4.7 Article

Ultrasenstive SERS biosensor based on Zn2+from ZnO nanoparticle assisted DNA enzyme amplification for detection of miRNA

期刊

ANALYTICA CHIMICA ACTA
卷 1228, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.aca.2022.340340

关键词

DNA enzyme amplification; SERS biosensor; ZnO nanoparticle amplification strategy; miRNA

资金

  1. Xihua University [RZ2000001351]
  2. Science and Technology Program of Sichuan Province [2022JDTD0028]

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In this study, a simple and sensitive SERS biosensor was proposed for ultrasensitive detecting miRNA 122 based on ZnO nanoparticle amplification strategy and the full utilization of DNA chain. The biosensor showed a low detection limit and a wide linear range, indicating great potential in clinical application and medical diagnosis.
In this work, a simple and sensitive SERS biosensor was proposed for ultrasensitive detecting miRNA 122 based on ZnO nanoparticle amplification strategy and the full utilization of DNA chain. Firstly, ZnO@S1/S2 and CoFe2O4@S3 complexes can flock together with the assistance of target miRNA. Accompanied with the incremental amount of miRNA, the quantity of ZnO@S1/S2 would increase. Therefore, a significant amplification capability can be obtained by converting ZnO complexes into Zn2+ with the assistance of HCl. In this case, the DNA chain S2 can be obtained by the ZnO dissolving. In addition, through a clever design, the obtained Zn2+ can be further utilized to induce DNA enzyme cycle amplification to cleave S5 into DNA chain which was similar with DNA S2. This step greatly avoided the waste of DNA chains and improved the utilization efficiency of DNA chains. The S2 and abundant S2 analogues can complement with S4 on the Raman sensing interface to imbed lots of Raman probe DOX for obtaining strong Raman signal. By this way, with the increased number of miRNA, the S2 and abundant S2 analogues would increase, so the amount of DOX would increase to produce strong Raman signal to quantitatively detect target miRNA. As a result, this SERS biosensor based on Zn+ amplification and high utilization efficiency of DNA chain can obtain a low detection limit of 6.82 aM and wide linear range from 10 aM to 10 pM, which shown great potential in the clinical application and medical diagnosis.

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