...
首页> 外文期刊>Acta Chimica Slovenica >In vitro assessment of potential bladder papillary neoplasm treatment with functionalized polyethyleneimine coated magnetic nanoparticles
【24h】

In vitro assessment of potential bladder papillary neoplasm treatment with functionalized polyethyleneimine coated magnetic nanoparticles

机译:功能化聚乙烯亚胺涂层磁性纳米粒子治疗膀胱乳头状肿瘤的体外评估

获取原文
   

获取外文期刊封面封底 >>

       

摘要

Normal porcine urothelial cells have been shown to have a much lower rate of endocytosis than urothelial papillary neoplasm cells. This could be used as a mechanism for selective delivery of toxic compounds, such as polyethyleneimine coated nanoparticles (NPs). However, these NPs induce nonselective toxicity through direct membrane disruption. This toxicity can be reduced by functionalization of NPs with L-glutathione reduced or bovine serum albumin by reducing their surface charge. Functionalization was confirmed with Fourier Transform Infrared Spectroscopy, Dynamic Light Scattering and Zeta potential measurements. Viability assays showed that bovine serum albumin coating reduced NPs cytotoxicity immediately after 3 h exposure and that such NPs were more toxic to urothelial papillary neoplasm cells compared to normal porcine urothelial cells at 50 μg/ml NPs concentration. However, 24 h after exposure, bovine serum albumin functionalized NPs had similar effect on viability of both cell lines. NPs showed some selective toxicity towards urothelial papillary neoplasm cells compared to normal cells after 3 h, however this was not confirmed after 24 h.
机译:正常猪尿路上皮细胞已显示出比尿路上皮乳头状瘤细胞低得多的内吞率。这可以用作选择性递送有毒化合物的机制,例如聚乙烯亚胺涂层的纳米颗粒(NPs)。然而,这些NP通过直接的膜破坏诱导非选择性毒性。可以通过将Ls-谷胱甘肽还原的NPs功能化或通过降低其表面电荷的牛血清白蛋白功能化来降低这种毒性。通过傅立叶变换红外光谱,动态光散射和Zeta电位测量证实了功能性。活力测定表明,牛血清白蛋白涂层在暴露3 h后立即降低了NPs的细胞毒性,并且与NP 50浓度的正常猪尿道上皮细胞相比,这些NPs对尿路上皮乳头状瘤细胞的毒性更大。然而,暴露后24小时,牛血清白蛋白功能化的NPs对两种细胞系的存活率具有相似的影响。与正常细胞相比,NP在3小时后对尿路上皮乳头状瘤细胞显示出一些选择性毒性,但是在24小时后未证实。

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