Lui J N, Sae-Lim V, Song K P, Chen N N
Department of Restorative Dentistry, Faculty of Dentistry, National University of Singapore, Singapore.
Int Endod J. 2004 Feb;37(2):105-13. doi: 10.1111/j.0143-2885.2004.00734.x.
To evaluate the in vitro antimicrobial effect of chlorhexidine-impregnated gutta percha points, Roeko activ point (Roeko, Langenau, Germany) on Enterococcus faecalis.
Human maxillary premolar roots were prepared with.04 rotary ProFile instruments to a master apical file size 40, autoclave-sterilized and then infected with E. faecalis (ATCC 29212) for 3 weeks. Baseline controls were carried out verifying negligible effects of plain gutta percha cones on E. faecalis. Subsequent to intracanal placement of calcium hydroxide, 'activ points' or saline (positive control) and the 2-week incubation in 54 root specimens, dentine sampling at depths of 100 and 250 micro m was carried out using.04 rotary ProFile instruments at sizes 60 and 90 to assess the quantity of bacteria present. Inactivating agents were used prior to sampling and the colony-forming units (CFU) of E. faecalis were then plate-counted after culturing. Statistical analysis was completed using the paired t-test.
In comparison to the positive control, treatment with calcium hydroxide (P = 0.000 and 0.000) or activ points (P = 0.000 and 0.002) produced significantly lower colony counts of E. faecalis at dentine depths of 100 and 250 micro m, respectively. Calcium hydroxide (2.10 x 102 CFU mL-1) was significantly more effective than activ points (1.58 x 103 CFU mL-1) at 100 micro m (P = 0.013), but not at 250 micro m (P = 0.353). Neither of these two medications was able to eliminate E. faecalis completely.
Chlorhexidine-impregnated activ points did not possess an in vitro inhibitory activity strong enough to eliminate E. faecalis completely from infected dentinal tubules.
评估含氯己定的牙胶尖(德国朗根瑙的罗伊科活性尖,Roeko activ point)对粪肠球菌的体外抗菌效果。
用.04旋转ProFile器械将人类上颌前磨牙牙根预备至主尖锉40号,高压灭菌后用粪肠球菌(ATCC 29212)感染3周。进行基线对照,验证普通牙胶尖对粪肠球菌的影响可忽略不计。在根管内放置氢氧化钙、“活性尖”或生理盐水(阳性对照)后,对54个牙根标本进行2周培养,然后用.04旋转ProFile器械在60号和90号规格下,于100和250微米深度进行牙本质取样,以评估细菌数量。取样前使用灭活剂,培养后对粪肠球菌的菌落形成单位(CFU)进行平板计数。采用配对t检验进行统计分析。
与阳性对照相比,在牙本质深度100微米和250微米处,用氢氧化钙(P = 0.000和0.000)或活性尖(P = 0.000和0.002)治疗后,粪肠球菌的菌落计数显著降低。在100微米处,氢氧化钙(2.10×10²CFU/mL)比活性尖(1.58×10³CFU/mL)显著更有效(P = 0.013),但在250微米处并非如此(P = 0.353)。这两种药物均不能完全消除粪肠球菌。
含氯己定的活性尖在体外不具有足够强的抑制活性,无法将感染的牙本质小管中的粪肠球菌完全消除。