Isfahan University of Medical Sciences

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Aptamer-Functionalized Localized Surface Plasmon Resonance Sensor for the Rapid and Affordable Detection of Staphylococcus Aureus Alpha-Toxin Publisher



Poudineh M1 ; Poudineh S1 ; Jalalifar T2 ; Vakili S3 ; Rostami A4 ; Samarenajaf M5, 6 ; Kakhaki HF7 ; Dehghanian A8, 9 ; Sabaghan M10 ; Behrouj H10
Authors
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Authors Affiliations
  1. 1. School of Medicine, Mashhad Azad University, Mashhad, Iran
  2. 2. Toxicology Department, Faculty of Pharmacy, Shahreza Branch, Islamic Azad University, Shahreza, Iran
  3. 3. Infertility Research Center, Shiraz University of Medical Sciences, Shiraz, Iran
  4. 4. Department of Internal Medicine, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran
  5. 5. Biochemistry Department, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran
  6. 6. Blood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Kerman Regional Blood Transfusion Center, Kerman, Iran
  7. 7. Mashhad Branch, Islamic Azad University, Mashhad, Iran
  8. 8. Trauma Research Center, Shiraz University of Medical Sciences, Shiraz, Iran
  9. 9. Molecular Pathology and Cytogenetics Division, Department of Pathology, Shiraz University of Medical Sciences, Shiraz, Iran
  10. 10. Behbahan Faculty of Medical Sciences, Behbahan, Iran

Source: Optik Published:2022


Abstract

The present study aimed to design a novel technique for detection of Staphylococcus aureus Alpha-toxin based on the aptamer-localized surface plasmon resonance (LSPR) to eliminate or reduce existing limitations. For this purpose, gold nanoparticles (GNPs) and the alpha-toxin-specific probe and aptamer were prepared. Nanoparticles were modified with optimal concentrations the aptamer and the performance of the aptasensor in the detection of different alpha-toxin concentrations was studied. Ultimately, spiked real samples with known concentrations of alpha-toxin were used to assess the analytical performance of the sensor. The results demonstrated that GNPs were synthesized and distributed equally. In concentrations of 40 nM and 5 pM, the performance of the probe and aptamer were optimized, respectively. Furthermore, the results regarding the linear range of detection (0–1400 nM), the limit of detection (LOD, 22 nM), and the limit of quantification (LOQ, 68 nM) demonstrated desired performance of the aptasensor. Additionally, the percent recovery between 98% and 106% and the relative standard deviation (RSD) between 0.51 and 1.35 were obtained. Taking together, the results achieved by the present aptamer-functionalized LSPR biosensor suggested a valid, simple, cost-effective, rapid, and reliable detection strategy to quantify alpha-toxin in human samples which is comparative with traditional S. aureus detection strategies. © 2022 Elsevier GmbH