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An ultra-sensitive and highly selective impedimetric sensor for vitamin D measurement based on a novel imprinted polymer synthesized utilizing template-derived functional monomer

Tutkimustuotos: LehtiartikkeliArticleScientificvertaisarvioitu

14 Sitaatiot (Scopus)

Abstrakti

A novel vitamin D3-imprinted (VD)-polymer was synthesized utilizing a functional monomer derived from vitamin D3. Acryloyl chloride reacted with VD leading to a functional monomer capable of interaction with VD during the molecularly imprinted polymer (MIP) synthesis step. Vitamin D3-derived functional monomer and divinylbenzene were copolymerized in the presence of vitamin D3 in order to create a new MIP, holding VD selective cavities, after template (VD) removal from the polymer. The MIP nanoparticles were used for the modification of a carbon paste electrode to fabricate VD selective sensor. The charge transfer resistance of Fe(CN)63-/Fe(CN)64−couple for the MIP-modified electrode increased significantly in the presence of VD; whereas, the non-imprinted polymer (NIP)-CPE electrode was not affected by VD, suggesting well acting of recognition sites of the MIP nanoparticles, incorporated into the electrode. The sensing mechanism was attributed to a gate effect principle. Interring of VD molecules to the selective sites of the MIP nanoparticles, existing on the electrode surface, makes the MIP particles swell and this leads to blocking the majority of routes via which the probe electroactive species accesses the carbon particles at the electrode surface. The MIP electrode was not sensitive to some molecules structurally similar to VD, suggesting a highly selective nature of the designed sensor. The new VD sensor impedimetric response as a function of the logarithm of VD concentration was found to be linear in the range of 1.0–100.0 pM. The detection limit of the sensor was estimated to be 0.22 pM. The sensor was used for VD level estimation in plasma samples.

AlkuperäiskieliEnglanti
Artikkeli340206
Sivumäärä8
JulkaisuAnalytica Chimica Acta
Vuosikerta1223
DOI - pysyväislinkit
TilaJulkaistu - 29 elok. 2022
OKM-julkaisutyyppiA1 Alkuperäisartikkeli tieteellisessä aikakauslehdessä

Rahoitus

Electrochemical impedance spectroscopy is a powerful tool to study the recognition events occurring at the modified electrode surfaces. EIS is categorized as a non-destructive technique. The impedance data can be recorded in the presence (faradaic impedance measurement) or absence (non-faradic impedance measurement) of a redox couple. The recognition events occurring at the electrode surface can be monitored by measuring the change in the interfacial electron transfer resistance, owing to the hindrance of the electroactive species in the supporting electrolyte to touch the electrode active sites [27]. Fig. 4 (I) and (II) illustrate EIS responses of the MIP- and NIP-modified carbon paste electrodes as the Nyquist plots in the presence and absence of VD3. It can be observed that the addition of a trace amount of VD3 results in a significant increase in the depressed semicircle diameter which is indicative of charge transfer resistance of probe ion species existing in the test solution. This observation clearly shows that VD3 has been recognized by the MIP nanoparticles within the MIP electrode surface. In spite of the very low concentration of VD3, added to the MIP electrode containing solution, the change in the EIS signal is considerably high, suggesting a very high affinity of the MIP sites to the VD3 molecules. On the other hand, the addition of the same amount of VD3 to the solution of the NIP-based electrode does not influence the charge transfer resistance of the NIP-CPE. This means that no recognition event happens in the NIP electrode when contacting the VD3 with the NIP electrode surface.The authors would like to appreciate the financial support of the research council of the University of Tehran. The authors would like to appreciate the financial support of the research council of the University of Tehran.

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