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用于牙齿和骨骼替代的多孔聚甲基丙烯酸甲酯树脂植入物。

Implantation of porous polymethylmethacrylate resin for tooth and bone replacement.

作者信息

Ashman A, Moss M L

出版信息

J Prosthet Dent. 1977 Jun;37(6):657-65. doi: 10.1016/0022-3913(77)90216-5.

Abstract

This study suggests that: 1. The porous plastic material tested is compatible with and showed no undesirable reactions in subcutaneous, intracerebral, intramuscular, and especially, intraosseous sites. 2. By standardizing porosity (e.g., a desired hole, any dimension, uniformly distributed) with the implant material (P.P.M.M.), one can predict with a degree of certainty that connective-tissue (collagen fibers) or hard-tissue (osteogenesis and reparative bone) ingrowth into these micropores will definitely occur. 3. The various shapes employed for implantation of the plastic material were not carcinogenic and did not cause a malignant reaction in any implanted region. 4. A close "amalgamation" with adjacent tissues was a result regardless of the implant site (e.g., intramuscular, intracerebral, or subcutaneous). Intraosseously, there was a variation. Depending upon the pore size, one observes either connective tissue or osseous ingrowth into the micropores. At a 100 micron pore size (B material), connective tissue ingrowth into the P.P.M.M. was seen. At the 450 micron size (E material), osseous tissue ingrowth into the P.P.M.M. was clearly observed. 5. The P.P.M.M. implant material can be used as a tooth replacement (e.g., for a root) at a small pore size (100 micron) and as a bone replacement (e.g., for bony defects) at a larger pore size (450 micron). 6. To secure vascularization of the implant material, porosity throughout is indicated at a large pore size. Surface porosity regardless of size will encourage only soft-tissue ingrowth into the implant material. 7. Any hard-tissue size or shape can be duplicated with the material, at any pore size, with compatibility to the adjacent tissue, regardless of the region of placement in the body. 8. There is a possibility of bone "induction" or stimulation of bone growth in predetermined directions with all its implications (e.g., periodontal disease). The replacement and repair of any hard tissue in the body (e.g., bone and teeth) are possibilities.

摘要

本研究表明

  1. 所测试的多孔塑料材料具有生物相容性,在皮下、脑内、肌肉内,尤其是骨内植入部位未出现不良反应。2. 通过对植入材料(多孔塑料微球)的孔隙率进行标准化(例如,所需的孔,任何尺寸,均匀分布),可以在一定程度上确定结缔组织(胶原纤维)或硬组织(骨生成和修复性骨)长入微孔隙中肯定会发生。3. 用于植入塑料材料的各种形状不具有致癌性,并且在任何植入区域均未引起恶性反应。4. 无论植入部位(例如肌肉内、脑内或皮下)如何,都会与相邻组织紧密“融合”。在骨内,情况有所不同。根据孔径大小,可观察到结缔组织或骨组织长入微孔隙中。在孔径为100微米(B材料)时,可见结缔组织长入多孔塑料微球。在450微米大小(E材料)时,清晰观察到骨组织长入多孔塑料微球。5. 多孔塑料微球植入材料在小孔径(100微米)时可用于牙齿替代(例如牙根),在大孔径(450微米)时可用于骨替代(例如骨缺损)。6. 为确保植入材料的血管化,大孔径时需整体具有孔隙率。无论大小,表面孔隙率只会促使软组织长入植入材料。7. 该材料可复制任何硬组织的大小和形状,在任何孔径下,与相邻组织具有相容性,无论在体内的植入部位如何。8. 有可能在预定方向上诱导骨生长或刺激骨生长,并带来所有相关影响(例如牙周病)。体内任何硬组织(例如骨和牙齿)的替代和修复都是可能的。

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