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[创伤与矫形外科中植入物的生物涂层]

[Biological coating of implants in trauma and orthopedic surgery].

作者信息

Raschke M J, Schmidmaier G

机构信息

Klinik für Unfall-, Hand- und Wiederherstellungschirurgie, Universitätsklinikum Münster.

出版信息

Unfallchirurg. 2004 Aug;107(8):653-63.

Abstract

In spite of improved operation techniques and optimized implants in trauma and orthopedic surgery complications like delayed fracture healing, non-unions or broad osseous infections may occur. This may be explained by more complex patterns of injuries, more extensive operative procedures and more complex fractures in cause of osteoporosis with increasing age. In the last years some growth factors for local application were approved (BMP-2, BMP-7), however not widely accepted. Reasons may be the high quantities of these limited and expensive proteins, which have to be implanted. Furthermore the local release from a bovine collagen carrier in tissue is not evident. The use of coated implants with incorporated active ingredients could release drugs locally and thereby obtain a high concentration in the area of interest without systemic side effects. Possible compounds for the improvement of fracture healing could be growth factors as well as antibiotics for prophylaxis of implant related infections. A biodegradable poly (D,L-lactid)-coating of implants could release incorporated growth factors in a controlled manner directly into the fracture. Furthermore the coated implant remains as a fracture treatment device. Different models are demonstrated (fracture healing--intervertebral fusion--infection model) to prove the efficiency of the coating technology. These findings seem to justify the transfer of this technology into clinic.

摘要

尽管创伤和骨科手术中的操作技术有所改进,植入物也得到了优化,但仍可能出现诸如骨折愈合延迟、骨不连或广泛的骨感染等并发症。这可能是由于随着年龄增长,骨质疏松导致损伤模式更复杂、手术操作更广泛以及骨折更复杂。近年来,一些用于局部应用的生长因子(骨形态发生蛋白-2、骨形态发生蛋白-7)已获批准,但尚未被广泛接受。原因可能是这些有限且昂贵的蛋白质需要大量植入。此外,从牛胶原蛋白载体在组织中的局部释放并不明显。使用含有活性成分的涂层植入物可以在局部释放药物,从而在感兴趣的区域获得高浓度而无全身副作用。用于改善骨折愈合的可能化合物可以是生长因子以及用于预防植入物相关感染的抗生素。植入物的可生物降解聚(D,L-丙交酯)涂层可以将所含生长因子以可控方式直接释放到骨折部位。此外,涂层植入物仍作为骨折治疗装置。展示了不同的模型(骨折愈合——椎间融合——感染模型)以证明涂层技术的有效性。这些发现似乎证明了将该技术转化到临床的合理性。

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