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

被引:113
作者
Anabousi, Samah
Bakowsky, Udo
Schneider, Marc
Huwer, Hanno
Lehr, Claus-Michael
Ehrhardt, Carsten [1 ]
机构
[1] Univ Dublin Trinity Coll, Sch Pharm & Pharmaceut Sci, Dublin 2, Ireland
[2] Univ Saarland, D-66123 Saarbrucken, Germany
[3] Univ Marburg, Dept Pharmaceut Technol & Biopharm, D-35037 Marburg, Germany
[4] Volkingen Heart Ctr, Dept Cardiothorac Surg, D-66333 Volklingen, Germany
关键词
liposomes; transferrin; lung cancer; pulmonary drug delivery; inhalation;
D O I
10.1016/j.ejps.2006.07.004
中图分类号
R9 [药学];
学科分类号
1007 ;
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. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:367 / 374
页数:8
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