Abstract
A novel internal standard electrochemiluminescence (ECL) sensor has been designed for the detection of ascorbic acid (AA). The adopted dual-emission luminophore (NSGQDs-PEI-luminol-Pt) is composed of nitrogen and sulfur double-doped graphene quantum dots (NSGQDs, as the main luminophore), luminol (as the auxiliary luminophore and internal standard), platinum nanoparticles (Pt NPs, as the co-reaction accelerator), and polyetherimide (PEI, as the linker of NSGQDs and luminol). The results suggest obviously enhanced ECL intensities by the Förster resonance energy transfer (FRET) between luminol (donor) and NSGQDs (acceptor). In this sensing system, the cathodic ECL intensities of NSGQDs (ECL-1, −1.8 V vs. Ag/AgCl) gradually decrease with increasing concentration of AA, while the anodic ECL intensities of luminol (ECL-2, 0.3 V vs. Ag/AgCl) almost remain essentially constant at a potential window from −2.0 to 0.4 V. The natural logarithm of the ratio between ECL-1 and ECL-2 (ln I (ECL-1/ECL-2)) shows a good linear relationship with AA concentration ranging from 10 to 360 nM. The regression equation is ln I (ECL-1/ECL-2) = − 0.0059 cAA + 3.55 (R2 = 0.992) with a limit of detection of 3.3 nM. Such sensor has also been applied for monitoring AA in human serum. The recovery range was 96.5–105.3% and the relative standard deviation was 1.3–3.3%.
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Introduction
Electrochemiluminescence (ECL) technology has become a powerful analytical tool due to the low cost, simple operation, fast analysis, and high sensitivity [1]. It is well known that the measurement accuracy and efficiency of ECL directly limit the wide application of ECL sensors. However, the self-annihilating ECL luminophore alone is unable to provide a high enough signal. Since C2O42− was first reported as a co-reactant, it has become a fashion to construct a binary system of ECL luminophores and co-reacting reagents in order to obtain significantly enhanced ECL signals. Commonly used co-reaction reagents include hydrogen peroxide, persulfate, and tripropylamine [2]. In addition, different methods have also been used to improve the ECL system, such as resonant energy transfer [3] and introduction of nanomaterials [4]. Förster resonance energy transfer (FRET) can improve the ECL intensity and stability of single luminescent material through energy transfer between donor and acceptor. Nanomaterials can play a variety of roles in ECL, for example, luminophores, co-reaction accelerators, and carriers.
Graphene quantum dots (GQDs), as a kind of novel zero-dimensional nanomaterials, possess some unique properties, such as low toxicity, excellent biocompatibility, good stability, and water solubility [5]. However, the primal GQDs without passivated surface often present low ECL efficiency [6]. Heteroatom doping is considered to be a valid method to tune the surface state, optical properties, and chemical features of GQDs [7]. For example, the electrochemical properties, surface chemical activity, and quantum yield are improved by sulfur or nitrogen doped GQDs [8, 9]. Therefore, GQDs doping with diverse elements are becoming a research topic.
To solve some potential systematic errors caused by single ECL technology and make the detection results more convincing, the ratiometric ECL sensors with dual-emission signals have been introduced [10]. For example, a ratiometric ECL sensor based on CdS nanocrystal and luminol has been developed for mp53 oncogene detection [11], and a dual-wavelength ratiometric electrochemiluminescence resonance energy transfer aptasensor has been constructed for amyloid-β protein detection, which based on the carbon nitride nanosheet as the energy donor and metal-organic framework as the acceptor [12]. However, when the dual signals change simultaneously, the reference signal cannot express the real status of the ECL system, which makes the reproducibility of the assay doubtful. The internal standard method has been introduced as an indirect or relative calibration method to solve this problem [13], which has been widely used in chromatography [14], fluorescence (FL) [15], Raman spectroscopy [16], and photoelectrochemical sensing [17]. That is to say, one ECL signal of the system remains constant as an internal reference while the other ECL signal changes sensitively according to the target, which can not only effectively avoid potential interferences but also greatly improve the reproducibility.
The dosage of ascorbic acid (AA) in human serum can be used as an indicator of some chronic diseases. The average level of AA in serum for a large number of people is 0.2 mg per 100 mL [18]. A series of methods have been developed to detect AA, including high-performance liquid chromatography [19], electroanalysis [20], ECL and so on [21].
Inspired by the above research, we present a novel composite (NSGQDs-PEI-luminol-Pt) to construct an internal standard ECL sensor for the detection of AA. Here, nitrogen and sulfur double doped graphene quantum dots (NSGQDs) and luminol are integrated into one nanostructure as the dual-emission luminophore, NSGQDs as the main luminophore, luminol as the auxiliary luminophore and internal standard, platinum nanoparticles (Pt NPs) as a co-reaction accelerator, and polyetherimide (PEI) as a linker of NSGQDs and luminol. The stable ECL signals corresponding to NSGQDs and luminol have been observed at − 2.0 V (ECL-1) and 0.4 V (ECL-2), respectively. With the increasing concentration of AA, the ECL-1 decreases gradually, whereas ECL-2 remains almost constant, which can be considered an internal standard calibration (Scheme 1). The internal standard ECL system can avoid the detection errors of the false positive or negative results generated by the single peak ECL. It will be a good choice for the detection of AA or other small molecules in organisms.
Experiment section
Reagents and materials
Ascorbic acid (AA, 99%), polyetherimide (PEI, 99%), and glutaric dialdehyde (GA, 50%), citric acid (99%), L-cysteine (97%), and chloroplatinic acid (H2PtCl6·6H2O, 99%) were got from Sigma-Aldrich Chem. Co. (St. Louis, MO, USA). N-Hydroxy succinimide (NHS, 99%) and N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (EDC, 99%) were acquired from J&k Chemical Co. (Beijing, China). 0.1 M phosphate buffer (PB, pH 7.4) was prepared by using 0.1 M Na2HPO4 and 0.1 M KH2PO4 containing 0.1 M KCl. 5.0 mM [Fe(CN)6]4−/3− solution (0.1 M PB, pH 7.4) was prepared by K4Fe(CN)6 and K3Fe(CN)6. Multi-walled carbon nanotubes (MWNTs, D = 40–60 nm) were purchased from Aladdin Reagent Co. Ltd. (Shanghai, China; www.aladdin-e.com). All chemicals were analytical grade and used as received without further purification. Ultrapure water (Millipore, 18.2 MΩ·cm) was used throughout this work.
Apparatus
Electrochemical determination was conducted on a CHI 660E electrochemical workstation (Shanghai Chenhua Instruments, China). ECL detection was performed using a model MPI-A electrochemiluminescence analyzer (Xi’an Remex Analysis Instruments Co. Ltd., China). The potential scanning range is from −2.0 to 0.4 V (vs. Ag/AgCl) and the photomultiplier tube was set at 600 V. A three-electrode system was employed: a glassy carbon electrode (GCE, Φ = 4.0 mm) or modified GCE as working electrode, a platinum wire as counter electrode, and an Ag/AgCl electrode (saturated KCl) as reference electrode. The UV 2600 spectrometer (Shimadzu, Japan) was used to record the UV-vis spectra in the range from 200 to 800 nm. JEM-1200EX transmission electron microscopy (TEM) was applied to receive the morphology and structure of the materials at an accelerating voltage of 120 kV (JEOL, Japan). Scanning electron microscopy (SEM) images and energy-dispersive spectra (EDS) were acquired on a field-emission SEM (ZEISS, Germany). The X-ray photoelectron spectroscopy (XPS) analysis was obtained using a VG Scientific ESCALAB 250 spectrometer (Thermoelectricity Instruments, USA).
Preparation of the different composites
PEI-luminol-Pt
PEI, an amino-rich polyelectrolyte, has been used as both a functional agent and a reductant with the assistance of formic acid to fabricate Pt NPs. First, PEI (4 mL, 0.05%), luminol (1.5 mL, 5 mM), GA (100 μL, 1%), and 5 mL of water were added into a 25-mL round-bottom flask and then stirred for 2 h at room temperature to make PEI and luminol cross-link sufficient. Next, H2PtCl6 solution (0.5 mL, 0.1 M) and 1 mL of formic acid were added into the above mixture. To accelerate the reaction, the above mixture was refluxed at 80 °C for 30 min (Scheme 1b).
NSGQDs-PEI-luminol-Pt
The dual-emission luminophore was obtained as follows. First, NSGQDs were prepared according to the literature with slight modification (Scheme 1a) [22]. Then, 500 μL of NSGQDs was activated by EDC/NHS (v/v = 4:1) solution for 40 min at 4 °C and mixed with 1 mL of PEI-luminol-Pt, which shortens the distance of the donor-receptor pair and produces an enhanced ECL luminescence signal, resulting in a significant quenching of the ECL of NSGQDs improving the sensitivity of the sensor. The mixture was stirred for 12 h at 4 °C. Last, the precipitates were collected by centrifugation and redispersed in 2 mL of water.
Fabrication of the ECL sensor
Prior to modification, each GCE was polished with 0.3 μm and 0.05 μm alumina respectively to achieve a mirror-like surface. Afterwards, 5 μL of MWCNTs dispersion was coated on the surface of the GCE and dried in air. Then, 10 μL NSGQDs-PEI-luminol-Pt was dropped on and dried in air (denoted as NSGQDs-PEI-luminol-Pt/MWCNTs/GCE). ECL analyses were executed in 0.1 M PB (pH 7.4) including 5 mM H2O2 and different concentrations of AA.
Results and discussion
Characterization of NSGQDs and NSGQDs-PEI-luminol-Pt
The morphologies of NSGQDs and NSGQDs-PEI-luminol-Pt composite were characterized by TEM and SEM, respectively. The NSGQDs show a spherical structure with the size around 1.5–5.5 nm (Fig. 1a). The high-resolution transmission electron microscope (HR-TEM) image exhibits that the lattice distance is 0.27 nm (Fig. 1b). The SEM image of the NSGQDs-PEI-luminol-Pt composite exhibits homogenously flower-like shape with an average diameter of 1 μm (Fig. 1c).The element type and chemical state of NSGQDs-PEI-luminol-Pt composite were examined by XPS. As depicted in Fig. 1d, the characteristic peaks at 284.5, 399.9, and 532.5 eV belong to C 1s, N 1s, and O 1s respectively, and the peak at 72.5 eV belongs to Pt 4f. The results prove the presence of C, N, O, and Pt in NSGQDs-PEI-luminol-Pt composite. Additionally, the proposed composite was analyzed by HR-XPS spectra. As shown in Fig. 1e, the raw data of C 1s spectra can be fitted by three components of C-C (284.6 eV), C-N (285.7 eV), and O-C=O (288.6 eV). As depicted in Fig. 1f, two peaks at 399.8 and 402.1 eV correspond to C-NH2 and -NR3+/-NH3+ respectively in high-resolution N 1s spectra. The above characterization indicates the successful preparation of NSGQDs-PEI-luminol-Pt composite.
Optical and electrical properties
The optical and electrical properties of the NSGQDs-PEI-luminol-Pt were also investigated via FL and ECL. As shown in Fig. 2A, a significant spectral overlap is observed from the FL emission spectrum of luminol (curve a) and the excitation spectrum of NSGQDs (curve b), indicating that the FRET between luminol (donor) and NSGQDs (acceptor) is possible. In other words, the NSGQDs can receive energy from luminol and can be excited to generate luminescence signal subsequently [23]. As shown in Fig. 2B, two ECL peaks are observed from NSGQDs-PEI-luminol-Pt, suggesting luminol and NSGQDs are co-existed in this dual-emission luminophore. The shoulder ECL peak located at 425 nm (ECL-2) is assigned to luminol, while the maximum ECL emission located at 484 nm (ECL-1) is raised from NSGQDs.
Furthermore, the ECL behaviors of luminol, PEI, NSGQDs, NSGQDs-PEI-luminol, and NSGQDs-PEI-luminol-Pt were studied comparatively at the potential window of −2.0 to 0.4 V (Fig. 3A). A small anodic ECL peak (0.4 V) is observed from luminol in 0.1 M PB (pH 7.4) containing 5 mM H2O2 as a co-reactant (curve a), while almost no obvious signal is detected in PEI solution (curve b). A weak cathodic ECL signal is obtained on NSGQDs (curve c), as well as a weak cathodic ECL signal and an anodic ECL signal are displayed on NSGQDs-PEI-luminol (curve d). Interestingly, a very high cathodic peak (ECL-1, −1.8 V, main emission from NSGQDs) accompanied by a weak anodic peak (ECL-2, 0.3 V, auxiliary emission from luminol) is appeared on NSGQDs-PEI-luminol-Pt (curve e). Compared with NSGQDs-PEI-luminol, dependent on the dual-emission luminophore NSGQDs-PEI-luminol-Pt, the ECL-1 is improved. Due to the presence of Pt NPs, the reaction between luminol and H2O2 was accelerated and further enhanced ECL-1 via FRET.
The effect of dissolved O2 to the ECL response has been investigated by comparing the signals before and after deaeration (Fig. 3B). No obvious change in ECL peak position and intensity has been observed, indicating that dissolved oxygen in solution has little effect on ECL reaction process.
ECL mechanism of NSGQDs-PEI-luminol-Pt
The possible ECL mechanism of the NSGQDs-PEI-luminol-Pt system is proposed (Scheme 1C). Since NSGQDs and luminol are integrated into one nanostructure, which can be oxidized synchronously on the surface of GCE. After the electrochemical oxidation, luminol anions (LH−) and NSGQDs are converted into luminol radicals (L•−) [24] and NSGQDs cations (NSGQDs+), respectively. Superoxide radical (O2•−) are produced by decomposition of H2O2. Afterwards, L•− reacts with O2•− to generate the excited state 3-aminophthalate (AP2−*). Next, AP2−* releases energy by giving an ECL emission at 425 nm (hν2) which can be absorbed by NSGQDs+ with a emission at 484 nm (hν1) based on the FRET between luminol and NSGQDs. Owing to the co-existence of luminol and NSGQDs, the energy transfer distance between luminol (donor) and NSGQDs (acceptor) is shortened, which makes FRET easy to realize. At the same time, Pt NPs have excellent catalytic performance which can accelerate the production of O2•− from H2O2. The corresponding ECL route is proposed as follows:
Measurement of AA
Under the optimal experimental conditions (Fig. S6), the ECL-1 decrease with the increasing AA concentration from 10 nM to 360 nM, while the ECL-2 as internal standard signal almost remain unchanged (Fig. 4A). The calibration plot was constructed by the natural logarithm of the ratio between ECL-1 and ECL-2 (ln I (ECL-1/ECL-2)) and the concentration of AA (Fig. 4B). The linear equation of this ECL system is ln I (ECL-1/ECL-2) = − 0.0059 cAA + 3.55 (R2 = 0.992) with a limit of detection (LOD) of 3.3 nM (S/N = 3). Compared with the previous method, the proposed sensor can detect AA with higher sensitivity and wider linear range (Table 1), but it is disposable.
Stability and selectivity of the ECL sensor
The stability of the present internal standard ECL sensor has been evaluated by the consecutive cyclic potential for 200 s in different AA concentrations (0.1 M PB containing 5 mM H2O2, pH 7.4) (Fig. 5a, Fig. S7). As depicted in Fig. 5a, the relative standard deviations (RSD) of ECL-1 and ECL-2 are 0.58% and 1.8% in 60 nM AA, indicating that reversibility and reliability of the system meet the regular requirements. The selectivity of the internal standard ECL system toward different interferences was investigated using various biologically relevant co-existing species including amino acid molecules of cysteine (Cys), phenylalanine (Phe), and tryptophan (Trp); small biological molecules of creatinine (Cre), glucose (Glu), and globulins (Glb); and common inorganic ions such as K+, Na+, Ca2+, Fe2+, and Fe3+ (Fig. 5b). The concentration of interference substances is100-fold (vs molecules) or even 1000-fold (vs common inorganic ions) that of AA (300 nM). Compared with the target AA, the small changes of ECL intensity appear with the addition of the interference substances, whereas a significantly decreased intensity present when AA is added (Fig. 5b).
Real applicability
To investigate the applicability of this strategy in real practice, human serum samples were selected for assay using the standard addition method. Prior to use, the samples were diluted 100-fold with 0.1 M PB (pH = 7.4) and spiked with different concentrations of AA. Under the same conditions as the standard sample, the ECL analyses were executed in 3 mL sample solution including 5 mM H2O2 with the proposed sensor. The results are listed in Table 2, and the recovery rates are in the range of 96.5–105.3% with the RSD ranged from 1.3 to 3.3%, indicating that the proposed method can be effectively used for AA detection in real sample.
Conclusion
In this work, an internal standard ECL sensor was prepared based on NSGQDs-PEI-luminol-Pt composite as a novel luminophore for sensitive detection of AA. The proposed internal standard ECL sensor exhibits a strong cathodic ECL-1 signal and an almost constant anodic ECL-2 signal and an improved sensitivity and accuracy for the detection of AA, possibility of employment in other ECL system.
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Funding
This work was supported by the National Natural Science Foundation of China (22077105) and Natural Science Foundation Project of CQ CSTC (cstc2020jcyj-msxmX0854), China.
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Liu, P., Meng, H., Han, Q. et al. Determination of ascorbic acid using electrochemiluminescence sensor based on nitrogen and sulfur doping graphene quantum dots with luminol as internal standard. Microchim Acta 188, 120 (2021). https://doi.org/10.1007/s00604-021-04761-w
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DOI: https://doi.org/10.1007/s00604-021-04761-w