物递送提供特异性。每种类型的功能化GNs的相对细胞生存力(%)大于80%,最高40μg/ mL。我们期望功能化的明胶球可以为靶向药物输送和直接成像确认提供有效的治疗方法。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号