Barriers to carrier mediated drug and gene delivery to brain tumors

被引:92
作者
Huynh, GH
Deen, DF
Szoka, FC
机构
[1] Univ Calif San Francisco, Dept Biopharmaceut Sci, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Pharmaceut Chem, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Joint Grad Grp Bioengn, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Brain Tumor Res Ctr, San Francisco, CA 94143 USA
[5] Univ Calif San Francisco, Dept Neurol Surg, San Francisco, CA 94143 USA
关键词
brain tumor; drug delivery; extracellular (CSF and ISF) fluid flow; gene therapy; liposome and polymer drug carriers;
D O I
10.1016/j.jconrel.2005.09.053
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Brain tumor patients face a poor prognosis despite significant advances in tumor imaging, neurosurgery and radiation therapy. Potent chemotherapeutic drugs fail when used to treat brain tumors because biochemical and physiological barriers limit drug delivery into the brain. In the past decade a number of strategies have been introduced to increase drug delivery into the brain parenchyma. In particular, direct drug administration into the brain tumor has shown promising results in both animal models and clinical trials. This technique is well suited for the delivery of liposome and polymer drug carriers, which have the potential to provide a sustained level of drug and to reach cellular targets with improved specificity. We will discuss the current approaches that have been used to increase drug delivery into the brain parenchyma in the context of fluid and solute transport into, through and from the brain, with a focus on liposome and polymer drug carriers. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:236 / 259
页数:24
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