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1.
Chemosphere ; 358: 142142, 2024 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-38677619

RESUMO

The presence of non-reactive phosphorus (NRP) in environmental waters presents a potential risk of eutrophication and poses challenges for the removal of all phosphorus (P) fractions. This study presents the first investigation on the removal performance and mechanism of three model NRP compounds, sodium tripolyphosphate (STPP), adenosine 5'-monophosphate (AMP) and 2-phosphonobutane-1,2,4-tricarboxylic acid (PBTC), in the sediment microbial fuel cell-floating treatment wetland (SMFC-FTW). Coupling SMFC with plants proved to be effective at removing NRP via electrochemical oxidation and plant uptake, particularly the challenging-to-degrade phosphonates that contain C-P bonds. Compared with the control group, the removal efficiencies of the model NRP in SMFC were observed to increase by 11.9%-20.8%. SMFC promoted the conversion of NRP to soluble reactive phosphorus (sRP) and the transfer of P to sediment. Furthermore, the electrochemical process enhanced both plant growth and P uptake, and increased P assimilation by 72.6%. The presence of plants in the bioelectrochemical system influenced the occurrence and fate of P by efficiently assimilating sRP and supporting microbial transformation of NRP. Consequently, plants enhanced the removal efficiencies of all P fractions in the overlying water. This study demonstrated that SMFC-FTW is a promising technology to remove various NRP species in environmental waters.


Assuntos
Fontes de Energia Bioelétrica , Sedimentos Geológicos , Fósforo , Poluentes Químicos da Água , Áreas Alagadas , Poluentes Químicos da Água/metabolismo , Poluentes Químicos da Água/análise , Sedimentos Geológicos/química , Biodegradação Ambiental , Eutrofização , Eliminação de Resíduos Líquidos/métodos
2.
Nat Prod Res ; 30(9): 1068-74, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-26539898

RESUMO

Two new triterpenoids (1-2) were isolated and elucidated from the roots of Gypsophila oldhamiana, together with four known triterpenoids (3-6). Their structures were identified to be 3ß-hydroxyolean-13(18)-ene-23, 28-dioic acid (1), 3ß, 12α-dihydroxy-23-carboxyolean-28, 13ß-olide (2), 3ß, 16α-dihydroxy-23-oxoolean-13(18)-en-28-oic acid (3), gypsogenin (4), quillaic acid (5) and gypsogenic acid (6) by spectral methods. All compounds were tested for their cytotoxicities against human tumour cell lines (lung cancer H460 and gastric cancer SGC-7901) and for their antiangiogenic effects using a zebra fish model. All compounds showed interesting antiangiogenic activities and the significant cytotoxicities against H460.


Assuntos
Caryophyllaceae/química , Triterpenos/análise , Inibidores da Angiogênese/farmacologia , Animais , Antineoplásicos Fitogênicos/farmacologia , Linhagem Celular Tumoral , Ensaios de Seleção de Medicamentos Antitumorais , Embrião não Mamífero , Humanos , Espectroscopia de Ressonância Magnética , Ácido Oleanólico/análogos & derivados , Extratos Vegetais/química , Raízes de Plantas/química , Espectrometria de Massas por Ionização por Electrospray , Peixe-Zebra
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