Septama Abdi Wira, Panichayupakaranant Pharkphoom
a Department of Pharmacognosy and Pharmaceutical Botany , Faculty of Pharmaceutical Sciences, Prince of Songkla University , Songkhla , Thailand and.
b Excellent Research Laboratory, Phytomedicine and Pharmaceutical Biotechnology Excellence Center, Faculty of Pharmaceutical Sciences, Prince of Songkla University , Songkhla , Thailand.
Pharm Biol. 2016;54(4):686-91. doi: 10.3109/13880209.2015.1072566. Epub 2015 Oct 1.
Antibacterial resistance has dramatically increased and resulted in serious health problems worldwide. One appealing strategy to overcome this resistance problem is the use of combinations of antibacterial compounds to increase their potency.
The objective of this study is to determine the synergistic effects of artocarpin for ampicillin, norfloxacin, and tetracycline against methicillin-resistant Staphylococcus aureus (MRSA) as well as the Gram-negative bacteria Pseudomonas aeruginosa and Escherichia coli.
A broth microdilution method (1.95-250 µg/mL) was used to determine the minimum inhibitory concentration (MIC) of artocarpin and the antibiotics. Any synergistic effects were evaluated at their own MIC using the checkerboard method and a time-kill assay at 37 °C for 24 h.
Artocarpin showed antibacterial activity against MRSA and E. coli with an MIC value of 62.5 µg/mL, and against P. aeruginosa with an MIC value of 250 µg/mL. The interaction of artocarpin with all tested antibiotics produced synergistic effects against MRSA with a fractional inhibitory concentration index (FICI) of 0.15-0.37. In addition, a combination of artocarpin and norfloxacin showed a synergistic effect against E. coli with an FICI value of 0.37, while the combinations of artocarpin and tetracycline as well as artocarpin and norfloxacin exhibited synergy interactions against P. aeruginosa with FICI values of 0.24 and 0.37, respectively. Time-kill assays indicated that artocarpin enhanced the antimicrobial activities of tetracycline, ampicillin, and norfloxacin against MRSA as well as Gram-negative bacteria.
抗菌耐药性已急剧增加,并在全球范围内导致严重的健康问题。一种有吸引力的克服这种耐药性问题的策略是使用抗菌化合物组合来提高其效力。
本研究的目的是确定面包果素与氨苄西林、诺氟沙星和四环素联合使用对耐甲氧西林金黄色葡萄球菌(MRSA)以及革兰氏阴性菌铜绿假单胞菌和大肠杆菌的协同作用。
采用肉汤微量稀释法(1.95 - 250μg/mL)测定面包果素和抗生素的最低抑菌浓度(MIC)。使用棋盘法并在37℃下进行24小时时间杀菌试验,在各自MIC水平评估任何协同作用。
面包果素对MRSA和大肠杆菌表现出抗菌活性,MIC值为62.5μg/mL,对铜绿假单胞菌的MIC值为250μg/mL。面包果素与所有测试抗生素的相互作用对MRSA产生协同作用,部分抑菌浓度指数(FICI)为0.15 - 0.37。此外,面包果素和诺氟沙星的组合对大肠杆菌表现出协同作用,FICI值为0.37,而面包果素和四环素以及面包果素和诺氟沙星的组合对铜绿假单胞菌表现出协同相互作用,FICI值分别为0.24和0.37。时间杀菌试验表明,面包果素增强了四环素、氨苄西林和诺氟沙星对MRSA以及革兰氏阴性菌的抗菌活性。