Targeted drug delivery for treatment and imaging of glioblastoma multiforme

被引:15
|
作者
Stukel, Jill M. [1 ]
Caplan, Michael R. [1 ]
机构
[1] Arizona State Univ, Ctr Intervent Biomat, Harrington Dept Bioengn, Tempe, AZ 85287 USA
关键词
convection enhanced delivery; drug delivery; glioblastoma; molecular targeting; CONVECTION-ENHANCED DELIVERY; BLOOD-BRAIN-BARRIER; POSITIVE-PRESSURE INFUSION; GROWTH-FACTOR RECEPTOR; QUANTUM DOTS; MALIGNANT GLIOMA; RAT-BRAIN; PHOTOTHERMAL ABLATION; EXTRACELLULAR-MATRIX; MOLECULAR-WEIGHT;
D O I
10.1517/17425240902988470
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Glioblastoma multiforme is a grade IV astrocytic tumor with a very high mortality rate. Although current treatment often includes surgical resection, this rarely removes all primary tumor cells, so is usually followed by radiation and/or chemotherapy. Remaining migratory tumor cells invade surrounding healthy tissue and contribute to secondary and tertiary tumor recurrence; therefore, despite significant research into glioma removal and treatment, prognosis remains poor. A variety of treatment modalities have been investigated to deliver drug to these cells, including systemic, diffusive and convection-enhanced delivery (CED). As systemic delivery is limited by molecules larger than similar to 500 Da being unable to cross the blood-brain barrier (BBB), therapeutic concentrations are difficult to attain; thus, localized delivery options relying on diffusion and CED have been used to circumvent the BBB. Although CED enables delivery to a greater volume of tissue than diffusive delivery alone, limitations still exist, requiring that these delivery strategies be improved. This review enumerates the strengths and weaknesses of these currently used strategies and details how predictive mathematical modeling can be used to aid investigators in optimizing these delivery modalities for clinical application.
引用
收藏
页码:705 / 718
页数:14
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