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含锌盐和三氯生的牙膏对牙龈炎和牙结石的控制

Control of gingivitis and calculus by a dentifrice containing a zinc salt and triclosan.

作者信息

Stephen K W, Saxton C A, Jones C L, Ritchie J A, Morrison T

机构信息

Department of Oral Medicine and Pathology, University of Glasgow Dental School, UK.

出版信息

J Periodontol. 1990 Nov;61(11):674-9. doi: 10.1902/jop.1990.61.11.674.

Abstract

The effect of unsupervised brushing with a dentifrice containing two antiplaque agents, 0.5% zinc citrate and 0.2% triclosan, on gingival health, plaque, supragingival calculus, and the oral flora was compared to brushing with a non-active control dentifrice. Volunteers were given oral hygiene instruction and their teeth were professionally cleaned. They then used a placebo dentifrice for a pre-experimental phase of 1 month, before being stratified into two groups on the basis of their initial plaque, gingival bleeding, and calculus levels, sex, and age. Over the following 6 months, one group used the control while the other used the test dentifrice. Plaque levels, gingival bleeding, and calculus were assessed at baseline and at 3 and 6 months. Supragingival plaque was sampled for microbiological analysis at the initial examination, at 3 and 6 months (conclusion of study period) and 3 months after the study. Representative oral bacteria and the development of bacterial resistance to triclosan were monitored. Results showed that plaque was reduced and gingival health significantly improved during the 1-month pre-experimental period. During the experimental period, this improvement was not maintained by the control group as gingival bleeding and calculus increased. In contrast, gingival bleeding and calculus levels of the test group were maintained significantly below those of the placebo group. Plaque levels were lower in the test group after 3 and 6 months, but the groups were not significantly (P = 0.05) different. No shifts in oral flora or development of bacterial resistance to triclosan were detected.

摘要

将含有两种防菌斑剂(0.5%柠檬酸锌和0.2%三氯生)的牙膏进行无监督刷牙对牙龈健康、牙菌斑、龈上牙石和口腔菌群的影响,与使用无活性对照牙膏刷牙进行了比较。志愿者接受了口腔卫生指导,并且他们的牙齿接受了专业清洁。然后他们在1个月的实验前期使用了安慰剂牙膏,之后根据他们最初的牙菌斑、牙龈出血和牙石水平、性别和年龄被分为两组。在接下来的6个月里,一组使用对照牙膏,而另一组使用测试牙膏。在基线以及3个月和6个月时评估牙菌斑水平、牙龈出血和牙石情况。在初始检查时、3个月和6个月(研究期结束时)以及研究结束后3个月采集龈上牙菌斑进行微生物分析。监测代表性口腔细菌以及细菌对三氯生耐药性的发展情况。结果显示,在1个月的实验前期牙菌斑减少,牙龈健康显著改善。在实验期,对照组未维持这种改善,因为牙龈出血和牙石增加。相比之下,测试组的牙龈出血和牙石水平显著维持在低于安慰剂组的水平。3个月和6个月后测试组的牙菌斑水平较低,但两组差异不显著(P = 0.05)。未检测到口腔菌群的变化或细菌对三氯生耐药性的发展。

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