4.7 Article

Design and Engineering of a Palm-Sized Optical Immunosensing Device for the Detection of a Kidney Dysfunction Biomarker

期刊

BIOSENSORS-BASEL
卷 12, 期 12, 页码 -

出版社

MDPI
DOI: 10.3390/bios12121118

关键词

optical sensing device; paper sensor; personalized diagnosis; surface chemistry; kidney dysfunction

资金

  1. Prime Minister's Research Fellowship (PMRF)
  2. Ministry of Education, Government of India
  3. INSPIRE Fellowship [IF170804]
  4. Department of Science and Technology, Government of India
  5. DST-funded I-DAPT Hub Foundation, IIT BHU [DST/NMICPS/TIH11/IIT(BHU)2020/02]

向作者/读者索取更多资源

Creatinine is a common and specific biomarker for renal diseases. Researchers have developed an optical sensing device that can quantitatively detect creatinine through a change in color. The sensor has been integrated with a smartphone to create a palm-sized device for personalized creatinine analysis. The fabricated biosensor has been thoroughly characterized and shown to have excellent sensitivity and selectivity, with no cross-reactivity from interfering molecules. The system has been validated for quantifying creatinine in spiked serum samples, showing high reproducibility and stability.
Creatinine is one of the most common and specific biomarkers for renal diseases, usually found in the serum and urine of humans. Its level is extremely important and critical to know, not only in the case of renal diseases, but also for various other pathological conditions. Hence, detecting creatinine in clinically relevant ranges in a simplistic and personalized manner is interesting and important. In this direction, an optical sensing device has been developed for the simple, point-of-care detection of creatinine. The developed biosensor was able to detect creatinine quantitatively based on optical signals measured through a change in color. The sensor has been integrated with a smartphone to develop a palm-sized device for creatinine analysis in personalized settings. The sensor has been developed following facile chemical modification steps to anchor the creatinine-selective antibody to generate a sensing probe. The fabricated sensor has been thoroughly characterized by FTIR, AFM, and controlled optical analyses. The quantitative analysis is mediated through the reaction between picric acid and creatinine which was detected by the antibody-functionalized sensor probe. The differences in color intensity and creatinine concentrations show an excellent dose-dependent correlation in two different dynamic ranges from 5 to 20 mu M and 35 to 400 mu M, with a detection limit of 15.37 (+/- 0.79) nM. Several interfering molecules, such as albumin, glucose, ascorbic acid, citric acid, glycine, uric acid, Na+, K+, and Cl-, were tested using the biosensor, in which no cross-reactivity was observed. The utility of the developed system to quantify creatinine in spiked serum samples was validated and the obtained percentage recoveries were found within the range of 89.71-97.30%. The fabricated biosensor was found to be highly reproducible and stable, and it retains its original signal for up to 28 days.

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