Evidence map›Paper›PMID 34078895›Full record

ArticleNature communications2021

Geometrically encoded SERS nanobarcodes for the logical detection of nasopharyngeal carcinoma-related progression biomarkers.

Duo Lin, Chang-Lin Hsieh, Keng-Chia Hsu, Pei-Hsuan Liao, Sufang Qiu, Tianxun Gong, Ken-Tye Yong, Shangyuan Feng, Kien Voon Kong

Abstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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

14 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

9 authors.

Duo Lin *Key Laboratory of OptoElectronic Science and Technology for Medicine, Ministry of Education, Fujian Provincial Key Laboratory for Photonics Technology, Fujian Normal University, Fuzhou, Fujian, China.ORCID 0000-0001-6959-5995
Chang-Lin Hsieh *Department of Chemistry, National Taiwan University, Taipei, Taiwan.
Keng-Chia HsuDepartment of Chemistry, National Taiwan University, Taipei, Taiwan.
Pei-Hsuan LiaoDepartment of Chemistry, National Taiwan University, Taipei, Taiwan.
Sufang QiuFujian Medical University Cancer Hospital, Fujian Cancer Hospital, Fuzhou, Fujian, China.
Tianxun GongState Key Laboratory of Electronic Thin Films and Integrated Devices, School of Electronic Science and Engineering (National Exemplary School of Microelectronics), University of Electronic Science and Technology of China, Chengdu, China.ORCID 0000-0001-9383-3666
Ken-Tye YongSchool of Biomedical Engineering, The University of Sydney, Sydney, NSW, Australia.
Shangyuan FengKey Laboratory of OptoElectronic Science and Technology for Medicine, Ministry of Education, Fujian Provincial Key Laboratory for Photonics Technology, Fujian Normal University, Fuzhou, Fujian, China.
Kien Voon KongDepartment of Chemistry, National Taiwan University, Taipei, Taiwan. kvkong@ntu.edu.tw.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The limited availability of nasopharyngeal carcinoma-related progression biomarker array kits that offer physicians comprehensive information is disadvantageous for monitoring cancer progression. To develop a biomarker array kit, systematic identification and differentiation of a large number of distinct molecular surface-enhanced Raman scattering (SERS) reporters with high spectral temporal resolution is a major challenge. To address this unmet need, we use the chemistry of metal carbonyls to construct a series of unique SERS reporters with the potential to provide logical and highly multiplex information during testing. In this study, we report that geometric control over metal carbonyls on nanotags can produce 14 distinct barcodes that can be decoded unambiguously using commercial Raman spectroscopy. These metal carbonyl nanobarcodes are tested on human blood samples and show strong sensitivity (0.07 ng/mL limit of detection, average CV of 6.1% and >92% degree of recovery) and multiplexing capabilities for MMPs.

Indexed as

Spectrum Analysis, RamanBiomarkers, TumorBiosensing TechniquesDisease ProgressionMatrix MetalloproteinasesMetal NanoparticlesNanogelsNasopharyngeal CarcinomaNasopharyngeal NeoplasmsOrganometallic CompoundsSensitivity and SpecificitySurface PropertiesBiomarkers, TumorMatrix MetalloproteinasesNanogelsOrganometallic Compounds

Identifiers

PMID34078895
PMCPMC8173014

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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.