Title of article
Targeting polymer therapeutics to bone
Author/Authors
Low، نويسنده , , Stewart A. and Kope?ek، نويسنده , , Jind?ich، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2012
Pages
16
From page
1189
To page
1204
Abstract
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.
Keywords
Cathepsin K , HPMA copolymer , PLGA copolymer , Hydroxyapatite , Poly(ethylene glycol) (PEG) , Prostaglandin , statins , Osteoporosis , Bone metastasis , rheumatoid arthritis , Bone fracture , Bone-targeting , PTH1–34 , DRUG DELIVERY
Journal title
Advanced Drug Delivery Reviews
Serial Year
2012
Journal title
Advanced Drug Delivery Reviews
Record number
1763447
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