Cunningham Bryan W, Atkinson Brent L, Hu Nianbin, Kikkawa Jun, Jenis Louis, Bryant Joseph, Zamora Paul O, McAfee Paul C
Orthopaedic Spinal Research Laboratory, St. Joseph Medical Center, Towson, MD, USA.
J Neurosurg Spine. 2009 Apr;10(4):300-7. doi: 10.3171/2009.1.SPINE08565.
New generations of devices for spinal interbody fusion are expected to arise from the combined use of bioactive peptides and porous implants. The purpose of this dose-ranging study was to evaluate the fusion characteristics of porous ceramic granules (CGs) coated with the bioactive peptide B2A2-K-NS (B2A) by using a model of instrumented lumbar interbody spinal fusion in sheep.
Instrumented spinal arthrodesis was performed in 40 operative sites in 20 adult sheep. In each animal, posterior instrumentation (pedicle screw and rod) and a polyetheretherketone cage were placed in 2 single-level procedures (L2-3 and L4-5). All cages were packed with graft material prior to implantation. The graft materials were prepared by mixing (1:1 vol/vol) CGs with or without a B2A coating and morselized autograft. Ceramic granules were coated with B2A at 50, 100, 300, and 600 microg/ml granules (50-B2A/CG, 100-B2A/CG, 300-B2A/CG, and 600-B2A/CG, respectively), resulting in 4 B2A-coated groups plus a control group (uncoated CGs). Graft material from each of these groups was implanted in 8 operative sites. Four months after arthrodesis, interbody fusion status was assessed with CT, and the interbody site was further evaluated with quantitative histomorphometry.
All B2A/CG groups had higher CT-confirmed interbody fusion rates compared with those in controls (CGs only). Seven of 8 sites were fused in the 50-B2A/CG, 100-B2A/CG, and 300-B2A/CG groups, whereas 5 of 8 sites were fused in the group that had received uncoated CGs. New woven and lamellar bone spanned the fusion sites with excellent osseointegration. There was no heterotopic ossification or other untoward events attributed to the use of B2A/CG in any group. Each B2A/CG treatment produced more new bone than that in the CG group.
Bioactive treatment with B2A effectively enhanced the fusion capacity of porous CGs. These findings suggest that B2A/CG may well represent a new generation of biomaterials for lumbar interbody fusion and indicate that additional studies are warranted.
新一代脊柱椎间融合装置有望通过生物活性肽与多孔植入物的联合使用而产生。本剂量范围研究的目的是通过使用绵羊腰椎椎间脊柱融合模型,评估涂有生物活性肽B2A2-K-NS(B2A)的多孔陶瓷颗粒(CGs)的融合特性。
在20只成年绵羊的40个手术部位进行器械辅助脊柱融合术。在每只动物中,通过两个单节段手术(L2-3和L4-5)放置后路器械(椎弓根螺钉和棒)和聚醚醚酮椎间融合器。所有椎间融合器在植入前均填充移植材料。移植材料通过将CGs与或不与B2A涂层以及碎骨自体移植混合(1:1体积/体积)制备。陶瓷颗粒分别以50、100、300和600μg/ml颗粒的浓度涂覆B2A(分别为50-B2A/CG、100-B2A/CG、300-B2A/CG和600-B2A/CG),从而形成4个B2A涂层组加一个对照组(未涂层的CGs)。这些组中的每组移植材料均植入8个手术部位。融合术后4个月,通过CT评估椎间融合状态,并通过定量组织形态计量学进一步评估椎间部位。
与对照组(仅CGs)相比,所有B2A/CG组的CT确认椎间融合率更高。50-B2A/CG、100-B2A/CG和300-B2A/CG组中8个部位有7个融合,而接受未涂层CGs的组中8个部位有5个融合。新的编织骨和板层骨跨越融合部位,骨整合良好。在任何组中均未发现因使用B2A/CG导致的异位骨化或其他不良事件。每种B2A/CG处理产生的新骨均比CG组多。
B2A的生物活性处理有效地增强了多孔CGs的融合能力。这些发现表明B2A/CG很可能代表了新一代用于腰椎椎间融合的生物材料,并表明有必要进行进一步研究。