1. Introduction
Butyl paraben (BP) has been widely used in humanity’s daily life. As the antimicrobial additive, it can be found in cosmetics, pharmaceuticals, as well as food products [1,2,3]. In consideration of the estrogenic effects caused by parabens, the application of parabens has aroused the increasing concerns on the latent hazards to health and environment [4,5]. It has been demonstrated that the chronic exposure to BP can cause breast cancer and breast tumors, as well as the impairment of the sperm quality and fecundity [6,7,8,9,10]. The European Union and China have stipulated the limit for BP at concentrations up to 0.14% (g/g) as the preservative in cosmetic products, including lotion, toilet water, face creams and rinse-off products, and so on [11].
Currently, some feasible methods have been applied for the BP detection, e.g., gas chromatography–mass spectrometry method (GC-MS) [12], high performance liquid chromatography (HPLC) [13], capillary electrophoresis (CE) [14], liquid chromatography -mass spectrometry (LC-MS) [15], and high-performance-liquid chromatography-photodiode array analysis (HPLC-PDA) [16,17] etc. Although these methods are sensitive and have wide measurement ranges, most of them need the expensive instruments, complicated sample preconcentration steps, as well as the experienced technicians, which are challenges for the real-time and rapid detection on the spot. Since the international trade is playing an increasingly important role, it is necessary to develop a sensor for the rapid spot screen of BP in the complicated samples. Especially, the portable visual sensor will be more welcome, because it can provide the intuitive and reasonable signal on-site.
The molecular imprinting polymers (MIPs) was proposed by Wulff in 1972. In the technique, the monomer(s) are frozen in polymeric structures with the presence of the template molecule [18,19,20]. After the removal of template molecule, the cavities complementary to the template in shape and binding sites are formed. Except specific recognition, the superiorities of the MIPs, such as easy preparation, physical robustness, low-cost, and thermal stability have resulted in increased researcher attraction [19,20,21]. MIPs have been widely employed in various areas, such as chromatographic separation, catalysis, and sensor platforms. Owing to the intuitiveness, different kind of colorimetric detection platforms have been developed by coupling with MIPs. For example, the MIP-based fluorescent sensor, enzyme assisted colorimetric method, and surface-enhanced Raman scattering (SERS), have been widely applied in clinic detection, food analysis, and environmental monitoring [22,23,24,25].
The photonic crystal (PC) materials have drawn increasing interests for endowing the MIPs with the self-reporting properties. PC is composed of several kinds of the regular shaped materials which have different dielectric constants and are periodically arranged in the PC skeleton [26,27,28]. Owing to the existence of photonic band gap in the PCs, only the light with certain wavelengths can be reflected from their surfaces, resulting in the characteristic structural colors of the PCs [29,30,31]. Any slight change of the lattice constant of the PC skeleton caused by the stimuli, such as the acidity, temperature, humidity, ionic strength as well as the concentration/speciation variations of the chemicals, will result in the shift of the Bragg reflection peak. And the shift of the Bragg reflection peak will consequently make the PC display the different colors according to the migration degree of the Bragg reflection peak [32]. The composite of PCs and MIPs, known as the MIPC, can integrate the advantages of both [33,34,35]. With the ability to transfer the molecular recognition process specifically into the spectral signals, MIPCs can be used to sense the targeted molecules visually, without needing the complex label techniques and expensive instruments. The MIPCs have been applied successfully in many fields such as poison analysis, clinical diagnosis, virus detection, customs security, and other fields [36,37,38,39,40].
In the present work, an MIPC sensor has been fabricated for the visual detection of BP in toner sample without sample pre-treatment. It can sense the trace BP with high sensitivity. Owing to the obvious regular color changes of MIPCs during the molecular recognition process, a “color guide” has been fabricated. The content of BPs in toner samples can be estimated by comparing the actual colors of the MIPCs with the “color guide”. Furthermore, the accurate concentration of BP can be obtained through the optical fiber spectrometer, since the shift value (∆λ) of the Bragg diffraction peak is positively correlated with the BP concentration. The factors that affect the analytical performance have been optimized and assessed.
2. Materials and Methods
2.1. Materials
Butyl paraben (BP, CAS 94-26-8), methyl paraben (MP, CAS 99-76-3), tetraethyl orthosilicate (TEOS, CAS 78-10-4), procaine (CAS 51-05-8), and benzocaine (CAS 94-09-7) were purchased from Aladdin (Shanghai, China). Acrylic acid (AA, CAS 79-10-7), 2, 2-Azobisisobutyronitrile (AIBN, CAS 78-67-1), and methacrylic acid (MAA, CAS 79-41-4) were obtained from Tianjin Damao chemical reagent factory (Tianjin, China). Hydrochloric acid (CAS 7647-01-0), absolute ethyl alcohol (CAS 64-17-5), glacial acetic acid (CAS 64-19-7), concentrated sulfuric acid (H2SO4, 98%, CAS 7664-93-9), and 25% ammonia water (NH3·H2O, CAS 1336-21-6) were purchased from Tianjin Zhiyuan chemical reagent Co., Ltd (Tianjin, China). Further, 30% hydrogen peroxide (CAS 7722-84-1) and 45% hydrofluoric acid (CAS 7664-39-3) were purchased from the Guangzhou chemical reagent factory (Guangzhou, China). Ethylene dimethacrylate (EDMA, CAS 97-90-5) was purchased from Alfa Aesar chemical Co., Ltd (Shanghai, China). Hydroxyisobutyric acid (CAS 594-61-6) was purchased from Shanghai Renxi technology Co., Ltd (Shanghai, China). All of the above chemicals were of analytical grade. Ultrapure water (18.2 MΩ·cm) was used in all solutions. The transparent soda–lime glass (Na2O·CaO·6SiO2) slides (50 × 9 × 1 mm3) were purchased from Jiangsu swift boat glass and plastic Co., Ltd (Yancheng, China). Additionally, polymethyl methacrylate (PMMA) slides (50 × 12 × 1.2 mm3) were used directly without any treatment. The PMMA slides were purchased from Yali organic process factory (Guangzhou, China).
2.2. Apparatus
The silica colloidal microspheres were collected by a centrifuging apparatus (TG18-WS, Hunan Xiangli instrument Co., Ltd. Changsha, China). Maya 2000 PRO fiber optic spectrometer (Ocean Optics, Orlando, FL, USA) with haloid lamp cold-light source (LS-3000, 360–2000 nm) was used to record the diffraction spectra. The self-assembly of the SiO2 based PC template was conducted by using a constant temperature and humidity chamber (WS-01Y, Hengfeng medical equipment Co. LTD, Huangshi, China). The JSM7001F field emission scanning electron microscope (Hitachi, Tokyo, Japan) was used for getting the SEM images. The HPLC analysis was performed with Shimadzu LC-20 AD with DAD detector (SPDM20A) (Tokyo, Japan).
2.3. Experimental Methods
2.3.1. Preparation and Self-Assembly of Silica Colloidal Microspheres
Anhydrous ethanol (16.25 mL), deionized water (24.75 mL), and aqueous ammonia (25%, 6.75 mL) were mixed in a conical flask and stirred at 1100 r/min for 5 min at room temperature. Next, 45.5 mL anhydrous ethanol and 6.75 mL tetraethyl orthosilicate (TEOS) were added. After stirring at 1100 r/min for 1 min, the speed was reset at 400 r/min for 2 h. Then, the resulted SiO2 particles were collected by centrifugation and rinsed five times with anhydrous ethanol. Subsequently, these silica particles were dispersed in anhydrous ethanol, and stored in vials in different weight concentration separately.
Basing on the SiO2, the PC films were fabricated on glass substrates through vertical deposition. The detailed procedures are as follows: firstly, the glass substrates were soaked in H2SO4/H2O2 (7/3, v/v) solution for 12 h to clean the glass plates and make them become hydrophilic. After being rinsed with ultrasonic water bath for 1 h, they were immersed vertically in the glass bottles which contained appropriate amount of SiO2 colloidal solution (8 mg·mL−1). Then, the bottles were putted in an incubator with temperature at 30 °C and humidity at 40%. With the evaporation of the solution, the SiO2 was self-assembled uniformly on the glass plate, resulting in the PC template with obvious structure color.
2.3.2. Fabrication of the Molecularly Imprinted Photonic Crystal (MIPC)
The fabrication approach (Scheme 1) is as following: First, 4 mmol AA and 1 mmol BP were dissolved with water/methanol (3:5, v/v). After storing overnight at 4 °C, EDMA (1 mmol) and AIBN (0.003 g) were added in the mixture. The resulted precursor solution was then degassed with nitrogen for several minutes to remove oxygen. In the meantime, a “sandwich” was prepared by sandwiching the PC template between two PMMA slides. Then, 10 µL precursor liquid was injected into the “sandwich” gaps gently. After that, the “sandwich” was put in the airtight container (60 °C) for 6 h for MIP polymerization.
Next, the “sandwich” was immersed in 1% hydrofluoric acid until the glass and PMMA slides were separated from each other. The obtained PMMA slides were then immersed in 4% hydrofluoric acid for 5 min to remove the SiO2 completely. This way, the molecular imprinted film with the inverse opal structure was formed on the PMMA slides. Then, the PMMA slides were subjected to the elution repeatedly with a mixture of methanol/water/acetic acid/hydrochloric acid (3.5:5.6:0.5:0.4, v/v/v/v) until no BP was detected in the eluent at 258 nm by using an UV spectrometer (Jinghua Technology Instrument Co. LTD, Shanghai, China).
2.4. Investigation of the Analytical Performance of the MIPCs
To investigate the effect of sample matrix on the sensing performance, different amount of methanol was mixed in the sample matrix with the final content changing from 10% to 30% (v/v). The corresponding diffraction spectra were recorded with fiber optic spectrometer.
To explore the response time and the reusability of MIPCs, the same piece of MIPC film was subjected to the adsorption and elution repeatedly, and the corresponding diffraction spectra were recorded.
Benzocaine, procaine and methyl paraben solution with concentrations ranging from 0.0001 to 0.003 mol·L−1 were prepared. The responses of the MIPC films to these structural analogues of BP were tested and compared to investigate the molecular recognition properties of the MIPCs.
2.5. The Application of MIPCs
A band of alcohol-free rose-water toner, which belongs to the skincare product, was bought from the supermarket. For the toner used in this work, the main ingredients are water, rose oil, nicotinamide and seaweed extract. It can be sprayed on the face for making the skin soft. Since it is non-viscous and almost transparent liquid, so no sample pretreatment procedures have been conducted. Before detection, some methanol was added in the toner to make methanol content achieve 20%. The MIPC film was dipped into the sample solution for 15 min, then the Bragg diffraction of the MIPC film was recorded by the optical fiber spectrometer, and the color change of the MIPC was recorded by a camera. The sensing performance of MIPC film was evaluated based on the peak shifts of the Bragg diffraction in response to the BP in real sample solution.
3. Results
Scheme 1 describes the overall procedures concerning the fabrication and application of BP MIPCs: (A) fabrication of PC template by self-assembly of silicon spheres; (B) injection of MIP precursor solution on the PC template; (C) thermal polymerization of BP imprinted membrane; (D) preparation of inverse opal MIPC via eliminating of the silica spheres and BP molecules; and (E) the utilization of MIPC in BP monitoring. Each step has been optimized in order to get the MIPCs with excellent properties, such as the acute color indication, fast response, high selectivity, and good reusability.
3.1. The Fabrication of PC Template and MIPC Sensor
Before the fabrication of a PC template, it is important to treat the glass plate with H2SO4/H2O2 solution to make the glass plate hydrophilic and clean. On this kind of glass plate, the SiO2 colloidal solution can be driven evenly to climb along the glass plate by the capillary action. Then, with the evaporation of the solvent, the SiO2 can be orderly arranged on the glass plate, and form the PC template with good quality.
Since the optical performance of PC is determined by the mono-dispersity and particle size of SiO2, the procedures for the fabrication of SiO2 should be optimized first. The Stöber method was modified to prepare the SiO2 microspheres. The purity of TEOS, the proportion of ammonia, ethanol, and TEOS, and even the formula for mixing TEOS with ammonia have been found to affect the shape, particle size, and mono-dispersity of silicon spheres in the previous work [40,41]. The proportion of TEOS showed positive effect on the particle size of the silicon sphere. It can be explained as the following: the more TEOS is used, the more silicic acid will be released through the hydrolyzation of TEOS. And the particle size of silica will increase accordingly owing to the subsequent condensation reaction of silicic acid. By changing the synthesis conditions, SiO2 particles with different size were produced. Further, the corresponding PCs were fabricated based on these SiO2 particles. The wavelength of the Bragg diffraction peaks (λmax) of PC is found positively correlated with the SiO2 particle size (d) and shows a linear correlation (λmax = 2.32d) with R2 as 0.95481 in the present work (Figure S1).
To achieve the naked-eye detection, the wavelength of the diffraction peaks of MIPCs needs to vary evidently in the different visible light regions (380–780 nm) during the sample responding. The MIPCs with structural color between green and yellow are preferable in the present work. As this kind of MIPCs is expected to produce the obvious visual color changes, no matter the color will red shift or blue shift in response to the target analytes.
In order to obtain the ideal MIPCs, the mono-dispersed SiO2 with average particle size of 365 nm and polydispersity index of 0.019 was selected to fabricate the PCs. The resulted PCs can display red color with the λmax of the Bragg diffraction at 750 nm (Figure 1a). As shown in the SEM picture (Figure 1a), the monodispersed silica nanoparticles are organized uniformly on the glass plate, producing the face-centered cubic (FCC) lattice. As there are many silicon spheres arranged on the surface, this morphology is vividly called “opal structure”.
After the polymerization of the precursor on the PC template, MIPs can form in the gap of silicon spheres. Then, through treating with HF, the SiO2 microspheres can be dissolved, resulting in the holes at the original position of these SiO2 microspheres in the MIP film as shown in Figure 1b. This kind of morphology is consequently called “inverse opal structure”. By this way, the shape and the arrangement of the SiO2 microspheres can be imprinted into the MIP film. Since the holes can keep the FCC arrangement, the MIP film can display the opal characteristics of the original PC lattice. Consequently, the MIP films are called MIPC.
Since the diameter of the hole in MIPCs is smaller than the original SiO2 sphere owing to the contraction, the corresponding MIPCs will becomes orange with λmax blue-moving to 646 nm. After further elution of the template BP, the molecular recognition sites can be formed on the MIPC film. Owing to the further reduction of diameter of the hole (Figure 1c), the λmax of MIPCs will approach to the boundary between green and yellow, which is 565 nm. It can be seen from Figure 1, even after removing the SiO2 microspheres and the imprinted templates, the inverse opal structure of the resulted MIPC still sustains the FCC arrangement. The periodic variation of refractive index of these porous films can give rise to Bragg optical properties.
The MIPCs accommodate interconnected macropore array, to which nanocavities complementary to BP in shape and binding sites are distributed. The presence of macropores in MIPCs not only provide more interaction sites but also decrease the molecular transport resistance, which is favorable for improving the MIPCs’ sensing efficiency. The obtained MIPCs not only have the ideal structural color (between green and yellow), which is conducive to change color in the visible light range, but have the stable and regular microporous structure. These features are helpful for achieving the evident color change in response to the slight shrinkage/swell of the cellular structure of the MIPC during sample monitoring. Thus, in the present study, the SiO2 with particle size of 365 nm was chosen for the fabrication of PCs and MIPCs.
It is known the recognition sites of MIPCs are resulted from the interactions between the functional monomers and template molecules during the polymerization. The rigidity of the MIPCs, which determines the swell/shrinkage properties of MIPCs, mainly depends on the dosage of the cross-linker used.
To obtain MIPCs with a satisfactory physical and chemical performance, the formula of precursor solution has been optimized in the present work. The insufficient functional monomer will cause the deficient binding with template molecules, but the overdose of functional monomer will produce a large amount of nonspecific binding sites through the interaction between the functional monomers during the polymerization. In order to obtain a smart MIPC sensor to convert the molecular recognition process acutely into a visible color change, the network skeleton should have good elasticity and durability, besides the molecular recognition specificity. It should be able to expand and shrink reversibly. Thus, the amount of MAA and EDMA has been investigated. Results (Figure 2a) indicate that the satisfying sensing performance can be obtained when the molar ratio of BP/AA/EDMA is 1:4:1. Thus, this condition has been used for producing the MIPCs in the present work.
Selecting a proper porogen is also key in order to improve the specific recognition property of MIPCs. It is known that the variation of polarity between the sample solution and the porogen that has been used to synthesize the MIPs will affect the polymer swelling or shrinking, and had a profound effect on the polymer recognition performance [42]. The interaction between the template molecule and the MIPs is governed by different molecular forces in organic solvents and in aqueous sample solution. The interactions that are predominant in the polar environment are mainly the hydrophobic interactions and ionic bonds [43]. Since this sensor are expected to be applied in aqueous sample solution, not only should the porogen dissolve BP, functional monomers, and cross-linkers completely, but provide the polarity approximating the real sample solution as closely as possible. Pure methanol was used as the porogen in the preliminary experiment. However, the resulted MIPCs can only display the weak response to BP. In addition, they will crack in the regeneration step, thus shortening the service time. Results (Figure 2b) indicate that the addition of a proper amount of water in the precursor solution will be helpful to improve the signal (Δλ) of the corresponding MIPCs in response to the BP sample. Through adjusting the methanol content in the precursor solution, it is found that the response sensitivity of the obtained MIPCs will decrease with the increase of methanol in precursor solution. In the experimental range, when the porogen contains 50 µL methanol and 30 µL water, the resulted MIPC can display the largest Δλ value. In order to avoid the further interruption of the hydrogen bond between BP and the functional monomers, the amount of water was not increased continually.
Similar porogen in preparation of MIPs has been used in literature [43]. In that work, the polymerization was conducted in the mixture of methanol/water (4:1, v/v). For the aqueous sample, the MIPs prepared in the mixed solvent has shown much better recognition properties than in the “classical” way in the presence of nonpolar solvents.
3.2. Analytical Performance for Sensing BPs
3.2.1. Effect of the Methanol Content in the Assayed Sample Solution
In the pure water samples, the MIPCs can only display the obscure peak-shift, because the hydrogen bond between BPs and the binding sites may be inhibited in the strong polar solution. Since methanol was used in the porogen to prepare the MIPCs in this work, the effect of methanol in the sample matrix on the sensing properties has been studied. Results show (Figure 3a) that the sensing signal can increase gradually with the addition of methanol. The shift (Δλ) of the diffraction peak can approach the maximum value when 20% (v/v) methanol is included in the sample matrix. Continue to increase methanol, the Δλ will decrease instead. Further, in pure methanol, the sensor shows no response at all because of the too high solubility of BPs in methanol. That is, the adsorption performance of MIPCs for BPs is poor when methanol content is high in the sample solution. Attributed to the competitive distribution of BPs between MIPC and solvent phase, the optimal concentration of methanol is 20% (v/v) in the sample solution. When the same MIPC is inserted in blank samples with methanol content changing from 0 to 30%, no change can be found for the Bragg diffraction.
3.2.2. The Effect of pH on the Performance of MIPC
The effect of pH on the performance of MIPC has been studied in 0.001 mol·L−1 BP solution by using the same piece of MIPC film. The phosphate buffer (10 mM) was used to control the pH in the present work. From Figure 3b, it can be seen that the shift value (Δλ) of the Bragg diffraction peak increases gradually as pH increases from 3 to 7, owing to the synergies of the hydrogen bond and the structural complementarity effect between BP and MIPC. However, when the pH is increased over 8, the Δλ of the diffraction peak of the MIPC tends to drop sharply. When pH value is greater than the pKa values of BP (8.41) and acrylic acid (4.26), owing to the acid dissociation effect, the COOH groups on the MIPC skeleton will turn into –COO- completely and the phenolic -−OH of BP will also become the negatively charged form. Thus, the hydrogen bond force between MIPC and BP will be weakened, leading to the decrease of the adsorption capacity for BP. Consequently, the Δλ of the diffraction peak of the MIPC has been found to decrease with the increase of pH in alkaline solution. Hence, the MIPCs is suitable to be used in the solution with pH 5–8.
3.2.3. The Effect of Temperature on the Performance of MIPCs
To investigate the effect of temperature on the response properties of MIPC membrane, the same piece of MIPC was operated in 0.001 mol·L−1 BP solution with the temperature ranging from 10 °C to 60 °C. It is found that the temperature between 10 °C and 35 °C can exert little influence on the performance of MIPCs (Figure 3c). However, when the temperature is over 35 °C, the peak shift (Δλ) of MIPCs in response to BPs will decrease gradually. When the temperature is higher than 60 °C, the Δλ approaches to zero, which means the well-aligned inverse opal structure can be demolished by the elevated temperature. Therefore, the MIPC prepared in this experiment is suitable for the practical application between 10 °C and 35 °C.
3.2.4. The Analytical Performance of MIPCs to BP
In BP solution, the analytes can be driven into the MIPC gel to combine with the imprinted binding sites by the concentration difference between the inside and outside the MIPC membrane. Owing to the augment of the ion strength and the swelling of the cavity of the MIPCs, the lattice constant of the PC skeleton will vary considerably along with the shifts of the Bragg diffraction peak. Results reveal that the Bragg diffraction peak of MIPC will red shift gradually with the increases of the soaking time in the sample solution. Then, the Δλmax can be achieved when the soaking time approaches 15 min. So, the analytical performance of the MIPCs were evaluated by immersing the same piece of MIPC film into BP solution with different concentration for 15 min. As shown in Figure 4, the wavelength of the Bragg diffraction can increase gradually with the increase of BP concentration. The peak shift (∆λ) is proportional to the concentration of BPs in the range of 0.1–3.0 mmol·L−1, and the detection limit is 0. 022 mmol·L−1 based on three times the ratio of signal/noise.
In addition to using the calibration curves between ∆λ and the concentration of BP for the quantitation of BP, in the present work, the color changes of the MIPC can also be used to estimate the concentration of the target analytes. In the blank solution the structure color of the MIPC is green. Along with the increase of the BP concentration, the film can display the colors changes regularly from the original green to yellow, and then to red. The pattern of color change can be used as the standard “color guide”. Through comparing the actual color of MIPC in the sample solution with the “color guide”, we can judge the presence of BP and estimate the change of BP concentration with the naked eyes, except by using the optical fiber spectrum.
3.2.5. The Selectivity of MIPCs Film to BP
As a sensor, the high selectivity is crucial to eliminate the interferences caused by the possible structural analogues. With the similar structure (Figure 5a) to BP, benzocaine, procaine, and methyl paraben (MP) were used to investigate the selectivity of the developed MIPCs. As shown in Figure 5, the response of the MIPC to BP is much stronger than the interferences, which means the MIPCs can recognize BP against these structure analogues.
It is known that the signal intensity of MIPC is related to the extent to which the lattice parameters of the PC skeleton can change during the response to analytes. Although methyl paraben is expected to nest in the cavity of the MIPCs easier owing to the smaller molecular size, it cannot occupy efficiently the cavity that is designed for the BP with bigger size. The insufficient swelling of the cavity cannot result in the obvious change of the lattice parameters of the PC skeleton. Thus, the response of MIPC to methyl paraben is much poorer than BP (Figure 5b).
Besides methyl paraben, other structure analogues such as benzocaine and procaine have been selected as the interferents in order to further investigate whether the anilne –NH2 group will cause interference. From Figure 5a, it can be seen that benzocaine and procaine have similar structures with paraben. The main difference is that the phenolic –OH is replaced with anilne –NH2. The selectivity experiment was conducted in the neutral solution (pH 7). In this solution, the –COOH exist mainly as the negative form, so the acid-base interaction between –COOH and anilne –NH2 can be ignored. Owing to the imprinting effect and the stronger hydrogen bond interaction between MIPC skeleton and BP, the response of the MIPC to BP is much stronger than benzocaine and procaine.
Given the outcome procured, it is distinct that the specific recognition sites have been fabricated in the lattice structure of the MIPC films. The MIPC can recognize BP against those with a similar structure.
Under the same conditions, non-imprinted photonic crystals (NIPCs) (Figure 5c) can only show the weak response to all the tested chemicals, and cannot differentiate BP from the interferences. It is demonstrated the imprinting technology has indeed played a positive role in the improvement of the selectivity and adsorption capacity of the PC sensors.
3.2.6. The Reusability of MIPCs Film
The reusability is an important indicator for evaluating a sensor. In order to regenerate the MIPCs efficiently without destroying the sensing film, the formula of the eluting solution has been optimized. The mixtures of methanol and acetic acid by 9:1 or 8:2 (v/v) have been commonly used to remove the template molecules in literature [39,44,45]. However, these kinds of elution solution showed damaging effects on the MIPCs. After repeated elution with the above solution, the MIPCs will crack, and the intensity of Bragg diffraction peak will decrease obviously and even disappear eventually.
After optimization, the mixture of methanol, water, acetic acid, and HCl with volume ratio as 3.5:5.5:0.5:0.5 was selected as the eluent in the subsequent experiment. With this eluent, the MIPCs can be regenerated successfully and exhibit a satisfying performance in sample detection. As is shown in Figure 6, after seven cycles of adsorption and elution, the diffraction peak shift of MIPCs can exhibit good repeatability with RSD below 5%, which indicates that the FCC lattice of MIPCs can be sustained after the repeated elution with the eluent.
4. Application
The European Union and China have stipulated the limit for BP in all cosmetic products, such as o/w lotion, toilet water, face creams, and rinse-off products, at concentrations up to 0.14% (g/g) [11]. As to the toner sample used in the present work, the main ingredient is water. Assuming the density of the toner is 1 g · L−1, the concentration limit of 0.14% (g/g) can be estimated to be 7.2 × 10−3 mol · L−1 according to the molecular weight of BP. Since the detection limit of the developed method is 325 times lower than the controlled value, the method is sensitive enough to be used for the detection of BPs in real samples. The lotion sample was purchased from the supermarket. No BP was found in the sample by using HPLC. Then the sample was divided into the control group and the spiked group. In the spiked group, 0.0015 mol · L−1 BP was added. As shown in Figure 7, neither the color or the diffraction spectrum of the MIPC changes in the control lotion sample. However, in the spiked lotion sample, a significant peak shift can be found along with the obvious color changing from green to orange for the same MIPC film. Based on the average peak shift value (∆λ) of 26.1 nm (n = 5), the BP concentration in the spiked sample is calculated to be 0.0016 mol · L−1 by using the linear regression equation of the MIPC film. In comparison with the spiked value, the standard addition recovery is indicated to be 107% for the real sample. In addition, though comparing the standard “color guide” with the actual color of MIPC film in the spiked sample solution, the concentration of BP can also be estimated to be about 0.0015 mol · L−1. Results demonstrate that the developed MIPC can be used as the credible visual sensor to realize the rapid screening and quality estimation for BP in the real samples. Therefore, the visual sensor could become a rapid, reliable, and effective supplement of the optic fiber method in toner samples evaluation.
5. Conclusions
A smart visual sensor based on MIPC was developed for the detection of BP in toner samples. In addition to its portability and good reusability, it could provide the intuitive visual signal in response to BP. Through comparing with the “color guide”, the content of BPs was estimated rapidly with the naked eye. In addition, the Bragg diffraction spectrum of the MIPC senor red shifted linearly with the increase of the concentration of BPs in sample solution with correlation coefficient as 0.9968. So, the quantitative detection for BPs was also be achieved. With good selectivity, it recognized BPs against the complex sample matrix, and showed a standard addition recovery of 107% in the real sample. After further optimization and integrating with the artificial intelligence device, the visual sensor could become a rapid, reliable, and effective supplement of the optic fiber method in the on-site customs inspection.
Y.L.: Conceptualization, Writing—original draft, Writing—review and editing. H.G.: Data curation, Methodology, Investigation. J.H.: Methodology, Visualization. A.C.: Validation. X.W.: Resources. J.L.: Supervision, Project administration. H.S.: Supervision, Project administration, Writing—review and editing. All authors have read and agreed to the published version of the manuscript.
This research was funded by he National Natural Science Foundation of China (21677053, 21876033), Scientific Research Projects in Colleges and Universities of Guangzhou Education Bureau (201831803).
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Data is contained within the article or
This work was supported by the National Natural Science Foundation of China (21677053, 21876033), Scientific Research Projects in Colleges and Universities of Guangzhou Education Bureau (201831803).
The authors declare no conflict of interest.
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Enlarge this image.Scheme 1. The schematic for the fabrication and application of the MIPC. (A) fabrication of PC template by self-assembly of silicon spheres; (B) injection of MIP precursor solution on the PC template; (C) thermal polymerization of BP imprinted membrane; (D) preparation of inverse opal MIPC via eliminating of the silica spheres and BP molecules; and (E) the utilization of MIPC in BP monitoring.
Enlarge this image.Figure 1. The Bragg diffraction, SEM images and colors (the inset pictures) of PC and MIPC. (a) PC, (b) MIPC before elution of BP, (c) MIPC after elution of BP.
Enlarge this image.Figure 2. Effect of the molar ratio of BP, AA and EDMA in the precursor solution (a) and the different porogen (b) on the peak shift of MIPCs (The upper and lower figures in Figure 2a indicate respectively the effect of EDMA and MAA on the peak shift of MIPCs; Concentration of BP: 0.001 mol·L−1).
Enlarge this image.Figure 3. Effect of the methanol content in the assayed sample solution (a), pH (b) and temperature (c) on the MIPC signal (Concentration of BP: 0.001 mol·L−1).
Enlarge this image.Figure 3. Effect of the methanol content in the assayed sample solution (a), pH (b) and temperature (c) on the MIPC signal (Concentration of BP: 0.001 mol·L−1).
Enlarge this image.Figure 4. The color changes (a), Bragg diffraction (b), and signal calibration curve (c) of MIPC film upon response to BPs.
Enlarge this image.Figure 4. The color changes (a), Bragg diffraction (b), and signal calibration curve (c) of MIPC film upon response to BPs.
Enlarge this image.Figure 5. The chemical formula (a) of BP and structural analogues; comparison of the sensing effect of MIPC (b) and NIPC (c) film.
Enlarge this image.Figure 7. (a)The color of MIPC in the control sample solution (left, green) and the spiked sample solution (right, orange); (b) The Bragg diffraction spectra of MIPC in different sample solution.
Enlarge this image.Figure 7. (a)The color of MIPC in the control sample solution (left, green) and the spiked sample solution (right, orange); (b) The Bragg diffraction spectra of MIPC in different sample solution.
Supplementary Materials
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