Breitenmoser T
Helv Odontol Acta. 1975 Apr;19(1):13-7.
The influence on the glycolytic activity of dental plaque of different amine-hydrochloride compounds 300, 315 and 356 (oleylamine) respectively at concentrations equimolar to their corresponding amine fluorides 297, 242 and 335 at 250 ppm F-concentrations and of hexetidine and sodium laurylsulfate was tested in an in vivo/in vitro combination. Hexetidine and sodium laurylsulfate were assessed at concentrations equimolar to compound 315. After having refrained from oral hygiene for three days four test subjects rinsed for 3 minutes with 10 ml H2O. Plaque was collected from interdental areas immediately after the control water rinse and 6 and 60 minutes after rinsing for 3 minutes with 10 ml of test solution. The plaque then was exposed in vitro to 10% glucose solution, and pH-decreases due to glycolysis were recorded for 30 minutes. Rinsing with amine chlorides resulted in strong inhibition of glycolytic activity 6 minutes as well as 1 hour after rinsing. Hexetidine and sodium laurylsulfate did not depress the fermentation of glucose.
在体内/体外联合实验中,测试了在250 ppm氟浓度下,不同胺盐酸盐化合物300、315和356(油胺)分别与其相应的胺氟化物297、242和335等摩尔浓度,以及洗必泰和十二烷基硫酸钠对牙菌斑糖酵解活性的影响。洗必泰和十二烷基硫酸钠的评估浓度与化合物315等摩尔。在三天不进行口腔卫生护理后,四名受试者用10毫升水冲洗3分钟。在对照水冲洗后以及用10毫升测试溶液冲洗3分钟后的6分钟和60分钟,立即从牙间隙区域收集牙菌斑。然后将牙菌斑在体外暴露于10%葡萄糖溶液中,并记录30分钟内由于糖酵解导致的pH值下降。用胺氯化物冲洗在冲洗后6分钟和1小时均导致糖酵解活性的强烈抑制。洗必泰和十二烷基硫酸钠没有抑制葡萄糖的发酵。