Strategies to target drugs to gliomas and CNS metastases of solid tumors

被引:14
作者
Kerklaan, B. Milojkovic [1 ,2 ]
van Tellingen, O. [3 ]
Huitema, A. D. R. [4 ]
Beijnen, J. H. [4 ,5 ]
Boogerd, W. [6 ]
Schellens, J. H. M. [1 ,2 ,5 ]
Brandsma, D. [6 ]
机构
[1] Netherlands Canc Inst Antoni van Leeuwenhoek, Dept Mol Pathol, NL-1066 CX Amsterdam, Netherlands
[2] Netherlands Canc Inst Antoni van Leeuwenhoek, Dept Clin Pharmacol, NL-1066 CX Amsterdam, Netherlands
[3] Netherlands Canc Inst Antoni van Leeuwenhoek, Dept Preclin Pharmacol, NL-1066 CX Amsterdam, Netherlands
[4] Netherlands Canc Inst Antoni van Leeuwenhoek, Dept Pharm & Pharmacol, NL-1066 CX Amsterdam, Netherlands
[5] Univ Utrecht, Utrecht Inst Pharmaceut Sci, Utrecht, Netherlands
[6] Netherlands Canc Inst Antoni van Leeuwenhoek, Dept Neurooncol, Plesmanlaan 121, NL-1066 CX Amsterdam, Netherlands
关键词
Glioma; Brain metastases; Nanoparticles; Polymer-based nanocarriers; siRNA; Antibodies; BLOOD-BRAIN-BARRIER; GLUTATHIONE-COATED NANOPARTICLES; P-GLYCOPROTEIN; RADIATION-THERAPY; BREAST-CANCER; PHASE-III; IN-VIVO; VINCRISTINE CHEMOTHERAPY; GLIOBLASTOMA-MULTIFORME; MULTIDRUG-RESISTANCE;
D O I
10.1007/s00415-015-7919-9
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The treatment for central nervous system metastases of solid tumors and gliomas is limited as the blood-brain barrier (BBB) is an obstacle to systemic therapy. Here, we review the physiochemical properties of the BBB and both current and new drug strategies to penetrate brain tumors. We focus on targeting receptor- or carrier-mediated transport mechanisms over the BBB used by drug conjugates, nanoparticles, polymer-based nanocarriers, siRNA, and antibodies.
引用
收藏
页码:428 / 440
页数:13
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