A water-stable luminescent metal-organic framework for effective detection of aflatoxin B1 in walnut and almond beverages.

Sensitive and rapid detection of aflatoxin B1 (AFB1) without using antibody or biomolecular modifications in water is achieved using a novel water-stable luminescent metal-organic framework (LMOF) termed Zr-CAU-24. The 1,2,4,5-tetrakis(4-carboxyphenyl) benzene (H4TCPB)-based LMOF with high water-stability has demonstrated drastic fluorescence fading in the presence of AFB1. The detection limit for AFB1 using this porous nanomaterial reaches as low as 19.97 ppb (64 nM), which is below the applicable action level for peanut and corn products set by the FDA and among the most sensitive sensors reported for AFB1. We further investigated its response to five other mycotoxins including AFB2, AFG1, AFG2, AFM and OTA and their Stern-Volmer quenching efficiencies are significantly below that of AFB1 (138 461 M-1). The prepared water-stable LMOF was directly used for the detection of AFB1 in spiked walnut and almond beverages. High recovery rates (91-108%) were achieved in 5 min. We found that the quenching of H4TCPB molecules towards mycotoxins was remarkably enhanced by anchoring them into the periodic framework and its mechanism was discussed. The presented method with acceptable detection limit is of potential for the development of low-cost, robust and sensitive sensors for the rapid detection of AFB1 in agricultural and food products. This journal is © The Royal Society of Chemistry.

Introduction

Mycotoxins are secondary metabolites produced by Aspergillus that are frequently found in spoiled agricultural commodities (such as peanuts, corns, rice, and milk), posing significant adverse health effects worldwide.[1] Among them, aflatoxins (AFs) and ochratoxin A (OTA) represent the most dominant and harmful mycotoxins,[2] which have been proved teratogenic, mutagenic, and carcinogenic to human beings and animals.[3] There are basically four types of AFs: B1, B2, G1, and G2 and AFB1 represents the most harmful one. In many countries, legislative limits were set for AFB1 in foodstuffs.[4] More importantly, AFB1 has demonstrated high chemical stability against elevated temperature through food processing, making the prevention of their entrance into the food supply chain difficult. Therefore, it is extremely important to detect their contamination at low concentration to ensure global food safety.[5] Nowadays, there are basically two methods for the detection of AFs: enzyme-linked immunoassays and chromatographic-based methods, including high performance liquid chromatography (HPLC) and immunoassay chromatography.[6] The former method provides a potable and rapid method for mycotoxins detection. However, low sensitivity and complex operation procedures has hampered its practical applications.[7] Chromatographic-based methods are considered as facile, sensitive and portable sensing method for AFs sensing.[8] Nevertheless, this method has some drawbacks such as high-cost, technique required operation and time-consuming sample preparation process. The incorporation of biomolecules in immunoassay chromatography also makes this method less robust. Thus, development of sensitive, low-cost and robust sensing methods for AFB1 is in high demand, especially in developing countries.[9] Metal–organic frameworks (MOFs), as an emerging class of porous materials with high surface area, flexible chemical properties, rich functionalities and tuneable pore structures, have demonstrated great potential in the detection of harmful residues, especially for small molecules.[10,11] For example, a series of luminescent Zr-based highly luminescent metal–organic frameworks (LOMF) were reported as sensitive chemical sensors for toxic chemicals detection and removal, including nitroaromatic explosives.[12-15] Two water-stable 3D florescent Zr(iv)-based metal–organic frameworks were constructed with different pore structures.[16] Both their florescence could be efficiently quenched with nitro compound, which enables the sensitive detection of organic explosives with the detection limit reaches as low as ppb level. 2D Cd-based LMOF was also reported for the selective detection of nitroaromatic explosives different –NO2 groups.[17] Furthermore, a LMOF-based method was reported for TNP selective detection with the presence of other nitro compounds based on the specific electrostatic interaction and electron and energy transfer between TNP and LMOF.[12] Taking advantage of the cation-exchange approach, a water-stable Eu-MOF was explored as sensitive and selective Fe3+ sensor with potential applications in biological system.[18] However, their potential as mycotoxins sensors was seldom investigated. Li et al. reported a highly sensitive Zn-based luminescent MOF (LMOF) towards mycotoxins that achieves a low detection limit of AFB1 (46 ppb) in 10 min. This novel sensing material is of potential for the development of applicable low-cost, rapid and sensitive mycotoxin sensors.[19] However, Zn-based MOFs suffered from poor water-stability due to the fragile Zn–O bond under the attack of H2O molecules,[20] which has generally limited its applications in industrial practices, such as water purification and sensing. Here, we present a robust Zr6-cluster based water-stable LMOF termed Zr-CAU-24 with sensitive response to AFs. With water-stable Zr4+ clusters and luminescent TCPB4− severing as second building units (SBU) and organic linkers, respectively, the prepared Zr-CAU-24 nanocrystals have demonstrated high structure stability in water due to their strong metal–ligand bond strength.[20-23] As-prepared Zr-LMOF crystals not only demonstrated high surface area but also revealed improved sensitivity towards AFB1 compared to free standing H4TCPB molecules in water. The limit of detection reaches as low as 19.97 ppb in 5 min, which is below the applicable action level set by Food and Drug Administration (FDA) for cottonseed meals intended for beef cattle (300 ppb) and corn and peanut products (20 ppb).[24,25]

Results and discussion

Characterization

Water-stable luminescent Zr-CAU-24 was synthesized according to a reported research with modifications.[26] In this study, benzoic acid was used as structure modulator to control the crystal size and morphology of prepared nanocrystals. Without benzoic acid, amorphous colloid-like polymer that is formed by the aggregation of nano-Zr-CAU-24 crystals (∼30 nm) is observed (Fig. S1†). Notably, we also found that the amorphous polymer has demonstrated negligible response towards AFB1. Thus, incorporating the H4TCPB into the long-range order periodic structure is necessary for its sensitive response towards AFB1. The as-prepared Zr-CAU-24 crystals have demonstrated a rod-like morphology with a size of ∼1 μm (Fig. 2A) with strong blue fluorescence. As shown in Fig. 1A, the Zr4+ are coordinated by eight carboxylate groups to form a C-centred orthorhombic arrangement cluster ([Zr6(μ3-O)4(μ3-OH)4]12+). The rest coordination sites at the Zr4+ ions are occupied by H2O and OH− molecules as mentioned in other Zr-based MOFs. As reported, the clusters are further bridged by TCPB4− linkers (Fig. 1B) in a SCU topology, giving rise to a porous framework with rhombic channels of ∼5.3 × 10.5 Å and ∼2.4 × 3.5 Å in diameter (Fig. 1C and D). For rapid and sensitive detection of mycotoxins in water, the structure stability of Zr-CAU-24 crystals in water is of great importance.

Fig. 2

Scanning electron microscopy images of prepared Zr-CAU-24 crystals with different magnification times. Scale bar: 1 μm ((A), inset). PXRD of Zr-CAU-24 crystals before and after water treatment and AFB1 absorption, (B) and N2 adsorption/desorption isotherms (C) of Zr-CAU-24 crystals before and after 24 h water treatment. TGA result of as-prepared Zr-CAU-24 crystals (D).

Fig. 1

Crystal structure of Zr-CAU-24 that is constructed from the [Zr6(μ3-O)4(μ3-OH)4]12+ clusters (A) and TCPB4+ molecules (B). Ball-stick models of Zr-CAU-24 crystals (C) and (D).

To prove its water-stability, the prepared Zr-CAU-24 crystals were immersed in water for 24 h before it is measured with Powder X-ray Diffraction (PXRD) and N2 adsorption/desorption isotherm. As shown in Fig. 2B, the XRD peaks before and after water treatment are in good agreement, indicating the intact pore structure after long time of operation in water. The PXRD pattern is also retained after the loading of AFB1, which proves that the Zr-MOF structure was well kept after its quenching of florescence by AFB1. Similar results can be found in its N2 adsorption/desorption isothermal curves before and after 24 h water treatment (Fig. 2C). We found that the Brunauer–Emmett–Teller (BET) surface area remained, which again proves its intact pore structure during water treatment. The isothermal curve of Zr-CAU-24 is in good agreement with type I adsorption/de-adsorption isothermal curve, which implies the uniform microporous structure of prepared Zr-CAU-24. Further pore size distribution analysis directly revealed that most of the micropores have an aperture of 1 nm (Fig. 2C, inset). Larger micropores of ∼2 nm with higher accessibility to mycotoxins can also be found. Thermal gravimetric analysis (TGA) was used to prove the thermal stability of Zr-CAU-24 (Fig. 2D). It first exhibited a weight loss of 3% in the temperature range 50–200 °C. Sequentially, further weight loss of 5% was observed between 200–420 °C (loss of internal solvent molecules). The decomposition of the thermal robust porous material starts at 420 °C with a total weight loss of ∼38% after degradation. With good water and thermal stability (∼420 °C), this robust sensing material is considered as an appropriate candidate for the development of low-cost, rapid and sensitive sensors for detection of mycotoxins.

Detection of mycotoxins

Mycotoxin detection was achieved by monitoring the PL signal fading of Zr-CAU-24 crystals after reacting with mycotoxins. We first determined the optimum LMOF dosage to harvest the highest FL fading by reacting with 50 μM AFB1 (Fig. S2†). When 50 μg mL−1 LMOF was applied, highest FL fading of 83% was achieved, while both lower and higher LMOF dosage decreased FL fading (73%). Sequentially, we examined its performance in the detection of AFB1 by adding given amount of toxins to the solution containing 50 μg mL−1 Zr-CAU-24 crystals. The strong blue-fluorescence-emission LMOF nanocrystals were significantly quenched in 5 min and the signal was monitored by a fluorimeter (Fig. 3A). Under the excitation of 340 nm wavelength, the fading of fluorescence intensity at 410 nm (Zr-CAU-24) is correlated linearly with the logarithmic molar volume of toxins (eqn (1))where y represents the relative florescence intensity, x represents the molar volume of AFB1, and F0 and F is the intensity of fluorescence with and without toxins, respectively. Good linear relationship between relative fluorescence ((F0 − F)/F0) and the logarithm of toxic concentration (>99%) is achieved for a wide range of toxin concentrations (0.075 to 25 μM), which is of advantage over its counterparts.[27] The detection limit reaches as low as 19.97 ppb (S/N = 3). The value of this detection limit is below the tolerant level of cottonseed meals intended for beef cattle (300 ppb) and corn and peanut products (20 ppb) (FDA) and among those of the most sensitive materials reported for AFB1 sensing. Furthermore, we applied the sensing material to the detection of other two aflatoxins (AFG1, AFM) and ochratoxin A (OTA). Drastic fluorescence quenching was also observed and the liner relationships were obtained as shown in the Fig. S3–S5.† They all demonstrated good linear relationship between relative fluorescence and the logarithm of toxic concentration (>98%), ranging from 0.075 to 25 μM. Stern–Volmer quenching efficiency is used to describe its sensitivity towards different mycotoxins.where I0 represents the initial emission peak of intensity, I is the emission peak intensity upon the addition of analyte, [Q] is molar intensity upon the addition of analyte (quencher) and Ksv is the quenching efficiency, which is used to quantitatively evaluate the performance of Zr-CAU-24 as a mycotoxin sensor. As shown in Fig. 3C, this porous nanomaterial has demonstrated sensitive quenching effect towards four kinds of mycotoxins including AFB1, AFG1, AFM and OTA and the Ksv reaches 138 461, 50 793, 68 119, 53 149 M−1, respectively. The Ksv for AFB1 is almost doubled compared with that for AFG1, AFM and OTA, indicating its higher selectivity toward AFB1. Stronger orbital overlap (π–π conjugation) between AFB1 and Zr-CAU-24 is reported responsible for the enhanced selectivity towards AFB1 compared with other kinds of mycotoxins.[14] To better reveal the different responses of Zr-CAU-24 toward different mycotoxins, we treated the analyst with a fixed concentration (50 μM) of AFB1, AFB2, AFG1, AFG2, AFM and OTA (Fig. 3D). The fluorescence intensity at 380 nm dropped drastically after adding of mycotoxins. Obvious red shift was observed in all test samples, which is due to the fluorescent properties of mycotoxins under the excitation of 340 nm.

Fig. 3

Emission spectra of Zr-CAU-24 with the incremental addition of AFB1 in water, with toxin concentrations given from 0 to 50 μM (A). Linear relationship between lg CAFB1 and FL intensity. Inset: optical photo of florescent Zr-CAU-24 crystals in water (left) and water (right) (B). Stern–Volmer curves acquired at λex = 340 nm and λem = 410 nm for AFB1, AFG1, AFM and OTA (C). FL intensity fading of Zr-CAU-24 towards 50 μM AFB1, AFB2, AFG1, AFG2, AFM and OTA (D).

Walnut and almond beverages are common products made from nuts, exposing them to the risk of being contaminated by AFB1. Therefore, we further applied this sensing material to the direct detection of AFB1 in the spiked samples (Table 1). AFB1 of three different concentrations (0.1 μM, 1 μM, 10 μM) were tested with Zr-CAU-24 and HPLC method is valued as a control to evaluate the recovery rates in real samples (Fig. S7†). High recoveries were achieved in all samples (91–108%), which is comparable to that of HPLC (95–102%). At low toxin concentration (0.1 μM), the recovery rates for walnut and almond beverages both reached 93%. It's noticed that this sensing method has demonstrated a wide liner range of 0.075–25 μM, while most of reported methods have narrow liner ranges.[28-30] These results have revealed the potential of this water-stable sensing material for the development of low-cost, rapid, and potable mycotoxin sensors.

Recovery rates of AFB1 in spiked walnut and almond beverages using fluorescent Zr-CAU-24 crystals (HPLC method was used as comparison)

	Spiked amount (μM)	HPLC (μM)	Proposed method (μM)	Recovery (%)
Walnut beverage	0.1	0.102	0.0975	98%
	1.0	1.007	1.079	108%
	10.0	9.969	9.73	97%
Almond beverage	0.1	0.0946	0.0966	97%
	1.0	0.956	1.041	104%
	10.0	9.73	9.06	91%

Mechanism of mycotoxin detection

By anchoring the fluorophore into the framework, the absorption wavelength presents a red shift from 280 nm to 330 nm (Fig. 4A) due to the strong π–π interaction in the framework, which is observed in other sensing materials reported. However, the emission wavelength of TCPB4− remained at 410 nm (Fig. 4B), which implies a higher energy transfer efficiency in Zr-CAU-24 crystals. TCPB4− is a strong fluorophore, but it has no strong interaction with AFs (Fig. 4C). Also, nano-Zr-CAU-24 crystals of ∼30 nm demonstrates negligible fluorescence quenching effect towards AFB1. Thus, incorporating the fluorophore into a long-range order structure of metal–organic framework is essential for sensitive and selective quenching of AFB1. The quenching mechanism of LMOF as a mycotoxin sensor was due to the electron transfer between the LMOF and mycotoxins because the LUMO energy state of MOF is above the LUMO state of mycotoxins.[19] However, the enhanced quenching efficiency of anchored TCPB4− molecules in the Zr-CAU-24 was barely discussed. N2 absorption/desorption curve demonstrates that the average pore size slightly decreases from 1 nm to 0.8 nm, which demonstrates that most pores of Zr-MOF is not occupied after AFB1 adsorption. Combined with the absorption testing result (Fig. S6†), it is found that the AFB1 was fully absorbed by the Zr-CAU-24 crystals and removed from the solution after sensing and the notable enhancement may be due to the amplified luminescence quenching of luminescent MOFs at the surface. The periodic structure of phosphorescent Zr-CAU-24 has allowed for long distance transfer of intra-MOF energy, which significantly enhances the electron-transfer quenching of fluorescence Zr-CAU-24 at the surface[31] and thereby causes higher quenching efficiency of micron level Zr-CAU-24 crystals compared with nano-Zr-CAU-24 of ∼30 nm.

Fig. 4

UV-visible spectrum (A) and emission spectra (λem = 410 nm) (B) of TCPB4+ molecules and Zr-CAU-24 crystals. FL intensity fading of Zr-CAU-24 crystals and TCPB4+ molecules with the existence of AFB1 (C).

Experimental

Instrumentation

Hitachi SU-8000 field-emission electron scanning microscope (Hitachi, Japan) was used to characterize the morphology and the EDS of MOF particles with an acceleration voltage of 3 kV (10 nm gold coating). Powder X-ray Diffraction was conducted on an X′ Pert PRO diffractometer (PANalytical, Netherland) equipped with Cu Kα radiation (λ = 0.15406 nm) (scan speed: 1° min−1; 2θ range: 2–50°; step size: 0.05°). The BET surface area of the MOF particles was measured using an AUTOSORB-1-C surface area and pore size analyzer (Quantachrome, USA) with samples degassed at 200 °C for 24 h in advance. The thermal stability of the MOF particles was determined on a Pyris 1 thermal gravimetric analyzer (Perkin Elmer, USA) with a ramp rate of 10° min−1 up to 600 °C. DU 800 UV-visible spectrometer (Beckman Coulter, USA) with 1 cm quartz cuvettes was used to measure the absorbance of TCPB4− and Zr-CAU-24. High Performance Liquid Chromatography (HPLC, Agilent 1260 Infinity, USA) was used to accurately determine the AFB1 concentration in both walnut and almond beverages. Analytical balance with an accuracy of 0.01 mg (Mettler Toledo, USA) was used.

Reagents

Zirconium chloride (97%), H4TCPB (99%) and benzoic acid (98%) were purchased from Sigma-Aldrich (USA). AFB1, AFB2, AFG1, AFG2, AFM, OTA, methanol (97%) and arsenic acid (80%) were purchased from Sinopharm Chemical Reagent Co., Ltd (Shanghai, China). Walnut and almond beverages were purchased from a local supermarket. All other chemicals were of analytical grade or better quality and used as received. Milli-Q ultrapure water (Millipore, USA; ≥ 18 MΩ cm) was used throughout.

Synthesis of Zr-CAU-24

Zr-CAU-24 was prepared according to a reported article with modifications.[21] 100 mg ZrCl4, 140 mg H4TCPB and 5400 mg benzoic acid were ultrasonically dissolved in 32 mL H2O : DMF (1 : 2) in a 50 mL Teflon vessel. The clear mixture was then kept in reaction kettle at 120 °C and maintained for 48 h. After cooling down to room temperature, the obtained white cloudy liquid was washed with DMF once and methanol twice and dried at 60 °C overnight. For the preparation of amorphous colloid-like polymer, 50 mg of H4TCPB was allowed to react with 70 mg of ZrCl4 in 8 mL of dimethyl formamide in a Teflon vessel baker for 24 h at 120 °C before washed with methanol for 3 times. The product was dried at 60 °C overnight.

AFB1 absorption

100 μM AFB1 and 0.5 mg mL−1 Zr-MOF were mixed for 10 min before being centrifugated at 8000 rpm for 10 min. The supernate was collected and measured using a fluorimeter.

Fluorescence detection

Typically, 4 mg of Zr-CAU-24 were simply dispersed in 10 mL of water at room temperature. The mixture was oscillated for 2 min to prepare the metal ion incorporated suspension for luminescent measurements. Then 90 μL of diluted Zr-CAU-24 (55 μg mL−1) aqueous solution was added with 10 μL of AFB1 solution with final concentrations of 0.075, 0.1, 0.25, 0.5, 0.75, 1.0, 2.5, 5.0, 7.5, 10, 25, and 50 μM. For specificity test, Zr-CAU-24 was mixed with 50 μM AFs (OTA, AFB1, AFB2, AFG1, AFG2, or AFM) or with 10 μL of water as a blank control. For the test on mechanism of mycotoxin detection, 90 μL of H4TCPB (55 μg mL−1) aqueous solution was added with 10 μL of AFB1 solution with final concentrations of 0.05, 0.1, 0.5, 1.0 and 5 μM.

Analysis of AFB1 in spiked samples

In this study, walnut and almond beverages without sprayed AFs were used for spiked experiments. The obtained spiked samples (5 mL) were added with 1 g of NaCl and then dissolved into 25 mL of methanol–water solution (volume ratio: methanol : H2O = 7 : 3). The mixed solution was filtrated and purified by immunoaffinity chromatography column, finally filtrated by 0.22 μm filter membrane before chromatographic determination.

Conclusions

We have presented a facile method for rapid and sensitive detection of microscale mycotoxins using a water-stable porous Zr-based luminescent MOF. It has demonstrated ultrasensitive response towards AFB1 with a detection limit of 19.97 ppb in 5 min (from sample detection to signal output) which is below the applicable action level set by FDA for cottonseed meals intended for beef cattle (300 ppb) and corn and peanut products (20 ppb). The quenching efficiency for AFB1 was as high as 138 461 M−1, which is almost a doubled value compared to that of AFG1, AFM and OTA, which indicates a higher selectivity for AFB1. Due to the good water-stability of prepared LMOF, we further applied the prepared Zr-CAU-24 without further modification to the detection of toxins in spiked samples of walnut and almond beverages. High recovery rates (≥91%) were achieved in the detection of different concentrations of AFB1. The amplified quenching effect of TCPB-based MOFs compared with unanchored TCPB4− molecules and nano-Zr-CAU-24 may be due to the amplified quenching on the surface of Zr-CAU-24 crystals. Thus, we have presented a simple, cost-saving, robust and sensitive method for the detection of AFB1 with acceptable detection limit and time, which has great potential for the development of innovative sensors for detection of mycotoxins in agriculture and food.

Conflicts of interest

There are no conflicts to declare.