6 research outputs found
Table_1_Toward revolutionizing water-energy-food nexus composite index model: from availability, accessibility, and governance.DOCX
The water-energy-food (WEF) nexus has emerged as a critical research interest to support integrated resource planning, management, and security. For this reason, many tools have been developed recently to evaluate the WEF nexus security and monitor progress toward the WEF-related sustainable development goals. Among these, calculating the WEF composite index model is critical since it can provide a quantitative approach to demonstrate the WEF nexus security status. However, the current WEF nexus index model framework needs to include the incorporation of governance indicators, neglecting the importance of governance in the WEF nexus framework. Thus, this article develops a new WEF nexus composite index model that incorporates governance indicators in each subpillar. The principal component analysis (PCA) is adopted to reduce the variables’ collinearity and the model’s dimensionality. A quasi-Monte Carlo-based uncertainty and global sensitivity analysis are applied to the index model to assess its effectiveness. Finally, the new WEF index model is applied to the 16 South African Development Community (SADC) countries as a case study. A critical synergy effect within the WEF nexus framework is identified that nations with better WEF governance ability tend to perform better in improving the WEF accessibility capability, suggesting the importance of governance in the WEF nexus security framework.</p
Diiodo-Bodipy-Encapsulated Nanoscale Metal–Organic Framework for pH-Driven Selective and Mitochondria Targeted Photodynamic Therapy
We
report herein a new ZIF-90-based PDT agent which was synthesized by
in situ assembly of imidazole-2-carboxaldehyde (IcaH), ZnÂ(NO<sub>3</sub>)<sub>2</sub>, and heavy atom iodine-attached Bodipy. The obtained
2I-BodipyPhNO<sub>2</sub>@ZIF-90 (<b>1</b>) host–guest
photosensitive system featured low cytotoxicity, good biocompatibility,
pH-driven selective cancer cell uptake and release, mitochondria targeting,
and highly efficient pH-triggered <sup>1</sup>O<sub>2</sub> generation.
Therefore, it can be used as a high-performing PDT agent to selectively
kill tumor cells. In comparison to free 2I-BodipyPhNO<sub>2</sub>, <b>1</b> exhibits a much higher antitumor efficacy and selectivity,
which was confirmed by in vitro cell experiments
A Multifunctional Covalent Organic Framework Nanozyme for Promoting Ferroptotic Radiotherapy against Esophageal Cancer
Radiotherapy
is inevitably accompanied by some degree of radiation
resistance, which leads to local recurrence and even therapeutic failure.
To overcome this limitation, herein, we report the room-temperature
synthesis of an iodine- and ferrocene-loaded covalent organic framework
(COF) nanozyme, termed TADI-COF-Fc, for the enhancement
of radiotherapeutic efficacy in the treatment of radioresistant esophageal
cancer. The iodine atoms on the COF framework not only exerted a direct
effect on radiotherapy, increasing its efficacy by increasing X-ray
absorption, but also promoted the radiolysis of water, which increased
the production of reactive oxygen species (ROS). In addition, the
ferrocene surface decoration disrupted redox homeostasis by increasing
the levels of hydroxyl and lipid peroxide radicals and depleting intracellular
antioxidants. Both in vitro and in vivo experiments substantiated the excellent radiotherapeutic response
of TADI-COF-Fc. This study demonstrates the potential
of COF-based multinanozymes as radiosensitizers and suggests a possible
treatment integration strategy for combination oncotherapy
New Family of Octagonal-Prismatic Lanthanide Coordination Cages Assembled from Unique Ln<sub>17</sub> Clusters and Simple Cliplike Dicarboxylate Ligands
Novel
high-nuclearity lanthanide clusters (Ln<sub>17</sub>) are generated
in situ in the coordination-driven self-assembly. A metal-cluster-directed
symmetry strategy for building metal coordination cages is successfully
applied to a lanthanide system for the first time. A new family of
octagonal-prismatic lanthanide coordination cages <b>UJN-Ln</b>, formulated as [LnÂ(μ<sub>3</sub>-OH)<sub>8</sub>]Â[Ln<sub>16</sub>(μ<sub>4</sub>-O)Â(μ<sub>4</sub>-OH)Â(μ<sub>3</sub>-OH)<sub>8</sub>(H<sub>2</sub>O)<sub>8</sub>(μ<sub>4</sub>-dcd)<sub>8</sub>]Â[(μ<sub>3</sub>-dcd)<sub>8</sub>]·22H<sub>2</sub>O (Ln = Gd, Tb, Dy, Ho, and Er; dcd = 3,3-dimethylcyclopropane-1,2-dicarboxylate
dianion), have been assembled from the unique Ln<sub>17</sub> clusters
and simple cliplike ligand H<sub>2</sub>dcd. Apart from featuring
aesthetically charming structures, all of the compounds present predominantly
antiferromagnetic coupling between the corresponding lanthanide ions.
Additionally, the intense-green photoluminescence for <b>UJN-Tb</b> and magnetic relaxation behavior for <b>UJN-Dy</b> have been
observed. Remarkably, <b>UJN-Gd</b> shows a large magnetocaloric
effect (MCE) with an impressive entropy change value of 42.3 J kg<sup>–1</sup> K<sup>–1</sup> for Δ<i>H</i> = 7.0 T at 2.0 K due to the high-nuclearity cluster and the lightweight
ligand. The studies highlight the structural diversity of multigonal-prismatic
metal coordination cages and provide a new direction in the design
of cagelike multifunctional materials by the introduction of lanthanide
clusters and other suitable cliplike ligands
One-Pot Synthetic Approach toward Porphyrinatozinc and Heavy-Atom Involved Zr-NMOF and Its Application in Photodynamic Therapy
Herein,
we report an iodine-attached ZnÂ(II)-porphyrinic dicarboxylic
building block (ZnDTPP-I<sub>2</sub>-2H, <b>1</b>) that can
be introduced into UiO-66 NMOF via one-pot synthetic approach to generate
a new ZnDTPP-I<sub>2</sub> doped UiO-66 type nano metal–organic
framework (NMOF) of ZnDTPP-I<sub>2</sub>⊂UiO-66 (<b>2</b>). Compared to its homologous iodine-free NMOF of ZnDTPP⊂UiO-66
(<b>4</b>), ZnDTPP-I<sub>2</sub>⊂UiO-66 (<b>2</b>) with heavy iodine atoms is a more effective nanosized photosensitizer
for singlet oxygen generation under physiological conditions. As expected, <b>2</b> displayed a high photodynamic therapy efficacy for treatment
of liver cancer cells in vitro
Needle-like Co<sub>3</sub>O<sub>4</sub> Anchored on the Graphene with Enhanced Electrochemical Performance for Aqueous Supercapacitors
We
synthesized the needle-like cobalt oxide/graphene composites with
different mass ratios, which are composed of cobalt oxide (Co<sub>3</sub>O<sub>4</sub> or CoO) needle homogeneously anchored on graphene
nanosheets as the template, by a facile hydrothermal method. Without
the graphene as the template, the cobalt precursor tends to group
into urchin-like spheres formed by many fine needles. When used as
electrode materials of aqueous supercapacitor, the composites of the
needle-like Co<sub>3</sub>O<sub>4</sub>/graphene (the mass ratio of
graphene oxideÂ(GO) and CoÂ(NO<sub>3</sub>)<sub>2</sub>·6H<sub>2</sub>O is 1:5) exhibit a high specific capacitance of 157.7 F g<sup>–1</sup> at a current density of 0.1 A g<sup>–1</sup> in 2 mol L<sup>–1</sup> KOH aqueous solution as well as good
rate capability. Meanwhile, the capacitance retention keeps about
70% of the initial value after 4000 cycles at a current density of
0.2 A g<sup>–1</sup>. The enhancement of excellent electrochemical
performances may be attributed to the synergistic effect of graphene
and cobalt oxide components in the unique multiscale structure of
the composites