Immobilization of horseradish peroxidase via an amino silane on oxidized ultrananocrystalline diamond
Source abstract
Abstract
We discuss the complete functionalization of nitrogen-doped ultrananocrystalline diamond (UNCD) films, starting from an oxidized surface. First, the presence of hydroxyl groups on oxidized nanocrystalline diamond (NCD) was confirmed by fluorescence microscopy. Next, the grafting of a linker molecule such as 3-aminopropylmethyldiethoxysilane on oxidized NCD was confirmed by fluorescence microscopy and X-ray photoelectron spectroscopy (XPS). Then the horseradish peroxidase (HRP) enzyme was immobilized on silane-modified initially oxidized UNCD. The HRP-modified UNCD was characterized by electrochemical techniques, such as faradaic cyclic voltammetry and the amperometric response to H2O2. This response to H2O2 is discussed in terms of the layer-by-layer configuration used and the electronic properties of conducting UNCD.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Diamond and Carbon-based Materials Research · Polymer Surface Interaction Studies · Nonlinear Optical Materials Studies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (22)
Show source-provided references
1. Swain · 2003 · 21
2. Bhattacharyya · Appl. Phys. Lett. · 2001 · 79 · 144110.1063/1.1400761 ↗
3. Yang · Nat. Mater. · 2002 · 1 · 25310.1038/nmat779 ↗
4. Härtl · Nat. Mater. · 2004 · 3 · 73610.1038/nmat1204 ↗
5. Sugata · Jpn. J. Appl. Phys. · 2002 · 41 · 498310.1143/JJAP.41.4983 ↗
6. Notsu · Electrochem. Solid-State Lett. · 2001 · 4 · H110.1149/1.1346556 ↗
7. Zhang · Jpn. J. Appl. Phys. · 2005 · 44 · L29510.1143/JJAP.44.L295 ↗
8. Moon · Langmuir · 1996 · 12 · 462110.1021/la9604339 ↗
9. Pallandre · Nano Lett. · 2004 · 4 · 36510.1021/nl035045n ↗
10. Ferapontova · J. Electroanal. Chem. · 2002 · 518 · 2010.1016/S0022-0728(01)00692-1 ↗
11. Freire · J. Braz. Chem. Soc. · 2003 · 14 · 23010.1590/S0103-50532003000200008 ↗
12. Ruzgas · Anal. Chim. Acta · 1996 · 330 · 12310.1016/0003-2670(96)00169-9 ↗
13. Kulys · Bioelectrochem. Bioenerg. · 1981 · 8 · 8110.1016/0302-4598(81)85009-X ↗
14. Ho · Biosens. Bioelectron. · 1995 · 10 · 68310.1016/0956-5663(95)96959-3 ↗
15. Tatsuma · Anal. Chem. · 2000 · 72 · 291910.1021/ac0000022 ↗
16. Granger · J. Electrochem. Soc. · 1999 · 146 · 455110.1149/1.1392673 ↗
17. Jia · Anal. Chem. · 2002 · 74 · 221710.1021/ac011116w ↗
18. Berggren · Anal. Chem. · 1997 · 69 · 365110.1021/ac970203e ↗
19. Xu · Sensors · 2003 · 3 · 35010.3390/s30900350 ↗
20. Imabayashi · Electroanalysis · 2001 · 13 · 40810.1002/1521-4109(200104)13:5<408::AID-ELAN408>3.0.CO;2-2 ↗
21. Li · J. Electroanal. Chem. · 1997 · 431 · 1910.1016/S0022-0728(97)00158-7 ↗
22. Chen · J. Electrochem. Soc. · 2001 · 148 · E4410.1149/1.1344550 ↗