Estrela C, Pimenta F C, Ito I Y, Bammann L L
Federal University of Goiás, Goiânia, Brazil.
J Endod. 1999 Jun;25(6):416-8. doi: 10.1016/S0099-2399(99)80269-6.
The objective of this study was to evaluate the antimicrobial activity of calcium hydroxide in infected dentinal tubules. Four microorganisms, strains of ATCC (Streptococcus faecalis (ATCC-29212), Staphylococcus aureus (ATCC-6538), Bacillus subtilis (ATCC-6633), and Pseudomonas aeruginosa (ATCC-27853)) and one mixture of these were used. These strains were inoculated in brain heart infusion (BHI) and incubated at 37 degrees C for 24 h. Sixty-three human maxillary central incisors were prepared and sterilized by autoclaving. Five groups of 12 teeth each were contaminated for 28 days using new 24-h cultures every 72 h, prepared and adjusted to tube 2 of the MacFarland scale (6 x 10(8) cells/ml). Root canals were then irrigated with 5 ml of saline, dried, and completely filled with calcium hydroxide paste. At intervals of 0, 48, and 72 h, and 7 days, dressings were removed and teeth were immersed in 5 ml of BHI and incubated at 37 degrees C for 48 h to observe the growth and multiplication of the microorganisms. Three uninoculated teeth were maintained in a humid environment as an aseptic control. These teeth were immersed in BHI and maintained at 37 degrees C for 7 days to determine microbial growth. Bacterial growth was shown by turbidity of the culture medium and confirmed by seeding these broths on BHI agar at 37 degrees C for 24 h. The positive BHI tubes were selected, and inoculum was spread on the surface of BHI agar, followed by the same incubation conditions. Gram stain was conducted from BHI growth and from colonies growing on solid medium. Calcium hydroxide in infected dentinal tubules showed no antimicrobial effect on S. faecalis, S. aureus, B. subtilis, P. aeruginosa, or on the bacterial mixture used throughout the experiment.
本研究的目的是评估氢氧化钙在感染牙本质小管中的抗菌活性。使用了四种微生物,即美国典型培养物保藏中心(ATCC)的菌株(粪肠球菌(ATCC - 29212)、金黄色葡萄球菌(ATCC - 6538)、枯草芽孢杆菌(ATCC - 6633)和铜绿假单胞菌(ATCC - 27853))以及它们的一种混合物。将这些菌株接种于脑心浸液(BHI)中,在37℃下培养24小时。制备63颗人上颌中切牙并通过高压灭菌进行消毒。将五组,每组12颗牙齿,每72小时使用新的24小时培养物污染28天,制备并调整至麦氏比浊法2号管(6×10⁸ 个细胞/毫升)。然后用5毫升生理盐水冲洗根管,干燥,并完全用氢氧化钙糊剂充填。在0、48和72小时以及7天时,取出敷料,将牙齿浸入5毫升BHI中,在37℃下培养48小时,以观察微生物的生长和繁殖。将三颗未接种的牙齿置于潮湿环境中作为无菌对照。将这些牙齿浸入BHI中并在37℃下保存7天以确定微生物生长。通过培养基的浑浊显示细菌生长,并通过将这些肉汤接种于37℃的BHI琼脂上24小时进行确认。选择阳性BHI管,将接种物铺展在BHI琼脂表面,然后在相同培养条件下培养。对BHI生长物和在固体培养基上生长的菌落进行革兰氏染色。感染牙本质小管中的氢氧化钙对粪肠球菌、金黄色葡萄球菌、枯草芽孢杆菌、铜绿假单胞菌或整个实验中使用的细菌混合物均未显示出抗菌作用。