A selective nitric oxide nanocomposite biosensor based on direct electron transfer of microperoxidase: Removal of interferences by co-immobilized enzymes

作者：Abdelwahab Adel A; Koh Wei Choon Alvin; Noh Hui Bog; Shim Yoon Bo^*

来源：Biosensors and Bioelectronics, 2010, 26(3): 1080-1086.

DOI：10.1016/j.bios.2010.08.070

• Cancer cells
• Catalase
• Microperoxidase
• Nitric oxide biosensor
• Rat liver
• Superoxide dismutase

A highly selective nitric oxide (NO) biosensor was developed by immobilizing microperoxidase (MP) onto the MWCNT-poly-5,2':5',2 ''-terthiophene-3'-carboxylic acid (PTTCA) nanocomposite. Catalase (CAS) and superoxide dismutase (SOD) co-immobilized on the probe successfully protected the interferences of H2O2 and O-2(-) during NO detection. The nanocomposite layer showed the direct electron transfer processes of the immobilized CAS, SOD, and MP simultaneously at -0.11/+0.04, -0.33/-0.27, and -0.47/-0.40 V vs. Ag/AgCl. Au nanoparticles (AuNPs) were electrodeposited on a glassy carbon surface to enhance the sensitivity of the sensor probe. The layers of CAS/SOD/MP/MWCNT-PTTCA/AuNPs were characterized using SEM, XPS, and QCM. The CAS/SOD/MP/MWCNT-PTTCA/AuNPs probe showed an excellent performance in the electrocatalytic reduction of NO which was attributed to the heme group of MP. Experimental conditions affecting the sensitivity of the biosensor were optimized in terms of pH, temperature, and applied potential. The dynamic range of NO analysis was from 1.0 to 40 mu M with the detection limit of 4.3 +/- 0.2 nM. The reliability of biosensor was examined for the determination of NO released from the real samples of rat liver, stomach (AGS), and intestinal (HT-29) cancer cells.