Sahdev Rohan, Ansari Tahera I, Higham Susan M, Valappil Sabeel P
Department of Health Services Research and School of Dentistry, University of Liverpool, Liverpool, UK.
Department of Surgical Research, Imperial College London, Watford Road, Harrow, UK.
J Biomater Appl. 2015 Jul;30(1):85-92. doi: 10.1177/0885328215571952. Epub 2015 Feb 12.
This study aimed at evaluating the potential effect of gallium-incorporated phosphate-based glasses towards periodontitis-associated bacteria, Porphyromonas gingivalis, and matrix metalloproteinase-13. Periodontitis describes a group of inflammatory diseases of the gingiva and supporting structures of the periodontium. They are initiated by the accumulation of plaque bacteria, such as the putative periodontal pathogen Porphyromonas gingivalis, but the host immune response such as elevated matrix metalloproteinases are the major contributing factor for destruction of periodontal tissues. Antibacterial assays of gallium-incorporated phosphate-based glasses were conducted on Porphyromonas gingivalis ATCC 33277 using disc diffusion assay on fastidious anaerobe agar and liquid broth assay in a modified tryptic soy broth. In vitro study investigated the effect of gallium on purified recombinant human matrix metalloproteinase-13 activity using matrix metalloproteinase assay kit. In vivo biocompatibility of gallium-incorporated phosphate-based glass was evaluated in rats as subcutaneous implants. Antibacterial assay of gallium displayed activity against Porphyromonas gingivalis (inhibition zone of 22 ± 0.5 mm compared with 0 mm for control glass, c-PBG). Gallium in the glass contributed to growth inhibitory effect on Porphyromonas gingivalis (up to 1.30 reductions in log 10 values of the viable counts compared with control) in a modified tryptic soy broth. In vitro study showed gallium-incorporated phosphate-based glasses inhibited matrix metalloproteinase activity significantly (p ≤ 0.01) compared with c-PBG. Evaluation of in vivo biocompatibility of gallium-incorporated phosphate-based glasses in rats showed a non-toxic and foreign body response after 2 weeks of implantation. The results indicate that gallium ions might act on multiple targets of biological mechanisms underlying periodontal disease. Moreover, gallium-incorporated phosphate-based glasses are biocompatible in a rat model. The findings warrant further investigation and will have important clinical implications in the future treatment and management of periodontitis.
本研究旨在评估含镓磷酸盐基玻璃对牙周炎相关细菌牙龈卟啉单胞菌以及基质金属蛋白酶-13的潜在作用。牙周炎是指牙龈及牙周支持组织的一组炎症性疾病。它们由菌斑细菌的积累引发,如假定的牙周病原体牙龈卟啉单胞菌,但宿主免疫反应如基质金属蛋白酶升高是破坏牙周组织的主要促成因素。采用对苛求厌氧菌琼脂的纸片扩散法以及在改良胰蛋白酶大豆肉汤中的液体肉汤法,对含镓磷酸盐基玻璃进行了针对牙龈卟啉单胞菌ATCC 33277的抗菌试验。体外研究使用基质金属蛋白酶检测试剂盒研究了镓对纯化的重组人基质金属蛋白酶-13活性的影响。在大鼠中作为皮下植入物评估了含镓磷酸盐基玻璃的体内生物相容性。镓的抗菌试验显示其对牙龈卟啉单胞菌具有活性(抑菌圈为22±0.5毫米,而对照玻璃c-PBG为0毫米)。玻璃中的镓在改良胰蛋白酶大豆肉汤中对牙龈卟啉单胞菌具有生长抑制作用(与对照相比,活菌计数的对数10值最多降低1.30)。体外研究表明,与c-PBG相比,含镓磷酸盐基玻璃显著抑制基质金属蛋白酶活性(p≤0.01)。对大鼠中含镓磷酸盐基玻璃的体内生物相容性评估显示,植入2周后无毒性且无异物反应。结果表明,镓离子可能作用于牙周疾病潜在生物学机制的多个靶点。此外,含镓磷酸盐基玻璃在大鼠模型中具有生物相容性。这些发现值得进一步研究,并将对未来牙周炎的治疗和管理具有重要的临床意义。