首页> 外文期刊>European journal of pharmaceutical sciences >In vitro assessment of transferrin-conjugated liposomes as drug delivery systems for inhalation therapy of lung cancer.
【24h】

In vitro assessment of transferrin-conjugated liposomes as drug delivery systems for inhalation therapy of lung cancer.

机译:体外评估转铁蛋白缀合的脂质体作为肺癌吸入治疗的药物递送系统。

获取原文
获取原文并翻译 | 示例
           

摘要

Most human tumours over-express receptors for growth factors and peptide hormones, which are being increasingly studied as a means to selectively deliver cytotoxic agents. An example being the transferrin receptor (TfR, CD71). Here, we studied expression levels and location of TfR in different lung epithelial cell types (i.e., bronchial and alveolar epithelial cells) by flow-cytometry and confocal laser scanning microscopy (CLSM). Furthermore, we assessed uptake levels and cytotoxicity of transferrin (Tf)-conjugated liposomes in vitro. TfR was found to be expressed at a significantly higher level in bronchial epithelial cells compared with their alveolar counterparts. Cells of cancerous origin (i.e., A549 cell line) showed a higher TfR expression level than healthy alveolar epithelial type II cells in primary culture. CLSM revealed TfR to be located primarily at the basolateral aspect of cells, with the exception of cells undergoing mitotic proliferation, which also showed TfR at their apical membranes, due to their loss of cell polarity. Higher expression levels of TfR correlated well with enhanced uptake of Tf-liposomes and increased levels of cytotoxicity. Liposome uptake was temperature-dependent and inhibitable by excess free Tf. Tf-conjugated liposomes appear as good candidates for an approach to deliver cytostatic drugs to sites of lung cancer by inhalation.
机译:大多数人类肿瘤过表达生长因子和肽激素的受体,正在日益研究它们作为选择性递送细胞毒剂的手段。一个例子是运铁蛋白受体(TfR,CD71)。在这里,我们通过流式细胞仪和共聚焦激光扫描显微镜(CLSM)研究了TfR在不同肺上皮细胞类型(即支气管和肺泡上皮细胞)中的表达水平和位置。此外,我们评估了转铁蛋白(Tf)偶联脂质体的摄取水平和细胞毒性。发现TfR在肺泡支气管上皮细胞中的表达水平明显高于其肺泡对应物。在原代培养中,癌起源的细胞(即A549细胞系)显示出比健康的II型肺泡上皮细胞更高的TfR表达水平。 CLSM揭示TfR主要位于细胞的基底外侧,除了有丝分裂增殖的细胞外,由于细胞极性的丧失,TfR在其顶膜也显示TfR。 TfR的较高表达水平与Tf-脂质体摄取增加和细胞毒性水平增加密切相关。脂质体的摄取是温度依赖性的,并且可以被过量的游离Tf抑制。结合有Tf的脂质体似乎是通过吸入将细胞抑制药物递送至肺癌部位的方法的良好候选者。

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