AI Article Synopsis

  • The study introduces molecularly imprinted polymers (MIPs) as synthetic antibodies for a microplate-based assay targeting human serum albumin (HSA), the most abundant plasma protein.
  • The MIPs were created using a surface imprinting method with a specific acrylic acid and vinylpyrrolidone ratio, achieving effective binding to HSA through the Bradford reaction.
  • The assay demonstrated high analytical accuracy and precision, with a detection range relevant to clinical needs, and the MIP-coated plates maintained their functionality for two months at room temperature.

Article Abstract

Herein we demonstrate molecularly imprinted polymers (MIP) as plastic antibodies for a microplate-based assay. As the most abundant plasma protein, human serum albumin (HSA) was selected as the target analyte model. Thin film MIP was synthesized by the surface molecular imprinting approach using HSA as the template. The optimized polymer consisted of acrylic acid (AA) and -vinylpyrrolidone (VP) in a 2:3 (/) ratio, crosslinked with -(1,2-dihydroxyethylene) bisacrylamide (DHEBA) and then coated on the microplate well. The binding of MIP toward the bound HSA was achieved via the Bradford reaction. The assay revealed a dynamic detection range toward HSA standards in the clinically relevant 1-10 g/dL range, with a 0.01 g/dL detection limit. HSA-MIP showed minimal interference from other serum protein components: γ-globulin had 11% of the HSA response, α-globulin of high-density lipoprotein had 9%, and β-globulin of low-density lipoprotein had 7%. The analytical accuracy of the assay was 89-106% at the 95% confidence interval, with precision at 4-9%. The MIP-coated microplate was stored for 2 months at room temperature without losing its binding ability. The results suggest that the thin film plastic antibody system can be successfully applied to analytical/pseudoimmunological HSA determinations in clinical applications.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8198403PMC
http://dx.doi.org/10.3390/polym13111763DOI Listing

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