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BME440 RAPOR X Merged
BME440 RAPOR X Merged
1.Introduction……………………………………………….…3
2.Method………………………………………………………..4
3.Discussion…………………………………………………..5
3.2.Articles Topics………………………………………….6
4.Result……………………………………………………….10
1.INTRODUCTION
This article report includes the research of the subject which is 'Visible-light-activated photo
electrical biosensor for the detection pathogens in blood bio liquids'.Also
includes,examining and filtering many different articles, comparing the articles and
determining the closest article on the subject. The strengths, deficiencies and contributions
of the research were investigated in the light of the relevant literature.As a result;the most
detailed article on the subject is which name is Visible light induced photoelectrochemic al
biosensing based on oxygen-sensitive quantum dots which is written by; Wenjing Wang,
Lei Bao, Jianping Lei,Wenwen Tu,Huangxian Ju
2.METHOD
3.DISCUSSION
neurotoxins( Qilin Huang, Hua Chen, Lili Xu, Danqin Lu,Linlin Tang ,
Zengyao Zheng , Jianying Yang , Min Chen , Qingwei Yao , Yaowen Chen ,
Wenhua Gao)
Shaojun Dong)
1.ARTICLE TOPIC:
2.ARTICLE TOPIC:
The subject of the second article is; A visible light induced photoelectrochemical biosensing
platform based on oxygen-sensitive near infrared quantum dots (NIR QDs) was developed
for detection of glucose. The NIR QDs were synthesized in an aqueous solution, and
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3.ARTICLE ARTICLE:
The subject of the third article is; A novel visible light driven self-powdered
(OPs). The biosensor was prepared by taking indium tin oxide (ITO) as the substrate,
4.ARTICLE TOPIC:
The subject of the fourth article is ; A ternary WO3/Au/CdS photocatalyst was prepared by
reversible redox and ionic adsorption for the first time. The photocatalyst exhibited high
WO3, CdS, WO3/Au and WO3/CdS, because the localized surface plasmon resonance
(LSPR) effect of Au nanoparticles (Au NPs) and the sensitization of CdS benefited the
spatial separation of photogenerated electron-hole pairs and the absorption of visible light.
5.ARTICLE TOPIC:
The subject of the last article is; A NADH and glucose biosensor based on thionine cross-
linked multiwalled carbon nanotubes (MWNTs) and Au nanoparticles (Au NPs) multilayer
functionalized indium-doped tin oxide (ITO) electrode were presented in this paper. The
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3.3.Contents and Methods of Articles:
1.ARTICLE:
The photoelectrode was prepared by three steps, as follows. At first, nitrogen and fluorine co-doped TiO2
nanotubes (TNs) were obtained by anodic oxidation of a Ti sheet. Secondly, silver nanoparticles (AgNPs)
were deposited onto the TNs through a microwave-assisted heating polyol (MAHP) process. At last, AChE
was immobilized on the obtained photoelectrode and the biosensor was marked as AChE/Ag/N–F–TNs.
Due to the nitrogen and fluorine co-doping, the photoelectrochemical biosensors can produce high
photocurrent under visible light irradiation. Moreover, the presence of AgNPs greatly increased the
photocurrent response of the biosensor. AChE/Ag/N–F–TNs hybrid system was used to study AChE
inhibition induced by (R)-Sal and (R)-NMSal. The result proved that both (R)-Sal and (R)-NMSal exhibited
mixed and reversible inhibition against AChE. This strategy is of great significance for the development of
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2.ARTICLE:
The as-prepared NIR QDs were employed to construct oxygen-sensitive photoelectrochemical biosensor
on a fluorine-doped tin oxide (FTO) electrode. The oxygen dependency ofthe photocurrent was
investigated at as-prepared electrode, which demonstrated the signal of photocurrent is suppressed with
the decreasing of oxygen. Coupling with the consumption of oxygen during enzymatic reaction, a pho-
toelectrochemical strategy was proposed for the detection of substrate. Using glucose oxidase (GOx) as a
model enzyme, that is, GOx was covalently attached to the surface of CdTe QDs, the resulting biosensor
showed the sensitive response to glucose. Under the irradiation of visible light of a wavelength at 505 nm,
the proposed photoelectrochemical method could detect glucose ranging from 0.1 mM to 11 mM with a
detection limit of 0.04 mM. The photoelectrochemical biosensor showed a good performance with high
upper detection limit, acceptable stability and accuracy, providing an alternative method for monitoring
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3.ARTICLE:
Because of the excellent optical performances of NCQDs, the photocurrent response of the NCQD/TiO2/ITO
electrode were improved obviously compared with TiO2/ITO electrode.The AChE immobilized on the surface of the
PEC biosensor can catalytic hydrolysis of acetylcholine chloride (ATCl) to generate thiocholine, which can serve as
the electron donor to enhance the separation of the photogenerated electron-hole pairs, therefore, the
photocurrent response of the PEC biosensor elevated greatly. The bioactivity of the AChE was inhibited by OPs
where chlorpyrifos was used as the model, the production of the thiocholine was declined, leading to a reduction of
the photocurrent response. The prepared PEC biosensor can achieve the sensitive detection of chlorpyrifos with the
board detection range varied from 0.001 mg mL1 to 1.5 mg mL1 and the detection limit was about 0.07 ng mL1
(S/N 1⁄4 3). It is the first time that NCQDs/TiO2 is adopted to construct the PEC biosensor for chlorpyrifos detection.
The obtained PEC biosensor can also achieve the detection of chlorpyrifos in the lake water and Chinese cabbage
samples, suggesting that the fabricated PEC biosensor had potential application for the detection of OPs in
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4.ARTICLE:
Thus, its photo-current response intensity was quite high, up to about 218-fold of WO3 and 87-fold of CdS under
430 nm LED light irradiation. Based on the large anodic photocurrent and the specific recognition between
carcinoembryonic antigen (CEA) and anti-CEA, a novel PEC immunosensor was constructed for the sensitive and
selective detection of CEA. Under the selected conditions, the change of photocurrent intensity was linear to the
logarithm of CEA concentration over the range from 0.01 to 10 ng/mL, and the detection limit was down to 1
pg/mL. The immunosensor also showed good stability, reproducibility and repeatability. It was successfully applied
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5.ARTICLE:
This bioelectrode exhibited excellent catalytic activity of the oxidation towards dihydronicotinamide adenine
dinucleotide (NADH). Most interesting, the performance of this NADH sensor could be tuned by the visible light.
When the biosensor was performed in the dark, the anodic current increased linearly with NADH concentration over
the range from 0.5 to 237 M with detection limit 0.1 M and sensitivity 17 nA M−1. The sensitivity became 115 nA
M−1 with detection limit 0.05 M with the light irradiation. Compared with the reaction in dark,the sensitivity
increased around 7 folds while the detection limit decreased 2 folds. The glucose biosensor also exhibited the
same behavior. The linear range was from 10 M to 2.56 mM with the sensitivity of 7.8 A mM−1 and detection limit
5.0 M in the dark. After the light irradiation, the linear range was from 1 M to 3.25 mM with the sensitivity of 18.5 A
mM−1 and detection limit 0.7 M. It indicated a potential to provide an operational access to develop new kinds of
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4.RESULTS AND COMPARISSON
4.1 RESULTS OF THE ARTICLES
1.ARTICLE:
AChE, which is a member of the large class of serine esterases,plays an important role in the signal transduction process of the
central nervous system. As a consequence, to study the activity change of AChE will contribute to the pathological study and
the drug screening about injury and disease of the central nervous system. Therefore, a sensitive and stable AChE biosensor
During the preparation process, the surface morphologies and chemical composition of the biosensor’s host materials
these modification processes and the morphology of prepared electrodes. Fig. 1(A) presents a top-view SEM image of the as
prepared porous TNs fabricated by anodic oxidation of a Ti sheet at 20 V for 2 h in 1 M (NH4)2SO4 electrolyte containing 0.1
MNH4F. As shown in the figure, an ordered porous structure of TNs is clearly observed, with an average pore diameter of 30–
50 nm and a wall thickness of 15–30 nm. Thus, the average pore spacing was estimated to be approximately 90 nm.
Therefore, the prepared TNs possess a self-organized structure with regular porous array. Fig. 1(E) presents the EDX spectrum
of the as prepared TNs. The strong diffraction peaks of elemental Ti at 0.45,4.51 and 4.92 KeV are clearly seen. The diffraction
peaks of elemental O, N and F are located at 0.52, 0.40 and 0.68 KeV, respectively. These results confirm that TNs were
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2.ARTICLE:
nm.
The second article gave us the most suitable method for our
knowledge.
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3.ARTICLE:
As shown in Fig. 1A, CQDs had the strong optical absorption in the UV region and weak absorption near to the visible range.
Compared with CQDs, NCQDs exhibited two characteristic peaks at around 238 nm and 340 nm respectively. The
representative absorption peak at 238 nm was due to the carbon core which belonged to p-p* electronic transitions of the
aromatic sp2 domains. The characteristic absorption peak at 340 nm was originated from the nep* electronic transition of C]O
and CeN bond, which was attributed to the formation of excited defect surface state caused by nitrogen-doping (N
heteroatoms) [32]. In other words, the nitrogen-doping made the surface groups of NCQDs more multitudinous. Under room
light, the transparent solutions of CQD and NCQD exhibited no fluorescence (inset left). Under UV excitation from 365 nm lamp,
the CQD solution showed low intense fluorescence, however, the NCQD solution exhibited the intense blue fluorescence (inset
right), that was possibly attributed to their small size effect and surface state effect.
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4.ARTICLE:
The morphology of as-synthesized materials was observed by SEM and TEM. As can be seen in Fig.1A, WO3 nanoplates
presented rectangular structure with average width of 150 nm; Au NPs were directly deposited on the surface of WO3
nanoplates, ensuring a good electrical contact and making full use of LSPR effect of Au NPs. After loading CdS, many
nanospheres aggregated on the surface of the WO3/Au composite (Fig. 1B), and the diameter of agglomerated CdS spheres
was around 30 nm (Fig. 1C). Fig. 1D showed the TEM image of WO3/Au NPs hybrid, WO3 was 2D nanoplate-like and Au NPs
located on the surface of WO3. The lattice spacing of 0.375 nm corresponded to the (020) plane of monoclinic-type WO3, while
the lattice spacing of 0.235 nm matched the (111) plane of Au NPs. The interface structures between WO3, Au and CdS were
depicted in Fig. 1E and F. CdS coated the surface of WO3 and Au NPs, and they formed WO3/CdS heterojunction and Au@CdS
core-shell nanostructure. The intimate contact effectively facilitated the spatial separation of charges during photoexcitation.
The lattice spacings of 0.336 and 0.316 nm were corresponding to the (111) and (101) planes of CdS, respectively.
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5.ARTICLE:
Thionine as a cross-linker to built a MWNTs and AuNPs multilayer has been shown in Scheme 1A. The formation of thionine
bridged MWNTs and AuNPs multilayer was confirmed and characterized by SEM image (the inset of Scheme 1A). The
sequential repetition of the deposition of MWNTs, thionine and AuNPs could produce a multilayer membrane with a porous
structure, which would be favorable for the approach of substrates to the enzyme molecules in internal layers. Further support
for the formation of (MWNTs/thionine/AuNPs)n multilayer can be provided by spectroscopy, electrochemistry (data not shown).
The absorption bandintensities at 267 and 512 nm increased gradually with increasing the number of MWNTs/thionine/AuNPs
layer, which could be attributed to the MWNTs and AuNPs, demonstrating that thionine had successfully cross-linked MWNTs
and Au NPs into multilayer. The peak currents of thionine in the multilayer and layer numbers exhibited good linear
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4.2COMPARISON OF THE ARTICLES
3.Article
the detection of the
substrate.
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4.Article
5.Article
NADH sensor can be tuned with visible
absorption of visible light. light.
Visible-light-
activated
This strategy is of
photoelectrochemic Qilin Huang, Silver nanoparticles (10–
Study of the great significance for
al biosensor for the Hua Chen, Lili 20 nm) TNs(30–50
acetylcholinesterase (AChE) , TNs pathogenesis of the development of
study Xu, Danqin https://drive.google.com/drive/folders/1mf8M9vwsM3wx7xQQlxDZh nm),TiO2 nanoparticles
1 410 nm AChE/Ag/N–F–TNs(TiO2) ,TiO2(387 neurodegenerative novel
of Lu,Linlin Tang , wJ-9wioMFp7?usp=sharing were quasi-spherical
biosensor nm) diseases such as photoelectrochemic
acetylcholinesterase Litong Jin,Zhiai with the size
Parkinson’s disease. al biosensors in the
inhibition induced by Xu, Wen Zhang range of 11.61e45.84 nm
future
endogenous
neurotoxins
The
photoelectrochemic
al biosensor showed
a good performance
with high
Wenjing Wang, upper detection
Visible light induced QDs show an
Lei Bao, limit, acceptable
photoelectrochemic Glucose,QDs-based absorption
Jianping https://drive.google.com/drive/folders/1mf8M9vwsM3wx7xQQlxDZh porphyrin-functionalized 0 to QDs peak 1543 Developed for stability and
2 al biosensing based 505 nm biosensor,CdS– shoulder
Lei,Wenwen wJ-9wioMFp7?usp=sharing ZnO 110Wm−2 at 650 nm cm−1 detection of glucose. accuracy, providing
on oxygen-sensitive polyamidoamine around
Tu,Huangxian an alternative
quantum dots 627nm
Ju method for
monitoring
biomolecules and
extending the
application of near-
infrared QDs
Under room
light, the
transparent
solutions of
CQD
and NCQD
PEC biosensor can
exhibited no
The visible light- also achieve the
fluorescence
driven and self- titanium dioxide CQDs, detection of
Wenjie Cheng (inset left).
powered (TiO2)=30-50 nm NCQDs elaborated visible chlorpyrifos in the
, Zengyao Under UV
photoelectrochemic nanoparticles were exhibited light-driven and lake water and
Zheng excitation
al biosensor for TİO2,CQDs,NCQDsPEC quasi-spherical with the two selfpowdered PEC Chinese cabbage
, Jianying Yang from 365 nm
organophosphate https://drive.google.com/drive/folders/1mf8M9vwsM3wx7xQQlxDZh biosensor size of 20 mW characteristi biosensor was samples, suggesting
3 , Min Chen 420 nm lamp, the
pesticides detection wJ-9wioMFp7?usp=sharing range of 11.61e45.84 cm2 c peaks at prepared for OPs that the fabricated
, Qingwei Yao CQD
based on nitrogen nm,Carbon quantum around 238 detection (for the PEC biosensor had
, solution
doped carbon dots nm and 340 biorecognition potential
Yaowen Chen showed low
quantum dots for (CQDs)=10nm,NCQDs nm molecule) application for the
, Wenhua Gao intense
the signal 1.47nm-3.95 nm respective detection of OPs in
fluorescence
amplification environment and
, however,
food.
the NCQD
solution
exhibited
the intense
blue
fluorescence
Absorption
edges of
WO3, CdS, The immunosensor
To the detection of
LED visible-light Au and NPs=20-nm- WO3/CdS, also showed good
CEA in serum
driven label-free sized,WO3 nanoplates WO3/Au, stability,
Bihong Zhang, samples,and can also
photoelectrochemic presented and reproducibility and
Hao Wang, https://drive.google.com/drive/folders/1mf8M9vwsM3wx7xQQlxDZh be applied in
4 al immunosensor 430 nm PEC biosensor rectangular structure WO3/Au/Cd 325 nm repeatability. It was
Faqiong Zhao, wJ-9wioMFp7?usp=sharing constructing
based on with average width of S were successfully applied
Baizhao Zeng highperformance
WO3/Au/CdS 150 nm,CdS spheres was about 460, to the detection of
PEC immunosensors
photocatalyst for the around 30 nm 540, 530, CEA in serum
for other targets.
sensitive detection 600 and 630 samples.
of carcinoembryonic nm,
antigen respectively.