百里香酚
伏立康唑
伊曲康唑
香芹酚
肉汤微量稀释
镰刀菌
卡斯波芬金
棋盘
两性霉素B
最小抑制浓度
泊沙康唑
抗真菌
微生物学
肉桂醛
生物
化学
精油
食品科学
抗菌剂
植物
生物化学
催化作用
作者
Tarcieli Pozzebon Venturini,Luana Rossato,Francieli Chassot,María Isabel de Azevedo,Abdullah M. S. Al‐Hatmi,Jânio Morais Santúrio,Sydney Hartz Alves
标识
DOI:10.1080/10412905.2021.1923580
摘要
Fusarium spp. are able to cause a wide range of opportunistic infections in both immunocompromised and immunocompetent individuals. Thus, new therapeutic options should be considered. We evaluated the antifungal activity of three phytocompounds (cinnamaldehyde, CIN; carvacrol, CRV; and thymol, THY), as well as their activities when combined with amphotericin B (AMB), caspofungin (CAS), itraconazole (ITC) and voriconazole (VRC) against 20 clinical isolates of Fusarium. Broth microdilution (M38-A2) and checkerboard methodologies were used to obtain MICs (Minimum inhibitory concentration) and FICIs (Fractional Inhibitory Concentration Index), respectively. The MICs observed for the phytocompounds were: 20–80 for CIN, 40-> 320 for CRV and 40–320 µg/mL for THY. The most effective combinations (synergism rates) were: THY + CAS (96%), CRV + CAS (88%), THY + AMB (76%), CRV + AMB (68%), THY + VRC (68%) and CRV + VRC (60%). Our findings suggest that CRV and THY have potent activity when combined with CAS, AMB or VRC.
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