Novel technologies for antiangiogenic drug delivery in the brain

被引:7
|
作者
Benny, Ofra [1 ]
Pakneshan, Pouya [1 ]
机构
[1] Harvard Univ, Childrens Hosp Boston, Karp Family Res Labs, Dept Surg,Vasc Biol Program,Med Sch, Boston, MA 02115 USA
关键词
angiogenesis; CNS; glioma; drug-delivery; brain; blood-brain-barrier; nanoparticles; lodamin;
D O I
10.4161/cam.3.2.7766
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Antiangiogenic therapies aimed at inhibiting the formation of tumor vasculature hold great promise for cancer therapy, with multiple compounds currently undergoing clinical trials. As with many forms of chemotherapy, antiangiogenic drugs face numerous hurdles in their translation to clinical use. Many such promising agents exhibit a short half-life, low solubility, poor bioavailability and multiple toxic side effects. Furthermore, when targeting malignant brain tumors the blood-brain barrier represents a formidable obstacle, preventing drugs from penetrating into the central nervous system (CNS). In this review, we discuss several preclinical antiangiogenic therapies and describe issues related to the unique conditions in the brain with regard to cancer treatment and neurotoxicity. We focus on the limitations of antiangiogenic drugs in the brain, along with numerous solutions that involve novel biomaterials and nanotechnological approaches. We also discuss an example in which modifying the properties of an antiangiogenic compound enhanced its clinical efficacy in treating tumors while simultaneously mitigating undesirable neurological side-effects.
引用
收藏
页码:224 / 229
页数:6
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