Mulligan A M, Wilson M, Knowles J C
Division of Biomaterials and Tissue Engineering, Eastman Dental Institute, University College London, 256 Gray's Inn Road, London, United Kingdom WC1X 8LD.
J Biomed Mater Res A. 2003 Nov 1;67(2):401-12. doi: 10.1002/jbm.a.10052.
Silver is a powerful antibacterial ion that may be useful for dealing with localized infections, such as periodontitis. However, the use of silver in this role could be significantly improved by the development of an effective means of delivery. Phosphate-based glasses may provide a means of delivering the ions in a controlled manner. In our study, we have examined the effect of increasing silver content in phosphate-based glasses on biofilms of Streptococcus sanguis. Glasses of nominally the same dissolution rate were doped with silver at 1, 5,10, and 15 mol % and the number of colony-forming units (CFUs) determined after 6 and 24 h in a constant depth film fermenter (CDFF). The 1 mol % silver showed little change between 6 and 24 h. However, only 0.5 log CFUs were present on the glass containing 5 mol % at 6 h, and this reduced to virtually zero at 24 h. Few viable bacteria were found on the 10 mol % glass at both 6 and 24 h. The 15 mol % glass was investigated in this experiment, but no viable counts were detected. In a second set of experiments, glasses with 10 and 15 mol % silver were tested in the CDFF for up to 192 h. For the 10 mol % silver glass, there was approximately 0.8 log CFUs on this glass, which dropped to almost zero at 50 h. This was approximately 1.5-2.0 log reduction in CFUs compared to controls, and this difference was maintained for the first 50 h. After 50 h, there was a slow increase in the CFUs on all samples. However, CFUs on the 10 mol % silver glass were still suppressed up to 192 h compared to the controls. However, both controls also exhibited a decrease in viable counts at 50 h; this may have been due to carryover of silver into the control sample holders. However, this was minimized by the specimen layout in the CDFF and by having gaps between specimen sets. For the 15 mol % silver glass, counts for both this glass and the controls decreased to virtually zero between 24 and 48 h, but the numbers slowly increased up to 170 h, but the number of CFUs was suppressed compared to the 10 mol % glass at the same time point. The decrease seen is clearly the effect of the silver ions; however, the slow increase in CFUs may be accounted for by the biofilms forming thick layers on top of the glass discs inhibiting the release of ions from the glass by forming a "sacrificial layer" through which further ions have to diffuse.
银是一种强效抗菌离子,可能有助于处理局部感染,如牙周炎。然而,通过开发一种有效的递送方式,银在这一作用中的应用可能会得到显著改善。磷酸盐基玻璃可能提供一种以可控方式递送离子的手段。在我们的研究中,我们研究了增加磷酸盐基玻璃中银含量对血链球菌生物膜的影响。将名义溶解速率相同的玻璃分别掺杂1、5、10和15摩尔%的银,并在恒深膜发酵罐(CDFF)中培养6小时和24小时后测定菌落形成单位(CFU)的数量。含1摩尔%银的玻璃在6小时和24小时之间变化不大。然而,含5摩尔%银的玻璃在6小时时仅有0.5个对数CFU,到24小时时几乎降至零。在含10摩尔%银的玻璃上,6小时和24小时时均未发现存活细菌。本实验对含15摩尔%银的玻璃进行了研究,但未检测到存活菌数。在第二组实验中,对含10和15摩尔%银的玻璃在CDFF中进行了长达192小时的测试。对于含10摩尔%银的玻璃,该玻璃上约有0.8个对数CFU,在50小时时降至几乎零。与对照组相比,CFU减少了约1.5 - 2.0个对数,且在最初50小时内这种差异一直保持。50小时后,所有样品上的CFU缓慢增加。然而,与对照组相比,含10摩尔%银的玻璃上的CFU在192小时内仍受到抑制。然而,两个对照组在50小时时存活菌数也都有所下降;这可能是由于银带入了对照样品架中。然而,通过CDFF中的样品布局以及样品组之间留出间隙,这种影响被最小化。对于含15摩尔%银的玻璃,该玻璃和对照组的菌数在24至48小时之间均降至几乎零,但数量在170小时前缓慢增加,不过在同一时间点,与含10摩尔%银的玻璃相比,CFU数量受到抑制。观察到的下降显然是银离子的作用;然而,CFU的缓慢增加可能是由于生物膜在玻璃盘顶部形成厚层,通过形成“牺牲层”抑制了玻璃中离子的释放——进一步的离子必须通过该“牺牲层”扩散。