Buergers Ralf, Rosentritt Martin, Schneider-Brachert Wulf, Behr Michael, Handel Gerhard, Hahnel Sebastian
Department of Prosthetic Dentistry, Regensburg University Medical Centre, Germany.
Acta Odontol Scand. 2008 Jun;66(3):174-80. doi: 10.1080/00016350802165614.
The aim of this study was to rank 10 denture disinfection methods according to their efficacy in reducing Candida albicans (C. albicans) colonization on soft denture relining material.
Circular specimens (diameter 8 mm) were made of soft denture relining material (Mucopren E, Kettenbach) and thermally aged. Specimens were incubated with C. albicans (strain 1386, DSMZ) followed by 1 of 10 disinfection procedures (6 soaks, 2 microwave irradiation regimes, 1 effervescent commercial cleansing product, and denture left dry overnight). Incubation with phosphate buffered saline (PBS) served as a control. Adhering fungi were quantified using a bioluminometric assay in combination with an automated plate reader for cell quantification. Scanning electron micrographs (SEMs) were made for validation.
Low median luminescence intensities indicated the presence of a few viable fungi after the soaking of specimens in sodium hypochlorite (10 relative luminescence units (rlu)), microwave irradiation immersed in water (8 rlu), and application of effervescent cleansing tabs (22 rlu). No statistically significant difference (p>0.05) to control PBS (200 rlu) was found after immersion in hydrogen peroxide (172 rlu), glutaraldehyde (103 rlu), household vinegar (196 rlu), Listerine coolmint (194 rlu), Plax (222 rlu), dry microwave irradiation (221 rlu) and specimens left dry overnight (165 rlu). SEM displayed C. albicans monolayers with different morphologic forms on each surface investigated.
Only soaking in sodium hypochlorite (1%; 10 min), microwave irradiation immersed in water (800 W; 6 min), and application of effervescent cleansing tabs (Blend-a-dent tabs; 10 min) proved to be effective against C. albicans colonization on soft denture relining material.
本研究旨在根据10种义齿消毒方法在减少白色念珠菌(白色假丝酵母菌)在软质义齿重衬材料上定植的效果进行排名。
用软质义齿重衬材料(Mucopren E,Kettenbach)制作圆形标本(直径8毫米)并进行热老化处理。将标本与白色念珠菌(菌株1386,德国微生物和细胞培养物保藏中心)共同孵育,然后进行10种消毒程序中的一种(6种浸泡法、2种微波照射方式、1种泡腾型商业清洁产品以及义齿干燥过夜)。用磷酸盐缓冲盐水(PBS)孵育作为对照。使用生物发光测定法结合自动酶标仪对细胞进行定量来对附着的真菌进行定量分析。制作扫描电子显微镜图像(SEM)用于验证。
较低的中位发光强度表明,将标本浸泡在次氯酸钠中(10相对发光单位(rlu))、浸入水中进行微波照射(8 rlu)以及使用泡腾清洁片(22 rlu)后存在少量活真菌。浸泡在过氧化氢(172 rlu)、戊二醛(103 rlu)、家用醋(196 rlu)、李施德林冰蓝(194 rlu)、普乐士(222 rlu)、干式微波照射(221 rlu)以及标本干燥过夜(165 rlu)后,与对照PBS(200 rlu)相比,未发现统计学上显著差异(p>0.05)。SEM显示在每个研究表面上白色念珠菌形成了具有不同形态的单层。
仅浸泡在次氯酸钠中(1%;10分钟)、浸入水中进行微波照射(800瓦;6分钟)以及使用泡腾清洁片(Blend-a-dent片;10分钟)被证明对软质义齿重衬材料上的白色念珠菌定植有效。