Zika virus (ZIKV) infection is a global threat associated to neurological disorders in adults and microcephaly in children born to infected mothers. No vaccine or drug is available against ZIKV. We herein report the anti‐ZIKV activity of 36 plant extracts containing polyphenols and/or triterpenes. ZIKV‐infected Vero CCL‐81 cells were treated with samples at non‐cytotoxic concentrations, determined by MTT and LDH assays. One third of the extracts elicited concentration‐dependent anti‐ZIKV effect, with viral loads reduction from 0.4 to 3.8 log units. The 12 active extracts were tested on ZIKV‐infected SH‐SY5Y cells and significant reductions of viral loads (in log units) were induced by Maytenus ilicifolia (4.5 log), Terminalia phaeocarpa (3.7 log), Maytenus rigida (1.7 log) and Echinodorus grandiflorus (1.7 log) extracts. Median cytotoxic concentration (CC50) of these extracts in Vero cells were higher than in SH‐SY5Y lineage. M. ilicifolia (IC50=16.8±10.3 μg/mL, SI=3.4) and T. phaeocarpa (IC50=22.0±6.8 μg/mL, SI=4.8) were the most active extracts. UPLC‐ESI‐MS/MS analysis of M. ilicifolia extract led to the identification of 7 triterpenes, of which lupeol and a mixture of friedelin/friedelinol showed no activity against ZIKV. The composition of T. phaeocarpa extract comprises phenolic acids, ellagitannins and flavonoids, as recently reported by us. In conclusion, the anti‐ZIKV activity of 12 plant extracts is here described for the first time and polyphenols and triterpenes were identified as the probable bioactive constituents of T. phaeocarpa and M. ilicifolia, respectively.
Hydrogen production using ethanol and Fe 2 O 3 /support in a redox cycle was investigated. The composites were prepared by impregnation of Al 2 O 3 and SiO 2 with Fe(NO 3 ) 3 , with different proportions of iron, i.e. 10, 30 and 50 wt.%, calcinated at 450 • C and characterized by Mössbauer spectroscopy, XRD, SEM, BET and TG. The redox cycle to produce and/or store hydrogen is a two step process (1) initially the ethanol is used to reduce the iron oxide to Fe • ; (2) and when H 2 is needed, Fe • reacts with H 2 O to produce CO-free hydrogen, and the iron oxide is reduced again to Fe • making this system cyclic. After the reactions it was interesting to observe that ethanol can directly reduce the iron oxide to produce metallic iron, with carbon deposition and iron-carbon as side product. Preliminary results indicate that it is possible to perform multiple redox cycles with the supported iron oxide without deactivation.
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