Electrochemical platform for anti-cardiolipin antibody detection in human syphilitic serum

Current research in biotechnology(2022)

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摘要
• We developed a biosensor platform based on an antigenic colloidal suspension as a biorecognition element. • The platform detects anti-cardiolipin (anti-C) antibodies in infected human serum. • The biosensor was able to detect the formation of immunocomplexes in serum samples. • We obtained a limit of detection of 1024 titer. Syphilis is a sexually transmitted disease with high morbidity and mortality rates. Venereal disease research laboratory (VDRL) and rapid plasma reagin (RPR) testing are the most commonly used syphilis identification methods; however, both have low specificity. The available molecular assays are expensive and time-consuming. Electrochemical biosensors are an innovative approach for detecting multiple target analytes present in syphilis complex samples. In this work, we used a self-assembled monolayer (3-mercaptopropyl)trimethoxysilane (MPTS) to immobilize an antigenic colloidal suspension (containing cardiolipin, cholesterol, and lecithin) as a biorecognition element in a platform for detecting anti-cardiolipin (anti-C) antibodies in infected human serum. The biosensor platform was evaluated through cyclic voltammetry, electrochemical impedance spectroscopy, and atomic force microscopy. Microscopic evaluation revealed the formation of small cardiolipin-anti-C complexes at the maximum titer of 1:32, thus indicating the serum’s syphilis infection positivity. Anti-C antibody detection was evaluated by blocking electron current and oxidation–reduction processes at the electrode–electrolyte interface. The proposed sensor yielded a linear response (serum dilutions ranging from 1:8 to 1:1024 titer) with a regression coefficient of 0.97. We obtained a limit of detection of 1:1024 titer and high selectivity against interfering biomolecules. The developed biosensor may provide a promising alternative for syphilis diagnosis and follow-up treatment.
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关键词
Biosensor,Syphilis,Cardiolipin,Cyclic voltammetry,Electrochemical impedance spectroscopy
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