Development of Bone Targeting Drugs

被引:83
作者
Stapleton, Molly [1 ,2 ]
Sawamoto, Kazuki [2 ]
Almeciga-Diaz, Carlos J. [3 ]
Mackenzie, William G. [2 ]
Mason, Robert W. [1 ,2 ]
Orii, Tadao [4 ]
Tomatsu, Shunji [1 ,2 ,4 ,5 ]
机构
[1] Univ Delaware, Dept Biol Sci, Newark, DE 19716 USA
[2] Nemours Alfred I duPont Hosp Children, Wilmington, DE 19803 USA
[3] Pontificia Univ Javeriana, Inst Study Inborn Errors Metab, Bogota 110231, Colombia
[4] Gifu Univ, Grad Sch Med, Dept Pediat, Gifu 5011193, Japan
[5] Thomas Jefferson Univ, Dept Pediat, Philadelphia, PA 19107 USA
关键词
bone targeting drugs; osteoporosis; metabolic skeletal dysplasia; bisphosphonates; nanoparticles; STEM-CELLS; ADIPOGENIC DIFFERENTIATION; RHEUMATOID-ARTHRITIS; TISSUE REGENERATION; PLGA NANOPARTICLES; DELIVERY-SYSTEM; BISPHOSPHONATES; MORQUIO; INTERFERENCE; OLIGOPEPTIDE;
D O I
10.3390/ijms18071345
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The skeletal system, comprising bones, ligaments, cartilage and their connective tissues, is critical for the structure and support of the body. Diseases that affect the skeletal system can be difficult to treat, mainly because of the avascular cartilage region. Targeting drugs to the site of action can not only increase efficacy but also reduce toxicity. Bone-targeting drugs are designed with either of two general targeting moieties, aimed at the entire skeletal system or a specific cell type. Most bone-targeting drugs utilize an affinity to hydroxyapatite, a major component of the bone matrix that includes a high concentration of positively-charged Ca2+. The strategies for designing such targeting moieties can involve synthetic and/or biological components including negatively-charged amino acid peptides or bisphosphonates. Efficient delivery of bone-specific drugs provides significant impact in the treatment of skeletal related disorders including infectious diseases (osteoarthritis, osteomyelitis, etc.), osteoporosis, and metabolic skeletal dysplasia. Despite recent advances, however, both delivering the drug to its target without losing activity and avoiding adverse local effects remain a challenge. In this review, we investigate the current development of bone-targeting moieties, their efficacy and limitations, and discuss future directions for the development of these specific targeted treatments.
引用
收藏
页数:15
相关论文
共 71 条
[1]  
Allgrove J., 2007, Paediatrics and child health, V17, P253
[2]  
Bassit A. C. F., 2015, J NANOMED NANOTECHNO, V6, P1
[3]   Targeting osteoclast-osteoblast communication [J].
Cao, Xu .
NATURE MEDICINE, 2011, 17 (11) :1344-1346
[4]   Multifunctional Eu3+/Gd3+ dual-doped calcium phosphate vesicle-like nanospheres for sustained drug release and imaging [J].
Chen, Feng ;
Huang, Peng ;
Zhu, Ying-Jie ;
Wu, Jin ;
Cui, Da-Xiang .
BIOMATERIALS, 2012, 33 (27) :6447-6455
[5]   Design of surface-modified poly(D,L-lactide-co-glycolide) nanoparticles for targeted drug delivery to bone [J].
Choi, Sung-Wook ;
Kim, Jung-Hyun .
JOURNAL OF CONTROLLED RELEASE, 2007, 122 (01) :24-30
[6]   Alendronate-decorated biodegradable polymeric micelles for potential bone-targeted delivery of vancomycin [J].
Cong, Yingying ;
Quan, Changyun ;
Liu, Meiqing ;
Liu, Jie ;
Huang, Gang ;
Tong, Guoquan ;
Yin, Yihua ;
Zhang, Chao ;
Jiang, Qing .
JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION, 2015, 26 (11) :629-643
[7]   Drug delivery and nanoparticles: Applications and hazards [J].
De Jong, Wim H. ;
Borm, Paul J. A. .
INTERNATIONAL JOURNAL OF NANOMEDICINE, 2008, 3 (02) :133-149
[8]   Bone marrow stromal cells (BMSCs) in bone engineering: Limitations and recent advances [J].
Derubeis, AR ;
Cancedda, R .
ANNALS OF BIOMEDICAL ENGINEERING, 2004, 32 (01) :160-165
[9]  
Edwards JR, 2012, DISCOV MED, V13, P201
[10]   The Influence of Tetracycline Inducible Targeting Rat PPARγ Gene Silencing on the Osteogenic and Adipogenic Differentiation of Bone Marrow Stromal Cells [J].
Feng, Xiaobo ;
Liu, Xianzhe ;
Cai, Xianyi ;
Lin, Tao ;
Xu, Weihua ;
Yang, Cao ;
Liu, Yongwei ;
Yang, Shuhua ;
Fu, Dehao .
CURRENT PHARMACEUTICAL DESIGN, 2016, 22 (41) :6330-6338