Drug targeting systems for inflammatory disease: One for all, all for one

被引:107
作者
Crielaard, Bart J. [1 ]
Lammers, Twan [2 ,3 ]
Schiffelers, Raymond M. [1 ,4 ]
Storm, Gert [1 ,3 ]
机构
[1] Univ Utrecht, Utrecht Inst Pharmaceut Sci UIPS, Dept Pharmaceut, NL-3508 TB Utrecht, Netherlands
[2] Rhein Westfal TH Aachen, Dept Expt Mol Imaging, Aachen, Germany
[3] Univ Twente, Dept Targeted Therapeut, NL-7500 AE Enschede, Netherlands
[4] Univ Med Ctr Utrecht, Dept Clin Chem & Haematol, Utrecht, Netherlands
关键词
Drug targeting; Nanomedicine; Inflammatory disease; Rheumatoid arthritis; Multiple sclerosis; EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS; COLLAGEN-INDUCED ARTHRITIS; ENDOTHELIAL GROWTH-FACTOR; FOLATE RECEPTOR ISOFORMS; SYNOVIAL LINING CELLS; MULTIPLE-SCLEROSIS; RHEUMATOID-ARTHRITIS; LIPOSOMAL GLUCOCORTICOSTEROIDS; MACROMOLECULAR THERAPEUTICS; INTEGRIN ALPHA(V)BETA(3);
D O I
10.1016/j.jconrel.2011.12.014
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
In various systemic disorders, structural changes in the microenvironment of diseased tissues enable both passive and active targeting of therapeutic agents to these tissues. This has led to a number of targeting approaches that enhance the accumulation of drugs in the target tissues, making drug targeting an attractive strategy for the treatment of various diseases. Remarkably, the strategic principles that form the basis of drug targeting are often employed for tumor targeting, while chronic inflammatory diseases appear to draw much less attention. To provide the reader with a general overview of the current status of drug targeting to inflammatory diseases, the passive and active targeting strategies that have been used for the treatment of rheumatoid arthritis (RA) and multiple sclerosis (MS) are discussed. The last part of this review addresses the dualism of platform technology-oriented ("one for all") and disease-oriented drug targeting research ("all for one"), both of which are key elements of effective drug targeting research. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:225 / 234
页数:10
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