Nanonetwork of Coordination Polymer AHMT-Ag for the Effective and Broad Spectrum Detection of 6-Mercaptopurine in Urine and Blood Serum.

Nanocrystalline coordination polymers (NCCPs) have been considered as an incredible electrochemical sensor for the effective detection of biologically dynamic drug 6-mercaptopurine (6-MP). In the present report, a significantly stable infinite arrayed coordination polymeric network was self-assembled via metal with efficient organic tecton 4-amino-3-hydrazino-5-mercapto-1,2,4,-triazole (AHMT) in which silver(I) ions are coordinated by AHMT via hydrazino and exocyclic thiol linkage to form AHMT-Ag NCCP. An efficient and highly sensitive detection of 6-MP is attained owing to eminent electron channeling via polymeric nanocrystallite pores. An effective charge transfer leads to an interface of the AHMT-Ag nano-pores and electrolyte anchored electrode via π-π electron coupling and hydrophobic interaction. The voltammogram exposes acute redox behavior of 6-MP and discloses an impeccable illustration for the AHMT-Ag facilitated oxidation of 6-MP. This unique signature was applied in voltammetric detection of 6-MP in blood serum, human urine, and pharmaceutical formulation (tablet) by a considerable high sensitivity of 0.074, 0.058, and 0.036 μA/μM and a detection limit of 87, 97, and 37 nM, respectively. Thus, the prepared AHMT-Ag NCCP can provide a valuable platform for fabrication of highly sensitive electrochemical devices to assay biologically essential drug molecules.

Introduction

Nanocrystalline coordination polymers-(NCCPs) are an attractive class of tailorable material and exhibit outstanding properties that expands the scope in various areas.[1] The significant research interest in the domain of these important scaffold are due to their specific size, structural regularity, high surface area, high porosity, design ability, and easy tunability results to a larger potential in different applications.[2−5] Nano size of these crystalline coordination polymeric regimes are of large significance in catalysis, thin film devices, and drug delivery.[6,7] Owing to these features recent research affords for the sketch of fashionable organization of metal ions with organic tecton results with a huge potential for various applications.[8−10] Geometry and coordination manner of organic tecton and metal center affects the properties and structure of NCCP, other secondary interactions, such as hydrogen bonding also results in the versatile properties of NCCPs.[11,12] In this regard, 4-amino-3-hydrazino-5-mercapto-1,2,4-triazole (AHMT), an efficient organic tecton used for the production of functional NCCP. Nitrogen and sulfur atoms facilitate coordination of organic tecton with a metal ion throughout the arrangement to create a functional structure. Because of structural tailorability of the organic tecton and capability to regulate the assembly with a metal ion at the nanoextent, they have fascinating applications in energy storage,[13] catalysis,[14] adsorption,[15] efficient contrast agents,[16] biotechnology,[17] nanofluids,[18] gas separation,[19] chemical sensing,[20,21] light harvesting,[22] device formation[23] and drug delivery,[24] selective catalysis,[25] fuel cells,[26] and so forth. The prominent interactions are metal–ligand interactions that create extra strong entities. Furthermore, the π–π stacking between polymer chains that inter- and intra-hydrogen bonding direct toward an organization and definite alignment of these structures.[27]

In the view of the above particulars, our research interest is preparation of unique nanosized coordination polymers with reasonable organic building blocks and electrochemical sensing of frequently used drugs; here we first time explore the development of AHMT-Ag NCCPs with an identical crystalline structure, high solvent dispersibility, and electrochemical activity for sensing application.

AHMT-Ag NCCP was formulated under optimal conditions at ambient temperature without any additional supplements. The optimization of reactant concentration is executed while synthesis and monitored by using appropriate characterization techniques. During synthesis the Ag(I) ions coordinate to nitrogen and sulfur atoms of the linker resulting in exceptional capability requisite for molecular amendment of the inner pore architecture. Thus, NCCPs cover huge advantages for the valuable application. This platform is advantageous for various sensing applications because of its multiple binding sites.

At present there is a number of lifesaving drugs frequently used every day, when their amount exceeds above a certain level it causes toxicity. 6-Meracaptopurine (6-MP), an excessively important immunosuppressive drug, is used in anticancer chemotherapy for dealing acute lymphoblastic leukemia and inflammatory bowel disease. Generally, the 6-MP concentration was found to be unpredictably high and low variable in plasma, with manifest individual differences. Hence, it is very essential to monitor the concentration of 6-MP.[28]

Numerous approaches have been devoted for the detection of 6-MP in biological preparation and pharmaceutical comprising capillary electrophoresis,[29] high-performance liquid chromatography,[30] laser-induced fluorescence,[31] spectrofluorimetry,[32] and chemiluminescence.[33] However, these methods require tedious experimentation. Electrochemical approaches have shown notable advantages in the investigation of drugs in human urine and pharmaceutical preparations. These methods in pharmaceutical analysis are studied owing to their accuracy and precision, low cost, simplicity and rapidity, sensitivity.

In this research work, the voltammetric method have been applied to depict the electrochemical nature of 6-MP on the carbon paste electrode (CPE) in the presence of highly electro-active AHMT-Ag NCCP as a suitable nanosensor in phosphate buffer (pH 7). Further, the developed sensor was also effectively explored to assay 6-mercaptopurine (6-MP) in real samples of blood serum, urine and tablet.

Results and Discussion

The coordination polymer AHMT-Ag is a remarkably symmetrical architecture which provides coordination position for bonding and construct a well-predictable network with various interactions and unique capacity to frame π stacking all over aromatic array. Here, sulfur and nitrogen atoms of AHMT coordinated with Ag(I) into a huge array of polymeric chain. The synthesized AHMT-Ag was characterized by UV–visible spectroscopy, X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), 1H NMR, high-resolution transmission electron microscopy (HR-TEM), high-resolution scanning electron microscope (HR-SEM), energy-dispersive system (EDS) mapping, energy dispersive X-ray (EDX), and thermal study.

Materials Characterizations

The FT-IR spectrum of AHMT shows various bands in the region 3270–2930 because of ν(N–H) and ν(NH2). The peak broadness recommends intramolecular hydrogen bonding (Figure I). The vibrational band at 3209 cm–1 is initiated because of ν(NH–NH2) of AHMT and remarkably attenuated to 3095 cm–1 in AHMT-Ag, spotting the connection of the exocyclic NH–NH2 with Ag. Additionally, the S–H stretching of AHMT evidenced at 2789 cm–1disappeared in AHMT-Ag; which indicates thiol ionization, bonding of sulfur via the silver atom. The thioamide band I at 1501 cm–1 in AHMT appeared at a higher wave number 1633 cm–1 in AHMT-Ag caused by a decrease in the major contributor ν(N–H), and a substantial increase in the minor contributor ν(C=N), respectively, because of sulfur and silver bonding. Furthermore, typical thioamide band II 1315–1346 cm–1 in AHMT with the significant contributor ν(C=N) increased considerably to 1365 cm–1 in AHMT-Ag, encouraging the bonding of silver with sulfur.

Figure 1

(I) FT-IR spectra (a) AHMT-Ag (b) AHMT and (II) Le-bail fit of AHMT-Ag.

Further XRD was executed in order to investigate the crystal structure. The XRD of AHMT-Ag and AHMT were correlated with Ag(0) attained from the JCPDS file (CAS number 87-0720). AHMT-Ag displays the crystalline nature as shown in S2 Figure S2. It is noticeable that structural characteristics of AHMT and Ag(0) are absent in AHMT-Ag. The crystallographic phase of AHMT-Ag, NCCP was examined at room temperature by XRD with a diffraction angle between 5° and 80°. The, DICVOL04.51 (auto-indexing program) was employed to index the XRD pattern of AHMT-Ag.[34] It was found that experimental diffraction peaks could be indexed using monoclinic, orthorhombic, and triclinic cells. In order to determine the correct crystallographic symmetry for the observed XRD spectra, AHMT-Ag was investigated by Le-Bail refinement through FullProf[35] for different probable crystal structures; for example, orthorhombic Pnma, monoclinic P21/m, Pm, and triclinic P1 space groups. It shows that the triclinic crystal structure has the closest fit between the calculated and experimentally observed profiles of AHMT-Ag with a good figure of merit, and it indexed all the diffraction peaks. Figure II reveals the experimentally observed data point which are indicated with dotted red circles, while the calculated pattern is shown as a continuous solid line and the variation of the observed from calculated pattern is shown by the continuous bottom green line obtained by the Le-Bail fit for space group “triclinic P1”. The vertical lines indicate the Bragg peak locations in the difference plot. From Figure II it can be clearly observed that the diffraction peaks emerge in the pattern representing a good crystalline nature of synthesized AHMT-Ag NCCP. The triclinic cell has the lattice parameters a = 11.055(1), b = 4.4964(1), c = 5.6471 (2), α = 91.62(4), β = 93.34(1), and γ = 90.28(2) and a unit cell volume 280.30(1) A3. The crystallinity of AHMT-Ag is again examined by selected area diffraction of transmission electron microscopy (TEM). The diffraction peaks of AHMT-Ag are indexed. The absorption spectra difference shows the interaction effect of metal (S3 Figure S3). AHMT has remarkable a absorbance at 360 nm, and the fellow AHMT-Ag reveals a characteristic absorbance at 270 nm. Signature of hypsochromic shift in the absorbance spectra is because the interaction between AHMT and Ag. XPS enlightens the chemical environment of the elements in AHMT-Ag and the oxidation state of the Ag center. The fitted peaks using software, XPS peak 4.1 (Figure ) imparts two doublets fitted for Ag (3d). The specific peak at 376.2 eV is the centered feature peak of the 3d3/2 Ag(I),[36] meanwhile the peak at 370.4 eV is the signature of the 3d5/2 Ag(I) supporting the oxidation state of silver. N (1s) peaks deliver 5 sets of the singlet in which the peak at 403.7 eV corresponds to the binding energy of endocyclic amine nitrogen (=N−). Binding energy of 402.7 eV attributed to −NH groups, superior binding energy acquainted to the bonding of silver with nitrogen of −NH. Additionally binding energy at 400.6, 402.1, and 401.4 eV correspond to nitrogen of −NH2, C–N–C, and C–NH–[37,38] The binding energy at 164.6 eV appears because of sulfur (2p3/2). A variation of binding energy favors coordination of the silver atom with exocyclic sulfur. Binding energy at 287.8 and 286.8 eV denotes that the C (1s) spectrum for the suitable fit analogous to N=C–N– and −N=C–S– bonding.[39]

Figure 2

XPS spectra of AHMT-Ag for Ag (3d), N (1s), S (2p), and C (1s) regions.

The 1H NMR spectrum of AHMT has signals at 12.8 that have significance for the ring NH, 7.13 for NH of the NHNH2, 5.4 for SH, and 5.264 ppm for NH2 of the NHNH2 protons relative to TMS. The absence of signal because the SH proton in AHMT-Ag NCCP establishes the bonding of silver through sulfur. The peak that appeared at 4.10 ppm is because of the NH2 of NNH2 in AHMT-Ag. The peak of NHNH2 and NH observed at a lower field, that is, 5.265 and 7.135 ppm, respectively, in AHMT-Ag furnishes bonding of silver with the NHNH2 group of AHMT. The signal corresponding to the S=C–NH proton at 8.406 diminishes in AHMT-Ag NCCP which may be because of bonding of the metal with the sulfur atom of C–S. The doublet at 5.438 also vanished in AHMT-Ag assigning interaction of the metal with the NH2 group of NH–NH2 . The signal corresponding to N–NH2 remained in AHMT-Ag emphasizes the unreacted proton of the amino group (S4 Figure S4).

The morphology and elemental investigation of AHMT-Ag, explored by the HR-TEM, HR-SEM, and SAED pattern shown in Figure provokes a crystalline nanoglobular shaped network structure (S5 Figure S5). The average particle size distribution of AHMT-Ag NCCP was analyzed with Image J software and it shows an average size 20–30 nm (Figure c). The irregular nanoglobules profile of the distinct AHMT-Ag was also captured in the HR-TEM micrograph Figure a,b. The SAED pattern illustrates the crystalline nature of the AHMT-Ag network (Figure d). The corresponding EDX measurements reveals the elemental composition of AHMT-Ag and verifies the presence of S,N, C, and Ag atoms in the selected area as presented in S6 Figure S6. The EDS mapping illustrate the elemental composition of AHMT-Ag. Here, the overlap image discloses homogeneous distribution of Ag, C, N, and S signifying the formation of the dense polymeric chain. The consequent images (S7 Figure. S7) reveal the mapping of discrete elements and evidences the higher nitrogen concentration.

Figure 4

HR TEM of AHMT-Ag (a,b), size distribution graph from the TEM image (c) and corresponding the SAED pattern (d).

Moreover, the molecular modeling is implemented to achieve the favored orientation of the ligand in the network which certifies antialignment, the favored orientation. (S8 Figure S8)

Furthermore, there could be three possible ways for coordination of Ag with ligand 4-amino-3-hydrazino-5-mercapto-1,2,4,-triazole (AHMT). Density functional theory (DFT) study was executed in order to assess the most probable way of interaction. Two ligand units were under investigation with the metal. Geometries of all the dimers were optimized in a water solvent using the B3LYP[40] functional and LanL2DZ basis set for the Ag atom and the 6–31g** basis set for the rest of the atoms. The genuineness of the calculated structures was confirmed by visually examining the vibrational modes related to all real vibration frequencies. All the calculations were accomplished by the Gaussian[41] program and GaussView program was used for visualization of optimized structures and vibrational modes. A most appropriate structure has been proposed after the coordination of Ag with AHMT. Three possible structural considerations were optimized using DFT (Figure ). Gibbs free energies of all the three structures of the Ag-coordinated AHMT dimer were obtained at the B3LYP/6-31G**+LanL2DZ level of theory in the water solvent. The N–Ag–S structure was more stable than N–Ag–N and S–Ag–S by 1.44 and 4.62 eV, respectively.

Figure 3

Three possible structures of the AHMT dimer coordinated with the Ag atom obtained at the B3LYP/6-31G**+LanL2DZ level of theory in water solvent.

Based on these findings the structure of nanocrystalline AHMT-Ag is proposed (Figure ). Ag(I) centers are linked with coordination sites of AHMT via sulfur and nitrogen atoms throughout the arrangement and adjacent layers are stabilized through π stacking of the aromatic ring and the intermolecular hydrogen bonding.

Figure 5

Proposed structural network of AHMT-Ag.

In order to investigate stability of the coordination network, zeta potential of prepared NCCP was measured by using the dynamic light scattering instrument. The charge on NCCP plays an important role in accumulation. Larger positive or negative charge repels each other and prevents accumulation. Zeta potential at −49 mV shows the extensively stable network of NCCP (S9 Figure S9).

Further, thermo-gravimetric properties of AHMT-Ag are studied under a nitrogen environment for analysis of the thermal stability and thermal decomposition activation energy. The thermal decomposition of AHMT and AHMT-Ag was illustrated by the thermal-gravimetric curve TGA (S10 Figure S10). AHMT-Ag shows a significant weight loss revealing thermally stable till 222 °C disclosing a thermally strong network of the coordination polymer. AHMT-Ag displays first degradation at a lower temperature than AHMT which explores the presence of the coordination linkage in AHMT-Ag. Here, first decomposition at 222 °C corresponds to the rupture of the coordination linkage. The minor degradation detected at 100 °C is due to uncoordinated water molecules in both AHMT and AHMT-Ag. Further, consecutive degradation in the TGA plot is due to the thermal breakdown of byproducts and is the same in both AHMT and AHMT-Ag.[42] Activation energy of AHMT-Ag related to thermal degradation is determined via the Broido equation[43] to be 11.39 kJ/mol (S11 Figure S11).

Electro Activity of AHMT-Ag

Electrode Active Surface Area

Electroactivity of the AHMT-Ag NCCP-modified CPE surface is probed by an Fe(III)/Fe(II) redox system and the unmodified CPE, AHMT-Ag/CPE active surface area are calculated to be 0.03 and 0.14 cm2. These reveal a substantial rise in the AHMT-Ag/CPE effective surface area by a factor of 4 caused by larger exposure and density in the nanoarchitecture modified electrode. (S12 Figure S12)

Electrochemical Detection of 6-MP

The remarkably efficient electroactivity of AHMT-Ag/CPE has been employed to quantify the immunosuppressive drug 6-MP in various media and for this, the reaction condition was monitored and optimized.

Optimization of Reaction Conditions

Effect of pH

Effect of pH on electrochemical detection of 6-MP was studied and the results are shown in S13 Figure S13. It shows that as pH increases the anodic potential displays a negative shift which leads to deprotonation before electron transfer in the electro-oxidation mechanism and is an obvious behavior of biological sulphydryl compounds.[44,45] The anodic current increases up to pH 7 and then decreases therefore, pH 7 is selected as optimum for 6-MP oxidation. The pH of the buffer was optimized to 7 for the whole quantification spectrum of the drug.

Effect of the Scan Rate

The plot of ip (anodic current) versus ν1/2(square root of the scan rate) displays the diffusion-controlled mechanism of 6-MP electro-oxidation on AHMT-Ag/CPE and explores adsorption on the surface of the electroactive electrode (S14 Figure S14b).

Number of Electrons Transferred (na)

The electrons involved in the electro-oxidation of 6-MP (na) is calculated to be 1.64 using the Laviron equation (S14, Figure S14a,c) and ensures that irreversible oxidation of 6-MP is a two electron procedure at AHMT-Ag/CPE, followed by the previous report.[46,47]

Effect of Matrix

Effect of matrix is the collective effect of several ingredient of the sample other than the analyte during quantitative analysis. It reduces or increases the analyte response. Dilution with solvent is the best approach to suppress the matrix effects. Therefore, mixed blank serum and phosphate-buffered saline (PBS) (pH 7.0) were both spiked with 6-MP (60 μM), diluted with PBS (pH 7.0) at 20, 50, 100, 120, and 150-fold, and analyzed, respectively, to explore the matrix effect. At 20-fold dilution, the serum discloses lower anodic peak current and higher anodic peak potential than PBS (Figure S15A,B). Increasing the dilution, the peak current remains stable and the anodic peak potential reduces from 50 to 100-fold in serum. Contrary, the peak current diminishes sharply while the peak potential rises slightly in PBS. For 100-fold onward dilution, anodic peak current and potential have almost constant values. These outcomes demonstrate the 100 times dilution which evidences the elimination of the matrix effect of serum and guarantees the high sensitivity and thus adopted for the consequent analysis.

The electroactivity of AHMT-Ag/CPE was explored for the thorough and broad spectrum voltammetric assay of 6-MP in PBS at optimized pH 7.0. A featured anodic signature exhibits at 0.48 V in the voltammogram of cyclic voltammetry (CV) and differential pulse voltammetric (DPV) using AHMT-Ag/CPE is a crucial signature of 6-MP electro-oxidation. In order to establish the complete experimentation, the plot for the consecutive addition was observed (Figure ) which shows anodic peak enhancement with the successive addition in both CV and DPV. The calibration graph for DPV, executes linear dependency of anodic current with drug concentration and provides the limit of detection as 21 nM and sensitivity 0.56 μA/μM with the regression value of 0.99 at the S/N ratio (signal/noise): 3.

Figure 6

(a) Differential pulse voltammogram recorded on AHMT-Ag/CPE in 0.1 M PBS (pH 7) by successive addition of 6-MP, the inset of (a) cyclic voltammogram recorded by successive addition of 6-MP, (b) corresponding calibration plot.

The anodic peak increases significantly with the sequential addition of drug because the AHMT-Ag modified electrode endorsed the electro-oxidation of 6-MP. Here 6-MP approaches to the modified electrode and gets attached. The driving force for the endorsement of attachment and electro-oxidation is (a) intermolecular hydrogen bonding between amino groups, (b) the effective electron channeling of AHMT-Ag which assist the faster electron transfer through the electrode, (c) the π–π electron coupling of aromatic rings, (d) hydrophobic interaction between duplex AHMT-Ag and 6-MP, (e) high surface area of AHMT-Ag, and (f) electro-catalytic efficiency of Ag promote the electro-oxidation of 6-MP. The schematics for electro-oxidation of 6-MP at the AHMT-Ag platform is presented, it occurs through transfer of two electrons and two protons and electron channeling occurs through the AHMT-Ag platform (Scheme ).

Scheme 2

Mechanism for Electro-Oxidation of 6-MP

In order to verify the broad spectrum applicability of the sensor, AHMT-Ag/CPE was used to assay 6-MP in pharmaceutical formulation of the drug. The sample solution was developed in buffer and pH was maintained at 7. This spiked solution of the tablet was utilized for the voltammetric assay under the same experimental conditions optimized for the ideal situation using both CV and DPV and shown in Figure . The CV and DPV response for the successive addition of the drug exhibit an anodic peak at 0.48 V with corresponding to 6-MP oxidation. The corresponding calibration plot for the detection shows a linear response of anodic current with a concentration of 6-MP up to 120 μM with a limit of detection 37 nM and a regression value 98% validating the sensing approach in clinical formulation.

Figure 7

(a) Differential pulse voltammogram recorded on AHMT-Ag/CPE in 0.1 M PBS (pH 7) by successive addition of the 6-MP tablet, the inset of (a) cyclic voltammogram recorded by successive addition of 6-MP, (b) corresponding calibration plot.

Validation of Method

Various constituents present in serum and urine coexist; therefore, the primary objective of this report was to assess and explore the ability of the sensor to assay 6-MP in urine and serum. The urine and serum samples were diluted and buffered to pH 7. The developed sensor explores the dependence of an anodic peak current of 6-MP on concentration. The plot for consecutive addition is displayed (Figures and 9) which provides a limit of detection 97 and 87 nM , respectively, using DPV results. The sensitivity diminished in urine and serum which may be because of the matrix effect. In the light of these results, the developed sensing platform is highly sensitive and versatile for detection of 6-MP which is authenticated in clinical formulation, human urine as well as serum samples. The characteristic envisioned anodic current event is figured at 0.48 V. Further, the proposed method was compared with various reported methods for 6-MP detection through a bar diagram (Table S2 and Figure S17). The proposed system provides the least detection limit among the existing literature for 6-MP assay and thus supports the better efficiency of the designed sensor.

Figure 8

(a) Differential pulse voltammogram recorded on AHMT-Ag/CPE in the urine sample by successive addition of 6-MP, the inset of (a) cyclic voltammogram recorded by successive addition of 6-MP, (b) corresponding calibration plot.

Figure 9

(a) Differential pulse voltammogram recorded on AHMT-Ag/CPE in the serum sample by successive addition of 6-MP, the inset of (a) cyclic voltammogram recorded by successive addition of 6-MP, (b) corresponding calibration plot.

The serum sample was investigated by the electrochemical assay. Pearson’s correlation analysis discloses a substantial relationship of 6-MP concentrations in serum analyzed by the electrochemical method (r = 0.9131, 0 < p < 1) (Figure ).

The matrix effect of serum has been studied with direct dilution and avoided the complex modification process. The sensitivity of the method was significant covering fairly low and lethal 6-MP concentrations. This encouraging work is to develop a simple, accurate, and practical electrochemical method for the determination of 6-MP in plasma for clinical diagnosis.

Interference and Repeatability Test

Interference study was performed to examine the specificity of the electrochemical sensor by using 6-MP (55 μM) with and without 100 μM solution of interfering substances through the designed electrochemical technique (Figure ). It can be noticed that the electrochemical current response deviation due to the interfering agent was <5% of without interferences, representing excellent selectivity of designed electrochemical sensors. Further, the reproducibility was confirmed by performing the repeatability test in both interday (1, 2, 3, and 4 days) and intraday (0, 2, 4, and 6 h). Figure S16a,b shows intra and interday repeatability test by differential pulse voltammogram at the fixed potential 0.48 V recorded on AHMT-Ag/CPE in 0.1 M PBS (pH 7) by successive addition of 6-MP.

Figure 10

DPV responses of the electrochemical sensor to 55 μM 6-MP, 55 μM 6-MP+ 100 μM ethanol, 55 μM 6-MP + 100 μM glucose, 55 μM 6-MP+ 100 μM starch, 55 μM 6-MP+ 100 μM ascorbic acid, 55 μM 6-MP+ 100 μM uric acid, and 55 μM 6-MP+ 100 μM dopamine. Error bar = RSD, (n = 5).

Conclusions

This article provides the development of an elegant nanocrystalline polymeric network of AHMT-Ag which provides a geometrically and symmetrically feasible highly sensitive platform for the ultra-trace and whole spectrum systematic and potential quantification of 6-MP. The effective electron channeling through the nanocrystalline architecture is essential for facile production of feature-centered events. The complete experimentation depicted that serendipitous use of AHMT-Ag is crucial for generating distinctive current patterns in characteristic events. This feature endows high confidence assay at an ultratrace level. The key of success of the sensing methodology is the feasible and faster electron channeling through the nanocrystalline polymeric platform. The potential of the study is enzymeless, cost-effective, and complete spectrum ultratrace detection of 6-MP. This strategy can be explored in the commercial portable device fabrication for a variety of anticancer drugs.

Experimental Section

Chemicals and Materials

AHMT was purchased from Sigma-Aldrich USA. Silver salt (AgNO3), 6-MP monohydrate (6-MP), TEMPO, sodium hydroxide, and BHT were bought from SRL chemical (India) and used as accepted unless mentioned otherwise. Aqua regia was used for cleaning of the glassware, after rinsing with the mixture of ultrapure water and ethanol, Merck India. 6-MP solution was freshly equipped by using doubly deionized water and ethanol mixture solution (1:1). The electrodes used to prepare the carbon-paste electrode were procured from bio-analytical organization. Human urine and blood serum samples were obtained from authorized hospitals. The tablet of 6-MP was acquired through a local supplier (Cipla Ltd. India); reaction solutions were exposed in pure nitrogen to remove oxygen and avoid any external oxidation during each electrochemical measurement.

Electrode Fabrication

1 mm diameter CPE used for modification was obtained from BASi (Indiana). Carbon paste was prepared by mixing 67% w/w graphite powder, 2.5% w/w paraffin oil, and 35% w/w AHMT-Ag then the cavity of the electrode was filled with a portion of the resulting paste. The surface of the CPE was smoothed against butter paper and rinsed with distilled water. The carbon paste was cautiously removed prior to pressing a new fraction into the electrode after each measurement.

Instrumentation

The PerkinElmer 783 spectrometer was used to record FT-IR spectra of AHMT-Ag and AHMT in the range of 3600–500 cm–1 on a KBr disc. Powder XRD were executed in the range of 5°–80° by using a Miniflex 600 diffractometer with Cu Kα radiation (Kα = 1.54056 Å) with a 2°/min scan rate. UV–vis was performed in a quartz cuvette (1 cm path length) by using a Biotech, Epoch 2 microplate reader spectrophotometer, USA. For elemental analysis XPS (X-ray photoelectron spectrometry) was executed with, Shimadzu Group Company, Kratos analytical instrument, XPS (UK), with 1.254 Å Mg Kα radiations. Nova, Nano-SEM 450 FEI (Netherlands) was used for the recording HR-SEM. An FEI TECHNAI G2 20 TWIN Czech Republic electron microscope was used for recording HR-TEM, EDS mapping, and EDX with 200 keV (accelerating voltage) on a copper grid (carbon-coated) prepared by 6 μL of polymer solution. A Mettler Toledo TGA/DSC 1 STARE System, Switzerland was used for thermal analysis. TGA and DTA were performed in an inert atmosphere with a heating rate of 10 °C min–1. All electrochemical measurements were accomplished on a Ω Metrohm, 797 VA, Computrace trace analyzer, Switzerland, using a three electrode assembly by electrochemical software 3.1 with AHMT-Ag-modified CPE (working electrode), Pt foil (counter electrode), Ag/AgCl (reference electrode), and pH 7.0 phosphate buffer used as supporting electrolytes for all electrochemical measurements.

Experimental Procedure for AHMT-Ag Synthesis

13.5 mM aqueous/ethanolic solution of AHMT and 100 mM ethanolic solution of AgNO3 were prepared. Further, the AgNO3 solution was dropwise added in the AHMT solution with continuous stirring for 24 h at atmospheric pressure and room temperature. A blackish-grey precipitate of AHMT-Ag NCCP was obtained then the obtained precipitate was washed three times after filtration followed by water–ethanol mixture solution (1:1 v/v %) to remove the unreacted AHMT and AgNO3. Removal of the solvent was regulated at 40 °C in vacuum and the obtained yield was 87%. (S1 Figure S1)

Radical Controlled Experiments

The radical-controlled experiments with BHT (2,6-di-t-butyl-4-hydroxytoluene) and TEMPO (2,2,6,6-tetramethyl-1-piperidinyl oxidanyl) trapping agents, endows the cationic pathway without any interference under standard conditions (Figure ). Mechanism involves silver ions as a cationic companion for initiating polymerization and launching the silver-associated monomeric segment which activates Ag oxidation to furnish AHMT-Ag.[47] (Scheme ). Thereafter structural and bonding information is reviewed under FT-IR, 1H NMR, and XPS analysis.

Figure 11

Schematic illustration of controlled experiments for the formation of AHMT-Ag using TEMPO and BHT.

Scheme 1

Possible Mechanism for Formation of AHMT-Ag