Ultrasensitive photoelectrochemical aptasensor for diclofenac sodium based on surface-modified TiO2-FeVO4 composite
Herein, a photoelectrochemical (PEC) aptasensing platform was designed by integrating surface oxygen vacancy (OV) defects, Ti 3+ self-doping, the heterojunction, and resonance energy transfer (RET) effect into one platform for the detection of diclofenac sodium (DCF). Briefly, OV defects were introd...
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Published in | Analytical and bioanalytical chemistry Vol. 413; no. 1; pp. 193 - 203 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Berlin/Heidelberg
Springer Berlin Heidelberg
01.01.2021
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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Summary: | Herein, a photoelectrochemical (PEC) aptasensing platform was designed by integrating surface oxygen vacancy (OV) defects, Ti
3+
self-doping, the heterojunction, and resonance energy transfer (RET) effect into one platform for the detection of diclofenac sodium (DCF). Briefly, OV defects were introduced on TiO
2
nanospheres with simultaneous Ti
3+
self-doping, followed by a well-separated deposition of FeVO
4
nanoparticles on TiO
2
to obtain a Ti
3+
-O-TiO
2
/FeVO
4
heterojunction. The surface modification of OVs, Ti
3+
doping, and deposition of FeVO
4
were confirmed by SEM, XPS, EPR, DRS, and PEC measurements. The surface OVs and doping of Ti
3+
species created a new donor (defect) energy level under the conduction band of TiO
2
, which minimized the bandgap and thereby improved the visible light absorption of TiO
2
. Moreover, the capture of photo-excited electrons by surface OVs could hinder the electron-hole recombination. Due to the intimate surface contact and perfect energy matching between TiO
2
and FeVO
4
, the formation of heterojunction decreased the bandgap and facilitated the electron-hole separation of TiO
2
. All these above events contributed to the enhancement of the PEC signals, which were then quenched by the RET effect between Ti
3+
-O-TiO
2
/FeVO
4
and Au nanoparticle (AuNP)–labeled cDNA that had been attached to its complementary DCF aptamer on Ti
3+
-O-TiO
2
/FeVO
4
|ITO. The addition of target-DCF detached AuNP-labeled cDNA from the electrode to recover the photocurrent, resulting in a “signal-on” PEC aptasensor that exhibited a 0.1–500-nM linear range and a detection limit of 0.069 nM for DCF, attributed to the excellent amplification of the proposed aptasensing platform. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 1618-2642 1618-2650 1618-2650 |
DOI: | 10.1007/s00216-020-02991-0 |