Mirth D B, Chite A F, Schuster G S
J Dent Res. 1978 Jan;57(1):65-71. doi: 10.1177/00220345780570012401.
8-Hydroxyquinolyl benzoate and 8-hydroxyquinolyl para-(fluorosulfonyl)benzoate have been synthesized and evaluated in vitro as antimicrobial and antiplaque agents. Both compounds inhibited the growth of cultures of the following genera: Streptococcus, Staphylococcus, Actinomyces, Lactobacillus, Veillonella, and Candida. Minimum inhibitory concentrations ranged from 0.98 to 62 microgram/ml. Extracted human teeth pretreated with 1% solutions of either compound and rinsed with distilled water exhibited reduced in vitro plaque formation for 48 hours. These results indicate that the in vitro antiplaque activity of 8-hydroxyquinolines can be enhanced by attaching the appropriate side chain in the 8-position.
苯甲酸8 - 羟基喹啉酯和对 -(氟磺酰基)苯甲酸8 - 羟基喹啉酯已被合成,并作为抗菌和抗牙菌斑剂进行了体外评估。两种化合物均抑制以下菌属培养物的生长:链球菌属、葡萄球菌属、放线菌属、乳杆菌属、韦荣氏菌属和念珠菌属。最低抑菌浓度范围为0.98至62微克/毫升。用任一种化合物的1%溶液预处理并经蒸馏水冲洗的离体人牙在48小时内显示出体外牙菌斑形成减少。这些结果表明,通过在8位连接适当的侧链,可以增强8 - 羟基喹啉的体外抗牙菌斑活性。