Targeting polymer therapeutics to bone

被引:139
作者
Low, Stewart A. [1 ]
Kopecek, Jindrich [1 ,2 ]
机构
[1] Univ Utah, Dept Bioengn, Salt Lake City, UT 84112 USA
[2] Univ Utah, Dept Pharmaceut & Pharmaceut Chem, Salt Lake City, UT 84112 USA
关键词
Bone-targeting; Drug delivery; Cathepsin K; HPMA copolymer; PLGA copolymer; Hydroxyapatite; Poly(ethylene glycol) (PEG); Prostaglandin; Statins; PTH1-34; Osteoporosis; Bone metastasis; Rheumatoid arthritis; Bone fracture; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; INDUCED OSTEOCLAST DIFFERENTIATION; ENZYMATICALLY DEGRADABLE BONDS; LUMBAR INTERBODY FUSION; CATHEPSIN K INHIBITORS; FORMATION IN-VIVO; NF-KAPPA-B; MORPHOGENETIC PROTEIN-2; RHEUMATOID-ARTHRITIS; HYDROXYAPATITE BINDING;
D O I
10.1016/j.addr.2012.01.012
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
An aging population in the developing world has led to an increase in musculoskeletal diseases such as osteoporosis and bone metastases. Left untreated many bone diseases cause debilitating pain and in the case of cancer, death. Many potential drugs are effective in treating diseases but result in side effects preventing their efficacy in the clinic. Bone, however, provides a unique environment of inorganic solids, which can be exploited in order to effectively target drugs to diseased tissue. By integration of bone targeting moieties to drug-carrying water-soluble polymers, the payload to diseased area can be increased while side effects decreased. The realization of clinically relevant bone targeted polymer therapeutics depends on (1) understanding bone targeting moiety interactions. (2) development of controlled drug delivery systems, as well as (3) understanding drug interactions. The latter makes it possible to develop bone targeted synergistic drug delivery systems. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:1189 / 1204
页数:16
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