Department of Bioengineering, University of Utah, Salt Lake City, UT 84112, USA.
Adv Drug Deliv Rev. 2012 Sep;64(12):1189-204. doi: 10.1016/j.addr.2012.01.012. Epub 2012 Jan 28.
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.
发展中国家人口老龄化导致肌肉骨骼疾病(如骨质疏松症和骨转移)的发病率上升。许多骨病如果得不到治疗,会导致衰弱性疼痛,在癌症的情况下,还会导致死亡。许多有潜力的药物在治疗疾病方面是有效的,但会产生副作用,从而降低其在临床上的疗效。然而,骨骼提供了一个独特的无机固体环境,可以加以利用,以便将药物有效地靶向患病组织。通过将骨靶向部分整合到载药的水溶性聚合物中,可以增加药物在患病部位的有效载荷,同时减少副作用。临床相关的骨靶向聚合物治疗的实现取决于:(1)了解骨靶向部分的相互作用;(2)开发控释药物输送系统;以及(3)了解药物相互作用。后者使得能够开发出骨靶向协同药物输送系统。