Abstract
The authors describe a fluorescent probe for sensitive and selective determination of quercetin, an indicator for the freshness of drinks. The probe consists of silica ball encapsulated graphitic carbon nitride (g-C3N4) modified with a molecularly imprinted polymer (MIP). It was synthesized via reverse microemulsion. The resulting MIP@g-C3N4 nanocomposite was characterized by fluorescence spectroscopy, transmission electron microscopy, Fourier transform infrared spectroscopy, and X-ray powder diffraction. Quercetin quenches the fluorescence of the MIP@g-C3N4 probe. The effect was used to quantify quercetin in grape juice, tea juice, black tea, and red wine by fluorometry (λexc = 350 nm, λem = 460 nm). Response is linear in the 10–1000 ng mL−1 quercetin concentration range. The detection limit is 2.5 ng mL−1, recoveries range between 90.7 and 94.1%, and relative standard deviations are between 2.1 and 5.5%.
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Introduction
Flavonoids are widely distributed in fruits, vegetables and some drinks [1,2,3]. Quercetin (Fig. S1) is a typical flavonol and can be detected in some daily food such as grape, tea, onion, nuts, berries, cauliflower and cabbage [4]. So it is significant to establish an effective approach for detecting quercetin.
A number of analytical methods are used for quantitative analysis of quercetin, for instance, high-performance liquid chromatography [5], liquid chromatography-mass spectrometry [6], capillary electrophoresis [7], electrochemical sensor [8] and fluorescence spectroscopy [9]. The above analytical methods have acquired good experimental results, but these methods have some disadvantages. For instance, the high-performance liquid chromatography method has a large reagent consumption and long analysis time. The capillary electrophoresis and electrochemical detection sometimes have poor reproducibility. Compared with other detection methods, fluorescence spectroscopy has the advantages of high sensitivity and low analysis cost.
Quantum dots (QDs), as novel fluorescent indicators, have unique optical properties that can be widely used in biomedical and pharmaceutical analysis. At present, a number of metal semiconductor QDs are applied as fluorophores in optical sensing, such as CdS [10], Mn-doped ZnS [11] and CdTe [12]. These metal semiconductor QDs have excellent fluorescence properties. But they have toxic and low selectivity. So how to fabricate benign nanomaterials with good optical properties is an interesting challenge.
In order to solve the problem of high toxicity of traditional metal QDs, some new fluorescent nanomaterials have been discovered, such as graphite carbon nitride (g-C3N4), carbon dots and graphene quantum dots. The synthetic steps of carbon dots and graphene quantum dots are relatively complex and the resulting product contains impurities. Comparatively speaking, g-C3N4 is a promising alternative to other QDs due to their advantages of strong fluorescence, uncomplex preparation process, low toxicity and excellent biocompatibility. G-C3N4, a kind of visible-light-response material similar to graphite, is a two-dimensional planar conjugation structure with unique electronic band [13]. Each layer of g-C3N4 consists of a repeating tri-s-triazine ring packaged together by van der Waals interactions [14, 15]. It has become of interest due to their unique optical properties.
In order to increase the selectivity of QDs, molecular imprinting technique was used. For example, Ren et al. used QDs coated with molecularly imprinted polymer (MIP) as fluorescence probe for detecting cyphenothrin [16]. Zhang et al. have synthesized MIP-g/r-QDs as a ratiometric fluorescent probe to detect melamine [17]. Their methods have achieved good results. It is a promising analytical method that QDs combined with molecularly imprinted technology. The method has attracted more and more attention.
In this work, an eco-friendly fluorescent probe was constructed which based on g-C3N4 combined with molecular imprinting for detecting quercetin. The g-C3N4 as a fluorescent signal is environmentally friendly and uncomplicated in preparation. The fluorescence probe can detect quercetin based on photoinduced electron transfer fluorescence quenching mechanism. Under the optimal conditions, the probe for quercetin assay was validated, and then was successfully applied to drink samples analysis.
Experimental
Materials and reagents
The standard reagent of melamine was purchased from Aladdin (Shanghai, China, http://www.aladdin-e.com). Dihydrate sodium citrate, citric acid monohydrate, 3-aminopropyltriethoxysilane, kaempferol, galangin, myricetin and bisphenol A were bought from Aladdin (Shanghai, China, http://www.aladdin-e.com). TEOS, n-amyl alcohol, ethanol, triton X-100, methanol, ammonium hydroxide, sodium hydroxide were purchased from Kermel (Tianjin, China, http://www.chemreagent.com/). Cyclohexane was purchased from Guangfu (Tianjin, China, http://tjguangfu.company.lookchem.cn). High-purity water was purchased from a Milli-Q water system (Millipore, Billerica, MA, USA, http://www.merckmilliporechina.com). Beverages and red wines were bought from Harbin supermarket. All reagents were analytical grade.
Preparation of the graphitic carbon nitride nanoparticles modified with a molecularly imprinted polymer (MIP@g-C3N4)
The g-C3N4 was synthesized according to the available methods in the literature [18]. The MIP@g-C3N4 composite was synthesized at room temperature via reverse microemulsion. First, 20 mL of cyclohexane, 3.6 mL of Triton X-100, 4.4 mL of n-amyl alcohol and 1.0 mL of distilled water were stirred for 5 min. The g-C3N4 (0.1 g) was added the above solution, then stirring 30 min in room temperature. Second, 200 μL of TEOS and 100 μL of NH3·H2O were added to above reaction solution. The mixture was stirred for 10 h so that the g-C3N4 was successfully encapsulated with silicon. Third, 0.1 g of quercetin (disperse in 20 mL of ethanol) and 250 μL of APTES were added to the system for stiring 1 h. Afterwards, 500 μL of TEOS and 1 mL of NH3·H2O were added in the microemulsion and stirred for 12 h under avoiding light. The MIP@g-C3N4 composite was synthesized, and washed with ethanol and water. Finally, methanol /acetic acid (9:1, v/v) was used to elute template molecule.
The same procedure was used to simultaneously prepare the non-imprinted appended to g-C3N4 (NIP@g-C3N4) without addition of the template quercetin.
Characterization
The Fourier transform infrared spectrum (FT-IR) was received by using FT-IR360 spectrometer (Nicolet, Madison, WI, USA, http://www.chem17.com). The X-ray diffraction (XRD) spectrum was received by using a Shimadzu XRD-600 diffractometer (Kyoto, Japan, https://www.shimadzu.com). Topography was received by using the H7650 transmission electron microscope (TEM) (Hitachi, Japan, http://www.hitachi.com). The ultraviolet spectrum (UV) was received by using TU-1901 spectrometer (PERSEE, Beijing, China, http://www.instrument.com). At the room temperature, fluorescence spectrum was received by using F-4600 fluorescence spectrophotometer (Hitachi, Japan, https://www.antpedia.com). X-ray Photoelectron Spectroscopy (XPS) spectrum (The United States, Minnesota, http://www.phi.com/index.html) was received by using PHI 5700 ESCA System, that the pass energy of wide scan and narrow scan were 187.85 eV and 23.50 eV, respectively. The MIP@g-C3N4 were dissolved in citric acid-sodium citrate buffer by A KQ5200E ultrasonic instrument (Kunshan Instrument, Kunshan, China, http://www.ks-csyq.com).
Fluorometry
By using a 400 nm excitation filter, a fluorescence spectrum was achieved in the wavelength range of 400–700 nm with an excitation wavelength of 350 nm. All measurements were performed under the following parameters: the slit width was 10 nm; the scan speed was 240 nm min−1; and photomultiplier tube voltage was 550 V. Moreover, every sample was repeated measurement three times under the same conditions, the Quartz cell of 1 cm path length was used for fluorescence measurement. The different concentrations of quercetin solutions were mixed with 0.1 mg mL−1 MIP@g-C3N4 solution (1:1, v/v) that adjusted to pH = 3 by citrate buffer (0.1 mol L−1). After the reaction was completed, the fluorescence analysis was carried out.
Analysis of quercetin in real samples
The quercetin content in the beverage and red wine are one of the signs of the quality of related products. Some kinds of juices and red wines from local supermarkets were analyzed for investigating the applicability of the MIP@g-C3N4 method. The red wine samples were diluted 10 times before fruther treatment due to the high content of quercetin. The samples were treated by the following process: MIP@g-C3N4 (0.1 mg mL−1) was dispersed in citric acid-sodium citrate buffer at pH = 3. The samples (10 mL) was mixed with the 0.1 mg mL−1 MIP@g-C3N4 (10 mL). After full shocking for 5 min, centrifuging and discarding the supernatant, the mixture was washed with distilled water (3 mL) to remove impurities for example sugar. Finally, the MIP@g-C3N4 adsorbing quercetin was redispersed in citrate buffer (20 mL) for fluorescence measurement. The fluorescence emission spectra were recorded under a 350 nm excitation wavelength and the fluorescence intensity of the maximum emission peak at 460 nm was used for the quantitative analysis of quercetin. Then the concentrations of quercetin in drink samples will be gained according to the linear equation.
Results and discussion
Choice of materials
Numerous nanomaterials are used as fluorescent probes for trace detection, such as metal QDs, g-C3N4, carbon dots and graphene QDs. The synthesis step of carbon dots is complicated and accompanied by a large amount of impurities [19]. The use of natural graphite or metal catalysts for the synthesis of graphene QDs can result in residual metal impurities (e.g., Fe, Co, and Ni) that are not easily removed [20]. Metal QDs are toxic and not environmentally friendly. In comparison, the synthesis step of g-C3N4 is uncomplex, and the product has high purity [18]. The surface of the g-C3N4 has many amino functional groups, which can further interact with the analyte. Therefore, g-C3N4 was selected as fluorescent component. In this experiment, molecular imprinting technique was also introduced to increase the selectivity of g-C3N4 (Fig. 1).
The emission wavelength of g-C3N4 was 460 nm. Quercetin had a weak peak at an emission wavelength of 530 nm. When quercetin and g-C3N4 were mixed, there was no interference to the experiment.
Characterizations of g-C3N4 and MIP@g-C3N4
As estimated from the TEM images in Fig. 2a, b, the diameter of g-C3N4 is approximately 10 nm. In this study, the bulk g-C3N4 turns into small nanoparticles by ultrasound for 10 h. The role of ultrasound is to destroy van der Waals forces among the layers of g-C3N4. Similar experimental phenomena also have been verified in the previous literature [21]. The diameter of MIP@g-C3N4 is 200–500 nm, and MIP@g-C3N4 have regular spherical shapes.
The characterization XRD patterns of g-C3N4 and MIP@g-C3N4 are presented in Fig. 2c, d. Figure 2c is consistent with the previous reports on g-C3N4 [22]. The strong shoulder peak around 27.4° represent the characteristic interplanar stacking peak of conjugated aromatic systems, index for the (002) peak of g-C3N4. Another the weak diffraction peak around 13.07° derives from an in-planar structural packing motif, index the (100) peak of g-C3N4. MIP@g-C3N4 appears widely peaks in Fig. 2d, it may be caused by wrapping the blotting membrane.
The chemical structures and composition of g-C3N4 and MIP@g-C3N4 are further investigated by XPS measurement. The obvious peaks of C, N and O can be seen in Fig. 2e. The binding energy peaks at 286.5, 402.1 and 534.9 eV correspond to C1s, N1 s and O1s, respectively. The XPS of the composites are shown in Fig. 2f, there are five obvious peaks can be clearly observed, their peaks appear on 287.3 (C1s), 535.6 (O1s), 401.8 (N1 s), 104.8 (Si2p), 157.2 (Si2s).
FT-IR (Fig. 2g, h) spectroscopy is acquired via a Fourier transform infrared spectrometer with the KBr pellet technique. The typical founctional group of g-C3N4 is shown in Fig. 2g. Distinct bands can be observed between 1200 and 1680 cm−1 and near 815 cm−1, it is the result of the organic molecules containing three azine ring structures. The absorption bands appear on 1570 and 1630 cm−1 are attributed to C=N stretching, the bands present to 1250, 1320 and 1410 cm−1 are consistent with aromatic C-N stretching, the terminal amino groups broad band appear in the 3000–3500 cm−1, for instance, -NH2 or = NH groups of g-C3N4. The sharp band of the bending vibration of characteristics of triazine rings appears in 815 cm−1. The FT-IR spectroscopy of MIP@g-C3N4 in Fig. 2h, the characteristic peak at 3270 cm−1 is corresponding to the stretching vibration of the N-H and O-H bonds. A wide peak located at 1060 cm−1 is corresponding to Si-O stretching vibration. The C=N stretching vibrations are observed at 1630 and 1570 cm−1, respectively. The stretching vibration of Si-H (2360 cm−1) and -CH3 of APTES (2920 cm−1), indicated MIP is successfully combined with g-C3N4.
Optimization of method
The following parameters were optimized: (a) Sample pH value; (b) Reaction time (c) Concentration of MIP@g-C3N4. Respective data and Figures are given in the Electronic Supporting Material in Fig. S2, Fig. S3 and Fig. S4. In short, the following experimental conditions were found to give best results: (a) Best sample pH value: pH = 3; (b) Optimal reaction time: 5 min; (c) Optimal concentration of MIP@g-C3N4: 0.1 mg mL−1.
The response of MIP@g-C3N4 and NIP@g-C3N4 to quercetin
The effects of different concentrations of quercetin on imprinted and nonimprinted probes (MIP@g-C3N4 and NIP@g-C3N4) is shown in Figure 3. It indicates that the fluorescenceof MIP@g-C3N4 and NIP@g-C3N4 decreased as the concentration of quercetin increased. The specific interactions between quercetin and MIP@g-C3N4 are the main reason of fluorescence quenching. It is obvious that the decline of the fluorescent intensity of the MIP@g-C3N4 is larger than that of NIP@g-C3N4 after adding the same concentration of quercetin. The different fluorescence quenching intensity can be explained by the Stern−Volmer [23]:
In the equation, F0 is the initial fluorescence of MIP@g-C3N4 without quercetin, F is the fluorescence of MIP@g-C3N4 after adding quercetin, KSV is the Stern−Volmer constant, and [Q] is the different quercetin concentrations added. Quercetin with a concentration range of 2–2000 ng mL−1 was tested. In the experiment, when the concentration of quercetin is less than 10 ng mL−1, the fluorescence quenching is too small and the repeatability is poor. When the concentration of quercetin is higher than 1000 ng mL−1, the linear plot greatly deviates. Quercetin shows a good linear relationship in a range of 10–1000 ng mL−1. As shown in Fig. S5, fluorescence changes of MIP@g-C3N4 after adding different quercetin concentrations can be confirmed a good linear correlation between F0 /F and quercetin concentration in the range of F0 /F = 0.000882[Q] + 1.00229, the correlation coefficient (R2) was 0.9994, the limit of detection (LOD) is the ratio of 3σ to K, where σ is the standard deviation of blank measurements (n = 11) and K is the slope of the calibration plot. The LOD of this method is 2.5 ng mL−1. The imprinting factor (IF) is also calculated, through defined by the ratio of KSV, MIP to KSV, NIP (IF = 5.04). The above results are shown wide linear range and low detection limit of the prepared fluorescence probe based on MIP@g-C3N4.
Selective responding on MIP@g-C3N4
To test the selectivity of the MIP@g-C3N4 prepared by our method, some substances were measured, for instance, kaempferol, galangin, myricetin as the similar structures analogue, and bisphenol A as the reference compound that also contained two benzene ring and hydroxy. Their chemical structures are shown in Fig. S6. The results of Fig. S7 indicate that the MIP@g-C3N4 displays the highest specific recognition ability for quercetin compare with other four substances. On account of the structures of four substances are different with quercetin, when the template molecule is removed, cavity sites that match quercetin are left, these analogues can’t retain in the recognition cavities of MIP@g-C3N4. So, quercetin can be specifically recognized by MIP@g-C3N4. The effect of interfering substances in the solution is investigated, and the results shows that within a certain concentration range is immune to interference (Table. S1).
Reuse is an important factor for fluorescent MIP. Fig. S8 shows the MIP@g-C3N4 can be used at least five times.
Fluorescence quenching mechanism
Fluorescence is reduced by various molecular interactions, excited-state reactions, molecular rearrangments, energy transfer, formation of ground state complexes, and collosional quenching, which is called fluorescence quenching. The mechanism of action of MIP@g-C3N4 and quercetin can be listed as follows:
-
(1)
There are some ways to cause fluorescence quenching such as fluorescence resonance energy transfer (FRET), photoinduced electron transfer (PET) and inner filter effect (IFE). Generally, in the FRET or IFE process, there should be a good spectral overlap between the absorption spectrum of quercetin and the emission spectrum of MIP@g-C3N4. It can be seen from Fig. S9, the peaks of the two substances do not overlap, which proves that their quenching mechanism are not FRET or IFE.
-
(2)
Fluorescence quenching usually has static quenching and dynamic quenching, which can be distinguished by measuring the relationship between quenching constant and temperature. The static quenching is caused by the formation of a non-luminescent ground state complex between the fluorescent molecule and the quencher. Therefore, when the temperature increases, the complex becomes unstable, resulting in the decreased of the quenching constant. The dynamic quenching is caused by collisions between quenchers and fluorophores. When the temperature rises, the collision is aggravated, leading to the quenching constant increases. As displays in Fig. S10, as the temperature increases, the quenching constant decreases. This imply that the reaction mechanism was static quenching [24].
-
(3)
Fluorescence quenching can also be discussed from molecular interactions (for electrostatic force, π-π, and hydrogen bonding interactions). The quercetin is added into the MIP@g-C3N4 solution, the molecular interactions between quercetin and MIP@g-C3N4 are occurred, such as electrostatic force and π-interactions, the interaction of quercetin and MIP@g-C3N4 is researched by using the Sterm-Volmer equation in different temperatures. The thermodynamic equation as follows [25]:
$$ \varDelta {G}^O=- RT\ln K\mathrm{sv} $$(2)$$ \varDelta {G}^O=\varDelta H- T\varDelta S $$(3)
By rearranging Eqs. 2 and 3, KSV can also be calculated:
Among them, ∆Go is free enthalpy change, ∆Ho is enthalpy change, and ∆So is entropy change. The thermodynamic equations can be used to calculate these values. The known quantities in the equation are temperature (quenching temperature in kelvin), the universal gas constant (R = 8.314 J mol−1 K−1), and equilibrium constant at the corresponding temperature. In Table 1, we can see the values of ∆Ho = −15.45 kJ mol−1 and ∆So = 52 J mol−1 K−1. These data show that the interaction between the two substances is electrostatic force [24]. When a large amount of cross-linking monomer is used in the presence of the template, special recognition pores are formed due to form hydrogen bonds between the amino group of APTES and the hydroxyl group of quercetin. Quercetin can be specifically identified by special pores.
Analytical application
To validate the practical utility of the fluorescent probe, three beverages samples and four red wines samples were selected for quantitative determination of quercetin. It can be seen that quercetin is detected in the green grape juice, black tea and four red wine samples in Table 2. The concentration of quercetin in the green grape juice is 18.0 ng mL−1 and black tea is 15.5 ng mL−1. four red wine samples’ concentration of quercetin are 3.0, 2.1, 2.7, 2.9 μg mL−1, respectively. Quercetin (10 ng mL−1 and 2000 ng mL−1) is added to beverages and red wines samples, respectively. The recoveries are 90.7–94.1% with relative standard deviations of 2.1–5.5%. The results indicate that MIP@g-C3N4 possesses good accuracy in real sample analysis.
Compared with the traditional method of detecting quercetin in Table 3, fluorescence analysis has many advantages, such as low analysis cost and short sample analysis time. Some HPLC detection methods are lower than our detection limit, but the instrument has some disadvantages of wasting reagents and requiring a long analysis time. At the same time, the specificity of detection is increased by using molecularly imprinted techniques.
The fluorescence analysis method has limitations, such as, the need for working in the UV (λexc = 350 nm) makes the probe prone to interferences by biomatter which always display strong background UV absorption and fluorescence. In addition, the UV light used for excitation may be screened off by UV absorbing biomolecules. In the future, we will find ways to solve these problems.
Conclusion
In conclusion, an effective fluorescence probe method is presented by using g-C3N4 combined with MIP and used to determine quercetin in beverages and red wines. The quercetin content is successfully detected in green grape juice, black tea and all kinds of red wines. Fluorescence spectroscopy has the advantages of low analysis cost and short sample analysis time. Compared with metal QDs, g-C3N4 has superior physicochemical and photochemical stabilities, nontoxicity, large surface area, plentiful material source and inexpensive to synthesize. In the future, we will devote to use the novel fluorescence probe to detect more food samples.
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Acknowledgments
This project was funded by the Fundamental Research Funds for the Central Universities (No. 2572017 EB08), Harbin science and technology innovation talent research special funds (2016RAQXJ151) and Natural Science Foundation of Heilongjiang Province (JJ2018ZR0081).
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Xu, S., Chen, L. & Ma, L. Fluorometric determination of quercetin by using graphitic carbon nitride nanoparticles modified with a molecularly imprinted polymer. Microchim Acta 185, 492 (2018). https://doi.org/10.1007/s00604-018-3016-y
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DOI: https://doi.org/10.1007/s00604-018-3016-y