Fabrication of multinuclear copper cluster-based coordination polymers as urease inhibitors.

This study focused on the design and synthesis of two Cu-based coordination polymers, [Cu2(4-dpye)(5-HSIP)(µ3-O)(H2O)2]·3H2O (Cu-CP-1) and [Cu(4-dpye)0.5(BCA)2] (Cu-CP-2), where 4-dpye = N,N'-bis(4-pyridinecarboxamide)-1,2-ethane, 5-H3SIP = 5-sulfoisophthalic acid, and HBCA = benzoic acid, by using a hydrothermal method. Single-crystal X-ray diffraction (SCXRD) study revealed that by adding various auxiliary ligands, the architectures of the Cu-CPs could be altered, yielding two distinct multinuclear Cu clusters. Moreover, the Cu-CPs can be used as urease inhibitors (UIs). In vitro experiments showed that the Cu-CPs had good urease inhibition effects with IC50 values of 0.53 ± 0.01 µM for Cu-CP-1 and 1.44 ± 0.01 µM for Cu-CP-2 and 98.48% (Cu-CP-1) and 96.27% (Cu-CP-2) inhibition of urease was achieved at a concentration of 100 µM, respectively. Furthermore, the inhibition effect of the tetranuclear Cu-CP was better than that of the binuclear Cu-CP. To better understand the potential mechanism of inhibition of the two copper complexes, we performed kinetic analysis using Lineweaver-Burk (L-B) plots in the presence of different concentrations of urea and different concentrations of inhibitors, and both Cu-CP-1 and Cu-CP-2 showed a non-competitive mode of inhibition. In addition, molecular docking analysis showed that the Cu-CPs were able to enter well into the urease binding pocket, thus interacting with key amino acid residues of urease to different degrees. Both kinetic and molecular docking studies theoretically explain and demonstrate the inhibition effect of both Cu-CPs on urease activity in vitro, which is expected to provide reasonable guidance and effective strategies for the development of novel, efficient, stable and safe CP-based UIs.

Black odorous water concentrating by forward osmosis: rejection performance of characteristic pollutants based on cation exchange.

This study aimed to investigate pollutant concentration and nitrogen interception characteristics of a forward osmosis (FO) process for concentrating black odorous water. The membrane cell was operated in active layer facing feed solution (AL-FS) mode with aquaporin (AQP) as the membrane material and NaCl solution as the draw solution (DS). The organic pollutants (COD), TP, NH+4-N, NO-3-N, TN, Fe and Mn in black odorous water were concentrated non-intermittently for 24 h, and their interception characteristics were investigated. The results showed that the average interception rates of COD, TP, NO- 3-N, TN, Fe and Mn were 97.2%, 98.0%, 58.7%, 54.3%, 61.8% and 60.0%, respectively, while the average interception rate of NH+4-N was only 1.27%-3.47%. To explore the characteristics of nitrogen interception, a comparison was conducted between AQP membrane and thin film composite (TFC) membrane. Because the surface electronegativity of AQP membrane was stronger than that of TFC, the effect of cation exchange on ammonia nitrogen interception was more serious with AQP membrane. With NaCl solution as DS, the reverse osmosis flux of Na+ was (0.53 ± 0.02 mol·m-2·h-1), which was significantly higher than that of Cl- (0.29 ± 0.03 mol·m-2·h-1) (P < 0.05). The interception effect of AQP membrane on TN was related to the proportion of NH+4-N in TN. The pretreatment of black odorous water by aeration could transform part of NH+4-N into NO-3-N, and reduce the negative effect of cation exchange effect on nitrogen interception. The TN interception rate increased from 54.3% to 66.1%.