Bone tissue engineering and regenerative medicine: Targeting pathological fractures

被引:18
|
作者
Nguyen, Duong T. [1 ]
Burg, Karen J. L.
机构
[1] Clemson Univ, Dept Bioengn, Clemson, SC 29634 USA
关键词
bone disease; bone substitutes; bone tissue engineering; fragility fracture; CALCIUM-PHOSPHATE CEMENT; IN-VITRO; ORTHOPEDIC IMPLANTS; DRUG-DELIVERY; OSTEOBLAST DIFFERENTIATION; OSTEOGENESIS IMPERFECTA; TRANSCRIPTION FACTORS; INTERNAL-FIXATION; LOCAL-DELIVERY; PAGET DISEASE;
D O I
10.1002/jbm.a.35139
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Patients with bone diseases have the highest risk of sustaining fractures and of suffering from nonunion bone healing due to tissue degeneration. Current fracture management strategies are limited in design and functionality and do not effectively promote bone healing within a diseased bone environment. Fracture management approaches include pharmaceutical therapy, surgical intervention, and tissue regeneration for fracture prevention, fracture stabilization, and fracture site regeneration, respectively. However, these strategies fail to accommodate the pathological nature of fragility fractures, leading to unwanted side effects, implant failures, and nonunions. To target fragility fractures, fracture management strategies should include bioactive bone substitutes designed for the pathological environment. However, the clinical outcome of these materials must be predictable within various disease environments. Initial development of a targeted treatment strategy should focus on simulating the physiological in vitro bone environment to predict clinical effectiveness of the engineered bone. An in vitro test system can facilitate reduction of implant failures and non-unions in fragility fractures. (c) 2014 Wiley Periodicals, Inc. J Biomed Mater Res Part A : 103A: 420-429, 2015.
引用
收藏
页码:420 / 429
页数:10
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