Abstract

A green electrodeposition method was firstly employed for the synthesis of round hairbrush-like gold nanostructure in the presence of cadaverine as a size and shape directing additive. The nanostructure which comprised of arrays of nanospindles was then applied as a transducer to fabricate a signal-on built in-marker electrochemical aptasensor for the detection of human prostate-specific antigen (PSA). The aptasensor detected PSA with a linear concentration range of 0.125 to 128 ng mL−1 and a limit of detection of 50 pg mL−1. The aptasensor was then successfully applied to detect PSA in the blood serum samples of healthy and patient persons.

Highlights

  • Prostate cancer (PCa) is the most common cancer in men and is the second-leading cause of cancer mortality in men

  • Prostate-specific antigen (PSA) is a biomarker that is most widely employed for the detection of PCa2

  • It has been shown that PSA is the most validated biomarker for the early detection of prostate cancer and monitoring the disease recurrence after treatment[3]

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Summary

Methods

All chemicals were of analytical grade from Scharlau (Spain) or Merck (Germany). All solutions were prepared by redistilled water. A specific aptamer sequence for PSA which was modified with methylene blue (MB) was employed with following sequence. It has been reported that this sequence has a high affinity to PSA46 and modified with MB in this study: 5′ SH-(CH2)[6] TT TT TA AT TA AA GC TC GC CA TC AA AT AG CT TT-3′-MB. The aptamer was purchased from Bioneer (Korea). PSA, hemoglobin and bovine serum albumin were purchased form Sigma (USA). The aptamer stock solutions were prepared with a 20 mmol dm−3 Tris-HCl buffer, pH 7.4 solution (Tris) and kept frozen

Microarray immunoassay
Additional Information
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