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Article

Synthesis of Gold-Platinum Core-Shell Nanoparticles Assembled on a Silica Template and Their Peroxidase Nanozyme Properties

by
Xuan-Hung Pham
1,
Van-Khue Tran
2,
Eunil Hahm
1,
Yoon-Hee Kim
1,
Jaehi Kim
1,
Wooyeon Kim
1 and
Bong-Hyun Jun
1,*
1
Department of Bioscience and Biotechnology, Konkuk University, Seoul 05029, Korea
2
VNUK Institute for Research and Executive Education, The University of Danang, Danang 550 000, Vietnam
*
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2022, 23(12), 6424; https://doi.org/10.3390/ijms23126424
Submission received: 27 April 2022 / Revised: 3 June 2022 / Accepted: 6 June 2022 / Published: 8 June 2022
(This article belongs to the Section Molecular Nanoscience)
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Abstract

:
Bimetallic nanoparticles are important materials for synthesizing multifunctional nanozymes. A technique for preparing gold-platinum nanoparticles (NPs) on a silica core template (SiO2@Au@Pt) using seed-mediated growth is reported in this study. The SiO2@Au@Pt exhibits peroxidase-like nanozyme activity has several advantages over gold assembled silica core templates (SiO2@Au@Au), such as stability and catalytic performance. The maximum reaction velocity (Vmax) and the Michaelis–Menten constants (Km) were and 2.1 × 10−10 M−1∙s−1 and 417 µM, respectively. Factors affecting the peroxidase activity, including the quantity of NPs, solution pH, reaction time, and concentration of tetramethyl benzidine, are also investigated in this study. The optimization of SiO2@Au@Pt NPs for H2O2 detection obtained in 0.5 mM TMB; using 5 µg SiO2@Au@Pt, at pH 4.0 for 15 min incubation. H2O2 can be detected in the dynamic liner range of 1.0 to 100 mM with the detection limit of 1.0 mM. This study presents a novel method for controlling the properties of bimetallic NPs assembled on a silica template and increases the understanding of the activity and potential applications of highly efficient multifunctional NP-based nanozymes.

1. Introduction

Nanozymes, a new functional nanomaterial with enzyme-like catalytic activity, have several advantages when compared with natural enzymes, including high stability in harsh environments, low production costs, large specific surface areas, and customizable catalytic activities based on size, morphology, and composition [1,2,3,4,5,6,7,8,9,10,11]. A series of nanomaterials made from metals, metal oxides, and other materials including Pt [12,13,14], Au [15,16,17,18], Ag [19], Cu [20], Fe3O4 [21], CeO2 [22], MnO2 [23], Mn3O4 [24,25], conducting polymers [26], metal–organic frameworks [27], carbon nanomaterials [28], and single-atom catalysts [29] have been prepared for use as nanozymes. These nanozymes have been used as bio(chemical) sensors, in immunoassays, for drug delivery, and as antibacterial agents [3,12,13,30,31,32,33,34]. While the physical and chemical properties of nanoparticles (NPs) can be adjusted by changing their size, shape, or structure, monometallic NPs are limited by other physical or chemical properties such as size-dependent optical properties, electronic properties, and thermal and catalytic effects that control the chemical compositions of NPs [35].
Several studies have been conducted on bimetallic NPs owing to the increased awareness of the options to adjust their physical and chemical properties. Compared with monometallic NPs, bimetallic NPs allow a greater adjustment of their magnetic, optical, and catalytic properties via adjustments of their composition and chemical configuration [36]. Bimetallic NPs have unique structure- and composition-dependent properties that allow the optimization of enzyme-like activities more than those of single-metal NPs [37,38]. The Pt family of bimetallic NPs has been developed using various morphologies including core–shell structures, solid solution alloys, intermetallic alloys, and phase-segregated structures. Owing to the synergistic effect caused by the presence of Pt NPs, a super catalyst for electrochemical reactions, which are designed to maximize Pt utilization, tune the energetics, and assemble the geometry of exposed Pt atoms for high catalytic reactivity and selectivity, has been created [39,40]. Bimetallic NPs exhibit various enzyme-like activities including peroxidase, catalase, polyphenol oxidase, ferroxidase, and superoxide dismutase activities [40,41,42,43,44]. Au@Pt bimetallic NPs have intrinsic peroxidase-like activities [45,46,47], have been studied extensively for electrochemical formic acid and alcohol oxidation, and Pt-rich compositions exhibit enhanced electrocatalytic activity [48,49]. Au@Pt NPs have extensive catalytic properties as they can effectively scavenge superoxide free radicals, H2O2, or formic acid, enabling their use in fuel cells, hydrogenation, air purification, anti-aging therapy, and cancer therapy [48,50,51,52]. However, Pt tends to aggregate in catalytic reactions, resulting in reduced catalytic activity [53].
Au@Ag or Au NPs immobilized on SiO2 NPs have been developed recently [54,55,56,57,58]. In these nanostructures, the SiO2 NPs serve as a template and the metal NPs are introduced to the surface using the seed-mediated growth method. Because of the SiO2 core, the metal NPs assembled on SiO2 nanostructures are cost-effective, more stable during surface modification, easily separatable from the reaction solution, aggregate less than fine metal NPs, and redisperse into solution with enhanced separation compared with single metal NPs. Furthermore, the effects of various synthesis factors on metal NPs assembled on SiO2 have been studied using near-infrared surface enhanced Raman scattering nanoprobes for bioimaging [55,56]. However, research regarding the high peroxidase-like activity of the metal NPs assembled on SiO2 is limited. Therefore, the development of an improved method for preparing metal NPs assembled on SiO2 templates is needed to enhance peroxidase activity. This study improves the understanding of the activity and applications of highly efficient multifunctional nanozymes.
In this study, gold-platinum NPs are prepared on a silica core template (SiO2@Au@Pt) using seed-mediated growth combined with the dropping method and utilize it as a nanomaterial to detect hydrogen peroxide (H2O2) as a model because H2O2 plays an important role in cellular metabolism and in various industry such as food industry, gas sensors, pharmaceuticals, catalysis, environment, and solar energy [59,60,61]. Therefore, the need to develop a low cost, simple, fast, and sensitive method for monitoring the concentration of H2O2 is of practical significance in both industry and academia. The preparation of SiO2@Au@Pt consists of two steps: tiny Au seeds are embedded on the SiO2 surface, and the addition of a Pt2+ precursor in the presence of ascorbic acid (AA) reductant allows the deposition and growth of the Pt layer. First, a suspension of Au seeds (approximately 2.5 nm) was prepared using tetrakis(hydroxymethyl)phosphonium chloride (THPC) and HAuCl4. Then, the Au seeds were mixed with aminated SiO2 NPs (approximately 160 nm) overnight to obtain SiO2@Au seeds, as previously reported [54,55,57,58,62,63,64]. On the SiO2@Au seeds, the reduction of Pt2+ to Pt(0) was directly induced using AA, a mild reducing agent, in the presence of polyvinylpyrrolidone (PVP). These mildly reducing conditions allow a greater control over the growth of the Pt layer as the reaction proceeds much slower than that in strongly reducing conditions [65]. A low concentration of the Pt2+ precursor and AA were added onto the SiO2@Au seeds in 5 min intervals to enable the precise control of the size of the Pt NPs. After the optimization of synthesis, SiO2@Au@Pt was used as a peroxidase-like nanomaterial to detect H2O2 efficiently.

2. Results and Discussion

2.1. Preparation of Au@Pt NPs-Assembled Silica Nanostructures

The seed-mediated growth from SiO2@Au seeds was used to prepare the gold-platinum-embedded silica nanospheres (SiO2@Au@Pt). First, the surface SiO2 template was assembled using small Au NPs (2.6 ± 0.52 nm) (Figure 1a). Then, 10 mM H2PtCl4 and AA solutions were added dropwise into the dispersion of SiO2@Au seeds to obtain a final Pt2+ concentration of 200 µM. The Au@Pt NPs on the surface of the SiO2 core were bigger (3.6 ± 0.56 nm) than SiO2@Au seeds. The presence of Pt on the surface of SiO2@Au was confirmed by the line energy dispersive X-ray (EDS) mapping of SiO2@Au@Pt (Figure 1b and Figure S1). In Figure 1b, the signal of both Pt and Au elements could obtain in the image. The quantitative EDS analysis in Table S1 of SiO2@Au@Pt synthesized at 200 µM Pt2+ consists of 74.6% Pt and 23.6% Au as mentioned in Table S1.
The UV-Vis spectroscopy of SiO2@Au@Pt was conducted when the Pt2+ solution was added into the SiO2@Au seed suspension in the presence of AA. The absorbance intensity of SiO2@Au showed a slight increase at ~500 nm. This peak was suppressed in the absorbance spectrum of SiO2@Au@Pt but the spectrum of SiO2@Au@Pt increased in the UV region (Figure 1c) owing to the Pt layer, consistent with previous results of pure Pt hydrosol [66,67]. The results of TEM, EDS mapping, UV-Vis spectrum of SiO2@Au@Pt indicated that Pt was deposited to the SiO2@Au.

2.2. Peroxidase-like Activity of SiO2@Au@Pt NPs

The peroxidase-like activity of SiO2@Au@Pt NPs was evaluated using the oxidation reaction of 3,3′,5,5′-tetramethylbenzidine (TMB) substrate prepared in a buffer (pH = 4) containing TMB or a TMB-H2O2 mixture. TMB oxidation involves the exchange of two electrons. When TMB transfers one electron to form TMB+, the solution changes from colorless to blue. However, TMB+ is unstable in acidic conditions and must oxidize to TMB2+, forming a yellow solution [68]. In this study, the TMB, H2O2, and TMB+H2O2 solutions without SiO2@Au@Pt NPs were colorless and no absorbance peaks were observed at 453 nm (Figure 1d), indicating that there was no peroxidase-like catalytic activity in the absence of SiO2@Au@Pt. A small absorbance band was observed for the SiO2@Au@Pt + TMB solution, and a strong absorbance band with peaks at 370 and 652 nm was observed for the SiO2@Au@Pt + TMB-H2O2 solution. The SiO2@Au@Pt + TMB-H2O2 solution changed from blue to yellow and an absorbance band with a peak at 453 nm was observed (Figure S2a). These results indicate that the conversion of TMB to TMB2+ was catalyzed by the SiO2@Au@Pt NPs with H2O2, suggesting that SiO2@Au@Pt NPs has a peroxidase-like activity. To confirm the synergic qualities of SiO2@Au@Pt, an Au layer was deposited on the surface of the SiO2@Au seeds using a 200 µM Au3+ solution. The peroxidase-like catalytic activity of SiO2@Au@Pt (5 µg) and SiO2@Au@Au (5 µg) in TMB and TMB-H2O2 solutions was then verified (Figure 2a and Figure S3b).
The blue color of the SiO2@Au@Pt in TMB-H2O2 is darker and the absorbance intensity at 370 and 652 nm is stronger than those of the SiO2@Au@Au suspension. The absorbance intensities of the SiO2@Au@Pt suspension were 5.7- and 7.7-fold of those of SiO2@Au@Au at 370 and 652 nm, respectively. Similarly, the absorbance intensity of the SiO2@Au@Pt suspension at 453 nm was stronger than that of SiO2@Au@Au (Figure S3b). In addition, the recycling of both SiO2@Au@Au and SiO2@Au@Pt in the TMB-H2O2 solution at 453 nm was compared when the NPs were reused five times. The absorbance intensity of SiO2@Au@Au in a TMB-H2O2 solution at 453 nm decreased to approximately 40% while that of SiO2@Au@Pt in a TMB-H2O2 solution at 453 nm decreased to 80%. These results indicate that the catalytic ability of SiO2@Au@Pt is better than that of SiO2@Au@Au, and that SiO2@Au@Pt NPs are reusable and separatable from the reaction mixture.
The catalytic performance of SiO2@Au@Pt NPs at TMB concentrations of 0–600 µM was also investigated as the absorbance intensity at 652 nm in TMB-H2O2 every 3 min (Figure 2b). The absorbance intensity of the oxidation of TMB increased as the TMB concentration increased, following Michaelis–Menten behavior. The signal of SiO2@Au@Pt NPs increased as the TMB concentration increased from 100 to 500 µM and reached saturation at 600 µM. The relationship of the TMB concentration and absorbance intensity at 652 nm after incubation for 180 s was plotted according to the Lineweaver–Burk equation to calculate the maximum reaction velocity (Vmax) and the Michaelis–Menten constants (Km) (Figure 2d). The kinetic activity of SiO2@Au@Pt at various TMB concentrations (100–500 µM) revealed a linear relationship. The Km was 417 µM and the Vmax was 2.1 × 10−10 M−1∙s−1. The Km of SiO2@Au@Pt indicates a higher affinity of SiO2@Au@Pt for TMB compared with that for horseradish peroxidase enzyme (Km = 438 µM). The Km of SiO2@Au@Pt was higher than those of Au NPs (Km = 123 µM), SiO2@Au@Au NPs (Km = 60 µM), glucose oxidase-conjugated Au-attached SiO2 microspheres (Km = 208 µM), MnO2 NPs (Km = 83 µM), and latex-conjugated MnO2 NPs (Km = 99 µM). The Km of SiO2@Au@Pt was lower than those of Au NPs-decorated porous silica microspheres (Km = 523 µM) and Prussian-blue-decorated latex NPs (Km = 2.19 mM) [55]. The Vmax of SiO2@Au@Pt was higher than that of SiO2@Au@Au (Vmax = 2.1 × 10−10 M−1∙s−1), indicating that SiO2@Au@Pt oxidizes TMB at a faster rate than SiO2@Au@Au. SiO2@Au@Pt had a comparatively more stable catalytic activity that remained at 80% after five reuses (Figure 2b).

2.3. Effects of Synthesis and Experimental Conditions on the Catalytic Activity of SiO2@Au@Pt NPs

Various concentrations of the Pt2+ precursor (100–400 μM) were added to the SiO2@Au seeds. The size of Pt increased as the Pt2+ concentration increased (Figure 3a and Figure S2). In particularly, the size of Au@Pt synthesized at 100, 200, 300, 400 µM Pt2+ were 3.1 ± 0.61; 3.6 ± 0.56; 3.9 ± 0.59; 4.6 ± 0.62 nm, respectively. At a high concentration of Pt2+ (>200 µM), the Au@Pt on the SiO2 surface partly merged. The quantitative EDS analysis of Pt and Au elements on the surface of SiO2 synthesized at various Pt2+ concentration was carried out to investigate the composition of the Au@Pt on the SiO2 surface and the results were shown in Table S1. All Au@Pt NPs contained both Pt and Au elements, but their Au and Pt components were different. The atomic Pt component increased from 71.59% to 87.07% while the atomic Au component decreased from 28.41 to 12.93% when Pt2+ increased from 100 µM to 400 µM. Therefore, the reciprocal of Pt and Au increased from 2.5 (at 100 µM Pt2+) to 6.7 (at 400 µM Pt2+). The results matched to the TEM images, and it indicated that Pt was gradually deposited on the surface of SiO2@Au.
The absorption spectra of SiO2@Au@Pt were collected (Figure 3b). The absorbance intensity at 300–800 nm increased as the concentration of the Pt2+ precursor increased, indicating the formation of larger Au@Pt NPs (Figure S2) that subsequently affected the proximate interparticle distance. The absorbance of the suspension broadened as the size of the Au@Pt NPs increased (Figure S2). The growth of Au@Pt NPs on SiO2 could be controlled well (Figure 3).
The correlation between the peroxidase-like activity of SiO2@Au@Pt NPs and the concentration of Pt2+ was investigated (Figure 3c). The peroxidase-like activity of SiO2@Au@Pt NPs synthesized with 100–400 μM Pt2+ was estimated using a TMB assay. The SiO2@Au seeds showed very weak peroxidase-like activity because of the lack of spaces on the SiO2@Au NPs and the small Au NPs on the SiO2 template, resulting an insufficient surface area for the catalytic reaction between the Au NPs and the TMB-H2O2 mixture [55]. The UV-Vis absorption spectra of all SiO2@Au@Pt NPs showed an absorbance peak at 453 nm (Figure 3c–e), indicating that all of the SiO2@Au@Pt NPs had peroxidase-like activity that was dependent on the initial Pt2+ concentration.
In contrast, SiO2@Au@Pt NPs treated with a Pt3+ precursor concentration >100 µM had high peroxidase-like activity. As the concentration of Pt2+ increased, the size of the Au@Pt NPs on the SiO2@Au@Pt NPs increased from 3.1 to 4.6 nm, which increased the surface area for reactions between NPs and reactants. Therefore, the catalytic activity of SiO2@Au@Pt NPs increased as the concentration of the Pt2+ precursor increased from 100 to 200 μM because of the formation of sublayers or a monolayer of Pt on the surface of SiO2@Pt [45,67]. This result consistent with the previous report where the increase of Pt component of Au-Pt led an better catalytic activity because the alloying of Pt with Au can change the electronic structure of Pt, leading the catalytic performance of Au@Pt changes [11,37,69]. Although the Au@Pt NPs grew as the concentration of the Pt2+ precursor increased, the peroxidase reaction of SiO2@Au@Pt treated with >200 µM of the Pt2+ precursor did not increase because TMB and H2O2 cannot gain access to inner part of the thick Pt layer [66]. It means that the catalytic activities of SiO2@Au@Pt reached the highest value at the Pt/Au ratio of 3.2 and decreased when Pt2+ concentration increased further. Therefore, 200 µM of Pt2+ precursor-treated SiO2@Au@Pt NPs, which exhibited high peroxidase-like activity, were used in subsequent experiments.
Reaction conditions affect the catalytic activity of nanozymes similarly to the effects of reaction conditions on enzymes [21,70,71,72,73,74]. Therefore, the peroxidase-like activity of different amounts of SiO2@Au@Pt NPs were investigated at different incubation times, pH values of the buffer solution, and TMB concentrations (Figure 4).
The amount of SiO2@Au@Pt varied from 0.02 to 20 μg (Figure 4a and Figure S3). The absorbance intensity of SiO2@Au@Pt in a TMB-H2O2 solution at 453 nm increased as the amount of SiO2@Au@Pt increased from 0.02 to 5 μg. When the amount of SiO2@Au@Pt increased to >10 μg, the poor solubility of TMB in the aqueous solution resulted in significant aggregation, inducing precipitation with oxidation [55].
The absorbance intensity increased as the incubation time increased from 5 to 15 min (Figure 4b and Figure S4). The absorbance intensity reached saturation after 15 min of incubation.
The highest peroxidase catalytic activity was obtained at a pH of 4.0, at which TMB dissolved maximally and H2O2 was the most stable (Figure 4c and Figure S5), which is consistent with the results of previous studies [17,21,75,76,77,78].
The absorbance of TMB2+ at 453 nm increased as the TMB concentration increased and reached the saturation at 600 μM TMB (Figure 4d and Figure S6).

2.4. Effects of H2O2 Concentration on Peroxidase-like Activity of SiO2@Au@Pt NPs

After optimizing the detection conditions, the absorbance intensity was measured at 0–400 nm for the SiO2@Au@Pt in 500 μM TMB with various concentrations of H2O2 (Figure 5). The yellow color of the 5 μg SiO2@Au@Pt suspension became darker as the H2O2 concentration increased to 200 mM, indicating that more TMB2+ was produced as the H2O2 concentration increased. The catalytic activity of SiO2@Au@Pt increased as the H2O2 concentration increased to 200 mM and reached saturation at 300 mM because of aggregation (Figure S7).
A linear curve-fitting procedure was used to calibrate the reaction (Figure 5c). A significant relationship was found between the absorbance intensity at 453 nm and the H2O2 concentration from 1.0 to 100 mM (calibration curve: y = 0.0185 x + 0.63285, where x is the H2O2 concentration, y is the absorbance intensity at 453 nm, and R2 = 0.99). The theoretical LOD was 1.0 mM, estimated using the 3sblank criterion. This LOD is higher than the LOD of silver NPs modified cellulose nanowhiskers [79], polyoxometalate [80], Ce2(WO4)3, papain [81], Ag-nanoparticle-decorated silica microspheres [82] and magnetic mesoporous silica nanoparticles [83]. These results suggest that this material can be used to detect H2O2.

3. Materials and Methods

3.1. Chemicals and Reagents

Tetraethylorthosilicate (TEOS), chloroauric acid (HAuCl4), THPC, chloroplatinic acid (H2PtCl6), 3-aminopropyltriethoxysilane (APTS), AA, TMB, and PVP (MW 40,000) were purchased from Sigma-Aldrich (St. Louis, MO, USA). Ammonium hydroxide (NH4OH, 27%), sodium hydroxide (NaOH), ethyl alcohol (EtOH, 99.9%), and sulfuric acid (H2SO4) were obtained from Samchun (Seoul, Korea). H2O2 was purchased from Daejung (Siheung, Gyeonggi-do, Korea). Phosphate buffer saline containing 0.1% Tween 20 (PBST, pH 7.4) was obtained from Dynebio (Seongnam, Gyeonggi-do, Korea).

3.2. Characterization

The TEM images of the samples were obtained using a JEM-F200 electron microscope (JEOL, Akishima, Tokyo, Japan) at an accelerated voltage of 200 kV. The UV-Vis spectra of the samples were recorded using an Optizen POP UV/Vis spectrometer (Mecasys, Seoul, Korea). The samples were centrifuged using a 1730R microcentrifuge (LaboGene, Lyngen, Denmark).

3.3. Synthesis of Gold-Platinum Nanoparticles Assembled on a SiO2 Nanostructure (SiO2@Au@Pt NPs)

The SiO2@Au seed NPs were synthesized as previously reported [54]. Briefly, colloidal Au NPs were prepared from HAuCl4 and THPC. Silica templates (approximately 160 nm) were prepared using the modified Stöber method [84]. The surfaces of 50 mg SiO2 NPs were modified using amino groups via incubation with 62 μL APTS overnight at 25°C. Animated SiO2 NPs (2 mg) were incubated with 10 mL colloidal Au (approximately 2.5 nm) for 12 h at 25°C. After the suspension was centrifuged for 10 min at 8500 rpm and washed with EtOH, 2 mg of SiO2@Au seed NPs were dispersed in 2 mL of 1 mg/mL PVP solution. Subsequently, 200 μL of SiO2@Au seed (1 mg/mL) suspension was mixed with 9.8 mL of PVP solution. Under stirring, 20 μL of 10 mM HPtCl6 solution (in water, Pt2+ precursor) and 40 μL of AA reducing agent (10 mM AA in water) were added to the mixture. The mixture was reacted for 5 min under stirring to convert Pt2+ to Pt(0). The same volumes of Pt2+ precursor and AA were added every 5 min to obtain the desired concentration of Pt2+. The SiO2@Au@Pt NPs were then carefully washed with EtOH several times using centrifugation at 8500 rpm for 10 min. The washed SiO2@Au@Pt NPs were redispersed in 0.1% PBST solution (1 mL) to obtain a 0.2 mg/mL SiO2@Au@Pt NP suspension.

3.4. Peroxidase-like Activity of SiO2@Au@Pt NPs

To verify the peroxidase-like catalytic activity of SiO2@Au@Pt NPs, TMB solution (6 mM in EtOH, 100 μL), the SiO2@Au@Pt NPs suspension (100 μL) synthesized with 100, 200, 300, and 400 μM Pt2+, and freshly prepared H2O2 solution (2 M in pH 4 buffer, 100 μL) were added to 700 μL of buffer (pH = 4.0). Then, the mixture was incubated at 25°C for 15 min. To terminate the reaction, 1 M H2SO4 solution (500 μL) was added to each mixture and the resulting mixture was incubated at 25°C for 10 min. The absorbances of the suspensions were measured at 300–1,000 nm using a UV-Vis spectrometer.

3.5. Peroxidase-like Activity of SiO2@Au@Pt in Various Reaction Conditions

3.5.1. Amount of SiO2@Au@Pt NPs

A mixture of 6 mM TMB solution in EtOH (100 μL), 2 M H2O2 (100 μL), and 700 μL buffer (pH = 4) was added to 100 μL PBST containing 0, 0.2, 2, 5, 10, or 20 μg of SiO2@Au@Pt. The resulting solution was incubated at 25 °C for 15 min, then terminated with 1 M H2SO4 (500 μL). The absorbances were measured at 453 nm using a UV-Vis spectrometer.

3.5.2. Reaction Time

A mixture of a 6 mM TMB (100 μL), a SiO2@Au@Pt NP suspension (0.05 mg/mL, 100 μL), and 2 M H2O2 (100 μL) was added to 700 μL buffer (pH = 4) then incubated at 25°C for various incubation times. The mixture was terminated using 1 M H2SO4 (500 μM). The absorbances of the mixtures were measured at 453 nm using a UV-Vis spectrometer.

3.5.3. PH Value of the Buffer

A mixture containing 6 mM TMB (100 μL), a SiO2@Au@Pt NP suspension (0.05 mg/mL, 100 μL), and 2 M H2O2 (100 μL) was added to 700 μL of buffer at a pH range from 3.0 to 11.0. The mixture was incubated for 15 min and terminated using 1 M H2SO4 (500 μL). The absorbances of the mixtures were measured at 453 nm using a UV-Vis spectrometer.

3.5.4. TMB Concentration

A mixture containing 700 μM buffer (pH 4.0), 2 M H2O2 (100 μL), and 0.05 mg/mL SiO2@Au@Pt suspension (100 μL) was added to various concentrations of TMB (1, 2, 3, 4, 5, and 6 mM). The final TMB concentration in the reaction mixture was 0.1, 0.2, 0.3, 0.4, 0.5, and 0.6 mM. After incubating the mixture for 15 min, the reaction was terminated using 1 M H2SO4 (500 μL). The absorbances of the mixtures were measured at 453 nm using a UV-Vis spectrometer.

4. Conclusions

In summary, SiO2@Au@Pt NPs were successfully synthesized using the seed-mediated growth method under mild conditions. Compared with SiO2@Au@Au, the SiO2@Au@Pt NPs exhibited more synergic and stable catalytic abilities that remained at 80% after five uses of 5 μg SiO2@Au@Pt NPs. In addition, the peroxidase-like activity of SiO2@Au@Pt NPs under various conditions such as the amount of SiO2@Au@Pt NPs, pH of the buffer solution, incubation time, and TMB concentration were also investigated, revealing optimized conditions of 5 μg SiO2@Au@Pt at pH 4.0, with 15 min of incubation in the presence of 500 μM TMB. SiO2@Au@Pt was used to detect H2O2. The dynamic linear range was obtained from 1 to 100 mM, with an LOD of 1.0 mM. Therefore, this study suggests novel uses of bimetallic metal-assembled silica nanostructures in various fields and provides a suitable method for the development of nanoparticle-based multi-functional nanozymes.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/ijms23126424/s1.

Author Contributions

Conceptualization, X.-H.P., V.-K.T., and B.-H.J.; methodology, V.-K.T. and X.-H.P.; investigation, W.K. and Y.-H.K.; formal analysis, X.-H.P., E.H., and J.K.; writing—original draft preparation, V.-K.T., X.-H.P., and E.H.; writing—review and editing, J.K. and B.-H.J.; supervisor, B.-H.J. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the KU Research Professor Program of Konkuk University and funded by the Ministry of Science and ICT (NRF-2022R1A2C2012883).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Data is available in the manuscript and supporting information.

Acknowledgments

The authors are grateful for the financial support from the NRF of Korea. Further, the authors give thanks for the financial support from Konkuk University.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Ragg, R.; Tahir, M.N.; Tremel, W. Solids Go Bio: Inorganic Nanoparticles as Enzyme Mimics. Eur. J. Inorg. Chem. 2016, 2016, 1906–1915. [Google Scholar] [CrossRef]
  2. Zhou, Y.; Liu, B.; Yang, R.; Liu, J. Filling in the Gaps between Nanozymes and Enzymes: Challenges and Opportunities. Bioconjug. Chem. 2017, 28, 2903–2909. [Google Scholar] [CrossRef] [PubMed]
  3. Wang, X.; Hu, Y.; Wei, H. Nanozymes in bionanotechnology: From sensing to therapeutics and beyond. Inorg. Chem. Front. 2016, 3, 41–60. [Google Scholar] [CrossRef]
  4. Wu, J.; Li, S.; Wei, H. Multifunctional nanozymes: Enzyme-like catalytic activity combined with magnetism and surface plasmon resonance. Nanoscale Horiz. 2018, 3, 367–382. [Google Scholar] [CrossRef] [PubMed]
  5. Wu, J.; Li, S.; Wei, H. Integrated nanozymes: Facile preparation and biomedical applications. Chem. Commun. 2018, 54, 6520–6530. [Google Scholar] [CrossRef]
  6. Jiang, D.; Ni, D.; Rosenkrans, Z.T.; Huang, P.; Yan, X.; Cai, W. Nanozyme: New horizons for responsive biomedical applications. Chem. Soc. Rev. 2019, 48, 3683–3704. [Google Scholar] [CrossRef]
  7. Wei, H.; Wang, E. Nanomaterials with enzyme-like characteristics (nanozymes): Next-generation artificial enzymes. Chem. Soc. Rev. 2013, 42, 6060–6093. [Google Scholar] [CrossRef]
  8. Gao, L.; Fan, K.; Yan, X. Iron Oxide Nanozyme: A Multifunctional Enzyme Mimetic for Biomedical Applications. Theranostics 2017, 7, 3207–3227. [Google Scholar] [CrossRef]
  9. Wu, J.; Wang, X.; Wang, Q.; Lou, Z.; Li, S.; Zhu, Y.; Qin, L.; Wei, H. Nanomaterials with enzyme-like characteristics (nanozymes): Next-generation artificial enzymes (II). Chem. Soc. Rev. 2019, 48, 1004–1076. [Google Scholar] [CrossRef]
  10. Wang, X.; Gao, X.J.; Qin, L.; Wang, C.; Song, L.; Zhou, Y.-N.; Zhu, G.; Cao, W.; Lin, S.; Zhou, L.; et al. eg occupancy as an effective descriptor for the catalytic activity of perovskite oxide-based peroxidase mimics. Nat. Commun. 2019, 10, 704. [Google Scholar] [CrossRef] [Green Version]
  11. Zhang, K.; Hu, X.; Liu, J.; Yin, J.-J.; Hou, S.; Wen, T.; He, W.; Ji, Y.; Guo, Y.; Wang, Q.; et al. Formation of PdPt Alloy Nanodots on Gold Nanorods: Tuning Oxidase-like Activities via Composition. Langmuir 2011, 27, 2796–2803. [Google Scholar] [CrossRef] [PubMed]
  12. Zhang, Y.; Wang, F.; Liu, C.; Wang, Z.; Kang, L.; Huang, Y.; Dong, K.; Ren, J.; Qu, X. Nanozyme Decorated Metal–Organic Frameworks for Enhanced Photodynamic Therapy. ACS Nano 2018, 12, 651–661. [Google Scholar] [CrossRef] [PubMed]
  13. Wang, X.; Qin, L.; Zhou, M.; Lou, Z.; Wei, H. Nanozyme Sensor Arrays for Detecting Versatile Analytes from Small Molecules to Proteins and Cells. Anal. Chem. 2018, 90, 11696–11702. [Google Scholar] [CrossRef]
  14. Han, L.; Zhang, H.; Li, F. Bioinspired Nanozymes with pH-Independent and Metal Ions-Controllable Activity: Field-Programmable Logic Conversion of Sole Logic Gate System. Part. Part. Syst. Charact. 2018, 35, 1800207. [Google Scholar] [CrossRef]
  15. Zhang, Z.; Wang, J.; Nie, X.; Wen, T.; Ji, Y.; Wu, X.; Zhao, Y.; Chen, C. Near infrared laser-induced targeted cancer therapy using thermoresponsive polymer encapsulated gold nanorods. J. Am. Chem. Soc. 2014, 136, 7317–7326. [Google Scholar] [CrossRef] [PubMed]
  16. Wang, F.; Ju, E.; Guan, Y.; Ren, J.; Qu, X. Light-Mediated Reversible Modulation of ROS Level in Living Cells by Using an Activity-Controllable Nanozyme. Small 2017, 13, 1603051. [Google Scholar] [CrossRef]
  17. He, W.; Zhou, Y.-T.; Wamer, W.G.; Hu, X.; Wu, X.; Zheng, Z.; Boudreau, M.D.; Yin, J.-J. Intrinsic catalytic activity of Au nanoparticles with respect to hydrogen peroxide decomposition and superoxide scavenging. Biomaterials 2013, 34, 765–773. [Google Scholar] [CrossRef]
  18. Das, R.; Dhiman, A.; Kapil, A.; Bansal, V.; Sharma, T.K. Aptamer-mediated colorimetric and electrochemical detection of Pseudomonas aeruginosa utilizing peroxidase-mimic activity of gold NanoZyme. Anal. Bioanal. Chem. 2019, 411, 1229–1238. [Google Scholar] [CrossRef]
  19. Pham, X.-H.; Seong, B.; Bock, S.; Hahm, E.; Huynh, K.-H.; Kim, Y.-H.; Kim, W.; Kim, J.; Kim, D.-E.; Jun, B.-H. Nonenzymatic Hydrogen Peroxide Detection Using Surface-Enhanced Raman Scattering of Gold–Silver Core–Shell-Assembled Silica Nanostructures. Nanomaterials 2021, 11, 2748. [Google Scholar] [CrossRef]
  20. Walther, R.; Winther, A.K.; Fruergaard, A.S.; van den Akker, W.; Sørensen, L.; Nielsen, S.M.; Jarlstad Olesen, M.T.; Dai, Y.; Jeppesen, H.S.; Lamagni, P.; et al. Identification and Directed Development of Non-Organic Catalysts with Apparent Pan-Enzymatic Mimicry into Nanozymes for Efficient Prodrug Conversion. Angew. Chem. Int. Ed. 2019, 58, 278–282. [Google Scholar] [CrossRef]
  21. Gao, L.; Zhuang, J.; Nie, L.; Zhang, J.; Zhang, Y.; Gu, N.; Wang, T.; Feng, J.; Yang, D.; Perrett, S.; et al. Intrinsic peroxidase-like activity of ferromagnetic nanoparticles. Nat. Nanotechnol. 2007, 2, 577–583. [Google Scholar] [CrossRef] [PubMed]
  22. Bhagat, S.; Srikanth Vallabani, N.V.; Shutthanandan, V.; Bowden, M.; Karakoti, A.S.; Singh, S. Gold core/ceria shell-based redox active nanozyme mimicking the biological multienzyme complex phenomenon. J. Colloid Interface Sci. 2018, 513, 831–842. [Google Scholar] [CrossRef] [PubMed]
  23. Huang, Y.; Liu, Z.; Liu, C.; Ju, E.; Zhang, Y.; Ren, J.; Qu, X. Self-Assembly of Multi-nanozymes to Mimic an Intracellular Antioxidant Defense System. Angew. Chem. Int. Ed. 2016, 55, 6646–6650. [Google Scholar] [CrossRef] [PubMed]
  24. Singh, N.; Savanur, M.A.; Srivastava, S.; D’Silva, P.; Mugesh, G. A Redox Modulatory Mn3O4 Nanozyme with Multi-Enzyme Activity Provides Efficient Cytoprotection to Human Cells in a Parkinson’s Disease Model. Angew. Chem. Int. Ed. 2017, 56, 14267–14271. [Google Scholar] [CrossRef] [PubMed]
  25. Singh, N.; Geethika, M.; Eswarappa, S.M.; Mugesh, G. Manganese-Based Nanozymes: Multienzyme Redox Activity and Effect on the Nitric Oxide Produced by Endothelial Nitric Oxide Synthase. Chem. A Eur. J. 2018, 24, 8393–8403. [Google Scholar] [CrossRef]
  26. Yang, Z.; Wang, C.; Lu, X. Conducting polymer-based peroxidase mimics: Synthesis, synergistic enhanced properties and applications. Sci. China Mater. 2018, 61, 653–670. [Google Scholar] [CrossRef] [Green Version]
  27. Zheng, H.-Q.; Liu, C.-Y.; Zeng, X.-Y.; Chen, J.; Lü, J.; Lin, R.-G.; Cao, R.; Lin, Z.-J.; Su, J.-W. MOF-808: A Metal–Organic Framework with Intrinsic Peroxidase-Like Catalytic Activity at Neutral pH for Colorimetric Biosensing. Inorg. Chem. 2018, 57, 9096–9104. [Google Scholar] [CrossRef]
  28. Garg, B.; Bisht, T. Carbon Nanodots as Peroxidase Nanozymes for Biosensing. Molecules 2016, 21, 1653. [Google Scholar] [CrossRef]
  29. Zhang, X.; Li, G.; Chen, G.; Wu, D.; Zhou, X.; Wu, Y. Single-atom nanozymes: A rising star for biosensing and biomedicine. Coordin. Chem. Rev. 2020, 418, 213376. [Google Scholar] [CrossRef]
  30. Huang, Y.; Ren, J.; Qu, X. Nanozymes: Classification, Catalytic Mechanisms, Activity Regulation, and Applications. Chem. Rev. 2019, 119, 4357–4412. [Google Scholar] [CrossRef]
  31. Sindhu, R.K.; Najda, A.; Kaur, P.; Shah, M.; Singh, H.; Kaur, P.; Cavalu, S.; Jaroszuk-Sierocińska, M.; Rahman, M.H. Potentiality of Nanoenzymes for Cancer Treatment and Other Diseases: Current Status and Future Challenges. Materials 2021, 14, 5965. [Google Scholar] [CrossRef] [PubMed]
  32. Wang, P.; Wang, T.; Hong, J.; Yan, X.; Liang, M. Nanozymes: A New Disease Imaging Strategy. Front. Bioeng. Biotechnol. 2020, 8, 15. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  33. Wang, Q.; Wei, H.; Zhang, Z.; Wang, E.; Dong, S. Nanozyme: An emerging alternative to natural enzyme for biosensing and immunoassay. Trends Anal. Chem. TrAC 2018, 105, 218–224. [Google Scholar] [CrossRef]
  34. Das, B.; Franco, J.L.; Logan, N.; Balasubramanian, P.; Kim, M.I.; Cao, C. Nanozymes in Point-of-Care Diagnosis: An Emerging Futuristic Approach for Biosensing. Nano-Micro Lett. 2021, 13, 193. [Google Scholar] [CrossRef] [PubMed]
  35. Sharma, G.; Kumar, A.; Sharma, S.; Naushad, M.; Prakash Dwivedi, R.; Alothman, Z.A.; Mola, G.T. Novel development of nanoparticles to bimetallic nanoparticles and their composites: A review. J. King Saud Univ. Sci. 2019, 31, 257–269. [Google Scholar] [CrossRef]
  36. Langlois, C.; Li, Z.L.; Yuan, J.; Alloyeau, D.; Nelayah, J.; Bochicchio, D.; Ferrando, R.; Ricolleau, C. Transition from core–shell to Janus chemical configuration for bimetallic nanoparticles. Nanoscale 2012, 4, 3381–3388. [Google Scholar] [CrossRef] [Green Version]
  37. Hu, X.; Saran, A.; Hou, S.; Wen, T.; Ji, Y.; Liu, W.; Zhang, H.; He, W.; Yin, J.-J.; Wu, X. Au@PtAg core/shell nanorods: Tailoring enzyme-like activities via alloying. RSC Adv. 2013, 3, 6095–6105. [Google Scholar] [CrossRef]
  38. Cai, S.; Qi, C.; Li, Y.; Han, Q.; Yang, R.; Wang, C. PtCo bimetallic nanoparticles with high oxidase-like catalytic activity and their applications for magnetic-enhanced colorimetric biosensing. J. Mater. Chem. B 2016, 4, 1869–1877. [Google Scholar] [CrossRef]
  39. Lapp, A.S.; Duan, Z.; Marcella, N.; Luo, L.; Genc, A.; Ringnalda, J.; Frenkel, A.I.; Henkelman, G.; Crooks, R.M. Experimental and Theoretical Structural Investigation of AuPt Nanoparticles Synthesized Using a Direct Electrochemical Method. J. Am. Chem. Soc. 2018, 140, 6249–6259. [Google Scholar] [CrossRef]
  40. Gawande, M.B.; Goswami, A.; Asefa, T.; Guo, H.; Biradar, A.V.; Peng, D.-L.; Zboril, R.; Varma, R.S. Core–shell nanoparticles: Synthesis and applications in catalysis and electrocatalysis. Chem. Soc. Rev. 2015, 44, 7540–7590. [Google Scholar] [CrossRef]
  41. He, W.; Wamer, W.; Xia, Q.; Yin, J.-j.; Fu, P.P. Enzyme-Like Activity of Nanomaterials. J. Environ. Sci. Health Part C 2014, 32, 186–211. [Google Scholar] [CrossRef] [PubMed]
  42. Liu, J.; Jiang, X.; Wang, L.; Hu, Z.; Wen, T.; Liu, W.; Yin, J.; Chen, C.; Wu, X. Ferroxidase-like activity of Au nanorod/Pt nanodot structures and implications for cellular oxidative stress. Nano Res. 2015, 8, 4024–4037. [Google Scholar] [CrossRef]
  43. Liu, Y.; Wu, H.; Chong, Y.; Wamer, W.G.; Xia, Q.; Cai, L.; Nie, Z.; Fu, P.P.; Yin, J.-J. Platinum Nanoparticles: Efficient and Stable Catechol Oxidase Mimetics. ACS Appl. Mater. Interfaces 2015, 7, 19709–19717. [Google Scholar] [CrossRef] [PubMed]
  44. Zhou, Y.-T.; He, W.; Wamer, W.G.; Hu, X.; Wu, X.; Lo, Y.M.; Yin, J.-J. Enzyme-mimetic effects of gold@platinum nanorods on the antioxidant activity of ascorbic acid. Nanoscale 2013, 5, 1583–1591. [Google Scholar] [CrossRef]
  45. Wu, Q.; Li, Y.; Xian, H.; Xu, C.; Wang, L.; Chen, Z. Ultralow Pt-loading bimetallic nanoflowers: Fabrication and sensing applications. Nanotechnology 2012, 24, 25501. [Google Scholar] [CrossRef]
  46. Tseng, C.-W.; Chang, H.-Y.; Chang, J.-Y.; Huang, C.-C. Detection of mercury ions based on mercury-induced switching of enzyme-like activity of platinum/gold nanoparticles. Nanoscale 2012, 4, 6823–6830. [Google Scholar] [CrossRef]
  47. Li, X.-R.; Xu, M.-C.; Chen, H.-Y.; Xu, J.-J. Bimetallic Au@Pt@Au core–shell nanoparticles on graphene oxide nanosheets for high-performance H2O2 bi-directional sensing. J. Mater. Chem. B 2015, 3, 4355–4362. [Google Scholar] [CrossRef]
  48. Li, D.; Meng, F.; Wang, H.; Jiang, X.; Zhu, Y. Nanoporous AuPt alloy with low Pt content: A remarkable electrocatalyst with enhanced activity towards formic acid electro-oxidation. Electrochim. Acta 2016, 190, 852–861. [Google Scholar] [CrossRef] [Green Version]
  49. Suntivich, J.; Xu, Z.; Carlton, C.E.; Kim, J.; Han, B.; Lee, S.W.; Bonnet, N.; Marzari, N.; Allard, L.F.; Gasteiger, H.A.; et al. Surface Composition Tuning of Au–Pt Bimetallic Nanoparticles for Enhanced Carbon Monoxide and Methanol Electro-oxidation. J. Am. Chem. Soc. 2013, 135, 7985–7991. [Google Scholar] [CrossRef]
  50. Kajita, M.; Hikosaka, K.; Iitsuka, M.; Kanayama, A.; Toshima, N.; Miyamoto, Y. Platinum nanoparticle is a useful scavenger of superoxide anion and hydrogen peroxide. Free Radic. Res. 2007, 41, 615–626. [Google Scholar] [CrossRef]
  51. Kim, J.; Takahashi, M.; Shimizu, T.; Shirasawa, T.; Kajita, M.; Kanayama, A.; Miyamoto, Y. Effects of a potent antioxidant, platinum nanoparticle, on the lifespan of Caenorhabditis elegans. Mech. Ageing Dev. 2008, 129, 322–331. [Google Scholar] [CrossRef] [PubMed]
  52. Hamasaki, T.; Kashiwagi, T.; Imada, T.; Nakamichi, N.; Aramaki, S.; Toh, K.; Morisawa, S.; Shimakoshi, H.; Hisaeda, Y.; Shirahata, S. Kinetic analysis of superoxide anion radical-scavenging and hydroxyl radical-scavenging activities of platinum nanoparticles. Langmuir 2008, 24, 7354–7364. [Google Scholar] [CrossRef] [PubMed]
  53. Li, J.; Xu, K.; Chen, Y.; Zhao, J.; Du, P.; Zhang, L.; Zhang, Z.; Lu, X. Pt Nanoparticles Anchored on NH2-MIL-101 with Efficient Peroxidase-Like Activity for Colorimetric Detection of Dopamine. Chemosensors 2021, 9, 140. [Google Scholar] [CrossRef]
  54. Seong, B.; Bock, S.; Hahm, E.; Huynh, K.-H.; Kim, J.; Lee, S.H.; Pham, X.-H.; Jun, B.-H. Synthesis of Densely Immobilized Gold-Assembled Silica Nanostructures. Int. J. Mol. Sci. 2021, 22, 2543. [Google Scholar] [CrossRef] [PubMed]
  55. Seong, B.; Kim, J.; Kim, W.; Lee, S.H.; Pham, X.-H.; Jun, B.-H. Synthesis of Finely Controllable Sizes of Au Nanoparticles on a Silica Template and Their Nanozyme Properties. Int. J. Mol. Sci. 2021, 22, 10382. [Google Scholar] [CrossRef]
  56. Bock, S.; Choi, Y.-S.; Kim, M.; Yun, Y.; Pham, X.-H.; Kim, J.; Seong, B.; Kim, W.; Jo, A.; Ham, K.-M.; et al. Highly sensitive near-infrared SERS nanoprobes for in vivo imaging using gold-assembled silica nanoparticles with controllable nanogaps. J. Nanobiotechnol. 2022, 20, 130. [Google Scholar] [CrossRef]
  57. Pham, X.-H.; Hahm, E.; Kang, E.; Ha, Y.N.; Lee, S.H.; Rho, W.-Y.; Lee, Y.-S.; Jeong, D.H.; Jun, B.-H. Gold-silver bimetallic nanoparticles with a Raman labeling chemical assembled on silica nanoparticles as an internal-standard-containing nanoprobe. J. Alloys Compd. 2019, 779, 360–366. [Google Scholar] [CrossRef]
  58. Pham, X.-H.; Hahm, E.; Huynh, K.-H.; Son, B.S.; Kim, H.-M.; Jeong, D.H.; Jun, B.-H. 4-Mercaptobenzoic Acid Labeled Gold-Silver-Alloy-Embedded Silica Nanoparticles as an Internal Standard Containing Nanostructures for Sensitive Quantitative Thiram Detection. Int. J. Mol. Sci. 2019, 20, 4841. [Google Scholar] [CrossRef] [Green Version]
  59. Yang, H.; Wang, J.; Li, X.; Zhang, L.; Yu, H.; Zhang, L.; Ge, S.; Yu, J.; Zhang, Y. Self-Circulation Oxygen–Hydrogen Peroxide–Oxygen System for Ultrasensitive Cathode Photoelectrochemical Bioassay Using a Stacked Sealed Paper Device. ACS Appl. Mater. Interfaces 2021, 13, 19793–19802. [Google Scholar] [CrossRef]
  60. Liu, H.; Weng, L.; Yang, C. A review on nanomaterial-based electrochemical sensors for H2O2, H2S and NO inside cells or released by cells. Microchim. Acta 2017, 184, 1267–1283. [Google Scholar] [CrossRef]
  61. Elias, H.; Vayssié, S. Reactive Peroxo Compounds Generated in Situ from Hydrogen Peroxide: Kinetics and Catalytic Application in Oxidation Processes. In Peroxide Chemistry; Wiley: Hoboken, NJ, USA, 2000; pp. 128–138. [Google Scholar] [CrossRef]
  62. Shim, S.; Pham, X.-H.; Cha, M.G.; Lee, Y.-S.; Jeong, D.H.; Jun, B.-H. Size effect of gold on Ag-coated Au nanoparticle-embedded silica nanospheres. RSC Adv. 2016, 6, 48644–48650. [Google Scholar] [CrossRef]
  63. Pham, X.-H.; Lee, M.; Shim, S.; Jeong, S.; Kim, H.-M.; Hahm, E.; Lee, S.H.; Lee, Y.-S.; Jeong, D.H.; Jun, B.-H. Highly sensitive and reliable SERS probes based on nanogap control of a Au-Ag alloy on silica nanoparticles. RSC Adv. 2017, 7, 7015–7021. [Google Scholar] [CrossRef] [Green Version]
  64. Pham, X.-H.; Hahm, E.; Kang, E.; Son, B.S.; Ha, Y.; Kim, H.-M.; Jeong, D.H.; Jun, B.-H. Control of Silver Coating on Raman Label Incorporated Gold Nanoparticles Assembled Silica Nanoparticles. Int. J. Mol. Sci. 2019, 20, 1258. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  65. Grzelczak, M.; Pérez-Juste, J.; Mulvaney, P.; Liz-Marzán, L.M. Shape control in gold nanoparticle synthesis. Chem. Soc. Rev. 2008, 37, 1783–1791. [Google Scholar] [CrossRef] [PubMed]
  66. Feng, R.; Li, M.; Liu, J. Synthesis of core–shell Au@Pt nanoparticles supported on Vulcan XC-72 carbon and their electrocatalytic activities for methanol oxidation. Colloid Surf. A Physicochem. Eng. Asp. 2012, 406, 6–12. [Google Scholar] [CrossRef]
  67. Kristian, N.; Yan, Y.; Wang, X. Highly efficient submonolayer Pt-decorated Au nano-catalysts for formic acid oxidation. Chem. Commun. 2008, 3, 353–355. [Google Scholar] [CrossRef]
  68. Josephy, P.D.; Eling, T.; Mason, R.P. The horseradish peroxidase-catalyzed oxidation of 3,5,3′,5′-tetramethylbenzidine. Free radical and charge-transfer complex intermediates. J. Biol. Chem. 1982, 257, 3669–3675. [Google Scholar] [CrossRef]
  69. He, W.; Han, X.; Jia, H.; Cai, J.; Zhou, Y.; Zheng, Z. AuPt Alloy Nanostructures with Tunable Composition and Enzyme-like Activities for Colorimetric Detection of Bisulfide. Sci. Rep. 2017, 7, 40103. [Google Scholar] [CrossRef]
  70. Asati, A.; Kaittanis, C.; Santra, S.; Perez, J.M. pH-Tunable Oxidase-Like Activity of Cerium Oxide Nanoparticles Achieving Sensitive Fluorigenic Detection of Cancer Biomarkers at Neutral pH. Anal. Chem. 2011, 83, 2547–2553. [Google Scholar] [CrossRef] [Green Version]
  71. Ge, C.; Fang, G.; Shen, X.; Chong, Y.; Wamer, W.G.; Gao, X.; Chai, Z.; Chen, C.; Yin, J.-J. Facet energy versus enzyme-like activities: The unexpected protection of palladium nanocrystals against oxidative damage. ACS Nano 2016, 10, 10436–10445. [Google Scholar] [CrossRef]
  72. Lin, L.; Song, X.; Chen, Y.; Rong, M.; Zhao, T.; Wang, Y.; Jiang, Y.; Chen, X. Intrinsic peroxidase-like catalytic activity of nitrogen-doped graphene quantum dots and their application in the colorimetric detection of H2O2 and glucose. Anal. Chim. Acta 2015, 869, 89–95. [Google Scholar] [CrossRef] [PubMed]
  73. Wang, H.; Zheng, L.; Peng, C.; Guo, R.; Shen, M.; Shi, X.; Zhang, G. Computed tomography imaging of cancer cells using acetylated dendrimer-entrapped gold nanoparticles. Biomaterials 2011, 32, 2979–2988. [Google Scholar] [CrossRef] [PubMed]
  74. Shah, V.; Shah, S.; Shah, H.; Rispoli, F.J.; McDonnell, K.T.; Workeneh, S.; Karakoti, A.; Kumar, A.; Seal, S. Antibacterial activity of polymer coated cerium oxide nanoparticles. PLoS ONE 2012, 7, e47827. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  75. Tian, J.; Liu, S.; Luo, Y.; Sun, X. Fe (III)-based coordination polymer nanoparticles: Peroxidase-like catalytic activity and their application to hydrogen peroxide and glucose detection. Catal. Sci. Technol. 2012, 2, 432–436. [Google Scholar] [CrossRef]
  76. Song, Y.; Qu, K.; Zhao, C.; Ren, J.; Qu, X. Graphene Oxide: Intrinsic Peroxidase Catalytic Activity and Its Application to Glucose Detection. Adv. Mater. 2010, 22, 2206–2210. [Google Scholar] [CrossRef]
  77. Lipinski, B. Hydroxyl Radical and Its Scavengers in Health and Disease. Oxid. Med. Cell. Longev. 2011, 2011, 809696. [Google Scholar] [CrossRef] [Green Version]
  78. Frey, A.; Meckelein, B.; Externest, D.; Schmidt, M.A. A stable and highly sensitive 3,3′,5,5′-tetramethylbenzidine-based substrate reagent for enzyme-linked immunosorbent assays. J. Immunol. Methods 2000, 233, 47–56. [Google Scholar] [CrossRef]
  79. Teodoro, K.B.R.; Migliorini, F.L.; Christinelli, W.A.; Correa, D.S. Detection of hydrogen peroxide (H2O2) using a colorimetric sensor based on cellulose nanowhiskers and silver nanoparticles. Carbohydr. Polym. 2019, 212, 235–241. [Google Scholar] [CrossRef]
  80. Tian, R.; Zhang, B.; Zhao, M.; Zou, H.; Zhang, C.; Qi, Y.; Ma, Q. Fluorometric enhancement of the detection of H2O2 using different organic substrates and a peroxidase-mimicking polyoxometalate. RSC Adv. 2019, 9, 12209–12217. [Google Scholar] [CrossRef] [Green Version]
  81. Chen, Y.; Zhong, Q.; Wang, Y.; Yuan, C.; Qin, X.; Xu, Y. Colorimetric detection of hydrogen peroxide and glucose by exploiting the peroxidase-like activity of papain. RSC Adv. 2019, 9, 16566–16570. [Google Scholar] [CrossRef] [Green Version]
  82. Zhang, Z.; Liu, Q.; Liu, Y.; Qi, R.; Zhou, L.; Li, Z.; Yun, J.; Liu, R.; Hu, Y. Colorimetric H2O2 Detection Using Ag-Nanoparticle-Decorated Silica Microspheres. Nano 2020, 15, 2050009. [Google Scholar] [CrossRef]
  83. Wang, Y.; Zhou, B.; Wu, S.; Wang, K.; He, X. Colorimetric detection of hydrogen peroxide and glucose using the magnetic mesoporous silica nanoparticles. Talanta 2015, 134, 712–717. [Google Scholar] [CrossRef] [PubMed]
  84. Deutsch, J.C. Ascorbic Acid Oxidation by Hydrogen Peroxide. Anal. Biochem. 1998, 255, 1–7. [Google Scholar] [CrossRef] [PubMed] [Green Version]
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Figure 1. (a) Transmission electronic microscopy images of SiO2@Au seed and gold-platinum-embedded silica nanospheres (SiO2@Au@Pt) at different magnifications. (b) Line energy dispersive X-ray mapping of SiO2@Au@Pt for Pt and Au elements. (c) UV-Vis absorbance spectroscopy of SiO2@Au seeds and SiO2@Au@Pt NPs. (d) UV-Vis absorbance spectroscopy of SiO2@Au@Pt in various solutions. The inset shows the colors of the solutions.
Figure 1. (a) Transmission electronic microscopy images of SiO2@Au seed and gold-platinum-embedded silica nanospheres (SiO2@Au@Pt) at different magnifications. (b) Line energy dispersive X-ray mapping of SiO2@Au@Pt for Pt and Au elements. (c) UV-Vis absorbance spectroscopy of SiO2@Au seeds and SiO2@Au@Pt NPs. (d) UV-Vis absorbance spectroscopy of SiO2@Au@Pt in various solutions. The inset shows the colors of the solutions.
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Figure 2. (a) UV-Vis absorbance spectroscopy of SiO2@Au@Pt and SiO2@Au@Au (5 µg) in TMB and in TMB-H2O2 solutions. The inset shows the colors of the solutions. (b) The absorbance of recycled SiO2@Au@Au and SiO2@Au@Pt is shown in a TMB-H2O2 solution. (c) UV-Vis absorbance spectroscopy and (d) Lineweaver-Burk plot at 652 nm for 5 μg SiO2@Au@Pt in a TMB-H2O2 solution (0–600 µM TMB).
Figure 2. (a) UV-Vis absorbance spectroscopy of SiO2@Au@Pt and SiO2@Au@Au (5 µg) in TMB and in TMB-H2O2 solutions. The inset shows the colors of the solutions. (b) The absorbance of recycled SiO2@Au@Au and SiO2@Au@Pt is shown in a TMB-H2O2 solution. (c) UV-Vis absorbance spectroscopy and (d) Lineweaver-Burk plot at 652 nm for 5 μg SiO2@Au@Pt in a TMB-H2O2 solution (0–600 µM TMB).
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Figure 3. (a) TEM images are shown at different magnifications. (b) UV–Vis absorbance spectroscopy images of SiO2@Au@Pt NPs fabricated with various concentrations of Pt2+. (c,d) Absorbance plots of SiO2@Au@Pt NPs and (e) Effect of Pt/Au ratio on the absorbance at 453 nm in the presence of TMB and H2O2 fabricated with various concentrations of Pt2+.
Figure 3. (a) TEM images are shown at different magnifications. (b) UV–Vis absorbance spectroscopy images of SiO2@Au@Pt NPs fabricated with various concentrations of Pt2+. (c,d) Absorbance plots of SiO2@Au@Pt NPs and (e) Effect of Pt/Au ratio on the absorbance at 453 nm in the presence of TMB and H2O2 fabricated with various concentrations of Pt2+.
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Figure 4. The effects of different conditions on the peroxidase-like catalytic activity of SiO2@Au@Pt NPs in a mixture of TMB and H2O2. (a) The amount of SiO2@Au@Pt, (b) incubation time, (c) pH of the solution, and (d) TMB concentration were varied.
Figure 4. The effects of different conditions on the peroxidase-like catalytic activity of SiO2@Au@Pt NPs in a mixture of TMB and H2O2. (a) The amount of SiO2@Au@Pt, (b) incubation time, (c) pH of the solution, and (d) TMB concentration were varied.
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Figure 5. (a) Colors of the solutions. (b) An absorbance signal plot at 453 nm and (c) the dynamic linear range of SiO2@Au@Pt@Pt at various H2O2 concentrations in the presence of 0.5 mM TMB. The optimized conditions were 5 µg SiO2@Au@Pt@Pt, 0.5 mM TMB, a 15 min incubation period, and a pH of 4.0.
Figure 5. (a) Colors of the solutions. (b) An absorbance signal plot at 453 nm and (c) the dynamic linear range of SiO2@Au@Pt@Pt at various H2O2 concentrations in the presence of 0.5 mM TMB. The optimized conditions were 5 µg SiO2@Au@Pt@Pt, 0.5 mM TMB, a 15 min incubation period, and a pH of 4.0.
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Pham, X.-H.; Tran, V.-K.; Hahm, E.; Kim, Y.-H.; Kim, J.; Kim, W.; Jun, B.-H. Synthesis of Gold-Platinum Core-Shell Nanoparticles Assembled on a Silica Template and Their Peroxidase Nanozyme Properties. Int. J. Mol. Sci. 2022, 23, 6424. https://doi.org/10.3390/ijms23126424

AMA Style

Pham X-H, Tran V-K, Hahm E, Kim Y-H, Kim J, Kim W, Jun B-H. Synthesis of Gold-Platinum Core-Shell Nanoparticles Assembled on a Silica Template and Their Peroxidase Nanozyme Properties. International Journal of Molecular Sciences. 2022; 23(12):6424. https://doi.org/10.3390/ijms23126424

Chicago/Turabian Style

Pham, Xuan-Hung, Van-Khue Tran, Eunil Hahm, Yoon-Hee Kim, Jaehi Kim, Wooyeon Kim, and Bong-Hyun Jun. 2022. "Synthesis of Gold-Platinum Core-Shell Nanoparticles Assembled on a Silica Template and Their Peroxidase Nanozyme Properties" International Journal of Molecular Sciences 23, no. 12: 6424. https://doi.org/10.3390/ijms23126424

APA Style

Pham, X. -H., Tran, V. -K., Hahm, E., Kim, Y. -H., Kim, J., Kim, W., & Jun, B. -H. (2022). Synthesis of Gold-Platinum Core-Shell Nanoparticles Assembled on a Silica Template and Their Peroxidase Nanozyme Properties. International Journal of Molecular Sciences, 23(12), 6424. https://doi.org/10.3390/ijms23126424

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