Evidence map›Paper›PMID 29601593›Full record

ArticlePloS one2018

A sensitive and innovative detection method for rapid C-reactive proteins analysis based on a micro-fluxgate sensor system.

Lei Guo, Zhen Yang, Shaotao Zhi, Zhu Feng, Chong Lei, Yong Zhou

Abstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Lei GuoKey Laboratory for Thin Film and Microfahrication of Ministry of Education, Research Institute of Micro/Nano Science and Technology, Shanghai JiaoTong University, Shanghai, China.ORCID 0000-0002-3520-7525
Zhen YangSchool of Physics and Electronic Engineering, Xinyang Normal University, Xinyang, China.
Shaotao ZhiKey Laboratory for Thin Film and Microfahrication of Ministry of Education, Research Institute of Micro/Nano Science and Technology, Shanghai JiaoTong University, Shanghai, China.
Zhu FengKey Laboratory for Thin Film and Microfahrication of Ministry of Education, Research Institute of Micro/Nano Science and Technology, Shanghai JiaoTong University, Shanghai, China.
Chong LeiKey Laboratory for Thin Film and Microfahrication of Ministry of Education, Research Institute of Micro/Nano Science and Technology, Shanghai JiaoTong University, Shanghai, China.
Yong ZhouKey Laboratory for Thin Film and Microfahrication of Ministry of Education, Research Institute of Micro/Nano Science and Technology, Shanghai JiaoTong University, Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A sensitive and innovative assay system based on a micro-MEMS-fluxgate sensor and immunomagnetic beads-labels was developed for the rapid analysis of C-reactive proteins (CRP). The fluxgate sensor presented in this study was fabricated through standard micro-electro-mechanical system technology. A multi-loop magnetic core made of Fe-based amorphous ribbon was employed as the sensing element, and 3-D solenoid copper coils were used to control the sensing core. Antibody-conjugated immunomagnetic microbeads were strategically utilized as signal tags to label the CRP via the specific conjugation of CRP to polyclonal CRP antibodies. Separate Au film substrates were applied as immunoplatforms to immobilize CRP-beads labels through classical sandwich assays. Detection and quantification of the CRP at different concentrations were implemented by detecting the stray field of CRP labeled magnetic beads using the newly-developed micro-fluxgate sensor. The resulting system exhibited the required sensitivity, stability, reproducibility, and selectivity. A detection limit as low as 0.002 μg/mL CRP with a linearity range from 0.002 μg/mL to 10 μg/mL was achieved, and this suggested that the proposed biosystem possesses high sensitivity. In addition to the extremely low detection limit, the proposed method can be easily manipulated and possesses a quick response time. The response time of our sensor was less than 5 s, and the entire detection period for CRP analysis can be completed in less than 30 min using the current method. Given the detection performance and other advantages such as miniaturization, excellent stability and specificity, the proposed biosensor can be considered as a potential candidate for the rapid analysis of CRP, especially for point-of-care platforms.

Indexed as

Limit of DetectionMicro-Electrical-Mechanical SystemsAnimalsBiosensing TechniquesCattleC-Reactive ProteinMagnetsMicrospheresPoint-of-Care SystemsTime FactorsC-Reactive Protein

Identifiers

PMID29601593
PMCPMC5877836

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.