Imprinted Proteins as a Receptor in Fluorescent Sensing Microplate Assay for Herbicide Determination

The manuscript describes an optical sensing microplate for the high-throughput screening of imidazolinone herbicides in soil extracts. As far as we know, imprinted proteins (IPs) specific to imidazolinone herbicides have not been synthesized and used as a recognition element for their solid-phase extraction before. Imprinted bovine serum albumin (BSA) and glucose oxidase (GOx) were synthesized in the presence of imazamox as a template and then these IPs were immobilized at the bottom of microplate wells. The sorption capacity (<i>Q</i>) of aminated silica nanoparticles modified by IPs (IP-BIS) was 6.38 mg g<sup>-1</sup> while the imprinting factor (IF) equaled 2.6. The concentration of imazamox was determined by a "turn-off" solid-phase assay using alloyed CdZnSeS/ZnS quantum dots (QDs) as a component of fluorescent substrate. Alloyed CdZnSeS/ZnS QDs were stabilized in an aqueous phase by positively charged cysteamine that, as far we know, had not been used as this type of ligand before. Our method allows for determining the concentration of imazamox in the range of 0.5-9.2 μg mL<sup>-1</sup>, with a limit of quantification limit of quantitation (LOQ) equal to 0.45 μg mL<sup>-1</sup> The sensing microplate enables parallel detection of up to 96 samples containing herbicides using standard fluorescence microplate readers or smartphones. The paper describes how such sensing microplates can be used for the analysis of artificially contaminated soil samples. The proposed approach combines pre-concentration of analyte at the IPs with its subsequent determination on a single analytical platform, thus allowing for both highly sensitive determination in laboratory conditions and mass screening in the field.

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Journal
Biosensors
Published
2026-03-03
DOI
https://doi.org/10.3390/bios16030149
Primary Topic
Analytical chemistry methods development
Type
article
Field-Weighted Citation Impact
0.00

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article

Imprinted Proteins as a Receptor in Fluorescent Sensing Microplate Assay for Herbicide Determination

Pavel S. Pidenko, Polina M. Ilicheva, Irina Yu. Goryacheva, Daria V. Tsyupka et al.
Biosensors
Analytical chemistry methods development
article

Imprinted Proteins as a Receptor in Fluorescent Sensing Microplate Assay for Herbicide Determination

Pavel S. Pidenko, Polina M. Ilicheva, Irina Yu. Goryacheva, Daria V. Tsyupka, Kirill Yu. Presnyakov, Н. А. Бурмистрова, M. V. Pozharov, Ivan S. Matlakhov, Daria G. Koganova, Svetlana A. Mescheryakova, Tatyana Yu. Rusanova, Ivan A. Reshetnik, Daniil D. Drozd
article en

Abstract

The manuscript describes an optical sensing microplate for the high-throughput screening of imidazolinone herbicides in soil extracts. As far as we know, imprinted proteins (IPs) specific to imidazolinone herbicides have not been synthesized and used as a recognition element for their solid-phase extraction before. Imprinted bovine serum albumin (BSA) and glucose oxidase (GOx) were synthesized in the presence of imazamox as a template and then these IPs were immobilized at the bottom of microplate wells. The sorption capacity (<i>Q</i>) of aminated silica nanoparticles modified by IPs (IP-BIS) was 6.38 mg g<sup>-1</sup> while the imprinting factor (IF) equaled 2.6. The concentration of imazamox was determined by a "turn-off" solid-phase assay using alloyed CdZnSeS/ZnS quantum dots (QDs) as a component of fluorescent substrate. Alloyed CdZnSeS/ZnS QDs were stabilized in an aqueous phase by positively charged cysteamine that, as far we know, had not been used as this type of ligand before. Our method allows for determining the concentration of imazamox in the range of 0.5-9.2 μg mL<sup>-1</sup>, with a limit of quantification limit of quantitation (LOQ) equal to 0.45 μg mL<sup>-1</sup> The sensing microplate enables parallel detection of up to 96 samples containing herbicides using standard fluorescence microplate readers or smartphones. The paper describes how such sensing microplates can be used for the analysis of artificially contaminated soil samples. The proposed approach combines pre-concentration of analyte at the IPs with its subsequent determination on a single analytical platform, thus allowing for both highly sensitive determination in laboratory conditions and mass screening in the field.

BiosensorsVol. 16(3)
Saratov State University (RU)
Russian Science Foundation
Openalex Percentile: Top 34%
Analytical chemistry methods development
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