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重组人骨形态发生蛋白-2(rhBMP-2)从脱矿牙本质基质中的假定释放曲线。

Postulated release profile of recombinant human bone morphogenetic protein-2 (rhBMP-2) from demineralized dentin matrix.

作者信息

Um In-Woong, Ku Jeong-Kui, Lee Bu Kyu, Yun Pil-Young, Lee Jeong Keun, Nam Jeong-Hun

机构信息

R&D Institute, Korea Tooth Bank, Seoul, Korea.

Department of Oral and Maxillofacial Surgery, Section of Dentistry, Armed Forces Capital Hospital, Seongnam, Korea.

出版信息

J Korean Assoc Oral Maxillofac Surg. 2019 Jun;45(3):123-128. doi: 10.5125/jkaoms.2019.45.3.123. Epub 2019 Jun 28.

Abstract

Demineralized dentin matrix (DDM) has been used as a recombinant human bone morphogenetic protein-2 (rhBMP-2) carrier in many clinical trials. To optimize the clinical safety and efficacy of rhBMP-2 with DDM, efforts have been made to improve the delivery of rhBMP-2 by 1) lowering the administered dose, 2) localizing the protein, and 3) prolonging its retention time at the action site as well as the bone forming capacity of the carrier itself. The release profile of rhBMP-2 that is associated with endogenous BMP in dentin has been postulated according to the type of incorporation, which is attributed to the loosened interfibrillar space and nanoporous dentinal tubule pores. Physically adsorbed and modified, physically entrapped rhBMP-2 is sequentially released from the DDM surface during the early stage of implantation. As DDM degradation progresses, the loosened interfibrillar space and enlarged dentinal tubules release the entrapped rhBMP-2. Finally, the endogenous BMP in dentin is released with osteoclastic dentin resorption. According to the postulated release profile, DDM can therefore be used in a controlled manner as a sequential delivery scaffold for rhBMP-2, thus sustaining the rhBMP-2 concentration for a prolonged period due to localization. In addition, we attempted to determine how to lower the rhBMP-2 concentration to 0.2 mg/mL, which is lower than the approved 1.5 mg/mL.

摘要

脱矿牙本质基质(DDM)在许多临床试验中已被用作重组人骨形态发生蛋白-2(rhBMP-2)的载体。为了优化rhBMP-2与DDM联合使用时的临床安全性和有效性,人们已做出努力通过以下方式改善rhBMP-2的递送:1)降低给药剂量;2)使蛋白质局部化;3)延长其在作用部位的保留时间以及载体本身的骨形成能力。根据结合类型推测了与牙本质中内源性骨形态发生蛋白相关的rhBMP-2的释放曲线,这归因于纤维间空间的疏松和纳米多孔牙本质小管孔隙。物理吸附和修饰、物理包裹的rhBMP-2在植入早期从DDM表面依次释放。随着DDM降解的进行,疏松的纤维间空间和扩大的牙本质小管释放出包裹的rhBMP-2。最后,牙本质中的内源性骨形态发生蛋白随着破骨细胞对牙本质的吸收而释放。根据推测的释放曲线,DDM因此可以作为rhBMP-2的顺序递送支架以可控方式使用,从而由于局部化而在较长时间内维持rhBMP-2的浓度。此外,我们试图确定如何将rhBMP-2浓度降低至0.2mg/mL,该浓度低于批准的1.5mg/mL。

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