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ZIF-65
SEPARATION AND PURIFICATION TECHNOLOGY · 2022 · IF 9.136

Zinc-based metal–organic framework nanofibers membrane ZIF-65/PAN as efficient peroxymonosulfate activator to degrade aqueous ciprofloxacin

Mengjie Pu,Daqi Ye,Jinquan Wan,Bentuo Xu,Wei Sun,Wei Li

A novel peroxymonosulfate (PMS) catalyst, zinc-based metal–organic framework electrospinning (ES) nanofibers membrane (short for ZIF-65/PAN) was firstly fabricated and used for the degradation of aqueous ciprofloxacin (CIP). Physicochemical properties, catalytic performance, stability, reusability, and the regeneration of ZIF-65/PAN was observed and conducted. Influence of various parameters including ZIF-65 loading content, reaction temperature, initial pH, and competitive organic molecules on CIP degradation was investigated. Reactive active species and degradation intermediates that involved in ZIF-65/PAN/PMS/CIP process were identified. Corresponding reaction mechanisms were speculated. The results indicate that the easy-separation ZIF-65/PAN nanofibers exhibit high efficiency for PMS activation, 89.2 % of CIP was degraded within 60 min, with up to 87.5 % of PMS utilization efficiency. ZIF-65/PAN was renewable through simple layer-by-layer self-assembly, thus shows good prospect in future applications. 26.4 % of surface Zn 2+ of ZIF-65/PAN exists in the form of + III oxidation state after activation, indicating the role of zinc catalytic site. Through activation, oxidative active species SO 4 ·− , ·OH, and 1 O 2 was generated, CIP was thus degraded through mainly-three pathways. This study provides novel ideas for the application of MOF-based membrane on PMS based advanced oxidation processes.

研究领域: 环境科学 · 化学工程 · 材料科学
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INORGANIC CHEMISTRY · 2025 · IF 4.7

Sulfolane as a Solvent for Nano-MOF Synthesis: Enabling Prolonged Nucleation and Controlled Growth

Saiyu Yang,Zicheng Yin,Xianchun Chen,Zhide Geng,Bo Wang,Junwen Zhou,Lu Wang

Conventional methods for synthesizing nano-sized metal-organic frameworks (nano-MOFs) often rely on additives or extra conditions, overlooking the critical role of solvents. Here, we highlight tetramethylene sulfone (TMS, or sulfolane) as a versatile solvent for nano-MOF synthesis. TMS forms strong solvation structures with metal ions and inhibits ligand deprotonation, enabling control over particle size. Using TMS, we synthesized ZIF-65 [Zn(2-nIm)2, 2-nIm = 2-nitroimidazole], ZIF-8 [Zn(2-mIm)2, 2-mIm = 2-methylimidazole], UiO-66 [Zr6O4(OH)4(BDC)6, BDC = 1,4-dicarboxybenzene acid], and MOF-199 [Cu3(BTC)2, BTC = 1,3,5-benzenetricarboxylic acid] with significantly smaller particle sizes compared to traditional solvents like ethanol (EtOH). Systematic analysis on the growth of ZIF-65 revealed distinct growth behaviors: in TMS, slower kinetics allowed the coexistence of nucleation and growth over an extended period, leading to an increase in particle number while maintaining relatively constant size; in contrast, EtOH promoted rapid growth followed by Ostwald ripening, resulting in larger particles and reduced particle number over time. By adjusting reactant concentration, metal-to-ligand ratio, and reaction temperature, we achieved facile size modulation of ZIF-65 nanoparticles. This work underscores the importance of solvents in nano-MOF synthesis and offers a robust strategy for tailoring MOF particle size, advancing applications in catalysis, biomedicine, and beyond.

CAS / MDL: 10026-11-6
研究领域: 材料科学 · 化学工程 · 纳米技术
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2023 · IF 9.9

Coenzyme-depleting nanocarriers for enhanced redox cancer therapy under hypoxia

Yao Li,Mengying Liu,Yan Zheng,Zheng Wang,Yanjun Zhao

Cancer cells show unique redox homeostasis . Glutathione (GSH) and reduced nicotinamide adenine dinucleotide phosphate (NADPH) play essential roles as coenzymes of multiple key antioxidant enzymes. Coenzyme depletion offers a unique opportunity for cancer treatment by inducing oxidative stress . Here, we report an innovative hybrid nanocarrier for cancer redox therapy via selective depletion of GSH and NADPH. The nanocarrier core is a sorafenib-loaded porous zeolitic imidazole framework (ZIF-65), and the shell is epigallocatechin gallate (EGCG)-Fe 3+ complex (EF). The nitroimidazole ligand in ZIF-65 could selectively deplete NADPH under hypoxia . Sorafenib diminished GSH by inhibiting cystine import and GSH biosynthesis. EGCG can reduce Fe 3+ to Fe 2+ , which aids the generation of hydroxyl radicals via the Fenton reaction . The reversible coordination between nitroimidazole and Zn 2+ , EGCG, and Fe 3+ enables triggered cargo release in acidic lysosomes . Tailored nanocarriers induced the depletion of both coenzymes (GSH and NADPH) and boosted reactive oxygen species in a 4T1 murine cancer cell line. The altered redox balance eventually resulted in efficient apoptotic cell death. The current work offers a novel means of redox cancer therapy via the selective depletion of key antioxidant enzymes in hypoxic cells.

研究领域: 癌症治疗 · 纳米技术 · 氧化还原生物学 · 药学
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