Nano Metal-organic Frameworks Research Articles

Multifunctional Dual Nano-MOF-Modified Decellularized Small Intestinal Submucosa Membrane Accelerates Healing of Infected Wound.

The treatment of complex or chronic skin wounds caused by burns, trauma, surgery, and genetic disorders has been a worldwide challenge. Small intestinal submucosa (SIS) is a biological material that is widely used in wound healing. How to further expand the wound healing application of SIS, especially in repairing infected wounds, remains a hot research topic for many tissue engineering and biomaterial scholars focusing on skin regeneration. This study uses nanometal-organic frameworks (nano-MOFs), which have not been applied to modify the SIS membrane before, to construct multifunctional dual nano-MOFs @ SIS membrane (dnMOF@SISm). Nano-MOFs are functionalized onto the nanofiber of SIS via in situ self-assembly under mild reaction conditions without any toxic reagent or complex instruments. The dnMOF@SISm can release Co2+, Zn2+, and bioactive factors, participating in the whole stage of the repair of infected wounds. In vitro, it can regulate the biological activities of various functional cells such as fibroblasts, endothelial cells, and macrophages and shows good antibacterial ability. In the infected full-thickness skin defect rat model, dnMOF@SISm can release metal ions and ligands, killing pathogenic bacteria colonized on the wound surface at the first stage, and then trigger and accelerate the skin repair process via angiogenesis, immune regulation, and collagen deposition. Above all, an efficient, nontoxic, mild self-assembly strategy realizes the functionalization of dual nano-MOFs on the nanofiber of SIS to expand its clinical application scenarios, especially in infected wounds.

A One-Nano MOF-Two-Functions Strategy Toward Self-healing, Anti-inflammatory, and Antibacterial Hydrogels for Infected Wound Repair

Porous metal–organic frameworks (MOF)-based hydrogels have recently attracted wide attention in sensing, catalysis, water treatment, and biomedicine. Yet, limited by challenges of insufficient stability, inordinate metal-ion leakage, and weak wound healing efficacy, the design of MOF-based hydrogel dressings for infected wounds has been rarely explored. Here, we propose a “one-nano MOF-two-functions” strategy to demonstrate the molecular engineering of a chemically stable nano MOF, which acts as both a carrier and a dynamic cross-linker, to fabricate functional composite hydrogels. The active amino groups of the MOF are employed to create dynamic networks with aldehyde-bearing alginate, ensuring excellent compatibility of the MOF with the polymer matrix and imparting effective self-healing properties to the resulting hydrogels. Simultaneously, two active ingredients, Cu nanoparticles (NPs) and curcumin, can be loaded into the nano MOF, achieving synergistic anti-inflammatory and antibacterial effects. Assisted by the mechanical stability and drug co-delivery in an infected full-thickness skin model, the MOF-based hydrogel can reduce the bacterial load on the wound by ∼103 times, and promote collagen deposition and angiogenesis by ∼1.5 and ∼3 times, compared with the control group. The “one-nano MOF-two-functions” design exhibits significant potential for high-performance infected wound dressings.

Carbon/copper oxide electrode materials with high atomic utilization constructed by in-situ induced growth strategy of nano metal-organic frameworks

Carbon/metal composites derived from metal-organic frameworks (MOFs) have attracted widespread attention due to their excellent electronic conductivity, adjustable porosity, and outstanding stability. However, traditional synthesis methods are limited by the dense stereo geometry and large crystal grain size of MOFs, resulting in many metals active sites are buried in the carbon matrix. While the common strategy involves incorporating additional dispersed media into material, this leads to a decrease in practical metal content. In this study, nanosized copper-metal-organic frameworks (Cu-MOFs) are in-situ grown on surface of carbon spheres by pre-anchoring copper ions, and the hybrid composite of porous carbon/copper oxide with high copper atom utilization rate is prepared through activation and pyrolysis methods. This strategy effectively addresses the issue of insufficient exposure of metal sites, and the obtained composite material exhibits high effective copper atom utilization rate, large specific surface area (2052.3 m2·g−1), diverse pore structure, outstanding specific capacity (1076.5F·g−1 at 0.5 A·g−1), and excellent cycle stability. Furthermore, this highly atom-economical universal method has positive significance in application fields of catalysis, energy storage, and adsorption.

Nano Metal–Organic Frameworks as Advanced Electrode Materials in Electrochemical Energy Storage

AbstractNano metal–organic frameworks as an attractive new class of porous materials, are synthesized via metal ions and organic ligands. With their desirable properties of abundant pores, high specific surface areas, fully exposed active sites and controllable structures, nano MOFs are acknowledged to be one of the most vital materials in electrochemical energy storages. However, in their practical applications, nano MOFs are still confronted with various difficulties and challenges because of their low conductivity, poor stability, and other disadvantages. The selection and development of MOF composites, MOF–derived materials and modified MOFs might be beneficial to use as better electrode materials to greatly improve the electrochemical properties of energy storage devices. This paper mainly focuses on the recent developments of nano MOFs as prospective materials in electrochemical energy storage applications, including lithium–ion batteries (LIB), lithium–sulfur batteries (LSB), zinc–ion batteries (ZIB), and supercapacitors (SCs). Finally, the challenges faced by these kinds of energy storage devices are proposed, along with the current directions and prospect.

Synthesis and Optimization of Ni-Based Nano Metal-Organic Frameworks as a Superior Electrode Material for Supercapacitor.

Metal-organic frameworks (MOFs) are hybrid materials that are being explored as active electrode materials in energy storage devices, such as rechargeable batteries and supercapacitors (SCs), due to their high surface area, controllable chemical composition, and periodic ordering. However, the facile and controlled synthesis of a pure MOF phase without impurities or without going through a complicated purification process (that also reduces the yield) are challenges that must be resolved for their potential industrial applications. Moreover, various oxide formations of the Ni during Ni-MOF synthesis also represent an issue that affects the purity and performance. To resolve these issues, we report the controlled synthesis of nickel-based metal-organic frameworks (NiMOFs) by optimizing different growth parameters during hydrothermal synthesis and by utilizing nickel chloride as metal salt and H2bdt as the organic ligand, in a ratio of 1:1 at 150 °C. Furthermore, the synthesis was optimized by introducing a magnetic stirring stage, and the reaction temperature varied across 100, 150, and 200 °C to achieve the optimized growth of the NiMOFs crystal. The rarely used H2bdt ligand for Ni-MOF synthesis and the introduction of the ultrasonication stage before putting it in the furnace led to the formation of a pure phase without impurities and oxide formation. The synthesized materials were further characterized by powder X-ray diffraction (XRD) technique, scanning electron microscopy (SEM), and UV-vis spectroscopy. The SEM images exhibited the formation of nano NiMOFs having a rectangular prism shape. The average size was 126.25 nm, 176.0 nm, and 268.4 nm for the samples (1:1)s synthesized at 100 °C, 150 °C, and 200 °C, respectively. The electrochemical performances were examined in a three-electrode configuration, in a wide potential window from -0.4 V to 0.55 V, and an electrolyte concentration of 2M KOH was maintained for each measurement. The charge-discharge galvanostatic measurement results in specific capacitances of 606.62 F/g, 307.33 F/g, and 287.42 F/g at a current density of 1 A/g for the synthesized materials at 100 °C, 150 °C, and 200 °C, respectively.

In-vitro and in-vivo assessment of pH-responsive core–shell nanocarrier system for sequential delivery of methotrexate and 5-fluorouracil for the treatment of breast cancer

Breast cancer (BC) is one of the leading fatal diseases affecting females worldwide. Despite the presence of tremendous chemotherapeutic agents, the resistance emergence directs the recent research towards synergistic drugs’ combination along with encapsulation inside biocompatible smart nanocarriers. Methotrexate (MTX) and 5-fluorouracil (Fu) are effective against BC and have sequential synergistic activity. In this study, a core–shell nanocarrier composed of mesoporous silica nanoparticles (MSN) as the core and zeolitic imidazolate framework-8 nano metal organic frameworks (ZIF-8 NMOF) as the shell was developed and loaded with Fu and MTX, respectively. The developed nanostructure; Fu-MSN@MTX-NMOF was validated by several characterization techniques and conferred high drugs’ entrapment efficiency (EE%). In-vitro assessment revealed a pH-responsive drug release pattern in the acidic pH where MTX was released followed by Fu. The cytotoxicity evaluation indicated enhanced anticancer effect of the Fu-MSN@MTX-NMOF relative to the free drugs in addition to time-dependent fortified cytotoxic effect due to the sequential drugs’ release. The in-vivo anticancer efficiency was examined using Ehrlich ascites carcinoma (EAC) animal model where the anticancer effect of the developed Fu-MSN@MTX-NMOF was compared to the sequentially administrated free drugs. The results revealed enhanced anti-tumor effect while maintaining the normal functions of the vital organs as the heart, kidney and liver.

PH/cellulase dual environmentally responsive nano-metal organic frameworks for targeted delivery of pesticides and improved biosafety

Environmentally responsive pesticide nanocarriers can respond to the metabolites of pathogenic fungi as well as the soil microenvironment to achieve intelligent release of pesticides. In this work, a smart pH and cellulase dual environmentally responsive pesticide delivery system (Tebu@ZnMOFs@CMC) was constructed by combining carboxymethyl cellulose (CMC) and Zn-based metal–organic frameworks (ZnMOFs), which are loaded with tebuconazole (Tebu). Physicochemical characterization indicates the successful preparation of Tebu@ZnMOFs@CMC nanoparticles. The Tebu loading capacity was approximately 18.26%. Release simulations showed a higher cumulative release of Tebu under acidic and cellulase-promoted conditions. The surface coverage of carboxymethyl cellulose could effectively improve its spread on wheat and rice leaves. Compared with tebuconazole suspension concentrate (Tebu@SC) and tebuconazole technical, Tebu@ZnMOFs@CMC nanoparticles showed higher antifungal activity. It also had lower acute toxicity to zebrafish, Daphnia magna and earthworms, and no significant effect on wheat and rice. Thus, the dual environmentally responsive Tebu@ZnMOFs@CMC nanoparticles have great potential for achieving on-demand and targeted pesticide delivery.

Novel composites of nano-metal–organic frameworks (IRMOF-3) and silver nanoparticles for the ultra-sensitive performance of SERS sensing and optical fiber modes

Rapid chemical detection of drugs of abuse in biological fluids such as blood and saliva is a concern within medicine and law enforcement. As an outcome, a label-free detection platform takes biological fluid samples with concentrations ranging from extremely high to very low. We obtained experimentally the limit of detection (LOD) of glycerol concentration, corresponding to a minimum resolvable refractive index of 3.4 × 10−7 RIU (refractive index unit). We applied the microfluidic device sensors to the quantitating concentration dopamine solutions. The experiment was recorded in real-time as the concentration of analyte injected exposed to the fiber core surface resulted in a sensitive change in optical power transmission. The presented sensors also exhibited reasonably good reproducibility and higher sensitivity, providing the LOD as 1.02 × 10−11 M. A relatively simple scheme procedure is proposed for the simultaneous detection and quantitative assessment of rhodamine B using surface-enhanced Raman spectroscopy with a limit of detection of 10−12 M and a relative standard deviation of 5.78% across a detection concentration range mainly from 10−5 M to 10−12 M. The obtained results demonstrate the potential of nano-metal–organic framework materials as large-area, label-free optical fiber sensors and SERS-based platforms for biomedical sensing and environmental applications.

Metal Nanoparticles as Novel Drug Delivery Systems: A Review of Current Challenges and Opportunities

Nanotechnology's intriguing characteristics have attracted a lot of study in recent years. Nanomaterials, nanoelectronics, and nanobiotechnology are all subfields of nanotechnology that share a great deal of common ground. The possibility for metal nanoparticles (MNPs) to completely transform treatment is what has made them so remarkable. In addition to avoid antibiotic resistance and improving medication delivery, MNPs have been shown to raise the efficacy index of medicines. Additionally, MNPs have applications in in vitro and in vivo tests, improved biodegradable substance production, and nutraceuticals. Improved targeting at the necessary target location is one major benefit of using metallic nanoparticles for drug delivery systems due to their improved durability and half-life in circulation. Bio-nanotechnology is expanding into the new field of green synthesis of MNPs, which is more environmentally friendly than traditional chemical and physical synthesis techniques. Focusing on environmentally friendly approaches to the preparation, surface modification, and applications of various MNPs like silver, gold, platinum, palladium, copper, zinc oxide, metal sulfide, and nanometal organic frameworks, this review seeks to present current insights into the challenges and perspectives of MNPs in drug delivery systems.

Organophosphate Level Evaluation for the Poisoning Treatment by Enzyme Activation Regeneration Strategy with Oxime-Functionalized ZIF-8 Nanoparticles.

In this work, two nanometal-organic frameworks (NMOFs) of ZIF-8-1 and ZIF-8-2 were designed and synthesized with a "missing linker" defects strategy by using Oxime-1 and Oxime-2 as coligands, respectively. ZIF-8-2 exhibited an excellent performance in comparison to that of ZIF-8-1 in activating and regenerating the activity of BChE suppressed by demeton-S-methyl (DSM) and could rapidly detoxify DSM in poisoned serum samples within 24 min. Additionally, the synthesized fluorescence probe of IND-BChE with high quantum yields, large Stokes shifts, and superior water solubility could be used for the detection of both butyrylcholinesterase (BChE) and DSM in a lower LOD of 0.63 mU/mL (BChE) and 0.086 μg/mL (DSM). By the difference in fluorescent intensity of IND-BChE with and without ZIF-8-2, a highly linear relationship of IND-BChE with DSM concentration was found (R2 = 0.9889), and the LOD was 0.073 μg/mL. In addition, an intelligent detection platform of ZIF-8-2@IND-BChE@agarose hydrogel combined with a smartphone formed a point-of-care test for DSM -poisoned serum samples and also realized satisfactory results. Unlike other detection methods of nerve agents, this assay first combined an NMOF reactivator for detoxification and detection of BChE enzyme activity and then quantification of OP nerve agents, which was of great significance in treatment of organophosphate poisoning.

Nano-metal-organic frameworks as corrosion inhibitors for strengthening anti-corrosion behavior of carbon steel in a sulfuric acid environment: from synthesis to applications.

In order to demonstrate the effect of Nano-metal organic frameworks, [Cu2(CN)4(Ph3Sn) (Pyz2-caH)2] (NMOF1) and [∞3[Cu(CN)2(Me3Sn)(Pyz)]] (NMOF2) as corrosion inhibitors for C-steel in 0.5 M sulfuric acid solutions, the following methods were utilized: mass reduction (MR), potentiodynamic polarization (PDP), and AC electrochemical impedance (EIS). The results of the experiments showed that by increasing the dose of these compounds, the inhibition efficacy (η%) of C-steel corrosion increased and reached 74.4-90% for NMOF2 and NMOF1 at a dose of 25 × 10-6 M, respectively. On the other hand, the η% decreased as the temperature range rose. Parameters for activation and adsorption were determined and discussed. Both NMOF2 and NMOF1 were physically adsorbed on the surface of C-steel and conformed to the Langmuir adsorption isotherm model. The PDP studies revealed that these compounds functioned as mixed type inhibitors, i.e. affecting both metal dissolution and hydrogen evolution reactions. Attenuated Total Reflection Infra-Red (ATR-IR) analysis was carried out to determine the morphology of the inhibited C-steel surface. There is good agreement between the findings of EIS, PDP and MR.

Nanoscale designing of metal organic framework moieties as efficient tools for environmental decontamination.

Environmental pollutants, being a major and detrimental component of the ecological imbalance, need to be controlled. Serious health issues can get intensified due to contaminants present in the air, water, and soil. Accurate and rapid monitoring of environmental pollutants is imperative for the detoxification of the environment and hence living beings. Metal-organic frameworks (MOFs) are a class of porous and highly diverse adsorbent materials with tunable surface area and diverse functionality. Similarly, the conversion of MOFs into nanoscale regime leads to the formation of nanometal-organic frameworks (NMOFs) with increased selectivity, sensitivity, detection ability, and portability. The present review majorly focuses on a variety of synthetic methods including the ex situ and in situ synthesis of MOF nanocomposites and direct synthesis of NMOFs. Furthermore, a variety of applications such as nanoabsorbent, nanocatalysts, and nanosensors for different dyes, antibiotics, toxic ions, gases, pesticides, etc., are described along with illustrations. An initiative is depicted hereby using nanostructures of MOFs to decontaminate hazardous environmental toxicants.

Efficient and green one‐pot synthesis of Knoevenagel condensation catalyzed nano metal–organic frameworks in water

Metal–organic frameworks (MOFs), Mlam‐NH‐66‐UiO and EtA‐NH‐66‐UiO, were prepared via post‐synthesis of the H2N‐66‐UiO and used as an efficient heterogeneous catalyst for Knoevenagel condensation of various aldehydes with malononitrile in water. The modified MOFs exhibited excellent catalyst activities in heterogeneous phase because of their large pore sizes and surface area, porosity, and the number of catalytically active sites (–NH2) on structures. In addition, the catalysts can be recycled and reused without decomposition of MOF structure and losing catalytic activity.

Amplifying Dendritic Cell Activation by Bioinspired Nanometal Organic Frameworks for Synergistic Sonoimmunotherapy.

Despite recent advancements of sonodynamic therapy (SDT) in cancer immunotherapy, challenges have yet to be surmounted to further boost its immunotherapeutic efficacy due to the low-level tumor antigens presentation of dendritic cells (DCs). Cell membrane camouflaged-nanoparticles can integrate the neoantigens of the cancer cell membrane with the multifunctionalities of synthetic nanocores. Herein, sono-responsive nanoparticles coated with DC-targeted antibody chimeric cancer cell membrane are investigated for multimodal therapy. The nanometal organic frameworks (MOFs) that respond to ultrasound are loaded successfully inside the vesicles displaying an anti-DEC205 antibody. The anti-DEC205 chimeric vesicles can directly target and activate DCs, promote tumor antigens cross-presentation, and then produce a cascade amplified T-cell immune response. Upon deep tissue-penetrating sonication, AMR-MOF@AuPt generates large amounts of reactive oxygen species that directly kill cancer cells, further initiating an anti-cancer T cell immune response. Such synergistic sono-immunotherapies effectually inhibit tumor growth and induce strong systemic and long-term immune memory against cancer recurrence and distant metastasis. The authors findings provide DCs and tumor cells of a dual active-targeting cell membrane-coated sono-immunotherapeutic nanoplatform for cancer therapy.

Infusion of Variable Chemical Structure to Tune Stacking among Metal-Organic Layers in 2D Nano MOF.

Thickness of two-dimensional (2D) metal-organic frameworks (MOFs) govern their intriguing functionalities. Primarily this thickness is controlled by the stacking between the metal-organic layers (MOL). It is observed that until now such modulating factors for stacking efficiency of MOL are not well studied. Here, we report a fundamental hypothesis to comprehend regulation of stacking efficiency among MOLs as a function of chemical structure of organic ligands (dicarboxylic acids and pillar linkers). This basically involves a series of isostructural three-dimensional (3D) MOFs which contain linkers of variable chemical nature that could be depillared to generate 2D stacked MOFs of different thickness. Depending on the linkers, we encountered the formation of single MOL to stacked multiple MOLs as evidenced from atomic force microscopic and other experimental analysis. The present study gives a concrete correlation between the stacking within 2D MOFs (from monolayer to multilayers), and their 3D counter parts, which may provide a thickness tuning pathway for 2D MOFs.

Porphyrin NanoMetal-Organic Frameworks as Cancer Theranostic Agents.

Metal-Organic Frameworks (MOFs) are hybrid multifunctional platforms that have found remarkable applications in cancer treatment and diagnostics. Independently, these materials can be employed in cancer treatment as intelligent drug carriers in chemotherapy, photothermal therapy, and photodynamic therapy; conversely, MOFs can further be used as diagnostic tools in fluorescence imaging, magnetic resonance imaging, computed tomography imaging, and photoacoustic imaging. One essential property of these materials is their great ability to fine-tune their composition toward a specific application by way of a judicious choice of the starting building materials (metal nodes and organic ligands). Moreover, many advancements were made concerning the preparation of these materials, including the ability to downsize the crystallites yielding nanoporous porphyrin MOFs (NMOFs) which are of great interest for clinical treatment and diagnostic theranostic tools. The usage of porphyrins as ligands allows a high degree of multifunctionality. Historically these molecules are well known for their reactive oxygen species formation and strong fluorescence characteristics, and both have proved helpful in cancer treatment and diagnostic tools. The anticipation that porphyrins in MOFs could prompt the resulting materials to multifunctional theranostic platforms is a reality nowadays with a series of remarkable and ground-breaking reports available in the literature. This is particularly remarkable in the last five years, when the scientific community witnessed rapid development in porphyrin MOFs theranostic agents through the development of imaging technologies and treatment strategies for cancer. This manuscript reviews the most relevant recent results and achievements in this particular area of interest in MOF chemistry and application.

Role of Lewis Acid Metal Centers in Metal–Organic Frameworks for Ultrafast Reduction of 4-Nitrophenol

Metal–Organic Frameworks (MOFs) can be a good alternative to conventional catalysts because they are non-toxic and can be selective without compromising efficiency. Nano MOFs such as UiO-66 have proven themselves to be competitive in the catalytic family. In this study, we report the excellent catalytic behavior of UiO-66 MOF in the reduction of a model reaction: 4-Nitrophenol (4-NP) to 4-Aminophenol (4-AP) over MOF-5 (Zn-BDC) and MIL-101 (Fe-BDC). Nano UiO-66 crystals were synthesized by a hydrothermal process and characterized by Powder X-ray Diffraction, Diffused Reflectance UV-Vis spectroscopy, Scanning Electron Microscopy, and Transmission Electron Microscopy. The catalysts’ performance during the hydrogenation reduction reaction from 4-NP to 4-AP was investigated in the presence of a reducer, NaBH4. The UiO-66 nano crystals exhibited excellent catalytic behavior owing to its large surface area and Lewis acidic nature at the metal nodes. Furthermore, UiO-66 showed excellent recyclability behavior, verified during repeated consecutive use in a sequence. The catalyst yielded similar catalytic behavior during the reduction of nitrophenols at each cycle, which is a novel finding.

Ultrasound Irradiation Assisted Synthesis of Luminescent Nano Amide-Functionalized Metal-Organic Frameworks; Application Toward Phenol Derivatives Sensing.

Two nano amide-functionalized metal-organic frameworks (MOFs) with molecular formula [Co(oba) (bpta)]·(DMF)2 TMU-50 and [Co2(oba)2 (bpfn)]·(DMF)2.5 TMU-51 obtained under ultrasonic method without any surfactants. The only difference between the two selected amide functionalized pillar ligands, N,N′-bis(4-pyridinyl)-terephthalamide (bpta), and N,N′-bis-(4-pyridylformamide)-1,5-naphthalenediamine (bpfn), is related to the naphthyl group, which led to the different luminescence properties of the nano frameworks. In this study, the special ability of the luminescent nano MOFs were investigated to sensitize nitroaromatic compounds. Due to its unique and porous framework, Nano TMU-50 shows a good sensitivity towards nitro phenol by strong fluorescence emission with a detection limit of 2 × 10–3 mM−1. Both nano MOF structures were characterized via many analyses such as powder X-ray diffraction, Field Emission Scanning Electron Microscopy (FE-SEM), elemental analysis, and FTIR spectroscopy. Moreover, the effect of a number of important parameters including initial reagent concentrations, power of ultrasound, time on morphology, and size of nano structures were examined. According to the fluorescence titration results, the activated nano-TMU-50 detected NP selectively with a quick response.

A Bibliometric Analysis of Nano Metal-Organic Frameworks Synthesis Research in Medical Science Using VOSviewer

Nano MOFs (nMOFs) have now evolved as a new class of MOF with exciting applications. The purpose of this research is to perform bibliometric analysis on nMOFs for medical science by combining mapping analysis using VOSviewer software. Application reference manager used to obtain research data. The data obtained is the result of a search based on the keyword "nano metal-organic framework and madical science". From the search results, 1000 relevant published articles were found in the range of 2017-2021. The results showed that research on nano metal-organic frameworks and medical science has increased in 2017-2020, but it decreases since 2021. The main reason for the increase is the need for human health which continues to increase along with the emergence of new diseases. Although the increase should continue to occur every year, the decline in 2021 is due to social restrictions due to the COVID-19 pandemic, thus limiting the work space in the field of research. This study shows the importance of bibliometric analysis in providing analytical data about what phenomena occur. This research is expected to help and become a reference for researchers in conducting and determining the research theme to be taken.

Construction of ultra-stable polypropylene membrane by in-situ growth of nano-metal–organic frameworks for air filtration

• MOFs were grown on the polypropylene fibers by the in-situ growth method. • Nano-sized MOFs have been synthesized to enhance the capture of PM particles. • Under the sonication of 600W, 80% of the MOFs were still loaded on the fibers. Air pollution, especially solid particulate pollution, seriously endangers people’s physical and mental health. As a result, the performance and stability of air filtration membranes are increasingly required. In this work, the nano-sized (sizes < 100 nm) polypropylene@zeolitic imidazolate framework-8 (PP@ZIF-8) membranes and polypropylene@copper(II) benzene-1,3,5-tricarboxylate (PP@Cu-BTC) membranes were designed in an in-situ growth method. These membranes can achieve efficient and stable filtration of PM2.5 particles in a practical environment. The PM1.0 quality factor and filtration efficiency of PP@Cu-BTC increased by 49.28% and 58.04%, respectively, compared to the PP membrane. In addition, more than 87% of metal–organic frameworks (MOFs) particles are still fixed on the fiber after ultrasonic treatment with ultrasonic power of 600 W for 30 min. Moreover, the membranes are recyclable and have excellent water resistance (>74.5% against PM1.0 after five washing cycles) and outstanding long-term storage performance (>94.9% against PM1.0 after storage for one month). This PP@MOFs membrane provides another idea for building stable and efficient air filtration membranes.