Magnetic Metal-organic Framework Research Articles

Magnetic Multienzyme@Metal-Organic Material for Sustainable Biodegradation of Insoluble Biomass.

Biodegradation of insoluble biomass such as cellulose via carbohydrase enzymes is an effective approach to break down plant cell walls and extract valuable materials therein. Yet, the high cost and poor reusability of enzymes are practical concerns. We recently proved that immobilizing multiple digestive enzymes on metal-organic materials (MOMs) allows enzymes to be reused via gravimetric separation, improving the cost efficiency of cereal biomass degradation [ACS Appl. Mater. Interfaces 2021, 13, 36, 43085-43093]. However, this strategy cannot be adapted for enzymes whose substrates or products are insoluble (e.g., cellulose crystals). Recently, we described an alternative approach based on magnetic metal-organic frameworks (MOFs) using model enzymes/substrates [ACS Appl. Mater. Interfaces 2020, 12, 37, 41794-41801]. Here, we aim to prove the effectiveness of combining these two strategies in cellulose degradation. We immobilized multiple carbohydrase enzymes that cooperate in cellulose degradation via cocrystallization with Ca2+, a carboxylate ligand (BDC) in the absence and presence of magnetic nanoparticles (MNPs). We then compared the separation efficiency and enzyme reusability of the resultant multienzyme@Ca-BDC and multienzyme@MNP-Ca-BDC composites via gravimetric and magnetic separation, respectively, and found that, although both composites were effective in cellulose degradation in the first round, the multienzyme@MNP-Ca-BDC composites displayed significantly enhanced reusability. This work provides the first experimental demonstration of using magnetic solid supports to immobilize multiple carbohydrase enzymes simultaneously and degrade cellulose and promotes green/sustainable chemistry in three ways: (1) reusing the enzymes saves energy/sources to prepare them, (2) the synthetic conditions are "green" without generating unwanted wastes, and (3) using our composites to degrade cellulose is the first step of extracting valuable materials from sustainable biomasses such as plants whose growth does not rely on nonregeneratable resources.

Structurally ordered core-shell MOFs in mixed matrix membrane as magnetic sieves for O2/N2 separation

Membrane separation technology has broad application prospects in O2/N2 separation, and improving the permselectivity of membranes remains a key problem to be solved. O2 and N2 have different magnetic properties and can be separated by magnetism. In addition, coupling magnetic separation with the use of a molecular sieve supported by metal-organic frameworks (MOFs) could further enhance the separation ability. In this work, a magnetic core-shell MOF (Fe3O4@ZIF-8) was prepared as a filler, and the impacts of the Fe3O4@ZIF-8 morphology, loading, channel magnetic properties and ordered arrangement on membrane O2/N2 selectivity were evaluated. To establish a magnetic-sieving O2 permeation channel, the preparation process was carried out in a magnetic field so that the fillers in the membrane were arranged orderly. Due to the synergistic impact of the structurally ordered MOF channel and magnetism, the gas transport performance of the resulting magnetic mixed matrix membranes (MMMs) was substantially improved. Therefore, the O2 permeability and O2/N2 selectivity of the 15 wt%Fe3O4@ZIF-8-8/Pebax MMMs reached 194 Barrer and 11.97, respectively. This study not only presents a novel approach for creating high-performance O2/N2 membranes but also plays a leading role in the development of magnetism-controlled multiscale (magnetic core-shell and filler-ordered) membrane structural engineering.

Just Soaping Them: The Simplest Method for Converting Metal Organic Frameworks into Superhydrophobic Materials.

The incorporation of superhydrophobic properties into metal organic framework (MOF) materials is highly desirable to enhance their hydrolytic stability, gas capture selectivity in the presence of humidity and efficiency in oil-water separations, among others. The existing strategies for inducing superhydrophobicity into MOFs have several weaknesses, such as increased cost, utilization of toxic reagents and solvents, applicability for limited MOFs, etc. Here, we report the simplest, most eco-friendly, and cost-effective process to impart superhydrophobicity to MOFs, involving a rapid (90 min) treatment of MOF materials with solutions of sodium oleate, a main component of soap. The method can be applied to both hydrolytically stable and unstable MOFs, with the porosity of modified MOFs approaching, in most cases, that of the pristine materials. Interestingly, this approach was used to isolate superhydrophobic magnetic MOF composites, and one of these materials formed stable liquid marbles, whose motion could be easily guided using an external magnetic field. We also successfully fabricated superhydrophobic MOF-coated cotton fabric and fiber composites. These composites exhibited exceptional oil sorption properties achieving rapid removal of floating crude oil from water, as well as efficient purification of oil-in-water emulsions. They are also regenerable and reusable for multiple sorption processes. Overall, the results described here pave the way for an unprecedented expansion of the family of MOF-based superhydrophobic materials, as virtually any MOF could be converted into a superhydrophobic compound by applying the new synthetic approach.

Orientation Growth of N-Doped and Iron-Based Metal-Organic Framework and Its Application for Removal of Cr(VI) in Wastewater.

A series of NH2-functionalized nano-sized magnetic metal-organic frameworks (MOFs) were prepared in this study for Cr(VI) removal from wastewater. It was observed that not only the morphological, i.e., orientation growth of N-doped and iron-based metal-organic frameworks, but also the adsorption of magnetic MOFs is largely related to the used amount of ammonium hydroxide in preparation. For example, with increasing amounts of ammonium hydroxide used in preparation, the morphology of magnetic MOFs changed from spherical to cube and triangular cone. Moreover, the maximum adsorption capacity of spherical-magnetic MOFs, cubic-magnetic MOFs and triangular cone-magnetic MOFs could be up to 204.08 mg/g, 232.56 mg/g and 270.27 mg/g, respectively. Under optimal conditions, the adsorption process of magnetic MOFs for Cr(VI) was consistent with the pseudo-second-order rate equation (R2 = 1) and Langmuir isotherm model (R2 > 0.99). Therefore, magnetic MOFs developed in this work offered a viable option for the removal of Cr(VI) from wastewater.

Enzymatic Synthesis of Indole-Based Imidazopyridine using α-Amylase.

The imidazo[1,2-a]pyridine scaffold has gained significant attention due to its presence as a lead structure in several commercially available pharmaceuticals like zolimidine, zolpidem, olprinone, soraprazan, etc. Further, indole-based imidazo[1,2-a]pyridine derivatives have been found interesting due to their anticancer and antibacterial activities. However, limited methods have been reported for the synthesis of indole-based imidazo[1,2-a]pyridines. In this study, we have successfully developed a biocatalytic process for synthesizing indole-based imidazo[1,2-a]pyridine derivatives using the α-amylase enzyme catalyzed Groebke-Blackburn-Bienayme (GBB) multicomponent reaction of 2-aminopyridine, indole-3-carboxaldehyde, and isocyanide. The generality and robustness of this protocol were shown by synthesizing differently substituted indole-based imidazo[1,2-a]pyridines in good isolated yields. Furthermore, to make α-amylase a reusable catalyst for GBB multicomponent reaction, it was immobilized onto magnetic metal-organic framework (MOF) materials [Fe3 O4 @MIL-100(Fe)] and found reusable up to four consecutive catalytic cycles without the significant loss in catalytic activity.

Integration of multienzyme co-immobilization and biomimetic catalysis in magnetic metal–organic framework nanoflowers for α-amylase detection in fermentation samples

Multiple enzymes induce biological cascade catalysis is essential in nature and industrial production. However, the shortcomings of enzymes, including unsatisfactory stability, reusability, and sensitivity in harsh microenvironment, have restricted their broader use. Here, we report a facile method for fabricating a cascade system by combining the benefits of immobilized enzymes and biomimetic catalysis based on magnetic metal–organic framework nanoflowers (mMOFNFs). mMOFNFs prepared through the layered double hydroxide-derived strategy exhibited remarkable peroxidase-like activity and accessible amino interface, enabling it to serve not only as a reliable carrier for α-glucosidase and glucose oxidase fixation, but also as a nanozyme participating in cascade. On this basis, a colorimetric biosensor of excellent sensitivity and selectivity for α-amylase detection was constructed with a wide range (2–225 U L−1), low detection limit (2.48 U L−1), and rapid operation (30 min). This work provides a versatile strategy for establishing multi-enzyme cascade systems and rapid analysis of α-amylase.

Development and application of a new deep eutectic solvent based magnetic metal–organic framework adsorbent for the detection of fluorotelomer alcohols in edible oils

The enrichment of per- and polyfluoroalkyl substances (PFASs) poses significant challenges for environmental and food safety monitoring, given their toxic and persistent nature, highly fluorinated character, and low concentration. This study focuses on the construction of a new deep eutectic solvent (DES)-functionalized magnetic metal–organic framework (MOF) adsorbent for fluorotelomer alcohols (FTOHs) analysis in foods. The DES, composed of levulinic acid and trifluoromethoxylbenzene, was modified onto the surface of magnetic UiO-66-NH2 to enable the specific adsorption of FTOHs during the pretreatment process, which was then followed by GC–MS analysis. The method exhibited a limit of detection (LOD) ranging from 31.51 to 185.76 pg g – 1 with satisfactory recoveries (73.83 %-128.55 %), and was successfully used in detecting FTOHs in 12 edible oils samples with the concentrations ranging from 401.89 to 8006.18 pg g − 1. The proposed adsorbent exhibited significantly improved enrichment performance for PFASs, primarily attributed to the cooperative enhancement of double hydrogen-bonding interactions and fluorine affinity via the elucidation of 1H nuclear magnetic resonance (1H NMR), 19F NMR, and quantum chemical calculations. This study provided new insights and directions for the design and fabrication of selective materials to pretreatment ultra-trace emerging contaminants in complex matrices.

Speciation analysis of inorganic selenium in food and water samples utilizing a 2,3-diaminonaphthalene post-synthetic modified magnetic metal–organic framework

In this work, a 2,3-diaminonaphthalene post-synthetic modified magnetic metal–organic framework was fabricated for fast and selective determination of inorganic selenium in real food and water samples. The results exhibited that selenium (IV) is adsorbed by the nano-material at a pH of 2.5, and in this way, selenium (IV) can be quantified selectively. After identifying the nanosorbent with FT-IR, CHNS, XRD, SEM, TEM, VSM, and BET surface analysis, parameters affecting the retention and desorption were optimized. Under optimal conditions, the detection limit of 8 ng/L was achieved for selenium (IV), and the method's precisions were less than 12.5 % intra-day RSD% and < 14.4 % for inter-day RSD%. The highest adsorption capacity was obtained as 264 mg/g. Finally, the desired adsorbent was used to extract and determine selenium species in water samples and total selenium in food samples. One of the most important advantages of the present method is its speed, ease, time-saving, and high accuracy.

A magnetic pore-confined catalyst with ionic liquids supported on MOFs for the synthesis of aryl-oxazolidinones: design, performance, and recyclability

Various methods have been explored for preparing heterogeneous catalysts using metal-organic framework (MOF) supported ionic liquids (ILs); however, it is challenging to develop such a synergistic catalyst that combines high efficiency, stability, the capability of maintaining immobilized ILs and active components, and high recovery efficiency. In this study, we successfully developed a magnetic MOF sub-nanostructured carrier by integrating organic UiO-66 with magnetic nanoparticles (MNPs). The resulting magnetic pore-confined catalyst, named MAG-UiO-66-IL(OAc), was prepared by in-situ self-assembly of pore-confining [C4mim] [OAc] within the nano-cavities of the magnetic MOF carrier. The morphology, structure, and thermal properties of the magnetic pore-confined catalyst were comprehensively characterized using various techniques. The novel catalyst MAG-UiO-66-IL(OAc) demonstrated remarkable catalytic efficiency in transforming cyclic carbonates and aryl amines to aryl-oxazolidinones, achieving yields up to 95% under mild solvent-free conditions. Furthermore, the catalyst showed exceptional recyclability, retaining its catalytic activity after ten successive reuses. Notably, the catalyst displayed excellent performance for reactions involving large-size reactants, expanding the range of substrate usability beyond previously reported solid-loading catalysts. Theoretical calculations were also conducted to complement the experimental results, providing valuable insights into the structure–activity relationship between the magnetic MOF carrier and the ionic liquid. These findings emphasize the significance of molecular-scale confinement on reactant diffusion and the overall reaction process, offering valuable guidance for the design of catalyst microstructures and the modulation of reaction performance.

Enhanced Electrochemical Characterization of the Immune Checkpoint Protein PD-L1 using Aptamer-Functionalized Magnetic Metal-Organic Frameworks.

Programmed death ligand 1 (PD-L1) is highly expressed in cancer cells and participates in the immune escape process of tumor cells. However, as one of the most promising biomarkers for cancer immunotherapy monitoring, the key problem ahead of practical usage is how to effectively improve the detection sensitivity of PD-L1. Herein, an electrochemical aptasensor for the evaluation of tumor immunotherapy is developed based on the immune checkpoint protein PD-L1. The fundamental principle of this method involves the utilization of DNA nanotetrahedron (NTH)-based capture probes and aptamer-modified magnetic metal-organic framework nanocomposites as signaling probes. A synergistic enhancement is observed in the electrocatalytic effect between Fe3O4 and UiO-66 porous shells in Fe3O4@UiO-66 nanocomposites. Therefore, the integration of aptamer-modified Fe3O4@UiO-66@Au with NTH-assisted target immobilization as an electrochemical sensing platform can significantly enhance sensitivity and specificity for target detection. This method enables the detection of targets at concentrations as low as 7.76 pgmL-1 over a wide linear range (0.01 to 1000ngmL-1). The authors have successfully employed this sensor for in situ characterization of PD-L1 on the cell surface and for monitoring changes in PD-L1 expression during drug therapy, providing a cost-effective yet robust alternative to highly expensive and expertise-dependent flow cytometry.

Novel advanced materials and magnetic solid phase extraction as approaches in sample preparation to enhance the analysis of ochratoxin A in peanuts.

Ochratoxin A (OTA) is a mycotoxin that can contaminate a variety of agricultural commodities, including fruit juices and wines. The capability of a magnetic solid-phase extraction (MSPE) method with a magnetic metal-organic framework (MOF) material having a three-layer core-shell structure to improve the detection of OTA in food matrices using high performance liquid chromatography is described. Analysis of the material through X-ray diffraction (XRD) indicated the successful synthesis of the magnetic nanomaterial Fe3O4@SiO2@UiO66-NH2. Scanning electron microscopy (SEM) and Zetasizer lab indicated its nano-sized morphological features. The conditions affecting the magnetic solid-phase extraction procedure, such as material dosage, pH, composition and amount of eluent, desorption solution and desorption time were investigated to obtain the optimal extraction conditions. Under optimized conditions, the recoveries of spiked analytes at three different concentrations ranged from 95.83 to 101.5%, and the relative standard deviations were below 5%. Coupling with HPLC allowed the limit of detection to be 0.3 μg kg-1. This method is simple and specific, and can effectively avoid the influence of coexisting elements and improve the sensitivity of determination through fast MSPE of OTA. It has broad development prospects in OTA detection pre-treatment.

Magnetic MOF composites for the electrocatalysis and biosensing of dopamine released from living cells.

Metal-organic frameworks (MOFs) with fit ligands and metals can be integrated into electrochemical biosensors for the detection of various biomolecules. In this study, we have synthesized novel magnetic MOF composites as electrocatalysts and constructed a novel biosensor for electrochemical detection of dopamine. The composites named Fe3O4@ZIF-8@AuNPs-COOH are synthesized through layer-by-layer assembly. They exhibit excellent stability and cooperative catalytic activity. In addition, green recycling is readily achieved through magnetizing/demagnetizing the electrode. The large specific surface area and ordered porous structures of the magnetic MOFs ensure good dispersion of gold nanoparticles, while the carboxyl group efficiently shields other redox-active interfering substances. The proposed electrochemical biosensor accomplishes the sensitive detection of dopamine in human serums and living cells. This study broadens the application of MOFs in electrochemical biosensing, validates the feasibility of biosensors for in vivo analysis, and provides new insights into green sensing.

Bioluminescence assay for rapid detection of live Staphylococcus aureus based on the enrichment of egg yolk antibody modified magnetic metal organic framework immunobeads.

Specific and rapid detection of live Staphylococcus aureus (S.A) in environmental and food samples is critically important for protecting human health. In order to fulfill this purpose, two kinds of novel egg yolk antibody (IgY) immobilized immunomagnetic beads (IMBs; mSiO2-IgY and mMOF-IgY), with core-shell mSiO2 and mMOF as substrate, were prepared for selectively enriching S.A from samples. Furthermore, the IMBs with captured S.A were collected and re-dissolved in 0.5 mL PBS. After that, a cotton swab coated with sodium dodecylsulfate (SDS) was put in the solution to lyse S.A cells and emit ATP bioluminescence of the luciferin/luciferase system. Finally, a portable bioluminescence detector was used for quantification of ATP corresponding to S.A concentration. The results demonstrated that mMOF-IgY can enrich more S.A than mSiO2-IgY and emit a stronger signal. The reasons may be due to the higher immobilization amount of IgY on the IMBs. Under optimal conditions, the calibration line of S.A concentration was 10-105 CFU mL-1 by mMOF-IgY within 30 min. The low detection limit of S.A was 3 CFU mL-1. The results demonstrated that the assay takes much shorter time than plate counting. Its portability and excellent detection capability are suitable for rapid monitoring of specific pathogens in foods.

Construction of core-shell magnetic metal-organic framework composites Fe3O4@MIL-101(Fe, Co) for degradation of RhB by efficiently activating PMS.

Low catalytic efficiency and catalyst recovery are the key factors limiting the practical application of advanced oxidation processes. In this work, a core-shell magnetic nanostructure Fe3O4@MIL-101(Fe, Co) was prepared via a simple solvothermal method. The core-shell structure and magnetic recovery performance were characterized by various technologies. The results of dye degradation experiments proved that within 10 minutes, the Fe3O4@MIL-101(Fe, Co)/PMS system can degrade more than 95% of 10 mg per L Rhodamine (RhB) at an initial pH of 7, which possesses higher catalytic activity than the Fe3O4/PMS system and the MIL-101(Fe, Co)/PMS system. The effects of initial solution pH and coexisting anions in water on the degradation of RhB were further discussed. The results showed that Fe3O4@MIL-101(Fe, Co) displayed excellent degradation efficiency in a wide pH range of 3-11 and capability of resisting coexisting anions. It is worth mentioning that after five cycles, the RhB removal rate can still be maintained at over 90% after 10 minutes of reaction. Free radical quenching experiments were further studied, confirming that ˙OH and SO4-˙ were involved in the degradation of RhB, while the dominating active free radical was SO4-˙. The possible reaction mechanism of the RhB degradation process was also inferred.

Effect of metal-ligand interactions on magnetic characteristics of two-dimensional Kagome structured perthiolated coronene (PTC) metal-organic frameworks (MOFs).

In recent years, the potential applications of two-dimensional (2D) metal-organic framework (MOF) materials in fields like spintronics have drawn increasing attention. Inspired by the successful synthesis of a perthiolated coronene (PTC)-Fe MOF structure, this study explores the fine-tuning of its electronic and magnetic structure by substituting Fe elements with various transition metals. Our calculations demonstrate a substantial increase in the Curie temperature (Tc) by a factor of 5 for Co and 10 for Mn when replacing Fe. This enhancement is attributed to the elevated electron density near the Fermi level, facilitating the generation of additional itinerant electrons crucial for the Ruderman-Kittel-Kasuya-Yosida (RKKY) exchange mechanism. However, substituting Fe with V, Cr, Ni, and Cu leads to a loss of ferromagnetic ground state. Our work enhances the understanding of the electronic and magnetic behavior of the 2D PTC-TM (transition metal) MOF family, and provides a promising avenue for engineering 2D magnetic MOF systems.

Hybridization of magnetic MOF composites with 3D terminal carboxyl hyperbranched polymers for dye wastewater treatment

A novel adsorbent obtained by hybridization of magnetic MOFs with three-dimensional terminal carboxyl hyperbranched polymers to achieve efficient dye removal.

Facile synthesis of Fe3O4@CS@ZIF-67 for the magnetic solid phase extraction-high performance liquid chromatographic determination of benzoylurea insecticides in tea infusions

In this paper, a novel magnetic metal–organic framework composite with chitosan as linker (Fe3O4@CS@ZIF-67) was synthesized by a facile method at normal pressure and normal temperature. After characterization, Fe3O4@CS@ZIF-67 was used as adsorbent for the magnetic solid phase extraction of benzoylurea insecticides (BUs) in tea infusions prior to high performance liquid chromatographic analysis. The effects of the amount of adsorbent, ionic strength, pH, adsorption time, type of eluent and elution time were investigated. The adsorption could be completed in 1.5 min with only 15 mg adsorbent for the extraction of 10 mL sample solution. Good linearity was obtained for the analysis of BUs with R2 between 0.9988 and 0.9999. The limits of detection were in the range of 0.72–1.48 μg·L−1. Relative standard deviations (RSDs) for intra-day precision and inter-day precision were in the range of 2.62–4.32 % and 3.60–6.29 %, respectively. RSDs for batch-to-batch precision of Fe3O4@CS@ZIF-67 were between 0.41 % and 7.52 %. The spiked recoveries ranged from 75.7 % to 112.5 %. The proposed method has been successfully applied to the determination of BUs in tea infusion samples.

Facile fabrication of Fe3O4@UiO-66-NH2/popcorn-like gold nanoparticles based SERS substrate for selective enrichment and real-time detection of residual enrofloxacin in milk

In this study, a magnetic metal-organic frameworks (MOFs) based hybrid substrate was designed and fabricated for SERS detection of enrofloxacin (ENR) in milk. The magnetic MOF (Fe3O4@UiO-66-NH2) was synthesized by a facile microwave-assisted method, then loaded with popcorn-like Au nanoparticles (NPs) through electrostatic interaction. The as-prepared SERS substrate (Fe3O4@UiO-66-NH2/Au NPs) integrated the abundant hot spots of popcorn-like Au NPs with porous Fe3O4@UiO-66-NH2, which greatly improved its SERS activity and stability. More importantly, benefiting from the fingerprint characteristics of SERS and adsorption performance of Fe3O4@UiO-66-NH2, the SERS substrate exhibited high selectivity and sensitivity in detecting ENR. Under the optimal detection condition, a good linearity (R2 = 0.996) was obtained with ENR concentration of 1.0 × 10−9–1.0 × 10−6 M in spiked milk, the LOD was as low as 5.26 × 10−10 M, and the recoveries were in the range of 76.1–86.1 % at three different spiking levels. The whole detection process including sample pretreatment took about 50 min, which indicating that the prepared substrate has great potential in sensitive and real-time detection of ENR in milk.

Magnetic solid phase extraction for the determination of Pb(II) and Cd(II) in high salt foods

The conventional method for the determination of heavy metals in food is acid digestion followed by atomic absorption spectrometry or induced coupled plasma mass spectrometry. However, for high salt foods, due to the strong matrix effect, the detection results are seriously inaccurate. In this work, sulfur-functionalized magnetic metal-organic frameworks (Fe3O4@UiO-66-SH) were synthesized by coating Fe3O4 nanospheres with sulfydryl-functionalized UiO-66. The Fe3O4@UiO-66-SH possesses both the magnetic properties of Fe3O4 and the diverse properties of metal-organic framework (MOF) in one material, which has the superiority of high surface area, easy-operation and strong adsorb ability with Pb (II) and Cd(II), is used to separate and determine Pb (II) and Cd(II) in high salt foods by magnetic solid phase extraction-induced plasma mass spectrometry. The detection limits (LODs) for Pb (II) and Cd(II) were 0.17 and 0.21µg/kg, respectively, and the quantification limits (LOQs) were 0.56 and 0.66µg/kg. Analyzing the certified reference material of soy sauce (CFAPA-QC1728-4, P41839) and estimating the spiked recoveries proved the accuracy and precision of the proposed method. The determined values agreed well with the reference values, and the recoveries for spiking sample varied from 85.8–100.5%.

Functionalized magnetic metal organic framework nanocomposites for high throughput automation extraction and sensitive detection of antipsychotic drugs in serum samples

Due to the complexity of biological sample matrix, the automated and high-throughput pretreatment technology is urgently needed for monitoring the antipsychotic drugs for mental patients. In this study, functionalized magnetic zirconium-based organic framework nanocomposites (Fe3O4@SiO2@Zr-MOFs) were successfully designed and synthesized by the layer-by-layer growth. Among them, Fe3O4@SiO2@UiO-67-COOH showed the best adsorption performance, and at the same time it exhibited excellent water dispersibility, high thermal stability, chemical stability and high hydrophobicity. Results of adsorption kinetics, isotherm and FT-IR showed that the adsorption process was dominated by chemical adsorption (hydrogen bond, electrostatic interaction, π-π interaction) and monolayer adsorption. Moreover, the smaller pore size improved the protein exclusion rate which reached 98.9–99.8%. Based on the above result, the synthesized magnetic nanoparticles were introduced to 96-well automatic extractor, antipsychotic drugs in 96 serum samples were automatically extracted within 9 min, which most greatly saved the time and labor costs and avoided artificial errors. By further integrating with ultra-high performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS), antipsychotic drugs can be detected in the range of 0.2–3.0 ng mL−1 with a quantitative limit of 0.06–0.9 ng mL−1. The recoveries of antipsychotic drugs and their metabolites in serum ranged from 95.7% to 112.3% within 1.4–6.5% of RSD. These features indicate that the proposed method is promising for high throughput and sensitively monitoring of drugs and other hazardous substances.